AU2008312631A1 - Thienopyrimidine and pyrazolopyrimidine compounds and their use as mTOR kinase and PI3 kinase inhibitors - Google Patents

Info

Publication number

AU2008312631A1

AU2008312631A1 AU2008312631A AU2008312631A AU2008312631A1 AU 2008312631 A1 AU2008312631 A1 AU 2008312631A1 AU 2008312631 A AU2008312631 A AU 2008312631A AU 2008312631 A AU2008312631 A AU 2008312631A AU 2008312631 A1 AU2008312631 A1 AU 2008312631A1

Authority

AU

Australia

Prior art keywords

phenyl

oxa

pyrimidin

azabicyclo

pyrazolo

Prior art date

2007-10-16

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Abandoned

Links

• Espacenet
• Global Dossier
• Discuss

• OGEBRHQLRGFBNV-RZDIXWSQSA-N chembl2036808 Chemical class C12=NC(NCCCC)=NC=C2C(C=2C=CC(F)=CC=2)=NN1C[C@H]1CC[C@H](N)CC1 OGEBRHQLRGFBNV-RZDIXWSQSA-N 0.000 title description 123
• RBNBDIMXFJYDLQ-UHFFFAOYSA-N thieno[3,2-d]pyrimidine Chemical compound C1=NC=C2SC=CC2=N1 RBNBDIMXFJYDLQ-UHFFFAOYSA-N 0.000 title description 30
• 239000003628 mammalian target of rapamycin inhibitor Substances 0.000 title description 12
• 239000002935 phosphatidylinositol 3 kinase inhibitor Substances 0.000 title 1
• -1 pyrazolopyrimidinyl group Chemical group 0.000 claims description 412
• 125000000217 alkyl group Chemical group 0.000 claims description 364
• 125000004943 pyrimidin-6-yl group Chemical group N1=CN=CC=C1* 0.000 claims description 324
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 319
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 238
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 237
• 125000001424 substituent group Chemical group 0.000 claims description 228
• 150000001875 compounds Chemical class 0.000 claims description 202
• 125000003118 aryl group Chemical group 0.000 claims description 138
• 125000001072 heteroaryl group Chemical group 0.000 claims description 131
• 125000005843 halogen group Chemical group 0.000 claims description 127
• 229910052736 halogen Inorganic materials 0.000 claims description 117
• 239000004202 carbamide Substances 0.000 claims description 114
• 150000002367 halogens Chemical class 0.000 claims description 114
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 113
• 229910052799 carbon Inorganic materials 0.000 claims description 102
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 95
• 150000003839 salts Chemical class 0.000 claims description 95
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 84
• 150000001721 carbon Chemical group 0.000 claims description 79
• 125000000623 heterocyclic group Chemical group 0.000 claims description 74
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 70
• SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 70
• 239000000203 mixture Substances 0.000 claims description 69
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 66
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 63
• 238000000034 method Methods 0.000 claims description 60
• 125000005530 alkylenedioxy group Chemical group 0.000 claims description 54
• 229910052739 hydrogen Inorganic materials 0.000 claims description 53
• 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 48
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 47
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 47
• 125000004432 carbon atom Chemical group C* 0.000 claims description 45
• 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 45
• 229910052757 nitrogen Inorganic materials 0.000 claims description 44
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 42
• 125000003545 alkoxy group Chemical group 0.000 claims description 42
• 125000005596 alkyl carboxamido group Chemical group 0.000 claims description 38
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 33
• 108010065917 TOR Serine-Threonine Kinases Proteins 0.000 claims description 33
• 102000013530 TOR Serine-Threonine Kinases Human genes 0.000 claims description 33
• DNUTZBZXLPWRJG-UHFFFAOYSA-M piperidine-1-carboxylate Chemical compound [O-]C(=O)N1CCCCC1 DNUTZBZXLPWRJG-UHFFFAOYSA-M 0.000 claims description 30
• 125000002911 monocyclic heterocycle group Chemical group 0.000 claims description 29
• 125000003710 aryl alkyl group Chemical group 0.000 claims description 28
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 25
• 206010028980 Neoplasm Diseases 0.000 claims description 24
• 125000004663 dialkyl amino group Chemical group 0.000 claims description 24
• 239000001257 hydrogen Substances 0.000 claims description 23
• 125000002619 bicyclic group Chemical group 0.000 claims description 21
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 21
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 20
• 125000005157 alkyl carboxy group Chemical group 0.000 claims description 19
• 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 18
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 18
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
• 208000035475 disorder Diseases 0.000 claims description 17
• 125000002950 monocyclic group Chemical group 0.000 claims description 17
• KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 16
• 125000003282 alkyl amino group Chemical group 0.000 claims description 16
• 229960005419 nitrogen Drugs 0.000 claims description 16
• 125000001188 haloalkyl group Chemical group 0.000 claims description 15
• 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims description 15
• 239000000470 constituent Substances 0.000 claims description 13
• 229940120638 avastin Drugs 0.000 claims description 12
• 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 11
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 11
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 11
• 125000002837 carbocyclic group Chemical group 0.000 claims description 11
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 11
• 125000001624 naphthyl group Chemical group 0.000 claims description 11
• 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims description 11
• 229910052717 sulfur Inorganic materials 0.000 claims description 11
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 10
• 201000011510 cancer Diseases 0.000 claims description 10
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
• 239000011593 sulfur Chemical group 0.000 claims description 10
• KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 9
• 150000001412 amines Chemical class 0.000 claims description 9
• 125000005842 heteroatom Chemical group 0.000 claims description 9
• 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 8
• AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 claims description 8
• 125000002252 acyl group Chemical group 0.000 claims description 8
• 230000002401 inhibitory effect Effects 0.000 claims description 8
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 8
• 229910052760 oxygen Inorganic materials 0.000 claims description 8
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
• 229960000397 bevacizumab Drugs 0.000 claims description 7
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 7
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 7
• 239000001301 oxygen Substances 0.000 claims description 7
• ULTTYPMRMMDONC-UHFFFAOYSA-N 5-[(2,5-dihydroxyphenyl)methyl-[(2-hydroxyphenyl)methyl]amino]-2-hydroxybenzoic acid Chemical compound C1=C(O)C(C(=O)O)=CC(N(CC=2C(=CC=CC=2)O)CC=2C(=CC=C(O)C=2)O)=C1 ULTTYPMRMMDONC-UHFFFAOYSA-N 0.000 claims description 6
• 201000001320 Atherosclerosis Diseases 0.000 claims description 6
• 102000014150 Interferons Human genes 0.000 claims description 6
• 108010050904 Interferons Proteins 0.000 claims description 6
• 208000008839 Kidney Neoplasms Diseases 0.000 claims description 6
• 241000124008 Mammalia Species 0.000 claims description 6
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 6
• 206010038389 Renal cancer Diseases 0.000 claims description 6
• 125000005529 alkyleneoxy group Chemical group 0.000 claims description 6
• 125000001769 aryl amino group Chemical group 0.000 claims description 6
• 239000003937 drug carrier Substances 0.000 claims description 6
• 229940079322 interferon Drugs 0.000 claims description 6
• 201000010982 kidney cancer Diseases 0.000 claims description 6
• 125000003386 piperidinyl group Chemical group 0.000 claims description 6
• BMIBJCFFZPYJHF-UHFFFAOYSA-N 2-methoxy-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine Chemical compound COC1=NC=C(C)C=C1B1OC(C)(C)C(C)(C)O1 BMIBJCFFZPYJHF-UHFFFAOYSA-N 0.000 claims description 5
• 150000002148 esters Chemical class 0.000 claims description 5
• 230000002194 synthesizing effect Effects 0.000 claims description 5
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
• FDKXTQMXEQVLRF-ZHACJKMWSA-N (E)-dacarbazine Chemical compound CN(C)\N=N\c1[nH]cnc1C(N)=O FDKXTQMXEQVLRF-ZHACJKMWSA-N 0.000 claims description 4
• QLHHRYZMBGPBJG-UHFFFAOYSA-N 1-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-pyrazolo[3,4-d]pyrimidinyl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCCO4)C2=N1 QLHHRYZMBGPBJG-UHFFFAOYSA-N 0.000 claims description 4
• WFXGXCPIPOZGHR-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethoxy]phenyl]-3-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(OCCN(C)C)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCF)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 WFXGXCPIPOZGHR-UHFFFAOYSA-N 0.000 claims description 4
• HMFRTKWUEKZJKW-UHFFFAOYSA-N 1-[4-[6-[(4-methylsulfonylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]-3-pyridin-4-ylurea Chemical compound C1CN(S(=O)(=O)C)CCN1CC1=CC2=NC(C=3C=CC(NC(=O)NC=4C=CN=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2S1 HMFRTKWUEKZJKW-UHFFFAOYSA-N 0.000 claims description 4
• WRCVEGVPVQBJJW-UHFFFAOYSA-N 1-methyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-oxocyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(=O)CC3)C2=N1 WRCVEGVPVQBJJW-UHFFFAOYSA-N 0.000 claims description 4
• DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 4
• 206010005003 Bladder cancer Diseases 0.000 claims description 4
• 208000003174 Brain Neoplasms Diseases 0.000 claims description 4
• 206010006187 Breast cancer Diseases 0.000 claims description 4
• 208000026310 Breast neoplasm Diseases 0.000 claims description 4
• DLGOEMSEDOSKAD-UHFFFAOYSA-N Carmustine Chemical compound ClCCNC(=O)N(N=O)CCCl DLGOEMSEDOSKAD-UHFFFAOYSA-N 0.000 claims description 4
• 206010009944 Colon cancer Diseases 0.000 claims description 4
• 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 4
• ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 claims description 4
• 206010033128 Ovarian cancer Diseases 0.000 claims description 4
• 206010061535 Ovarian neoplasm Diseases 0.000 claims description 4
• 229930012538 Paclitaxel Natural products 0.000 claims description 4
• 206010061902 Pancreatic neoplasm Diseases 0.000 claims description 4
• 206010060862 Prostate cancer Diseases 0.000 claims description 4
• 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 4
• 208000000453 Skin Neoplasms Diseases 0.000 claims description 4
• 208000005718 Stomach Neoplasms Diseases 0.000 claims description 4
• 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims description 4
• 208000002495 Uterine Neoplasms Diseases 0.000 claims description 4
• RJURFGZVJUQBHK-UHFFFAOYSA-N actinomycin D Natural products CC1OC(=O)C(C(C)C)N(C)C(=O)CN(C)C(=O)C2CCCN2C(=O)C(C(C)C)NC(=O)C1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)NC4C(=O)NC(C(N5CCCC5C(=O)N(C)CC(=O)N(C)C(C(C)C)C(=O)OC4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-UHFFFAOYSA-N 0.000 claims description 4
• VSRXQHXAPYXROS-UHFFFAOYSA-N azanide;cyclobutane-1,1-dicarboxylic acid;platinum(2+) Chemical compound [NH2-].[NH2-].[Pt+2].OC(=O)C1(C(O)=O)CCC1 VSRXQHXAPYXROS-UHFFFAOYSA-N 0.000 claims description 4
• ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims description 4
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
• 229960004562 carboplatin Drugs 0.000 claims description 4
• DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims description 4
• 229960004316 cisplatin Drugs 0.000 claims description 4
• 208000029742 colonic neoplasm Diseases 0.000 claims description 4
• 229960003901 dacarbazine Drugs 0.000 claims description 4
• 229960004679 doxorubicin Drugs 0.000 claims description 4
• 229960005420 etoposide Drugs 0.000 claims description 4
• VJJPUSNTGOMMGY-MRVIYFEKSA-N etoposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@H](C)OC[C@H]4O3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 VJJPUSNTGOMMGY-MRVIYFEKSA-N 0.000 claims description 4
• 206010017758 gastric cancer Diseases 0.000 claims description 4
• 208000032839 leukemia Diseases 0.000 claims description 4
• 201000005202 lung cancer Diseases 0.000 claims description 4
• 208000020816 lung neoplasm Diseases 0.000 claims description 4
• 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 4
• 229960001592 paclitaxel Drugs 0.000 claims description 4
• 208000008443 pancreatic carcinoma Diseases 0.000 claims description 4
• 201000000849 skin cancer Diseases 0.000 claims description 4
• 201000011549 stomach cancer Diseases 0.000 claims description 4
• RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 claims description 4
• 229940121358 tyrosine kinase inhibitor Drugs 0.000 claims description 4
• 201000005112 urinary bladder cancer Diseases 0.000 claims description 4
• 206010046766 uterine cancer Diseases 0.000 claims description 4
• SGRCPPFHVNOJSS-UHFFFAOYSA-N 1-[4-(4-methylpiperazin-1-yl)phenyl]-3-[4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3C4CCC3COC4)N=2)C=C1 SGRCPPFHVNOJSS-UHFFFAOYSA-N 0.000 claims description 3
• IZEKUGZAKDZVTI-UHFFFAOYSA-N 1-[4-(4-methylpiperazin-1-yl)phenyl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 IZEKUGZAKDZVTI-UHFFFAOYSA-N 0.000 claims description 3
• DBNVNMWEQKXYJD-UHFFFAOYSA-N 1-[4-(dimethylamino)phenyl]-3-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(N(C)C)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCF)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 DBNVNMWEQKXYJD-UHFFFAOYSA-N 0.000 claims description 3
• CCJBBQMLLPYZTR-UHFFFAOYSA-N 1-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(4-methylpiperazin-1-yl)phenyl]urea Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCF)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 CCJBBQMLLPYZTR-UHFFFAOYSA-N 0.000 claims description 3
• LDOKUGHHYHVRRK-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethoxy]phenyl]-3-[4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(OCCN(C)C)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3C4CCC3COC4)N=2)C=C1 LDOKUGHHYHVRRK-UHFFFAOYSA-N 0.000 claims description 3
• BRFGDDGSUBMDBH-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1h-pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound C=1C=C(C=2N=C3NN=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1=CC=CN=C1 BRFGDDGSUBMDBH-UHFFFAOYSA-N 0.000 claims description 3
• MDAFZGAXBHQRNG-UHFFFAOYSA-N 1-[4-[6-[(4-methylsulfonylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]-3-pyridin-3-ylurea Chemical compound C1CN(S(=O)(=O)C)CCN1CC1=CC2=NC(C=3C=CC(NC(=O)NC=4C=NC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2S1 MDAFZGAXBHQRNG-UHFFFAOYSA-N 0.000 claims description 3
• WVOQTENOLWJVRB-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CCF)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1CC1 WVOQTENOLWJVRB-UHFFFAOYSA-N 0.000 claims description 3
• KPSKKPDRNSLZRB-HOTGVXAUSA-N 1-cyclopropyl-3-[4-[4-[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C([C@]1(OC[C@]2([H])C1)[H])N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C(C=C1)=CC=C1NC(=O)NC1CC1 KPSKKPDRNSLZRB-HOTGVXAUSA-N 0.000 claims description 3
• YKHJGTINLIVMSH-UHFFFAOYSA-N 1-methyl-3-[4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2C3CCC2COC3)=C(C=NN2CC(F)(F)F)C2=N1 YKHJGTINLIVMSH-UHFFFAOYSA-N 0.000 claims description 3
• 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 3
• FZSZWXZCXGPTKY-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CC(F)(F)F)C2=N1 FZSZWXZCXGPTKY-UHFFFAOYSA-N 0.000 claims description 3
• QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 3
• 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 3
• 208000020084 Bone disease Diseases 0.000 claims description 3
• RIWKUMGHZXCSPC-BZKVGYQJSA-N C1C[C@@H](OC)CC[C@@H]1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 Chemical compound C1C[C@@H](OC)CC[C@@H]1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 RIWKUMGHZXCSPC-BZKVGYQJSA-N 0.000 claims description 3
• 206010012689 Diabetic retinopathy Diseases 0.000 claims description 3
• 108010072051 Glatiramer Acetate Proteins 0.000 claims description 3
• 206010061218 Inflammation Diseases 0.000 claims description 3
• 206010033645 Pancreatitis Diseases 0.000 claims description 3
• 208000004403 Prostatic Hyperplasia Diseases 0.000 claims description 3
• 201000004681 Psoriasis Diseases 0.000 claims description 3
• FHEAIOHRHQGZPC-KIWGSFCNSA-N acetic acid;(2s)-2-amino-3-(4-hydroxyphenyl)propanoic acid;(2s)-2-aminopentanedioic acid;(2s)-2-aminopropanoic acid;(2s)-2,6-diaminohexanoic acid Chemical compound CC(O)=O.C[C@H](N)C(O)=O.NCCCC[C@H](N)C(O)=O.OC(=O)[C@@H](N)CCC(O)=O.OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 FHEAIOHRHQGZPC-KIWGSFCNSA-N 0.000 claims description 3
• 230000033115 angiogenesis Effects 0.000 claims description 3
• 229940045719 antineoplastic alkylating agent nitrosoureas Drugs 0.000 claims description 3
• 206010003246 arthritis Diseases 0.000 claims description 3
• 229960003776 glatiramer acetate Drugs 0.000 claims description 3
• ZQDWXGKKHFNSQK-UHFFFAOYSA-N hydroxyzine Chemical compound C1CN(CCOCCO)CCN1C(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 ZQDWXGKKHFNSQK-UHFFFAOYSA-N 0.000 claims description 3
• 229960000930 hydroxyzine Drugs 0.000 claims description 3
• 208000026278 immune system disease Diseases 0.000 claims description 3
• 125000001041 indolyl group Chemical group 0.000 claims description 3
• 230000004054 inflammatory process Effects 0.000 claims description 3
• 208000017169 kidney disease Diseases 0.000 claims description 3
• KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 claims description 3
• 229960001156 mitoxantrone Drugs 0.000 claims description 3
• 229960005027 natalizumab Drugs 0.000 claims description 3
• 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
• 208000037803 restenosis Diseases 0.000 claims description 3
• VUCWMAJEUOWLEY-UHFFFAOYSA-N 1-$l^{1}-azanylpiperidine Chemical group [N]N1CCCCC1 VUCWMAJEUOWLEY-UHFFFAOYSA-N 0.000 claims description 2
• RWXHOFCUCAVRSM-UHFFFAOYSA-N 1-(2-fluoroethyl)-3-[4-[1-[1-(2-methylpropanoyl)piperidin-4-yl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C(=O)C(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCF)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 RWXHOFCUCAVRSM-UHFFFAOYSA-N 0.000 claims description 2
• VNRJYXRJFNRQRD-UHFFFAOYSA-N 1-(2-fluoroethyl)-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCF)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CC(F)(F)F)C2=N1 VNRJYXRJFNRQRD-UHFFFAOYSA-N 0.000 claims description 2
• RRNFUKFNHGBQEF-UHFFFAOYSA-N 1-(2-fluoroethyl)-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCF)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 RRNFUKFNHGBQEF-UHFFFAOYSA-N 0.000 claims description 2
• DNHBBMBOUVXRJF-UHFFFAOYSA-N 1-(2-hydroxyethyl)-3-[4-[1-[1-(2-methylpropanoyl)piperidin-4-yl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C(=O)C(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCO)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 DNHBBMBOUVXRJF-UHFFFAOYSA-N 0.000 claims description 2
• VTZPAZFULIFFPW-UHFFFAOYSA-N 1-(2-hydroxyethyl)-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 VTZPAZFULIFFPW-UHFFFAOYSA-N 0.000 claims description 2
• FGCPYNHZGVJJLS-UHFFFAOYSA-N 1-(4-morpholin-4-ylphenyl)-3-[4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC(F)(F)F)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCOCC1 FGCPYNHZGVJJLS-UHFFFAOYSA-N 0.000 claims description 2
• BYGOEBYVFYSDGF-UHFFFAOYSA-N 1-(4-morpholin-4-ylphenyl)-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC(F)(F)F)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCOCC1 BYGOEBYVFYSDGF-UHFFFAOYSA-N 0.000 claims description 2
• LERUIIPTVXHCLN-GOTSBHOMSA-N 1-(4-morpholin-4-ylphenyl)-3-[4-[4-[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C([C@]1(OC[C@]2([H])C1)[H])N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCOCC1 LERUIIPTVXHCLN-GOTSBHOMSA-N 0.000 claims description 2
• QKQRJVLKJZATTP-UHFFFAOYSA-N 1-(6-aminopyridin-3-yl)-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(N)N=C1 QKQRJVLKJZATTP-UHFFFAOYSA-N 0.000 claims description 2
• XAZGVAFGYQYKTL-UHFFFAOYSA-N 1-(6-morpholin-4-ylpyridin-3-yl)-3-[4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC(F)(F)F)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC(C=N1)=CC=C1N1CCOCC1 XAZGVAFGYQYKTL-UHFFFAOYSA-N 0.000 claims description 2
• MONILLGMGZKJNK-UHFFFAOYSA-N 1-(6-morpholin-4-ylpyridin-3-yl)-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC(F)(F)F)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=N1)=CC=C1N1CCOCC1 MONILLGMGZKJNK-UHFFFAOYSA-N 0.000 claims description 2
• RYWMQCNZWXNHIB-UHFFFAOYSA-N 1-(dimethylamino)-3-[4-[6-[(4-methylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NN(C)C)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC(CN2CCN(C)CC2)=C2)C2=N1 RYWMQCNZWXNHIB-UHFFFAOYSA-N 0.000 claims description 2
• ALUBESIHOJVCDK-UHFFFAOYSA-N 1-[2-(2-aminoethoxy)ethyl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NCCOCCN)C=C1 ALUBESIHOJVCDK-UHFFFAOYSA-N 0.000 claims description 2
• UCGFKGIOOUVIOP-UHFFFAOYSA-N 1-[2-(dimethylamino)ethyl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NCCN(C)C)C=C1 UCGFKGIOOUVIOP-UHFFFAOYSA-N 0.000 claims description 2
• OQALSGXMCNMPKF-UHFFFAOYSA-N 1-[2-(dimethylamino)ethyl]-3-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCN(C)C)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C)C2=N1 OQALSGXMCNMPKF-UHFFFAOYSA-N 0.000 claims description 2
• WOGPOVFUVILBEW-UHFFFAOYSA-N 1-[3-(dimethylamino)phenyl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound CN(C)C1=CC=CC(NC(=O)NC=2C=CC(=CC=2)C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)=C1 WOGPOVFUVILBEW-UHFFFAOYSA-N 0.000 claims description 2
• UMSDHBZXTINUSP-UHFFFAOYSA-N 1-[3-(dimethylamino)propyl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NCCCN(C)C)C=C1 UMSDHBZXTINUSP-UHFFFAOYSA-N 0.000 claims description 2
• ZTLYDMQLSAICDR-UHFFFAOYSA-N 1-[3-(dimethylamino)propyl]-3-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCCN(C)C)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C)C2=N1 ZTLYDMQLSAICDR-UHFFFAOYSA-N 0.000 claims description 2
• WAOKYKONZRCFJW-UHFFFAOYSA-N 1-[3-(hydroxymethyl)phenyl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound OCC1=CC=CC(NC(=O)NC=2C=CC(=CC=2)C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)=C1 WAOKYKONZRCFJW-UHFFFAOYSA-N 0.000 claims description 2
• UHVGWFGAZNCSFU-UHFFFAOYSA-N 1-[4-(2-hydroxyethoxy)phenyl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(OCCO)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 UHVGWFGAZNCSFU-UHFFFAOYSA-N 0.000 claims description 2
• SAXVGQAUJGTTDG-UHFFFAOYSA-N 1-[4-(2-hydroxyethyl)phenyl]-3-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CCO)C=C1 SAXVGQAUJGTTDG-UHFFFAOYSA-N 0.000 claims description 2
• CKICPWIYCQZPMV-UHFFFAOYSA-N 1-[4-(2-hydroxyethyl)phenyl]-3-[4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(CCO)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3C4CCC3COC4)N=2)C=C1 CKICPWIYCQZPMV-UHFFFAOYSA-N 0.000 claims description 2
• MURNNMKLHXSXQC-UHFFFAOYSA-N 1-[4-(2-hydroxyethyl)phenyl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(CCO)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 MURNNMKLHXSXQC-UHFFFAOYSA-N 0.000 claims description 2
• ZYENMTFOLXJCOD-SFTDATJTSA-N 1-[4-(2-hydroxyethyl)phenyl]-3-[4-[4-[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C([C@]1(OC[C@]2([H])C1)[H])N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CCO)C=C1 ZYENMTFOLXJCOD-SFTDATJTSA-N 0.000 claims description 2
• RBVTXOAIFJHNSX-UHFFFAOYSA-N 1-[4-(4-methylpiperazin-1-yl)phenyl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-oxocyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(C4CCC(=O)CC4)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 RBVTXOAIFJHNSX-UHFFFAOYSA-N 0.000 claims description 2
• JCDUVMKYALYSCA-UHFFFAOYSA-N 1-[4-(4-methylpiperazin-1-yl)phenyl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-propoxycyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CC(OCCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(=CC=4)N4CCN(C)CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 JCDUVMKYALYSCA-UHFFFAOYSA-N 0.000 claims description 2
• OGQRLNMAEQPGJF-UHFFFAOYSA-N 1-[4-(aminomethyl)phenyl]-3-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CN)C=C1 OGQRLNMAEQPGJF-UHFFFAOYSA-N 0.000 claims description 2
• QDQFNJOBXNDVPS-UHFFFAOYSA-N 1-[4-(dimethylamino)phenyl]-3-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(N(C)C)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(C)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 QDQFNJOBXNDVPS-UHFFFAOYSA-N 0.000 claims description 2
• QRPPJJFFSLQATD-UHFFFAOYSA-N 1-[4-(hydroxymethyl)phenyl]-3-[4-[1-(4-methoxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CC(OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(CO)=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 QRPPJJFFSLQATD-UHFFFAOYSA-N 0.000 claims description 2
• WXBFFWOJWOEYEC-UHFFFAOYSA-N 1-[4-(hydroxymethyl)phenyl]-3-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CO)C=C1 WXBFFWOJWOEYEC-UHFFFAOYSA-N 0.000 claims description 2
• BQEVGAXHNFPCTP-UHFFFAOYSA-N 1-[4-(hydroxymethyl)phenyl]-3-[4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(CO)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3C4CCC3COC4)N=2)C=C1 BQEVGAXHNFPCTP-UHFFFAOYSA-N 0.000 claims description 2
• UKWDHIDULSJIRO-UHFFFAOYSA-N 1-[4-(hydroxymethyl)phenyl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(CO)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 UKWDHIDULSJIRO-UHFFFAOYSA-N 0.000 claims description 2
• TZFINOAGXDAXAO-PMACEKPBSA-N 1-[4-(hydroxymethyl)phenyl]-3-[4-[4-[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C([C@]1(OC[C@]2([H])C1)[H])N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CO)C=C1 TZFINOAGXDAXAO-PMACEKPBSA-N 0.000 claims description 2
• MVWGPMLPVKVJOK-UHFFFAOYSA-N 1-[4-[(dimethylamino)methyl]phenyl]-3-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CN(C)C)C=C1 MVWGPMLPVKVJOK-UHFFFAOYSA-N 0.000 claims description 2
• XHNJXQFICQUYRG-UHFFFAOYSA-N 1-[4-[(dimethylamino)methyl]phenyl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CN(C)C)C=C1 XHNJXQFICQUYRG-UHFFFAOYSA-N 0.000 claims description 2
• GYOUBQRXSAHJQZ-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-morpholin-4-ylphenyl)urea Chemical compound C=1C=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC(C=C1)=CC=C1N1CCOCC1 GYOUBQRXSAHJQZ-UHFFFAOYSA-N 0.000 claims description 2
• VLWYJTAQQPZAJL-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(6-morpholin-4-ylpyridin-3-yl)urea Chemical compound C=1C=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC(C=N1)=CC=C1N1CCOCC1 VLWYJTAQQPZAJL-UHFFFAOYSA-N 0.000 claims description 2
• PYMQNCNMPKYHRR-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(2-hydroxyethyl)phenyl]urea Chemical compound C1=CC(CCO)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 PYMQNCNMPKYHRR-UHFFFAOYSA-N 0.000 claims description 2
• ZLEWXVNORLUUGZ-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(4-methylpiperazin-1-yl)phenyl]urea Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 ZLEWXVNORLUUGZ-UHFFFAOYSA-N 0.000 claims description 2
• XONAXDSGGBMHNG-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(hydroxymethyl)phenyl]urea Chemical compound C1=CC(CO)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 XONAXDSGGBMHNG-UHFFFAOYSA-N 0.000 claims description 2
• UMLKHSOFLLPNQK-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-[2-(dimethylamino)ethoxy]phenyl]urea Chemical compound C1=CC(OCCN(C)C)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 UMLKHSOFLLPNQK-UHFFFAOYSA-N 0.000 claims description 2
• NFFZXYXQSLXDSU-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]urea Chemical compound C1CN(C)CCN1C(N=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 NFFZXYXQSLXDSU-UHFFFAOYSA-N 0.000 claims description 2
• YXYABVGBCDZUIA-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-cyclopropylurea Chemical compound C=1C=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1CC1 YXYABVGBCDZUIA-UHFFFAOYSA-N 0.000 claims description 2
• HJLBILJRSZZKJL-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CCC#N)C2=N1 HJLBILJRSZZKJL-UHFFFAOYSA-N 0.000 claims description 2
• YFADXJFERUTOIB-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound C=1C=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1=CC=CN=C1 YFADXJFERUTOIB-UHFFFAOYSA-N 0.000 claims description 2
• RMJJDRYOMQIVJI-UHFFFAOYSA-N 1-[4-[1-(2-cyanoethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound C=1C=C(C=2N=C3N(CCC#N)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1=CC=NC=C1 RMJJDRYOMQIVJI-UHFFFAOYSA-N 0.000 claims description 2
• SDRFXWMDVIHAMJ-UHFFFAOYSA-N 1-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-morpholin-4-ylphenyl)urea Chemical compound N1=C2N(CCF)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCOCC1 SDRFXWMDVIHAMJ-UHFFFAOYSA-N 0.000 claims description 2
• LOKZPATYWMCLBT-UHFFFAOYSA-N 1-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(hydroxymethyl)phenyl]urea Chemical compound C1=CC(CO)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CCF)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 LOKZPATYWMCLBT-UHFFFAOYSA-N 0.000 claims description 2
• MXKMECPPQGOGLO-UHFFFAOYSA-N 1-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CCF)C2=N1 MXKMECPPQGOGLO-UHFFFAOYSA-N 0.000 claims description 2
• WPNZFLVLMWYSPE-UHFFFAOYSA-N 1-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound N1=C2N(CCF)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 WPNZFLVLMWYSPE-UHFFFAOYSA-N 0.000 claims description 2
• BBWGIVSPCZCRPJ-UHFFFAOYSA-N 1-[4-[1-(3,3-dimethyl-1,5-dioxaspiro[5.5]undecan-9-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCC(C)(C)CO4)C2=N1 BBWGIVSPCZCRPJ-UHFFFAOYSA-N 0.000 claims description 2
• DCBCEXPXWXJOKW-UHFFFAOYSA-N 1-[4-[1-[1-(3-acetylbenzoyl)piperidin-4-yl]-4-morpholin-4-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CCOCC2)=C(C=NN2C3CCN(CC3)C(=O)C=3C=C(C=CC=3)C(C)=O)C2=N1 DCBCEXPXWXJOKW-UHFFFAOYSA-N 0.000 claims description 2
• UPBUHFORXUZSRN-UHFFFAOYSA-N 1-[4-[1-benzyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-ethylurea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CC=3C=CC=CC=3)C2=N1 UPBUHFORXUZSRN-UHFFFAOYSA-N 0.000 claims description 2
• NCKXTAXYVPUKBK-UHFFFAOYSA-N 1-[4-[1-benzyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CC=3C=CC=CC=3)C2=N1 NCKXTAXYVPUKBK-UHFFFAOYSA-N 0.000 claims description 2
• NIHOWXYNRHYKFX-UHFFFAOYSA-N 1-[4-[1-benzyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound C=1C=C(C=2N=C3N(CC=4C=CC=CC=4)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1=CC=NC=C1 NIHOWXYNRHYKFX-UHFFFAOYSA-N 0.000 claims description 2
• ZKHQUVNCZZHVBY-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(2-pyrrolidin-1-ylethoxy)phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1OCCN1CCCC1 ZKHQUVNCZZHVBY-UHFFFAOYSA-N 0.000 claims description 2
• REAZWRUWNZTALY-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(4-methylpiperazin-1-yl)phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCN(C)CC1 REAZWRUWNZTALY-UHFFFAOYSA-N 0.000 claims description 2
• IYRBVBTWGPIKNS-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(pyrrolidin-1-ylmethyl)phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1CN1CCCC1 IYRBVBTWGPIKNS-UHFFFAOYSA-N 0.000 claims description 2
• UFTUVGIEUVBLOO-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-[(4-methylpiperazin-1-yl)methyl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1CN1CCN(C)CC1 UFTUVGIEUVBLOO-UHFFFAOYSA-N 0.000 claims description 2
• VZPAKKAWVXZJOO-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC(C=N1)=CC=C1N1CCN(C)CC1 VZPAKKAWVXZJOO-UHFFFAOYSA-N 0.000 claims description 2
• MKVPTYVBNXITMH-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C1=CC=C(NC(=O)NC)C=C1 MKVPTYVBNXITMH-UHFFFAOYSA-N 0.000 claims description 2
• ISKUMKPOLBEELU-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-phenylurea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CC=C1 ISKUMKPOLBEELU-UHFFFAOYSA-N 0.000 claims description 2
• XRIMHGBOUOLHBI-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CN=C1 XRIMHGBOUOLHBI-UHFFFAOYSA-N 0.000 claims description 2
• AWTBEQWBRRKGKB-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 AWTBEQWBRRKGKB-UHFFFAOYSA-N 0.000 claims description 2
• FVTTWLQASNZXBO-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-3-(pyrrolidin-1-ylmethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C12=C(N3CC4CCC(O4)C3)N=C(C=3C=CC(NC(=O)NC)=CC=3)N=C2N(CC)N=C1CN1CCCC1 FVTTWLQASNZXBO-UHFFFAOYSA-N 0.000 claims description 2
• FFSFJYJABLLMKY-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(1-methylpiperidin-4-yl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1CCN(C)CC1 FFSFJYJABLLMKY-UHFFFAOYSA-N 0.000 claims description 2
• PTVAHFLJYTVLPN-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(2-fluoroethyl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NCCF)C=C1 PTVAHFLJYTVLPN-UHFFFAOYSA-N 0.000 claims description 2
• SBGTVFMGDAHBNE-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(2-hydroxyethyl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NCCO)C=C1 SBGTVFMGDAHBNE-UHFFFAOYSA-N 0.000 claims description 2
• UBTJIBVOHICGEY-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(2-morpholin-4-ylethyl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NCCN1CCOCC1 UBTJIBVOHICGEY-UHFFFAOYSA-N 0.000 claims description 2
• MHEFFNLOVMOWPU-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-morpholin-4-ylphenyl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCOCC1 MHEFFNLOVMOWPU-UHFFFAOYSA-N 0.000 claims description 2
• WLTGGZJCDZMNBZ-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-pyrrolidin-1-ylphenyl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCCC1 WLTGGZJCDZMNBZ-UHFFFAOYSA-N 0.000 claims description 2
• WTXTUPLZVSNWLB-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[(1-methylpiperidin-4-yl)methyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NCC1CCN(C)CC1 WTXTUPLZVSNWLB-UHFFFAOYSA-N 0.000 claims description 2
• XGIZKKOTRRCGLQ-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NCC(=O)N1CCN(C)CC1 XGIZKKOTRRCGLQ-UHFFFAOYSA-N 0.000 claims description 2
• CXNZGMDFFGLRLY-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[2-(4-methylpiperazin-1-yl)ethyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NCCN1CCN(C)CC1 CXNZGMDFFGLRLY-UHFFFAOYSA-N 0.000 claims description 2
• KJAJGXINFQAKHZ-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[2-(methylamino)ethyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NCCNC)C=C1 KJAJGXINFQAKHZ-UHFFFAOYSA-N 0.000 claims description 2
• UTMQDJIIJVAEMU-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[3-(4-methylpiperazin-1-yl)-3-oxopropyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NCCC(=O)N1CCN(C)CC1 UTMQDJIIJVAEMU-UHFFFAOYSA-N 0.000 claims description 2
• NEMWIAVOKJWJCS-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[3-(methylamino)propyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NCCCNC)C=C1 NEMWIAVOKJWJCS-UHFFFAOYSA-N 0.000 claims description 2
• JQGIMHVWTOXCTP-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(2-hydroxyethoxy)phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(OCCO)C=C1 JQGIMHVWTOXCTP-UHFFFAOYSA-N 0.000 claims description 2
• JGCLMPLLEOAPAC-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(pyrrolidin-1-ylmethyl)phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1CN1CCCC1 JGCLMPLLEOAPAC-UHFFFAOYSA-N 0.000 claims description 2
• YDFWAAMONNHYQX-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[6-(2-hydroxyethoxy)pyridin-3-yl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(OCCO)N=C1 YDFWAAMONNHYQX-UHFFFAOYSA-N 0.000 claims description 2
• LSPYTXAQSKEIJE-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[6-(2-morpholin-4-ylethoxy)pyridin-3-yl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=N1)=CC=C1OCCN1CCOCC1 LSPYTXAQSKEIJE-UHFFFAOYSA-N 0.000 claims description 2
• DPFONBIFXAOZIL-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NC)C=C1 DPFONBIFXAOZIL-UHFFFAOYSA-N 0.000 claims description 2
• ADCADUHNSKXDGZ-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-phenylurea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CC=C1 ADCADUHNSKXDGZ-UHFFFAOYSA-N 0.000 claims description 2
• AUXKCHHCFDLRBV-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CN=C1 AUXKCHHCFDLRBV-UHFFFAOYSA-N 0.000 claims description 2
• OIUUQUNTDMZTRN-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 OIUUQUNTDMZTRN-UHFFFAOYSA-N 0.000 claims description 2
• UGUVKBXJXFNVFA-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-methylsulfonylphenyl)urea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(S(C)(=O)=O)C=C1 UGUVKBXJXFNVFA-UHFFFAOYSA-N 0.000 claims description 2
• HOYKWWOQTAMPCR-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-morpholin-4-ylphenyl)urea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCOCC1 HOYKWWOQTAMPCR-UHFFFAOYSA-N 0.000 claims description 2
• UFQYFACWJGZKBQ-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(6-morpholin-4-ylpyridin-3-yl)urea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=N1)=CC=C1N1CCOCC1 UFQYFACWJGZKBQ-UHFFFAOYSA-N 0.000 claims description 2
• IEWKJELUKQVDKG-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(2-piperidin-1-ylethylsulfonyl)phenyl]urea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1S(=O)(=O)CCN1CCCCC1 IEWKJELUKQVDKG-UHFFFAOYSA-N 0.000 claims description 2
• YQGJXFKRKDSFOO-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(4-methylpiperazin-1-yl)phenyl]urea Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(C)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 YQGJXFKRKDSFOO-UHFFFAOYSA-N 0.000 claims description 2
• POANRMCBZWELLZ-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]urea Chemical compound C1CN(C)CCN1C(N=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(C)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 POANRMCBZWELLZ-UHFFFAOYSA-N 0.000 claims description 2
• GIQRDHHCACLCDO-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-phenylurea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CC=C1 GIQRDHHCACLCDO-UHFFFAOYSA-N 0.000 claims description 2
• MAMRCWLIONFVJH-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CN=C1 MAMRCWLIONFVJH-UHFFFAOYSA-N 0.000 claims description 2
• GHDIKFLCCIGIID-UHFFFAOYSA-N 1-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 GHDIKFLCCIGIID-UHFFFAOYSA-N 0.000 claims description 2
• SUAHTQMBINZOHP-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethoxy]phenyl]-3-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(OCCN(C)C)C=C1 SUAHTQMBINZOHP-UHFFFAOYSA-N 0.000 claims description 2
• OCKKJHVJQPASQW-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethoxy]phenyl]-3-[4-[4-(3-oxa-7,9-diazabicyclo[3.3.1]nonan-9-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(OCCN(C)C)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3C4CNCC3COC4)N=2)C=C1 OCKKJHVJQPASQW-UHFFFAOYSA-N 0.000 claims description 2
• UNZFOPJEYOHDHE-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethyl-methylamino]phenyl]-3-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(N(C)CCN(C)C)C=C1 UNZFOPJEYOHDHE-UHFFFAOYSA-N 0.000 claims description 2
• KKONFQGHFMWUNZ-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethyl-methylamino]phenyl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(N(C)CCN(C)C)C=C1 KKONFQGHFMWUNZ-UHFFFAOYSA-N 0.000 claims description 2
• FZMJPJHMNXGZCE-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethylamino]phenyl]-3-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(NCCN(C)C)C=C1 FZMJPJHMNXGZCE-UHFFFAOYSA-N 0.000 claims description 2
• JEJCRWFEOZVUSQ-UHFFFAOYSA-N 1-[4-[3-ethenyl-1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound N1=C2N(CC)N=C(C=C)C2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NC)C=C1 JEJCRWFEOZVUSQ-UHFFFAOYSA-N 0.000 claims description 2
• IDJREHHFYLMPLX-UHFFFAOYSA-N 1-[4-[4-(3,7-dioxa-9-azabicyclo[3.3.1]nonan-9-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2C3COCC2COC3)=C(C=NN2CC(F)(F)F)C2=N1 IDJREHHFYLMPLX-UHFFFAOYSA-N 0.000 claims description 2
• LVOMIMOWTKHHCX-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-pyrrolidin-1-ylcyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound C=1C=CN=CC=1NC(=O)NC(C=C1)=CC=C1C(N=C12)=NC(N3CC4CCC(O4)C3)=C1C=NN2C(CC1)CCC1N1CCCC1 LVOMIMOWTKHHCX-UHFFFAOYSA-N 0.000 claims description 2
• IEUHFTUDDSBTPZ-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-piperidin-4-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-phenylurea Chemical compound C=1C=C(C=2N=C3N(C4CCNCC4)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1=CC=CC=C1 IEUHFTUDDSBTPZ-UHFFFAOYSA-N 0.000 claims description 2
• JXMJEHGYAODUJF-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-propan-2-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-phenylurea Chemical compound N1=C2N(C(C)C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CC=C1 JXMJEHGYAODUJF-UHFFFAOYSA-N 0.000 claims description 2
• VROHDVQPMGULKN-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]-3-phenylurea Chemical compound C=1C=C(C=2N=C3C=CSC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1=CC=CC=C1 VROHDVQPMGULKN-UHFFFAOYSA-N 0.000 claims description 2
• MUHQNYNRDBOJBC-UHFFFAOYSA-N 1-[4-[6-[(4-methylsulfonylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]-3-phenylurea Chemical compound C1CN(S(=O)(=O)C)CCN1CC1=CC2=NC(C=3C=CC(NC(=O)NC=4C=CC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2S1 MUHQNYNRDBOJBC-UHFFFAOYSA-N 0.000 claims description 2
• 102100025573 1-alkyl-2-acetylglycerophosphocholine esterase Human genes 0.000 claims description 2
• FIVUWKNIZDVMKE-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-(4-ethoxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CC(OCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 FIVUWKNIZDVMKE-UHFFFAOYSA-N 0.000 claims description 2
• ZTNUCBXTEODPOV-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-[1-(2-methylpropanoyl)piperidin-4-yl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C(=O)C(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 ZTNUCBXTEODPOV-UHFFFAOYSA-N 0.000 claims description 2
• XCQIYNDFAUQWDO-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1CC1 XCQIYNDFAUQWDO-UHFFFAOYSA-N 0.000 claims description 2
• IDZYCKDHMUMZKA-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC(F)(F)F)N=CC2=C(N2C3CCC2COC3)N=C1C(C=C1)=CC=C1NC(=O)NC1CC1 IDZYCKDHMUMZKA-UHFFFAOYSA-N 0.000 claims description 2
• QXXPDHWWQICWNI-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC(F)(F)F)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1CC1 QXXPDHWWQICWNI-UHFFFAOYSA-N 0.000 claims description 2
• DFLDYTVHZHLCAT-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-oxocyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C=1C=C(C=2N=C3N(C4CCC(=O)CC4)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1CC1 DFLDYTVHZHLCAT-UHFFFAOYSA-N 0.000 claims description 2
• WJZXICWAUVFQMS-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-propoxycyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CC(OCCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 WJZXICWAUVFQMS-UHFFFAOYSA-N 0.000 claims description 2
• AQBXSLRCNIYGJZ-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(CC(F)(F)F)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 AQBXSLRCNIYGJZ-UHFFFAOYSA-N 0.000 claims description 2
• HBZPGFLLAMADHT-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C=1C=C(C=2N=C3C=CSC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1CC1 HBZPGFLLAMADHT-UHFFFAOYSA-N 0.000 claims description 2
• ASHVJCPRWLMYPH-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[6-[(4-methylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1CN(C)CCN1CC1=CC2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2S1 ASHVJCPRWLMYPH-UHFFFAOYSA-N 0.000 claims description 2
• NLNIZBXJXWGGBP-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[6-[(4-methylsulfonylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1CN(S(=O)(=O)C)CCN1CC1=CC2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2S1 NLNIZBXJXWGGBP-UHFFFAOYSA-N 0.000 claims description 2
• FDLVQFRXPKVPPN-UHFFFAOYSA-N 1-ethyl-3-[4-[1-(4-methoxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(CC3)OC)C2=N1 FDLVQFRXPKVPPN-UHFFFAOYSA-N 0.000 claims description 2
• CUNNEAHMWONEIJ-UHFFFAOYSA-N 1-ethyl-3-[4-[1-[1-(2-methylpropanoyl)piperidin-4-yl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)C(C)C)C2=N1 CUNNEAHMWONEIJ-UHFFFAOYSA-N 0.000 claims description 2
• FZZHKLCKAGUQLD-UHFFFAOYSA-N 1-ethyl-3-[4-[1-ethyl-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2C3CCC2COC3)=C(C=NN2CC)C2=N1 FZZHKLCKAGUQLD-UHFFFAOYSA-N 0.000 claims description 2
• KQLINRHJAKDXAU-UHFFFAOYSA-N 1-ethyl-3-[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C)C2=N1 KQLINRHJAKDXAU-UHFFFAOYSA-N 0.000 claims description 2
• XQXVCGDWWAHZSJ-UHFFFAOYSA-N 1-ethyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 XQXVCGDWWAHZSJ-UHFFFAOYSA-N 0.000 claims description 2
• NVKWDJVYEJIVAC-UHFFFAOYSA-N 1-ethyl-3-[4-[6-[(4-methylsulfonylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC(CN2CCN(CC2)S(C)(=O)=O)=C2)C2=N1 NVKWDJVYEJIVAC-UHFFFAOYSA-N 0.000 claims description 2
• IWBFIWBQNCLJEG-UHFFFAOYSA-N 1-methyl-3-[4-[1-[1-(2-methylpyridine-3-carbonyl)piperidin-4-yl]-4-morpholin-4-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CCOCC2)=C(C=NN2C3CCN(CC3)C(=O)C=3C(=NC=CC=3)C)C2=N1 IWBFIWBQNCLJEG-UHFFFAOYSA-N 0.000 claims description 2
• QFUOOPGLNQIHSJ-UHFFFAOYSA-N 1-methyl-3-[4-[1-[1-(4-methylpyridine-3-carbonyl)piperidin-4-yl]-4-morpholin-4-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CCOCC2)=C(C=NN2C3CCN(CC3)C(=O)C=3C(=CC=NC=3)C)C2=N1 QFUOOPGLNQIHSJ-UHFFFAOYSA-N 0.000 claims description 2
• XCELLIQJDGNQAC-UHFFFAOYSA-N 1-methyl-3-[4-[4-(2-oxa-5-azabicyclo[2.2.2]octan-5-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2C3CCC(OC3)C2)=C(C=NN2CC(F)(F)F)C2=N1 XCELLIQJDGNQAC-UHFFFAOYSA-N 0.000 claims description 2
• LYTWPZIIWFVNTB-UHFFFAOYSA-N 1-methyl-3-[4-[4-(3-oxa-9-azabicyclo[3.3.1]nonan-9-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2C3CCCC2COC3)=C(C=NN2CC(F)(F)F)C2=N1 LYTWPZIIWFVNTB-UHFFFAOYSA-N 0.000 claims description 2
• LHKWYVSHKLEEJS-UHFFFAOYSA-N 1-methyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CC(F)(F)F)C2=N1 LHKWYVSHKLEEJS-UHFFFAOYSA-N 0.000 claims description 2
• QUMQCWMSCSDDMX-UHFFFAOYSA-N 1-methyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-pyrrolidin-1-ylcyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(CC3)N3CCCC3)C2=N1 QUMQCWMSCSDDMX-UHFFFAOYSA-N 0.000 claims description 2
• DLOCQUMLEMAOPE-UHFFFAOYSA-N 1-methyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC(F)(F)F)CC3)C2=N1 DLOCQUMLEMAOPE-UHFFFAOYSA-N 0.000 claims description 2
• WOZYVVSCKUPLTE-UHFFFAOYSA-N 1-methyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(pyridin-3-ylmethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC=4C=NC=CC=4)CC3)C2=N1 WOZYVVSCKUPLTE-UHFFFAOYSA-N 0.000 claims description 2
• QAQUVBOSSUCOMU-UHFFFAOYSA-N 1-methyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-propan-2-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C(C)C)C2=N1 QAQUVBOSSUCOMU-UHFFFAOYSA-N 0.000 claims description 2
• ITYGQBOCBCGBAV-UHFFFAOYSA-N 1-methyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 ITYGQBOCBCGBAV-UHFFFAOYSA-N 0.000 claims description 2
• QYBNTJVELFYLOM-UHFFFAOYSA-N 1-methyl-3-[4-[6-[(4-methylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC(CN2CCN(C)CC2)=C2)C2=N1 QYBNTJVELFYLOM-UHFFFAOYSA-N 0.000 claims description 2
• XUYPPKAYBHIWJO-UHFFFAOYSA-N 1-methyl-3-[4-[6-[(4-methylsulfonylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC(CN2CCN(CC2)S(C)(=O)=O)=C2)C2=N1 XUYPPKAYBHIWJO-UHFFFAOYSA-N 0.000 claims description 2
• RPABADYMEMUBEC-UHFFFAOYSA-N 1-oxaspiro[4.5]decan-8-one Chemical compound C1CC(=O)CCC11OCCC1 RPABADYMEMUBEC-UHFFFAOYSA-N 0.000 claims description 2
• VSNHCAURESNICA-NJFSPNSNSA-N 1-oxidanylurea Chemical compound N[14C](=O)NO VSNHCAURESNICA-NJFSPNSNSA-N 0.000 claims description 2
• 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 2
• SSRSJJMKLQVXAL-UHFFFAOYSA-N 2-hydroxyethyl N-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound OCCOC(NC1=CC=C(C=C1)C1=NC(=C2C(=N1)N(N=C2)C1CCC2(OCCO2)CC1)N1CC2CCC(C1)O2)=O SSRSJJMKLQVXAL-UHFFFAOYSA-N 0.000 claims description 2
• DLAORXOIJUEBDN-GJZGRUSLSA-N 2-hydroxyethyl N-[4-[4-[(1S,4S)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound [C@@H]12OC[C@@H](N(C1)C1=C3C(=NC(=N1)C1=CC=C(C=C1)NC(OCCO)=O)N(N=C3)CC(F)(F)F)C2 DLAORXOIJUEBDN-GJZGRUSLSA-N 0.000 claims description 2
• ZYFPWCMHPFHLMP-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[4-(2-oxa-5-azabicyclo[2.2.2]octan-5-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2C3CCC(OC3)C2)=C(C=NN2CC(F)(F)F)C2=N1 ZYFPWCMHPFHLMP-UHFFFAOYSA-N 0.000 claims description 2
• TZDRFMIJSUPKFI-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[4-(3,7-dioxa-9-azabicyclo[3.3.1]nonan-9-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2C3COCC2COC3)=C(C=NN2CC(F)(F)F)C2=N1 TZDRFMIJSUPKFI-UHFFFAOYSA-N 0.000 claims description 2
• VYXYJPINWJYXFT-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[4-(3-oxa-7,9-diazabicyclo[3.3.1]nonan-9-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2C3CNCC2COC3)=C(C=NN2CC(F)(F)F)C2=N1 VYXYJPINWJYXFT-UHFFFAOYSA-N 0.000 claims description 2
• BTWPJYMNOQYWJN-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[4-(3-oxa-9-azabicyclo[3.3.1]nonan-9-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2C3CCCC2COC3)=C(C=NN2CC(F)(F)F)C2=N1 BTWPJYMNOQYWJN-UHFFFAOYSA-N 0.000 claims description 2
• NOEWLHJDVOJKDS-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC(F)(F)F)CC3)C2=N1 NOEWLHJDVOJKDS-UHFFFAOYSA-N 0.000 claims description 2
• FYVMMORNSWLXJS-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(pyridin-3-ylmethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC=4C=NC=CC=4)CC3)C2=N1 FYVMMORNSWLXJS-UHFFFAOYSA-N 0.000 claims description 2
• FYRWDDLFFQNOKF-ARWYELJZSA-N 2-hydroxyethyl n-[4-[4-[(6r)-6-hydroxy-8-oxa-3-azabicyclo[3.2.1]octan-3-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2CC3[C@H](O)CC(O3)C2)=C(C=NN2CC(F)(F)F)C2=N1 FYRWDDLFFQNOKF-ARWYELJZSA-N 0.000 claims description 2
• JMQPGBQRHYWIGC-UHFFFAOYSA-N 3-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenol Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=CC(O)=C1 JMQPGBQRHYWIGC-UHFFFAOYSA-N 0.000 claims description 2
• GVUAZTSFHDKFPH-UHFFFAOYSA-N 3-[1-ethyl-6-(1h-indol-5-yl)pyrazolo[3,4-d]pyrimidin-4-yl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C1C(O2)CCC2CN1C1=C2C=NN(CC)C2=NC(C=2C=C3C=CNC3=CC=2)=N1 GVUAZTSFHDKFPH-UHFFFAOYSA-N 0.000 claims description 2
• CMNWKFRKWPPELQ-UHFFFAOYSA-N 3-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenol Chemical compound N1=C2N(C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=CC(O)=C1 CMNWKFRKWPPELQ-UHFFFAOYSA-N 0.000 claims description 2
• XGYOLCHTMBWRGA-UHFFFAOYSA-N 3-[2-(1h-indol-5-yl)thieno[3,2-d]pyrimidin-4-yl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C1=C2NC=CC2=CC(C=2N=C(C=3SC=CC=3N=2)N2CC3CCC(C2)O3)=C1 XGYOLCHTMBWRGA-UHFFFAOYSA-N 0.000 claims description 2
• XHIBKBRCVQLOJC-UHFFFAOYSA-N 3-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-phenylpyrazolo[3,4-d]pyrimidin-6-yl]phenol Chemical compound OC1=CC=CC(C=2N=C3N(C=4C=CC=CC=4)N=CC3=C(N3CC4CCC(O4)C3)N=2)=C1 XHIBKBRCVQLOJC-UHFFFAOYSA-N 0.000 claims description 2
• DCQVJAZICZPUFT-UHFFFAOYSA-N 3-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenol Chemical compound OC1=CC=CC(C=2N=C3C=CSC3=C(N3CC4CCC(O4)C3)N=2)=C1 DCQVJAZICZPUFT-UHFFFAOYSA-N 0.000 claims description 2
• JWHDDZUUGOBHNV-UHFFFAOYSA-N 3-[6-(1h-indol-5-yl)-1-[1-(pyridin-3-ylmethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-4-yl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C1CC(N2C3=NC(=NC(=C3C=N2)N2CC3CCC(O3)C2)C=2C=C3C=CNC3=CC=2)CCN1CC1=CC=CN=C1 JWHDDZUUGOBHNV-UHFFFAOYSA-N 0.000 claims description 2
• AOJJSUZBOXZQNB-VTZDEGQISA-N 4'-epidoxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-VTZDEGQISA-N 0.000 claims description 2
• UDLFOGHOIIYABT-UHFFFAOYSA-N 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]aniline Chemical compound C1=CC(N)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 UDLFOGHOIIYABT-UHFFFAOYSA-N 0.000 claims description 2
• IRLOZVLSUVCEIJ-UHFFFAOYSA-N 4-[[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]amino]phenol Chemical compound C1=CC(O)=CC=C1NC1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 IRLOZVLSUVCEIJ-UHFFFAOYSA-N 0.000 claims description 2
• YTNADJDHKAORBK-UHFFFAOYSA-N 5-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]pyridin-2-amine Chemical compound C1=NC(N)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 YTNADJDHKAORBK-UHFFFAOYSA-N 0.000 claims description 2
• RQUSSQSOEJOAEP-UHFFFAOYSA-N 5-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]pyrimidin-2-amine Chemical compound C1=NC(N)=NC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 RQUSSQSOEJOAEP-UHFFFAOYSA-N 0.000 claims description 2
• WYWHKKSPHMUBEB-UHFFFAOYSA-N 6-Mercaptoguanine Natural products N1C(N)=NC(=S)C2=C1N=CN2 WYWHKKSPHMUBEB-UHFFFAOYSA-N 0.000 claims description 2
• VVIAGPKUTFNRDU-UHFFFAOYSA-N 6S-folinic acid Natural products C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-UHFFFAOYSA-N 0.000 claims description 2
• STQGQHZAVUOBTE-UHFFFAOYSA-N 7-Cyan-hept-2t-en-4,6-diinsaeure Natural products C1=2C(O)=C3C(=O)C=4C(OC)=CC=CC=4C(=O)C3=C(O)C=2CC(O)(C(C)=O)CC1OC1CC(N)C(O)C(C)O1 STQGQHZAVUOBTE-UHFFFAOYSA-N 0.000 claims description 2
• 108010024976 Asparaginase Proteins 0.000 claims description 2
• 108010006654 Bleomycin Proteins 0.000 claims description 2
• QRFAFGCAVNGXKY-IJDVVPKISA-N C1C[C@@H](O)CC[C@@H]1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 Chemical compound C1C[C@@H](O)CC[C@@H]1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 QRFAFGCAVNGXKY-IJDVVPKISA-N 0.000 claims description 2
• RIWKUMGHZXCSPC-OIRDZHBESA-N C1C[C@@H](OC)CC[C@H]1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 Chemical compound C1C[C@@H](OC)CC[C@H]1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 RIWKUMGHZXCSPC-OIRDZHBESA-N 0.000 claims description 2
• GAGWJHPBXLXJQN-UORFTKCHSA-N Capecitabine Chemical compound C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1[C@H]1[C@H](O)[C@H](O)[C@@H](C)O1 GAGWJHPBXLXJQN-UORFTKCHSA-N 0.000 claims description 2
• GAGWJHPBXLXJQN-UHFFFAOYSA-N Capecitabine Natural products C1=C(F)C(NC(=O)OCCCCC)=NC(=O)N1C1C(O)C(O)C(C)O1 GAGWJHPBXLXJQN-UHFFFAOYSA-N 0.000 claims description 2
• CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims description 2
• UHDGCWIWMRVCDJ-CCXZUQQUSA-N Cytarabine Chemical compound O=C1N=C(N)C=CN1[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O1 UHDGCWIWMRVCDJ-CCXZUQQUSA-N 0.000 claims description 2
• 229940123780 DNA topoisomerase I inhibitor Drugs 0.000 claims description 2
• 108010092160 Dactinomycin Proteins 0.000 claims description 2
• HTIJFSOGRVMCQR-UHFFFAOYSA-N Epirubicin Natural products COc1cccc2C(=O)c3c(O)c4CC(O)(CC(OC5CC(N)C(=O)C(C)O5)c4c(O)c3C(=O)c12)C(=O)CO HTIJFSOGRVMCQR-UHFFFAOYSA-N 0.000 claims description 2
• GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 claims description 2
• MCAHMSDENAOJFZ-UHFFFAOYSA-N Herbimycin A Natural products N1C(=O)C(C)=CC=CC(OC)C(OC(N)=O)C(C)=CC(C)C(OC)C(OC)CC(C)C(OC)C2=CC(=O)C=C1C2=O MCAHMSDENAOJFZ-UHFFFAOYSA-N 0.000 claims description 2
• XDXDZDZNSLXDNA-TZNDIEGXSA-N Idarubicin Chemical compound C1[C@H](N)[C@H](O)[C@H](C)O[C@H]1O[C@@H]1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2C[C@@](O)(C(C)=O)C1 XDXDZDZNSLXDNA-TZNDIEGXSA-N 0.000 claims description 2
• XDXDZDZNSLXDNA-UHFFFAOYSA-N Idarubicin Natural products C1C(N)C(O)C(C)OC1OC1C2=C(O)C(C(=O)C3=CC=CC=C3C3=O)=C3C(O)=C2CC(O)(C(C)=O)C1 XDXDZDZNSLXDNA-UHFFFAOYSA-N 0.000 claims description 2
• FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 claims description 2
• HLFSDGLLUJUHTE-SNVBAGLBSA-N Levamisole Chemical compound C1([C@H]2CN3CCSC3=N2)=CC=CC=C1 HLFSDGLLUJUHTE-SNVBAGLBSA-N 0.000 claims description 2
• GQYIWUVLTXOXAJ-UHFFFAOYSA-N Lomustine Chemical compound ClCCN(N=O)C(=O)NC1CCCCC1 GQYIWUVLTXOXAJ-UHFFFAOYSA-N 0.000 claims description 2
• 229930192392 Mitomycin Natural products 0.000 claims description 2
• NWIBSHFKIJFRCO-WUDYKRTCSA-N Mytomycin Chemical compound C1N2C(C(C(C)=C(N)C3=O)=O)=C3[C@@H](COC(N)=O)[C@@]2(OC)[C@@H]2[C@H]1N2 NWIBSHFKIJFRCO-WUDYKRTCSA-N 0.000 claims description 2
• FAUNBOBDFJICCL-XVJQKTIWSA-N N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)N[C@@H]1CC[C@H](N)CC1 Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)N[C@@H]1CC[C@H](N)CC1 FAUNBOBDFJICCL-XVJQKTIWSA-N 0.000 claims description 2
• 239000000365 Topoisomerase I Inhibitor Substances 0.000 claims description 2
• JXLYSJRDGCGARV-WWYNWVTFSA-N Vinblastine Natural products O=C(O[C@H]1[C@](O)(C(=O)OC)[C@@H]2N(C)c3c(cc(c(OC)c3)[C@]3(C(=O)OC)c4[nH]c5c(c4CCN4C[C@](O)(CC)C[C@H](C3)C4)cccc5)[C@@]32[C@H]2[C@@]1(CC)C=CCN2CC3)C JXLYSJRDGCGARV-WWYNWVTFSA-N 0.000 claims description 2
• OUOHHCCUVWTREN-UHFFFAOYSA-N [3-(dimethylamino)phenyl] n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound CN(C)C1=CC=CC(OC(=O)NC=2C=CC(=CC=2)C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)=C1 OUOHHCCUVWTREN-UHFFFAOYSA-N 0.000 claims description 2
• RJURFGZVJUQBHK-IIXSONLDSA-N actinomycin D Chemical compound C[C@H]1OC(=O)[C@H](C(C)C)N(C)C(=O)CN(C)C(=O)[C@@H]2CCCN2C(=O)[C@@H](C(C)C)NC(=O)[C@H]1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)N[C@@H]4C(=O)N[C@@H](C(N5CCC[C@H]5C(=O)N(C)CC(=O)N(C)[C@@H](C(C)C)C(=O)O[C@@H]4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-IIXSONLDSA-N 0.000 claims description 2
• 229960000473 altretamine Drugs 0.000 claims description 2
• 125000005001 aminoaryl group Chemical group 0.000 claims description 2
• 125000004429 atom Chemical group 0.000 claims description 2
• 229960001561 bleomycin Drugs 0.000 claims description 2
• OYVAGSVQBOHSSS-UAPAGMARSA-O bleomycin A2 Chemical compound N([C@H](C(=O)N[C@H](C)[C@@H](O)[C@H](C)C(=O)N[C@@H]([C@H](O)C)C(=O)NCCC=1SC=C(N=1)C=1SC=C(N=1)C(=O)NCCC[S+](C)C)[C@@H](O[C@H]1[C@H]([C@@H](O)[C@H](O)[C@H](CO)O1)O[C@@H]1[C@H]([C@@H](OC(N)=O)[C@H](O)[C@@H](CO)O1)O)C=1N=CNC=1)C(=O)C1=NC([C@H](CC(N)=O)NC[C@H](N)C(N)=O)=NC(N)=C1C OYVAGSVQBOHSSS-UAPAGMARSA-O 0.000 claims description 2
• 229960004117 capecitabine Drugs 0.000 claims description 2
• 229960005243 carmustine Drugs 0.000 claims description 2
• QVNZNYAMDUBKRR-UHFFFAOYSA-N chembl595288 Chemical compound C1=CC(O)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 QVNZNYAMDUBKRR-UHFFFAOYSA-N 0.000 claims description 2
• 229960004397 cyclophosphamide Drugs 0.000 claims description 2
• 229960000684 cytarabine Drugs 0.000 claims description 2
• 229960000640 dactinomycin Drugs 0.000 claims description 2
• STQGQHZAVUOBTE-VGBVRHCVSA-N daunorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(C)=O)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 STQGQHZAVUOBTE-VGBVRHCVSA-N 0.000 claims description 2
• 229960000975 daunorubicin Drugs 0.000 claims description 2
• 229960003668 docetaxel Drugs 0.000 claims description 2
• 229960001904 epirubicin Drugs 0.000 claims description 2
• SIHZWGODIRRSRA-ONEGZZNKSA-N erbstatin Chemical compound OC1=CC=C(O)C(\C=C\NC=O)=C1 SIHZWGODIRRSRA-ONEGZZNKSA-N 0.000 claims description 2
• FRPJXPJMRWBBIH-RBRWEJTLSA-N estramustine Chemical compound ClCCN(CCCl)C(=O)OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 FRPJXPJMRWBBIH-RBRWEJTLSA-N 0.000 claims description 2
• 229960001842 estramustine Drugs 0.000 claims description 2
• HTKIKBBDXDCWIQ-UHFFFAOYSA-N ethyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(1h-pyrazol-5-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4NN=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 HTKIKBBDXDCWIQ-UHFFFAOYSA-N 0.000 claims description 2
• YAJHBFQMEJCMRC-UHFFFAOYSA-N ethyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(phenylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 YAJHBFQMEJCMRC-UHFFFAOYSA-N 0.000 claims description 2
• UCOYKQWWADNOMC-UHFFFAOYSA-N ethyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(piperidin-4-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CCNCC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 UCOYKQWWADNOMC-UHFFFAOYSA-N 0.000 claims description 2
• XYMNBNRKXWAQHM-UHFFFAOYSA-N ethyl 4-[6-[4-(2-fluoroethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCF)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 XYMNBNRKXWAQHM-UHFFFAOYSA-N 0.000 claims description 2
• NDQQSMRHYSAWQW-UHFFFAOYSA-N ethyl 4-[6-[4-[3-(methylamino)propylcarbamoylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCCNC)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 NDQQSMRHYSAWQW-UHFFFAOYSA-N 0.000 claims description 2
• RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims description 2
• 229960002949 fluorouracil Drugs 0.000 claims description 2
• VVIAGPKUTFNRDU-ABLWVSNPSA-N folinic acid Chemical compound C1NC=2NC(N)=NC(=O)C=2N(C=O)C1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 VVIAGPKUTFNRDU-ABLWVSNPSA-N 0.000 claims description 2
• 235000008191 folinic acid Nutrition 0.000 claims description 2
• 239000011672 folinic acid Substances 0.000 claims description 2
• SDUQYLNIPVEERB-QPPQHZFASA-N gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 claims description 2
• 229960005277 gemcitabine Drugs 0.000 claims description 2
• 229940045109 genistein Drugs 0.000 claims description 2
• TZBJGXHYKVUXJN-UHFFFAOYSA-N genistein Natural products C1=CC(O)=CC=C1C1=COC2=CC(O)=CC(O)=C2C1=O TZBJGXHYKVUXJN-UHFFFAOYSA-N 0.000 claims description 2
• 235000006539 genistein Nutrition 0.000 claims description 2
• ZCOLJUOHXJRHDI-CMWLGVBASA-N genistein 7-O-beta-D-glucoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=C2C(=O)C(C=3C=CC(O)=CC=3)=COC2=C1 ZCOLJUOHXJRHDI-CMWLGVBASA-N 0.000 claims description 2
• BEBCJVAWIBVWNZ-UHFFFAOYSA-N glycinamide Chemical compound NCC(N)=O BEBCJVAWIBVWNZ-UHFFFAOYSA-N 0.000 claims description 2
• MCAHMSDENAOJFZ-BVXDHVRPSA-N herbimycin Chemical compound N1C(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@@H](OC)[C@@H](OC)C[C@H](C)[C@@H](OC)C2=CC(=O)C=C1C2=O MCAHMSDENAOJFZ-BVXDHVRPSA-N 0.000 claims description 2
• UUVWYPNAQBNQJQ-UHFFFAOYSA-N hexamethylmelamine Chemical compound CN(C)C1=NC(N(C)C)=NC(N(C)C)=N1 UUVWYPNAQBNQJQ-UHFFFAOYSA-N 0.000 claims description 2
• 150000002431 hydrogen Chemical class 0.000 claims description 2
• 229960000908 idarubicin Drugs 0.000 claims description 2
• HOMGKSMUEGBAAB-UHFFFAOYSA-N ifosfamide Chemical compound ClCCNP1(=O)OCCCN1CCCl HOMGKSMUEGBAAB-UHFFFAOYSA-N 0.000 claims description 2
• 229960001101 ifosfamide Drugs 0.000 claims description 2
• 229960003685 imatinib mesylate Drugs 0.000 claims description 2
• YLMAHDNUQAMNNX-UHFFFAOYSA-N imatinib methanesulfonate Chemical compound CS(O)(=O)=O.C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 YLMAHDNUQAMNNX-UHFFFAOYSA-N 0.000 claims description 2
• UWKQSNNFCGGAFS-XIFFEERXSA-N irinotecan Chemical compound C1=C2C(CC)=C3CN(C(C4=C([C@@](C(=O)OC4)(O)CC)C=4)=O)C=4C3=NC2=CC=C1OC(=O)N(CC1)CCC1N1CCCCC1 UWKQSNNFCGGAFS-XIFFEERXSA-N 0.000 claims description 2
• 229960004768 irinotecan Drugs 0.000 claims description 2
• 229960001691 leucovorin Drugs 0.000 claims description 2
• 229960001614 levamisole Drugs 0.000 claims description 2
• 229960002247 lomustine Drugs 0.000 claims description 2
• GLVAUDGFNGKCSF-UHFFFAOYSA-N mercaptopurine Chemical compound S=C1NC=NC2=C1NC=N2 GLVAUDGFNGKCSF-UHFFFAOYSA-N 0.000 claims description 2
• 229960001428 mercaptopurine Drugs 0.000 claims description 2
• 229960000485 methotrexate Drugs 0.000 claims description 2
• 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
• 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
• ZLTZVXHHZMAUET-UHFFFAOYSA-N methyl 4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-[4-(phenylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC=CC=4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 ZLTZVXHHZMAUET-UHFFFAOYSA-N 0.000 claims description 2
• YCSUYVMGFIAGHE-UHFFFAOYSA-N methyl 4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-[4-(pyridin-3-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=NC=CC=4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 YCSUYVMGFIAGHE-UHFFFAOYSA-N 0.000 claims description 2
• ONLFLKPDLQRBJU-UHFFFAOYSA-N methyl 4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-[4-(pyridin-4-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CN=CC=4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 ONLFLKPDLQRBJU-UHFFFAOYSA-N 0.000 claims description 2
• XDDGEBPZEULJTI-UHFFFAOYSA-N methyl 4-[4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-6-[4-[(4-piperazin-1-ylphenyl)carbamoylamino]phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(=CC=4)N4CCNCC4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 XDDGEBPZEULJTI-UHFFFAOYSA-N 0.000 claims description 2
• BGAJRBIZGPXHGM-UHFFFAOYSA-N methyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(2-pyrrolidin-1-ylethoxycarbonylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)OCCN4CCCC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 BGAJRBIZGPXHGM-UHFFFAOYSA-N 0.000 claims description 2
• SOJUZOLCVDOSFG-UHFFFAOYSA-N methyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(phenylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 SOJUZOLCVDOSFG-UHFFFAOYSA-N 0.000 claims description 2
• ATPLVZHZSJDMFY-UHFFFAOYSA-N methyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(pyridin-3-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=NC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 ATPLVZHZSJDMFY-UHFFFAOYSA-N 0.000 claims description 2
• JCRXZPWPABMNMW-UHFFFAOYSA-N methyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(pyridin-4-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CN=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 JCRXZPWPABMNMW-UHFFFAOYSA-N 0.000 claims description 2
• LWWQQEOPPRLEFS-UHFFFAOYSA-N methyl 4-[6-[4-(2-aminoethoxycarbonylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)OCCN)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 LWWQQEOPPRLEFS-UHFFFAOYSA-N 0.000 claims description 2
• VQOAMYUHUCBWFS-UHFFFAOYSA-N methyl 4-[6-[4-(2-fluoroethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCF)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 VQOAMYUHUCBWFS-UHFFFAOYSA-N 0.000 claims description 2
• HLEAOICRACUZDD-UHFFFAOYSA-N methyl 4-[6-[4-(2-morpholin-4-ylethoxycarbonylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)OCCN4CCOCC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 HLEAOICRACUZDD-UHFFFAOYSA-N 0.000 claims description 2
• RJVKBOCLBAWFEI-UHFFFAOYSA-N methyl 4-[6-[4-(cyclopropylcarbamoylamino)phenyl]-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 RJVKBOCLBAWFEI-UHFFFAOYSA-N 0.000 claims description 2
• OUSDGHINODPQOK-UHFFFAOYSA-N methyl 4-[6-[4-(cyclopropylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 OUSDGHINODPQOK-UHFFFAOYSA-N 0.000 claims description 2
• BQTUXBMTUNHMOS-UHFFFAOYSA-N methyl 4-[6-[4-(ethylcarbamoylamino)phenyl]-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2C3CCC2COC3)=C(C=NN2C3CCN(CC3)C(=O)OC)C2=N1 BQTUXBMTUNHMOS-UHFFFAOYSA-N 0.000 claims description 2
• JHNAQAVZQKWQRE-UHFFFAOYSA-N methyl 4-[6-[4-(ethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OC)C2=N1 JHNAQAVZQKWQRE-UHFFFAOYSA-N 0.000 claims description 2
• DHEXCUIEBAVGJU-UHFFFAOYSA-N methyl 4-[6-[4-(methoxycarbonylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)OC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OC)C2=N1 DHEXCUIEBAVGJU-UHFFFAOYSA-N 0.000 claims description 2
• PMAPHSJLODNDBF-UHFFFAOYSA-N methyl 4-[6-[4-(methylcarbamoylamino)phenyl]-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2C3CCC2COC3)=C(C=NN2C3CCN(CC3)C(=O)OC)C2=N1 PMAPHSJLODNDBF-UHFFFAOYSA-N 0.000 claims description 2
• JORHBQYMPMJLJA-UHFFFAOYSA-N methyl 4-[6-[4-(methylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OC)C2=N1 JORHBQYMPMJLJA-UHFFFAOYSA-N 0.000 claims description 2
• IMPICVCTUFPJTI-UHFFFAOYSA-N methyl 4-[6-[4-[2-(4-methylpiperazin-1-yl)ethoxycarbonylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)OCCN4CCN(C)CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 IMPICVCTUFPJTI-UHFFFAOYSA-N 0.000 claims description 2
• KUASFPYMWBHZSZ-UHFFFAOYSA-N methyl 4-[6-[4-[2-(4-methylpiperazin-1-yl)ethylcarbamoylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCN4CCN(C)CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 KUASFPYMWBHZSZ-UHFFFAOYSA-N 0.000 claims description 2
• FKNILBMCHFSHHH-UHFFFAOYSA-N methyl 4-[6-[4-[[3-(hydroxymethyl)phenyl]carbamoylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=C(CO)C=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 FKNILBMCHFSHHH-UHFFFAOYSA-N 0.000 claims description 2
• WEOJREKAZINAJS-UHFFFAOYSA-N methyl 4-[6-[4-[[4-(2-hydroxyethyl)phenyl]carbamoylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(CCO)=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 WEOJREKAZINAJS-UHFFFAOYSA-N 0.000 claims description 2
• AXZSIXBWDZGMJU-UHFFFAOYSA-N methyl 4-[6-[4-[[4-(4-methylpiperazin-1-yl)phenyl]carbamoylamino]phenyl]-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(=CC=4)N4CCN(C)CC4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 AXZSIXBWDZGMJU-UHFFFAOYSA-N 0.000 claims description 2
• RVIJIHVNPDEZMT-UHFFFAOYSA-N methyl 4-[6-[4-[[4-(4-methylpiperazin-1-yl)phenyl]carbamoylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(=CC=4)N4CCN(C)CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 RVIJIHVNPDEZMT-UHFFFAOYSA-N 0.000 claims description 2
• JBLDDEVRKCGASR-UHFFFAOYSA-N methyl 4-[6-[4-[[4-[(4-methylpiperazin-1-yl)methyl]phenyl]carbamoylamino]phenyl]-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(CN5CCN(C)CC5)=CC=4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 JBLDDEVRKCGASR-UHFFFAOYSA-N 0.000 claims description 2
• KUAVRCJQPQCFJA-UHFFFAOYSA-N methyl 4-[6-[4-[[4-[(dimethylamino)methyl]phenyl]carbamoylamino]phenyl]-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(CN(C)C)=CC=4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 KUAVRCJQPQCFJA-UHFFFAOYSA-N 0.000 claims description 2
• CFCUWKMKBJTWLW-BKHRDMLASA-N mithramycin Chemical compound O([C@@H]1C[C@@H](O[C@H](C)[C@H]1O)OC=1C=C2C=C3C[C@H]([C@@H](C(=O)C3=C(O)C2=C(O)C=1C)O[C@@H]1O[C@H](C)[C@@H](O)[C@H](O[C@@H]2O[C@H](C)[C@H](O)[C@H](O[C@@H]3O[C@H](C)[C@@H](O)[C@@](C)(O)C3)C2)C1)[C@H](OC)C(=O)[C@@H](O)[C@@H](C)O)[C@H]1C[C@@H](O)[C@H](O)[C@@H](C)O1 CFCUWKMKBJTWLW-BKHRDMLASA-N 0.000 claims description 2
• 229960004857 mitomycin Drugs 0.000 claims description 2
• MMVNGBAMDGGFQY-UHFFFAOYSA-N n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]acetamide Chemical compound C1=CC(NC(=O)C)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(SC=C2)C2=N1 MMVNGBAMDGGFQY-UHFFFAOYSA-N 0.000 claims description 2
• LEFZXBFLARQTIC-UHFFFAOYSA-N n-[4-[[4-[1-methyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamoylamino]phenyl]acetamide Chemical compound C1=CC(NC(=O)C)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(C)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 LEFZXBFLARQTIC-UHFFFAOYSA-N 0.000 claims description 2
• 239000006186 oral dosage form Substances 0.000 claims description 2
• DWAFYCQODLXJNR-BNTLRKBRSA-L oxaliplatin Chemical compound O1C(=O)C(=O)O[Pt]11N[C@@H]2CCCC[C@H]2N1 DWAFYCQODLXJNR-BNTLRKBRSA-L 0.000 claims description 2
• 229960001756 oxaliplatin Drugs 0.000 claims description 2
• 229960003171 plicamycin Drugs 0.000 claims description 2
• CPTBDICYNRMXFX-UHFFFAOYSA-N procarbazine Chemical compound CNNCC1=CC=C(C(=O)NC(C)C)C=C1 CPTBDICYNRMXFX-UHFFFAOYSA-N 0.000 claims description 2
• 229960000624 procarbazine Drugs 0.000 claims description 2
• YGVBZDNRJZCFEJ-UHFFFAOYSA-N propan-2-yl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(pyridin-3-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=NC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 YGVBZDNRJZCFEJ-UHFFFAOYSA-N 0.000 claims description 2
• CYMDKPVILORHBA-UHFFFAOYSA-N propan-2-yl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(pyridin-4-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CN=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 CYMDKPVILORHBA-UHFFFAOYSA-N 0.000 claims description 2
• DOXVKYODDWHSHW-UHFFFAOYSA-N propan-2-yl 4-[6-[4-(2-fluoroethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCF)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 DOXVKYODDWHSHW-UHFFFAOYSA-N 0.000 claims description 2
• QHNDLILSMLASIP-UHFFFAOYSA-N propan-2-yl 4-[6-[4-(2-hydroxyethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCO)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 QHNDLILSMLASIP-UHFFFAOYSA-N 0.000 claims description 2
• OPHGZLAGIVIGAR-UHFFFAOYSA-N propan-2-yl 4-[6-[4-(cyclopropylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 OPHGZLAGIVIGAR-UHFFFAOYSA-N 0.000 claims description 2
• 125000004076 pyridyl group Chemical group 0.000 claims description 2
• 229940063683 taxotere Drugs 0.000 claims description 2
• NRUKOCRGYNPUPR-QBPJDGROSA-N teniposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@@H](OC[C@H]4O3)C=3SC=CC=3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 NRUKOCRGYNPUPR-QBPJDGROSA-N 0.000 claims description 2
• 229960001278 teniposide Drugs 0.000 claims description 2
• YEAJWKDUTFGREI-UHFFFAOYSA-N tert-butyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(pyridin-3-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=NC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 YEAJWKDUTFGREI-UHFFFAOYSA-N 0.000 claims description 2
• XNNQUUOPAJPUIM-UHFFFAOYSA-N tert-butyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(pyridin-4-ylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CN=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 XNNQUUOPAJPUIM-UHFFFAOYSA-N 0.000 claims description 2
• CEPZLSYRIXXARR-UHFFFAOYSA-N tert-butyl 4-[6-[4-(methylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OC(C)(C)C)C2=N1 CEPZLSYRIXXARR-UHFFFAOYSA-N 0.000 claims description 2
• PFZPGGIJNWGLEN-UHFFFAOYSA-N tert-butyl 4-[[4-[1-(1-ethoxycarbonylpiperidin-4-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamoylamino]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CCN(CC4)C(=O)OC(C)(C)C)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 PFZPGGIJNWGLEN-UHFFFAOYSA-N 0.000 claims description 2
• QXDYWHWVGFMFNY-UHFFFAOYSA-N tert-butyl 7-[6-[4-(pyridin-4-ylcarbamoylamino)phenyl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-4-yl]-9-oxa-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate Chemical compound C1C(O2)CN(C(=O)OC(C)(C)C)CC2CN1C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 QXDYWHWVGFMFNY-UHFFFAOYSA-N 0.000 claims description 2
• XCNFVVCWUVWYEG-UHFFFAOYSA-N tert-butyl 9-[6-[4-(2-hydroxyethoxycarbonylamino)phenyl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-4-yl]-3-oxa-7,9-diazabicyclo[3.3.1]nonane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CC2COCC1N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C1=CC=C(NC(=O)OCCO)C=C1 XCNFVVCWUVWYEG-UHFFFAOYSA-N 0.000 claims description 2
• UBCOHNDNSCGERK-UHFFFAOYSA-N tert-butyl 9-[6-[4-(methylcarbamoylamino)phenyl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-4-yl]-3-oxa-7,9-diazabicyclo[3.3.1]nonane-7-carboxylate Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2C3COCC2CN(C3)C(=O)OC(C)(C)C)=C(C=NN2CC(F)(F)F)C2=N1 UBCOHNDNSCGERK-UHFFFAOYSA-N 0.000 claims description 2
• CKCPUOWKNWAVAW-UHFFFAOYSA-N tert-butyl 9-[6-[4-[[4-[2-(dimethylamino)ethoxy]phenyl]carbamoylamino]phenyl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-4-yl]-3-oxa-7,9-diazabicyclo[3.3.1]nonane-7-carboxylate Chemical compound C1=CC(OCCN(C)C)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3C4COCC3CN(C4)C(=O)OC(C)(C)C)N=2)C=C1 CKCPUOWKNWAVAW-UHFFFAOYSA-N 0.000 claims description 2
• MNRILEROXIRVNJ-UHFFFAOYSA-N tioguanine Chemical compound N1C(N)=NC(=S)C2=NC=N[C]21 MNRILEROXIRVNJ-UHFFFAOYSA-N 0.000 claims description 2
• 229960003087 tioguanine Drugs 0.000 claims description 2
• UCFGDBYHRUNTLO-QHCPKHFHSA-N topotecan Chemical compound C1=C(O)C(CN(C)C)=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 UCFGDBYHRUNTLO-QHCPKHFHSA-N 0.000 claims description 2
• 229960000303 topotecan Drugs 0.000 claims description 2
• 239000005483 tyrosine kinase inhibitor Substances 0.000 claims description 2
• 229960003048 vinblastine Drugs 0.000 claims description 2
• JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-N 0.000 claims description 2
• OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 claims description 2
• 229960004528 vincristine Drugs 0.000 claims description 2
• OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 claims description 2
• GBABOYUKABKIAF-GHYRFKGUSA-N vinorelbine Chemical compound C1N(CC=2C3=CC=CC=C3NC=22)CC(CC)=C[C@H]1C[C@]2(C(=O)OC)C1=CC([C@]23[C@H]([C@]([C@H](OC(C)=O)[C@]4(CC)C=CCN([C@H]34)CC2)(O)C(=O)OC)N2C)=C2C=C1OC GBABOYUKABKIAF-GHYRFKGUSA-N 0.000 claims description 2
• 229960002066 vinorelbine Drugs 0.000 claims description 2
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 7
• ZFCBTTPZBOLLNM-UHFFFAOYSA-N 1-(2-fluoroethyl)-3-[4-[1-[4-(4-methylpiperazin-1-yl)cyclohexyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C)CCN1C1CCC(N2C3=NC(=NC(=C3C=N2)N2CC3CCC(O3)C2)C=2C=CC(NC(=O)NCCF)=CC=2)CC1 ZFCBTTPZBOLLNM-UHFFFAOYSA-N 0.000 claims 1
• XBLBSXOUHOVQPA-UHFFFAOYSA-N 1-(2-hydroxyethyl)-3-[4-[1-(2-hydroxyethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CCO)C2=N1 XBLBSXOUHOVQPA-UHFFFAOYSA-N 0.000 claims 1
• NRFWZNMEBOVDDF-DNQXCXABSA-N 1-[4-(4-methylpiperazin-1-yl)phenyl]-3-[4-[4-[(1r,4r)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C([C@@]1(OC[C@@]2([H])C1)[H])N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCN(C)CC1 NRFWZNMEBOVDDF-DNQXCXABSA-N 0.000 claims 1
• NRFWZNMEBOVDDF-ZEQRLZLVSA-N 1-[4-(4-methylpiperazin-1-yl)phenyl]-3-[4-[4-[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C([C@]1(OC[C@]2([H])C1)[H])N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCN(C)CC1 NRFWZNMEBOVDDF-ZEQRLZLVSA-N 0.000 claims 1
• UDAWZLGMHSEQAG-UHFFFAOYSA-N 1-[4-(dimethylaminocarbamoyl)phenyl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C(=O)NN(C)C)C=C1 UDAWZLGMHSEQAG-UHFFFAOYSA-N 0.000 claims 1
• HXNLDHXVQFPKQT-UHFFFAOYSA-N 1-[4-[1-(1,3-dimethoxypropan-2-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-piperazin-1-ylphenyl)urea Chemical compound N1=C2N(C(COC)COC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCNCC1 HXNLDHXVQFPKQT-UHFFFAOYSA-N 0.000 claims 1
• IJQBGHXJLLTXPZ-UHFFFAOYSA-N 1-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(4-methylpiperazin-1-yl)phenyl]urea Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(C4CCC5(CC4)OCCO5)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 IJQBGHXJLLTXPZ-UHFFFAOYSA-N 0.000 claims 1
• QEZCXGHWXXLBFJ-UHFFFAOYSA-N 1-[4-[1-(1,5-dioxaspiro[5.5]undecan-9-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCCCO4)C2=N1 QEZCXGHWXXLBFJ-UHFFFAOYSA-N 0.000 claims 1
• RZERWDKPRCXFKM-UHFFFAOYSA-N 1-[4-[1-(4,4-dimethoxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(CC3)(OC)OC)C2=N1 RZERWDKPRCXFKM-UHFFFAOYSA-N 0.000 claims 1
• GTWCTQSVXFCJEK-UHFFFAOYSA-N 1-[4-[1-[4-(2-hydroxyethylamino)cyclohexyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(CC3)NCCO)C2=N1 GTWCTQSVXFCJEK-UHFFFAOYSA-N 0.000 claims 1
• WYTADYJFVUAVOT-UHFFFAOYSA-N 1-[4-[1-[4-(4-methylpiperazin-1-yl)cyclohexyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound C1CN(C)CCN1C1CCC(N2C3=NC(=NC(=C3C=N2)N2CC3CCC(O3)C2)C=2C=CC(NC(=O)NC=3C=NC=CC=3)=CC=2)CC1 WYTADYJFVUAVOT-UHFFFAOYSA-N 0.000 claims 1
• JQEACQXIVNPOGS-UHFFFAOYSA-N 1-[4-[1-ethyl-3-(4-methylpiperazin-1-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C12=C(N3CC4CCC(O4)C3)N=C(C=3C=CC(NC(=O)NC)=CC=3)N=C2N(CC)N=C1N1CCN(C)CC1 JQEACQXIVNPOGS-UHFFFAOYSA-N 0.000 claims 1
• RCHWHILZANOZHZ-UHFFFAOYSA-N 1-[4-[1-ethyl-3-[(4-methylpiperazin-1-yl)methyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C12=C(N3CC4CCC(O4)C3)N=C(C=3C=CC(NC(=O)NC)=CC=3)N=C2N(CC)N=C1CN1CCN(C)CC1 RCHWHILZANOZHZ-UHFFFAOYSA-N 0.000 claims 1
• DDPCJPFCPSGJOG-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-methoxyphenyl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(OC)C=C1 DDPCJPFCPSGJOG-UHFFFAOYSA-N 0.000 claims 1
• YFUIEEMMAVGYTI-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-methylphenyl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C)C=C1 YFUIEEMMAVGYTI-UHFFFAOYSA-N 0.000 claims 1
• OIZVMINJTWHORX-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(4-piperazin-1-ylphenyl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCNCC1 OIZVMINJTWHORX-UHFFFAOYSA-N 0.000 claims 1
• RCWCYHYCUNPFSO-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-(6-morpholin-4-ylpyridin-3-yl)urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=N1)=CC=C1N1CCOCC1 RCWCYHYCUNPFSO-UHFFFAOYSA-N 0.000 claims 1
• ATLHTKSZGMIXLX-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(2-hydroxyethyl)phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CCO)C=C1 ATLHTKSZGMIXLX-UHFFFAOYSA-N 0.000 claims 1
• KYUFDBIYWRJMMF-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-(4-methylpiperazin-1-yl)phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1N1CCN(C)CC1 KYUFDBIYWRJMMF-UHFFFAOYSA-N 0.000 claims 1
• FTRSKAKWKUDZKU-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[4-[(4-methylpiperazin-1-yl)methyl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1CN1CCN(C)CC1 FTRSKAKWKUDZKU-UHFFFAOYSA-N 0.000 claims 1
• VKSCSFHLPAAEGS-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=N1)=CC=C1N1CCN(C)CC1 VKSCSFHLPAAEGS-UHFFFAOYSA-N 0.000 claims 1
• ARKRGLDVMPXTLI-UHFFFAOYSA-N 1-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-[6-(methylamino)pyridin-3-yl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(NC)N=C1 ARKRGLDVMPXTLI-UHFFFAOYSA-N 0.000 claims 1
• GWQJCRNIPKKUFO-UHFFFAOYSA-N 1-[4-[3-bromo-1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound N1=C2N(CC)N=C(Br)C2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NC)C=C1 GWQJCRNIPKKUFO-UHFFFAOYSA-N 0.000 claims 1
• XFXAJYFCPLMACD-UHFFFAOYSA-N 1-[4-[4-(3-acetyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound C1C(O2)CN(C(=O)C)CC2CN1C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 XFXAJYFCPLMACD-UHFFFAOYSA-N 0.000 claims 1
• DJPJTACLFRPTPA-UHFFFAOYSA-N 1-[4-[4-(7-formyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound N1=C2N(CC(F)(F)F)N=CC2=C(N2CC3CN(CC(O3)C2)C=O)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 DJPJTACLFRPTPA-UHFFFAOYSA-N 0.000 claims 1
• QGMKUMYDPUQICJ-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-propan-2-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound N1=C2N(C(C)C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CN=C1 QGMKUMYDPUQICJ-UHFFFAOYSA-N 0.000 claims 1
• IYEVLTXSGWCTAD-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-propan-2-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound N1=C2N(C(C)C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 IYEVLTXSGWCTAD-UHFFFAOYSA-N 0.000 claims 1
• YCEUUXAHOHKAHA-UHFFFAOYSA-N 1-[4-[4-(9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound N1=C2N(CC(F)(F)F)N=CC2=C(N2CC3CNCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=NC=C1 YCEUUXAHOHKAHA-UHFFFAOYSA-N 0.000 claims 1
• MTIARLQVNAAYGF-UHFFFAOYSA-N 1-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C)CCN1C(N=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=C1 MTIARLQVNAAYGF-UHFFFAOYSA-N 0.000 claims 1
• ZRLCNRCZZGRZFX-UHFFFAOYSA-N 1-[6-(dimethylamino)pyridin-3-yl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(N(C)C)N=C1 ZRLCNRCZZGRZFX-UHFFFAOYSA-N 0.000 claims 1
• ZWGYTSYJEZHODU-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-(2-hydroxyethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CCO)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1CC1 ZWGYTSYJEZHODU-UHFFFAOYSA-N 0.000 claims 1
• XYMCMQNRZAYJFU-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-[4-(4-methylpiperazin-1-yl)cyclohexyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CN(C)CCN1C1CCC(N2C3=NC(=NC(=C3C=N2)N2CC3CCC(O3)C2)C=2C=CC(NC(=O)NC3CC3)=CC=2)CC1 XYMCMQNRZAYJFU-UHFFFAOYSA-N 0.000 claims 1
• ZXXBGPFLOBZGTR-UHFFFAOYSA-N 1-ethyl-3-[4-[1-[4-(4-methylpiperazin-1-yl)cyclohexyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(CC3)N3CCN(C)CC3)C2=N1 ZXXBGPFLOBZGTR-UHFFFAOYSA-N 0.000 claims 1
• DZCKHQBHPTXSEC-UHFFFAOYSA-N 1-ethyl-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CC)C2=N1 DZCKHQBHPTXSEC-UHFFFAOYSA-N 0.000 claims 1
• OCEMYPICVNLEAL-UHFFFAOYSA-N 1-methyl-3-[4-[1-[4-(4-methylpiperazin-1-yl)cyclohexyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(CC3)N3CCN(C)CC3)C2=N1 OCEMYPICVNLEAL-UHFFFAOYSA-N 0.000 claims 1
• QUKPALAWEPMWOS-UHFFFAOYSA-N 1h-pyrazolo[3,4-d]pyrimidine Chemical compound C1=NC=C2C=NNC2=N1 QUKPALAWEPMWOS-UHFFFAOYSA-N 0.000 claims 1
• 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims 1
• ZOOSIANKMLTUPB-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[1-[4-(4-methylpiperazin-1-yl)cyclohexyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1CN(C)CCN1C1CCC(N2C3=NC(=NC(=C3C=N2)N2CC3CCC(O3)C2)C=2C=CC(NC(=O)OCCO)=CC=2)CC1 ZOOSIANKMLTUPB-UHFFFAOYSA-N 0.000 claims 1
• DLAORXOIJUEBDN-HUUCEWRRSA-N 2-hydroxyethyl n-[4-[4-[(1r,4r)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2[C@@H]3C[C@@H](OC3)C2)=C(C=NN2CC(F)(F)F)C2=N1 DLAORXOIJUEBDN-HUUCEWRRSA-N 0.000 claims 1
• QWUNRYMMAGVRMS-UHFFFAOYSA-N 4-[[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamoylamino]-n-pyrrolidin-1-ylbenzamide Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC(C=C1)=CC=C1C(=O)NN1CCCC1 QWUNRYMMAGVRMS-UHFFFAOYSA-N 0.000 claims 1
• SYKXTQULDCRVJS-DPJKZYHESA-N C1C[C@@H](OC)CC[C@@H]1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(=CC=4)N4CCN(C)CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 Chemical compound C1C[C@@H](OC)CC[C@@H]1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(=CC=4)N4CCN(C)CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 SYKXTQULDCRVJS-DPJKZYHESA-N 0.000 claims 1
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
• 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
• OYRYVAGSZOFIQH-UHFFFAOYSA-N methyl 4-[6-[4-(2-fluoroethylcarbamoylamino)phenyl]-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCF)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 OYRYVAGSZOFIQH-UHFFFAOYSA-N 0.000 claims 1
• ZYMJMBRIYJFQRV-UHFFFAOYSA-N methyl 4-[6-[4-(2-hydroxyethoxycarbonylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)OCCO)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 ZYMJMBRIYJFQRV-UHFFFAOYSA-N 0.000 claims 1
• DNMGUTGVKHLEHC-UHFFFAOYSA-N methyl 4-[6-[4-(2-methoxyethoxycarbonylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)OCCOC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OC)C2=N1 DNMGUTGVKHLEHC-UHFFFAOYSA-N 0.000 claims 1
• UYTGQQFNCGMMEC-UHFFFAOYSA-N methyl 4-[6-[4-[[4-[2-(dimethylamino)ethoxy]phenyl]carbamoylamino]phenyl]-4-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(OCCN(C)C)=CC=4)=CC=3)=NC(N3C4CCC3COC4)=C2C=N1 UYTGQQFNCGMMEC-UHFFFAOYSA-N 0.000 claims 1
• VVAJIQKINOMMAW-UHFFFAOYSA-N methyl 4-[6-[4-[[6-(4-methylpiperazin-1-yl)pyridin-3-yl]carbamoylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=NC(=CC=4)N4CCN(C)CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 VVAJIQKINOMMAW-UHFFFAOYSA-N 0.000 claims 1
• VMAMMBJWQIMCRO-UHFFFAOYSA-N methyl n-[4-[1-(1,3-dimethoxypropan-2-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound N1=C2N(C(COC)COC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)OC)C=C1 VMAMMBJWQIMCRO-UHFFFAOYSA-N 0.000 claims 1
• FTFGELDMGOAGIK-UHFFFAOYSA-N methyl n-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)OC)C=C1 FTFGELDMGOAGIK-UHFFFAOYSA-N 0.000 claims 1
• DJCYVDOYEUQNLJ-UHFFFAOYSA-N propan-2-yl 4-[6-[4-(ethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OC(C)C)C2=N1 DJCYVDOYEUQNLJ-UHFFFAOYSA-N 0.000 claims 1
• ZWGIXYUVTRWCSG-UHFFFAOYSA-N tert-butyl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(phenylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 ZWGIXYUVTRWCSG-UHFFFAOYSA-N 0.000 claims 1
• ZXCQAXLUYKCYPH-UHFFFAOYSA-N tert-butyl 4-[6-[4-(2-fluoroethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCF)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 ZXCQAXLUYKCYPH-UHFFFAOYSA-N 0.000 claims 1
• OOMIGCLMYAHKFM-UHFFFAOYSA-N tert-butyl 4-[6-[4-(ethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OC(C)(C)C)C2=N1 OOMIGCLMYAHKFM-UHFFFAOYSA-N 0.000 claims 1
• 235000002639 sodium chloride Nutrition 0.000 description 94
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 69
• 235000013877 carbamide Nutrition 0.000 description 61
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 45
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 38
• 239000000243 solution Substances 0.000 description 38
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 36
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 36
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 31
• 235000019439 ethyl acetate Nutrition 0.000 description 30
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 27
• 125000002768 hydroxyalkyl group Chemical group 0.000 description 26
• 239000007787 solid Substances 0.000 description 26
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
• KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 24
• UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 description 21
• LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 20
• 239000003814 drug Substances 0.000 description 20
• 239000000463 material Substances 0.000 description 20
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 18
• 239000011734 sodium Substances 0.000 description 18
• 229940124597 therapeutic agent Drugs 0.000 description 17
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
• 239000000546 pharmaceutical excipient Substances 0.000 description 15
• 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 description 14
• 125000003342 alkenyl group Chemical group 0.000 description 14
• 230000000694 effects Effects 0.000 description 14
• 238000013270 controlled release Methods 0.000 description 13
• 239000011541 reaction mixture Substances 0.000 description 13
• IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 12
• 229910000041 hydrogen chloride Inorganic materials 0.000 description 12
• 239000007924 injection Substances 0.000 description 12
• 238000002347 injection Methods 0.000 description 12
• 239000007788 liquid Substances 0.000 description 12
• 238000013268 sustained release Methods 0.000 description 12
• 239000012730 sustained-release form Substances 0.000 description 12
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
• 239000003795 chemical substances by application Substances 0.000 description 11
• 229940124302 mTOR inhibitor Drugs 0.000 description 11
• BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 10
• 125000000304 alkynyl group Chemical group 0.000 description 10
• 239000002775 capsule Substances 0.000 description 10
• 239000003921 oil Substances 0.000 description 10
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 9
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
• CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 9
• 108091007960 PI3Ks Proteins 0.000 description 9
• 102000038030 PI3Ks Human genes 0.000 description 9
• 238000010438 heat treatment Methods 0.000 description 9
• 235000019198 oils Nutrition 0.000 description 9
• 239000000741 silica gel Substances 0.000 description 9
• 229910002027 silica gel Inorganic materials 0.000 description 9
• DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 9
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
• SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 8
• FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
• 239000002552 dosage form Substances 0.000 description 8
• 238000004128 high performance liquid chromatography Methods 0.000 description 8
• NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 8
• 239000000843 powder Substances 0.000 description 8
• 239000000829 suppository Substances 0.000 description 8
• 239000000725 suspension Substances 0.000 description 8
• 239000003826 tablet Substances 0.000 description 8
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 7
• 238000006243 chemical reaction Methods 0.000 description 7
• QOPVNWQGBQYBBP-UHFFFAOYSA-N chloroethyl chloroformate Chemical compound CC(Cl)OC(Cl)=O QOPVNWQGBQYBBP-UHFFFAOYSA-N 0.000 description 7
• 238000002360 preparation method Methods 0.000 description 7
• 239000000047 product Substances 0.000 description 7
• 239000002904 solvent Substances 0.000 description 7
• 239000000758 substrate Substances 0.000 description 7
• JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 7
• WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 6
• VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 6
• CUYKNJBYIJFRCU-UHFFFAOYSA-N 3-aminopyridine Chemical compound NC1=CC=CN=C1 CUYKNJBYIJFRCU-UHFFFAOYSA-N 0.000 description 6
• VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 6
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
• 241001465754 Metazoa Species 0.000 description 6
• 229920002472 Starch Polymers 0.000 description 6
• 239000004480 active ingredient Substances 0.000 description 6
• 239000000839 emulsion Substances 0.000 description 6
• 238000009472 formulation Methods 0.000 description 6
• 229940002612 prodrug Drugs 0.000 description 6
• 239000000651 prodrug Substances 0.000 description 6
• 125000006413 ring segment Chemical group 0.000 description 6
• 239000011780 sodium chloride Substances 0.000 description 6
• 235000019698 starch Nutrition 0.000 description 6
• 230000001225 therapeutic effect Effects 0.000 description 6
• YVHBSYTYLQYTOU-UHFFFAOYSA-N 3,6-diazabicyclo[3.1.1]heptane Chemical compound C1NCC2CC1N2 YVHBSYTYLQYTOU-UHFFFAOYSA-N 0.000 description 5
• ZANPJXNYBVVNSD-UHFFFAOYSA-N 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline Chemical compound O1C(C)(C)C(C)(C)OB1C1=CC=C(N)C=C1 ZANPJXNYBVVNSD-UHFFFAOYSA-N 0.000 description 5
• FYTFCKSXUKINKK-UHFFFAOYSA-N 6,8-dioxa-3-azabicyclo[3.2.1]octane Chemical compound C1NCC2COC1O2 FYTFCKSXUKINKK-UHFFFAOYSA-N 0.000 description 5
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
• 101100520660 Drosophila melanogaster Poc1 gene Proteins 0.000 description 5
• 102000004190 Enzymes Human genes 0.000 description 5
• 108090000790 Enzymes Proteins 0.000 description 5
• 101100520662 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) PBA1 gene Proteins 0.000 description 5
• CBPNZQVSJQDFBE-FUXHJELOSA-N Temsirolimus Chemical compound C1C[C@@H](OC(=O)C(C)(CO)CO)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 CBPNZQVSJQDFBE-FUXHJELOSA-N 0.000 description 5
• 239000012141 concentrate Substances 0.000 description 5
• 235000008504 concentrate Nutrition 0.000 description 5
• 229940088598 enzyme Drugs 0.000 description 5
• 238000011534 incubation Methods 0.000 description 5
• 239000012528 membrane Substances 0.000 description 5
• 210000004379 membrane Anatomy 0.000 description 5
• 239000002207 metabolite Substances 0.000 description 5
• 230000037361 pathway Effects 0.000 description 5
• 239000012071 phase Substances 0.000 description 5
• 238000010992 reflux Methods 0.000 description 5
• 238000010898 silica gel chromatography Methods 0.000 description 5
• 239000008107 starch Substances 0.000 description 5
• 238000011282 treatment Methods 0.000 description 5
• 238000010626 work up procedure Methods 0.000 description 5
• KCDXWVLANOYMJG-UHFFFAOYSA-N 2,6-dioxa-8-azabicyclo[2.2.2]octane Chemical compound C1OC2CNC1CO2 KCDXWVLANOYMJG-UHFFFAOYSA-N 0.000 description 4
• JNYWVERKQKRXSL-UHFFFAOYSA-N 2-oxa-5-azabicyclo[2.2.2]octane Chemical compound C1NC2CCC1OC2 JNYWVERKQKRXSL-UHFFFAOYSA-N 0.000 description 4
• AYNOATFQHAEZHR-UHFFFAOYSA-N 3,6-dioxa-8-azabicyclo[3.2.1]octane Chemical compound C1OCC2COC1N2 AYNOATFQHAEZHR-UHFFFAOYSA-N 0.000 description 4
• VCRZEBCHQMOGQZ-UHFFFAOYSA-N 3-(6-chloro-1h-pyrazolo[3,4-d]pyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C1C(O2)CCC2CN1C1=C(C=NN2)C2=NC(Cl)=N1 VCRZEBCHQMOGQZ-UHFFFAOYSA-N 0.000 description 4
• BXMGZQQTBBJSPP-UHFFFAOYSA-N 3-oxa-6-azabicyclo[3.1.1]heptane Chemical compound C1OCC2CC1N2 BXMGZQQTBBJSPP-UHFFFAOYSA-N 0.000 description 4
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 4
• YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 4
• FMCLKHXUTROOEV-UHFFFAOYSA-N 5-oxa-2,8-diazabicyclo[2.2.2]octane Chemical compound C1NC2CNC1OC2 FMCLKHXUTROOEV-UHFFFAOYSA-N 0.000 description 4
• HYJHBSPJETTWEH-UHFFFAOYSA-N 6-oxa-3,8-diazabicyclo[3.2.1]octane Chemical compound C1NCC2COC1N2 HYJHBSPJETTWEH-UHFFFAOYSA-N 0.000 description 4
• WDJAQSJMDRFZIX-UHFFFAOYSA-N 6-oxa-3-azabicyclo[3.1.1]heptane Chemical compound C1NCC2CC1O2 WDJAQSJMDRFZIX-UHFFFAOYSA-N 0.000 description 4
• GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 4
• QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
• 241000282326 Felis catus Species 0.000 description 4
• 108010010803 Gelatin Proteins 0.000 description 4
• OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
• GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 4
• 241000872931 Myoporum sandwicense Species 0.000 description 4
• JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 4
• GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
• DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 4
• 150000001298 alcohols Chemical class 0.000 description 4
• WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 4
• 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 4
• 230000037396 body weight Effects 0.000 description 4
• 230000010261 cell growth Effects 0.000 description 4
• 235000010980 cellulose Nutrition 0.000 description 4
• 229920002678 cellulose Polymers 0.000 description 4
• 239000001913 cellulose Substances 0.000 description 4
• 239000003085 diluting agent Substances 0.000 description 4
• ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
• 201000010099 disease Diseases 0.000 description 4
• 239000006260 foam Substances 0.000 description 4
• 229920000159 gelatin Polymers 0.000 description 4
• 235000019322 gelatine Nutrition 0.000 description 4
• 235000011852 gelatine desserts Nutrition 0.000 description 4
• 238000001802 infusion Methods 0.000 description 4
• 239000003112 inhibitor Substances 0.000 description 4
• 238000001990 intravenous administration Methods 0.000 description 4
• 239000008101 lactose Substances 0.000 description 4
• 239000002502 liposome Substances 0.000 description 4
• HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
• 229910052943 magnesium sulfate Inorganic materials 0.000 description 4
• 235000019341 magnesium sulphate Nutrition 0.000 description 4
• 239000012044 organic layer Substances 0.000 description 4
• 125000005010 perfluoroalkyl group Chemical group 0.000 description 4
• 239000008194 pharmaceutical composition Substances 0.000 description 4
• UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 4
• 150000003915 phosphatidylinositol 4,5-bisphosphates Chemical class 0.000 description 4
• VVWRJUBEIPHGQF-MDZDMXLPSA-N propan-2-yl (ne)-n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)\N=N\C(=O)OC(C)C VVWRJUBEIPHGQF-MDZDMXLPSA-N 0.000 description 4
• 230000002829 reductive effect Effects 0.000 description 4
• 230000001105 regulatory effect Effects 0.000 description 4
• 238000004007 reversed phase HPLC Methods 0.000 description 4
• 229920006395 saturated elastomer Polymers 0.000 description 4
• 229960002930 sirolimus Drugs 0.000 description 4
• 229910052708 sodium Inorganic materials 0.000 description 4
• 229910000104 sodium hydride Inorganic materials 0.000 description 4
• 125000004434 sulfur atom Chemical group 0.000 description 4
• 238000002560 therapeutic procedure Methods 0.000 description 4
• RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
• KVJIRFGNHAAUNQ-UHFFFAOYSA-N 2,4,6-trichloropyrimidine-5-carbaldehyde Chemical compound ClC1=NC(Cl)=C(C=O)C(Cl)=N1 KVJIRFGNHAAUNQ-UHFFFAOYSA-N 0.000 description 3
• UKHJNJFJCGBKSF-UHFFFAOYSA-N 2,5-diazabicyclo[2.2.1]heptane Chemical compound C1NC2CNC1C2 UKHJNJFJCGBKSF-UHFFFAOYSA-N 0.000 description 3
• DJWDAKFSDBOQJK-UHFFFAOYSA-N 2,5-diazabicyclo[2.2.2]octane Chemical compound C1NC2CCC1NC2 DJWDAKFSDBOQJK-UHFFFAOYSA-N 0.000 description 3
• UBUBIMQAMCKQCX-UHFFFAOYSA-N 2,5-dioxa-8-azabicyclo[2.2.2]octane Chemical compound C1OC2CNC1OC2 UBUBIMQAMCKQCX-UHFFFAOYSA-N 0.000 description 3
• RSEBUVRVKCANEP-UHFFFAOYSA-N 2-pyrroline Chemical compound C1CC=CN1 RSEBUVRVKCANEP-UHFFFAOYSA-N 0.000 description 3
• LKDJYZBKCVSODK-UHFFFAOYSA-N 3,8-diazabicyclo[3.2.1]octane Chemical compound C1NCC2CCC1N2 LKDJYZBKCVSODK-UHFFFAOYSA-N 0.000 description 3
• LDCONZAKYQXURF-UHFFFAOYSA-N 3-[1-(1-benzylpiperidin-4-yl)-6-chloropyrazolo[3,4-d]pyrimidin-4-yl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C12=NC(Cl)=NC(N3CC4CCC(O4)C3)=C2C=NN1C(CC1)CCN1CC1=CC=CC=C1 LDCONZAKYQXURF-UHFFFAOYSA-N 0.000 description 3
• 229960000549 4-dimethylaminophenol Drugs 0.000 description 3
• USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 3
• 239000005695 Ammonium acetate Substances 0.000 description 3
• KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
• HKVAMNSJSFKALM-GKUWKFKPSA-N Everolimus Chemical compound C1C[C@@H](OCCO)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 HKVAMNSJSFKALM-GKUWKFKPSA-N 0.000 description 3
• 238000005481 NMR spectroscopy Methods 0.000 description 3
• RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
• 208000006265 Renal cell carcinoma Diseases 0.000 description 3
• DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
• 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 description 3
• 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 description 3
• XJLXINKUBYWONI-DQQFMEOOSA-N [[(2r,3r,4r,5r)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2s,3r,4s,5s)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate Chemical compound NC(=O)C1=CC=C[N+]([C@@H]2[C@H]([C@@H](O)[C@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](OP(O)(O)=O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 XJLXINKUBYWONI-DQQFMEOOSA-N 0.000 description 3
• 238000010521 absorption reaction Methods 0.000 description 3
• 239000002253 acid Substances 0.000 description 3
• 230000009471 action Effects 0.000 description 3
• 230000004913 activation Effects 0.000 description 3
• 229940043376 ammonium acetate Drugs 0.000 description 3
• 235000019257 ammonium acetate Nutrition 0.000 description 3
• 239000008280 blood Substances 0.000 description 3
• 210000004369 blood Anatomy 0.000 description 3
• 239000000872 buffer Substances 0.000 description 3
• 239000000969 carrier Substances 0.000 description 3
• 230000003197 catalytic effect Effects 0.000 description 3
• 210000004027 cell Anatomy 0.000 description 3
• 239000003086 colorant Substances 0.000 description 3
• 239000006071 cream Substances 0.000 description 3
• 125000004122 cyclic group Chemical group 0.000 description 3
• 238000013461 design Methods 0.000 description 3
• 238000001035 drying Methods 0.000 description 3
• 238000001914 filtration Methods 0.000 description 3
• 239000008273 gelatin Substances 0.000 description 3
• 235000011187 glycerol Nutrition 0.000 description 3
• 238000007914 intraventricular administration Methods 0.000 description 3
• 238000002955 isolation Methods 0.000 description 3
• 239000010410 layer Substances 0.000 description 3
• 230000007246 mechanism Effects 0.000 description 3
• 125000002757 morpholinyl group Chemical group 0.000 description 3
• TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
• 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 description 3
• 238000007911 parenteral administration Methods 0.000 description 3
• 239000003208 petroleum Substances 0.000 description 3
• 125000004193 piperazinyl group Chemical group 0.000 description 3
• 239000002244 precipitate Substances 0.000 description 3
• 230000000069 prophylactic effect Effects 0.000 description 3
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
• 125000000719 pyrrolidinyl group Chemical group 0.000 description 3
• ZVJHJDDKYZXRJI-UHFFFAOYSA-N pyrroline Natural products C1CC=NC1 ZVJHJDDKYZXRJI-UHFFFAOYSA-N 0.000 description 3
• 239000000377 silicon dioxide Substances 0.000 description 3
• 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
• 239000003381 stabilizer Substances 0.000 description 3
• 238000003756 stirring Methods 0.000 description 3
• 239000000126 substance Substances 0.000 description 3
• 238000001356 surgical procedure Methods 0.000 description 3
• 238000003786 synthesis reaction Methods 0.000 description 3
• 230000009885 systemic effect Effects 0.000 description 3
• 239000000454 talc Substances 0.000 description 3
• 229910052623 talc Inorganic materials 0.000 description 3
• 235000012222 talc Nutrition 0.000 description 3
• YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
• 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 description 3
• 229940100411 torisel Drugs 0.000 description 3
• 239000003643 water by type Substances 0.000 description 3
• ZZCHUBZBYAFNPJ-UHFFFAOYSA-N (1-benzylpiperidin-4-yl)hydrazine;dihydrochloride Chemical compound Cl.Cl.C1CC(NN)CCN1CC1=CC=CC=C1 ZZCHUBZBYAFNPJ-UHFFFAOYSA-N 0.000 description 2
• AXKGIPZJYUNAIW-UHFFFAOYSA-N (4-aminophenyl)methanol Chemical compound NC1=CC=C(CO)C=C1 AXKGIPZJYUNAIW-UHFFFAOYSA-N 0.000 description 2
• IMLSAISZLJGWPP-UHFFFAOYSA-N 1,3-dithiolane Chemical compound C1CSCS1 IMLSAISZLJGWPP-UHFFFAOYSA-N 0.000 description 2
• PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 2
• ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
• AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
• LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
• CGHIBGNXEGJPQZ-UHFFFAOYSA-N 1-hexyne Chemical compound CCCCC#C CGHIBGNXEGJPQZ-UHFFFAOYSA-N 0.000 description 2
• JRZJOMJEPLMPRA-UHFFFAOYSA-N 1-nonene Chemical compound CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
• KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
• OXBLVCZKDOZZOJ-UHFFFAOYSA-N 2,3-Dihydrothiophene Chemical compound C1CC=CS1 OXBLVCZKDOZZOJ-UHFFFAOYSA-N 0.000 description 2
• JKTCBAGSMQIFNL-UHFFFAOYSA-N 2,3-dihydrofuran Chemical compound C1CC=CO1 JKTCBAGSMQIFNL-UHFFFAOYSA-N 0.000 description 2
• JECYNCQXXKQDJN-UHFFFAOYSA-N 2-(2-methylhexan-2-yloxymethyl)oxirane Chemical compound CCCCC(C)(C)OCC1CO1 JECYNCQXXKQDJN-UHFFFAOYSA-N 0.000 description 2
• RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 2
• JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 2
• XNMQEEKYCVKGBD-UHFFFAOYSA-N 2-butyne Chemical compound CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 2
• UUNLPKLFGVUVSN-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CCF)C2=N1 UUNLPKLFGVUVSN-UHFFFAOYSA-N 0.000 description 2
• DIQOUXNTSMWQSA-UHFFFAOYSA-N 2-oxa-5-azabicyclo[2.2.1]heptane Chemical compound C1OC2CNC1C2 DIQOUXNTSMWQSA-UHFFFAOYSA-N 0.000 description 2
• NKTDTMONXHODTI-UHFFFAOYSA-N 2-pentyne Chemical compound CCC#CC NKTDTMONXHODTI-UHFFFAOYSA-N 0.000 description 2
• MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 2
• BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 2
• BOCNZKTXQKRHBT-UHFFFAOYSA-N 3-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-6-(1h-indol-5-yl)pyrazolo[3,4-d]pyrimidin-4-yl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound O1CCOC11CCC(N2C3=NC(=NC(=C3C=N2)N2CC3CCC(O3)C2)C=2C=C3C=CNC3=CC=2)CC1 BOCNZKTXQKRHBT-UHFFFAOYSA-N 0.000 description 2
• VYMZKBNBRXLBDU-UHFFFAOYSA-N 3-[6-chloro-1-(oxan-2-yl)pyrazolo[3,4-d]pyrimidin-4-yl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C12=NC(Cl)=NC(N3CC4CCC(O4)C3)=C2C=NN1C1CCCCO1 VYMZKBNBRXLBDU-UHFFFAOYSA-N 0.000 description 2
• PWVHZVWNAGLZFH-UHFFFAOYSA-N 3-azabicyclo[3.1.1]heptane Chemical compound C1C2CC1CNC2 PWVHZVWNAGLZFH-UHFFFAOYSA-N 0.000 description 2
• MOZNZNKHRXRLLF-UHFFFAOYSA-N 4-(4-methylpiperazin-1-yl)aniline Chemical compound C1CN(C)CCN1C1=CC=C(N)C=C1 MOZNZNKHRXRLLF-UHFFFAOYSA-N 0.000 description 2
• PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
• DENNCEQUAZKJGC-UHFFFAOYSA-N 6-azabicyclo[3.1.1]heptane Chemical compound C1CCC2CC1N2 DENNCEQUAZKJGC-UHFFFAOYSA-N 0.000 description 2
• BUROJSBIWGDYCN-GAUTUEMISA-N AP 23573 Chemical compound C1C[C@@H](OP(C)(C)=O)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 BUROJSBIWGDYCN-GAUTUEMISA-N 0.000 description 2
• ZKHQWZAMYRWXGA-UHFFFAOYSA-N Adenosine triphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C(O)C1O ZKHQWZAMYRWXGA-UHFFFAOYSA-N 0.000 description 2
• NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 2
• VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
• 208000005623 Carcinogenesis Diseases 0.000 description 2
• 108091007959 Class II PI3Ks Proteins 0.000 description 2
• 108091007963 Class III PI3Ks Proteins 0.000 description 2
• FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
• BUDQDWGNQVEFAC-UHFFFAOYSA-N Dihydropyran Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 description 2
• XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
• 239000012591 Dulbecco’s Phosphate Buffered Saline Substances 0.000 description 2
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
• WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
• DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
• 229920000084 Gum arabic Polymers 0.000 description 2
• 241000282412 Homo Species 0.000 description 2
• 229930195725 Mannitol Natural products 0.000 description 2
• 229920000168 Microcrystalline cellulose Polymers 0.000 description 2
• IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
• PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
• UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
• 229910019142 PO4 Inorganic materials 0.000 description 2
• NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
• 102000004022 Protein-Tyrosine Kinases Human genes 0.000 description 2
• 108090000412 Protein-Tyrosine Kinases Proteins 0.000 description 2
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
• CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
• 229930006000 Sucrose Natural products 0.000 description 2
• 238000006069 Suzuki reaction reaction Methods 0.000 description 2
• YPWFISCTZQNZAU-UHFFFAOYSA-N Thiane Chemical compound C1CCSCC1 YPWFISCTZQNZAU-UHFFFAOYSA-N 0.000 description 2
• 230000002159 abnormal effect Effects 0.000 description 2
• 235000010489 acacia gum Nutrition 0.000 description 2
• DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
• PBCJIPOGFJYBJE-UHFFFAOYSA-N acetonitrile;hydrate Chemical compound O.CC#N PBCJIPOGFJYBJE-UHFFFAOYSA-N 0.000 description 2
• 125000004450 alkenylene group Chemical group 0.000 description 2
• 125000002947 alkylene group Chemical group 0.000 description 2
• 125000004419 alkynylene group Chemical group 0.000 description 2
• 239000003708 ampul Substances 0.000 description 2
• 239000007864 aqueous solution Substances 0.000 description 2
• 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
• WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
• PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
• WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
• 239000011230 binding agent Substances 0.000 description 2
• 230000015572 biosynthetic process Effects 0.000 description 2
• 239000004305 biphenyl Substances 0.000 description 2
• 235000010290 biphenyl Nutrition 0.000 description 2
• ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 2
• GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
• KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical compound CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 description 2
• OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
• 230000036952 cancer formation Effects 0.000 description 2
• 239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
• 239000001768 carboxy methyl cellulose Substances 0.000 description 2
• 231100000504 carcinogenesis Toxicity 0.000 description 2
• 238000007906 compression Methods 0.000 description 2
• 230000006835 compression Effects 0.000 description 2
• PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
• FAMRKDQNMBBFBR-BQYQJAHWSA-N diethyl azodicarboxylate Substances CCOC(=O)\N=N\C(=O)OCC FAMRKDQNMBBFBR-BQYQJAHWSA-N 0.000 description 2
• 229940079593 drug Drugs 0.000 description 2
• 238000012377 drug delivery Methods 0.000 description 2
• 239000003995 emulsifying agent Substances 0.000 description 2
• 239000002158 endotoxin Substances 0.000 description 2
• 125000005677 ethinylene group Chemical group [*:2]C#C[*:1] 0.000 description 2
• 229960005167 everolimus Drugs 0.000 description 2
• 239000000796 flavoring agent Substances 0.000 description 2
• 235000013312 flour Nutrition 0.000 description 2
• 235000013355 food flavoring agent Nutrition 0.000 description 2
• 235000003599 food sweetener Nutrition 0.000 description 2
• 210000001035 gastrointestinal tract Anatomy 0.000 description 2
• 239000000499 gel Substances 0.000 description 2
• 238000007429 general method Methods 0.000 description 2
• YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 2
• SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 2
• 239000008187 granular material Substances 0.000 description 2
• PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 2
• 150000002430 hydrocarbons Chemical group 0.000 description 2
• 239000007943 implant Substances 0.000 description 2
• 238000000338 in vitro Methods 0.000 description 2
• 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 description 2
• 239000004615 ingredient Substances 0.000 description 2
• 230000005764 inhibitory process Effects 0.000 description 2
• CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 2
• 150000002576 ketones Chemical class 0.000 description 2
• 229920006008 lipopolysaccharide Polymers 0.000 description 2
• 210000001853 liver microsome Anatomy 0.000 description 2
• 239000000314 lubricant Substances 0.000 description 2
• 235000019359 magnesium stearate Nutrition 0.000 description 2
• 239000000594 mannitol Substances 0.000 description 2
• 235000010355 mannitol Nutrition 0.000 description 2
• 238000002844 melting Methods 0.000 description 2
• 230000008018 melting Effects 0.000 description 2
• NNYFZOCDWHHJHK-UHFFFAOYSA-N methyl n-[4-[1-[2-(dimethylamino)ethyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CCN(C)C)C2=N1 NNYFZOCDWHHJHK-UHFFFAOYSA-N 0.000 description 2
• 235000019813 microcrystalline cellulose Nutrition 0.000 description 2
• 239000011859 microparticle Substances 0.000 description 2
• QYLYZBBYMWXQRX-UHFFFAOYSA-N n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(oxan-2-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]acetamide Chemical compound C1=CC(NC(=O)C)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3OCCCC3)C2=N1 QYLYZBBYMWXQRX-UHFFFAOYSA-N 0.000 description 2
• GIFKOQWKTYICIC-UHFFFAOYSA-N n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1h-pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]acetamide Chemical compound C1=CC(NC(=O)C)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2)C2=N1 GIFKOQWKTYICIC-UHFFFAOYSA-N 0.000 description 2
• 238000011580 nude mouse model Methods 0.000 description 2
• QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
• 239000002674 ointment Substances 0.000 description 2
• YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
• QMMOXUPEWRXHJS-UHFFFAOYSA-N pentene-2 Natural products CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 2
• 235000021317 phosphate Nutrition 0.000 description 2
• 239000002953 phosphate buffered saline Substances 0.000 description 2
• 150000003911 phosphatidylinositol 4-phosphates Chemical class 0.000 description 2
• 150000003905 phosphatidylinositols Chemical class 0.000 description 2
• 239000006187 pill Substances 0.000 description 2
• 239000003755 preservative agent Substances 0.000 description 2
• 230000008569 process Effects 0.000 description 2
• QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
• 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
• 238000000746 purification Methods 0.000 description 2
• 150000003217 pyrazoles Chemical class 0.000 description 2
• 108700042226 ras Genes Proteins 0.000 description 2
• 230000009467 reduction Effects 0.000 description 2
• 238000006722 reduction reaction Methods 0.000 description 2
• 230000004044 response Effects 0.000 description 2
• 238000012552 review Methods 0.000 description 2
• 239000012279 sodium borohydride Substances 0.000 description 2
• 229910000033 sodium borohydride Inorganic materials 0.000 description 2
• 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
• 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
• 239000012453 solvate Substances 0.000 description 2
• 239000005720 sucrose Substances 0.000 description 2
• 235000000346 sugar Nutrition 0.000 description 2
• 150000008163 sugars Chemical class 0.000 description 2
• 239000000375 suspending agent Substances 0.000 description 2
• 239000003765 sweetening agent Substances 0.000 description 2
• 239000006188 syrup Substances 0.000 description 2
• 235000020357 syrup Nutrition 0.000 description 2
• 229960000235 temsirolimus Drugs 0.000 description 2
• RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 2
• 239000002562 thickening agent Substances 0.000 description 2
• VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 2
• 238000004809 thin layer chromatography Methods 0.000 description 2
• 230000000699 topical effect Effects 0.000 description 2
• VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
• 239000001993 wax Substances 0.000 description 2
• OZFAFGSSMRRTDW-UHFFFAOYSA-N (2,4-dichlorophenyl) benzenesulfonate Chemical compound ClC1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=CC=C1 OZFAFGSSMRRTDW-UHFFFAOYSA-N 0.000 description 1
• JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
• GGSSKVJAJPNEPM-UHFFFAOYSA-N (3-aminophenyl)methyl n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound NC1=CC=CC(COC(=O)NC=2C=CC(=CC=2)C=2N=C3N(CC(F)(F)F)N=CC3=C(N3CC4CCC(O4)C3)N=2)=C1 GGSSKVJAJPNEPM-UHFFFAOYSA-N 0.000 description 1
• VYEWTHXZHHATTA-UHFFFAOYSA-N (4-acetamidophenyl)boronic acid Chemical compound CC(=O)NC1=CC=C(B(O)O)C=C1 VYEWTHXZHHATTA-UHFFFAOYSA-N 0.000 description 1
• 125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 1
• 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 1
• GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 1
• YCTDZYMMFQCTEO-FNORWQNLSA-N (E)-3-octene Chemical compound CCCC\C=C\CC YCTDZYMMFQCTEO-FNORWQNLSA-N 0.000 description 1
• GVRWIAHBVAYKIZ-FNORWQNLSA-N (e)-dec-3-ene Chemical compound CCCCCC\C=C\CC GVRWIAHBVAYKIZ-FNORWQNLSA-N 0.000 description 1
• SOVOPSCRHKEUNJ-VQHVLOKHSA-N (e)-dec-4-ene Chemical compound CCCCC\C=C\CCC SOVOPSCRHKEUNJ-VQHVLOKHSA-N 0.000 description 1
• IICQZTQZQSBHBY-HWKANZROSA-N (e)-non-2-ene Chemical compound CCCCCC\C=C\C IICQZTQZQSBHBY-HWKANZROSA-N 0.000 description 1
• WIKBZUXHNPONPP-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoro-2-iodo-2-(trifluoromethyl)propane Chemical compound FC(F)(F)C(I)(C(F)(F)F)C(F)(F)F WIKBZUXHNPONPP-UHFFFAOYSA-N 0.000 description 1
• CXWGKAYMVASWDQ-UHFFFAOYSA-N 1,2-dithiane Chemical compound C1CCSSC1 CXWGKAYMVASWDQ-UHFFFAOYSA-N 0.000 description 1
• WORJRXHJTUTINR-UHFFFAOYSA-N 1,4-dioxane;hydron;chloride Chemical compound Cl.C1COCCO1 WORJRXHJTUTINR-UHFFFAOYSA-N 0.000 description 1
• VKRKCBWIVLSRBJ-UHFFFAOYSA-N 1,4-dioxaspiro[4.5]decan-8-one Chemical compound C1CC(=O)CCC21OCCO2 VKRKCBWIVLSRBJ-UHFFFAOYSA-N 0.000 description 1
• YSVBDTHDOXANQI-UHFFFAOYSA-N 1-(1-benzylpiperidin-4-yl)-4,6-dichloropyrazolo[3,4-d]pyrimidine Chemical compound C12=NC(Cl)=NC(Cl)=C2C=NN1C(CC1)CCN1CC1=CC=CC=C1 YSVBDTHDOXANQI-UHFFFAOYSA-N 0.000 description 1
• NTJQREUGJKIARY-UHFFFAOYSA-N 1-(2,5-dimethoxy-4-methylphenyl)propan-2-amine Chemical compound COC1=CC(CC(C)N)=C(OC)C=C1C NTJQREUGJKIARY-UHFFFAOYSA-N 0.000 description 1
• JDEYBJHOTWGYFE-UHFFFAOYSA-N 1-(4-aminophenyl)ethanol Chemical compound CC(O)C1=CC=C(N)C=C1 JDEYBJHOTWGYFE-UHFFFAOYSA-N 0.000 description 1
• BGAKGLPYUURGAR-UHFFFAOYSA-N 1-[2-(dimethylamino)ethyl]-3-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCCN(C)C)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCCO4)C2=N1 BGAKGLPYUURGAR-UHFFFAOYSA-N 0.000 description 1
• ODSKIIXTBSXLGG-UHFFFAOYSA-N 1-[4-(aminomethyl)phenyl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(CN)C=C1 ODSKIIXTBSXLGG-UHFFFAOYSA-N 0.000 description 1
• RSKRPMNJXANSOH-UHFFFAOYSA-N 1-[4-[1-ethyl-3-formyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound N1=C2N(CC)N=C(C=O)C2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)NC)C=C1 RSKRPMNJXANSOH-UHFFFAOYSA-N 0.000 description 1
• ZGHQYQZGCBQBIH-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethoxy]phenyl]-3-[4-[1-(4-methoxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CC(OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC(OCCN(C)C)=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 ZGHQYQZGCBQBIH-UHFFFAOYSA-N 0.000 description 1
• OVJNWPYSQKFXRB-UHFFFAOYSA-N 1-[4-[2-(dimethylamino)ethylamino]phenyl]-3-[4-[1-ethyl-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(NCCN(C)C)C=C1 OVJNWPYSQKFXRB-UHFFFAOYSA-N 0.000 description 1
• ZWBNLUMFYUXGMK-UHFFFAOYSA-N 1-[4-[4-(6-hydroxy-3-oxa-8-azabicyclo[3.2.1]octan-8-yl)-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-methylurea Chemical compound C1=CC(NC(=O)NC)=CC=C1C1=NC(N2C3C(O)CC2COC3)=C(C=NN2CC(F)(F)F)C2=N1 ZWBNLUMFYUXGMK-UHFFFAOYSA-N 0.000 description 1
• YXLIUTQVEMJFQR-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(pyridin-3-ylmethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-phenylurea Chemical compound C=1C=C(C=2N=C3N(C4CCN(CC=5C=NC=CC=5)CC4)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1=CC=CC=C1 YXLIUTQVEMJFQR-UHFFFAOYSA-N 0.000 description 1
• LCHYMODHMGJDEG-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(pyridin-3-ylmethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-3-ylurea Chemical compound C=1C=CN=CC=1NC(=O)NC(C=C1)=CC=C1C(N=C12)=NC(N3CC4CCC(O4)C3)=C1C=NN2C(CC1)CCN1CC1=CC=CN=C1 LCHYMODHMGJDEG-UHFFFAOYSA-N 0.000 description 1
• YHOJJHQLBNYACI-UHFFFAOYSA-N 1-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(pyridin-3-ylmethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound C=1C=C(C=2N=C3N(C4CCN(CC=5C=NC=CC=5)CC4)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1=CC=NC=C1 YHOJJHQLBNYACI-UHFFFAOYSA-N 0.000 description 1
• SJZKULRDWHPHGG-UHFFFAOYSA-N 1-benzylpiperidin-4-one Chemical compound C1CC(=O)CCN1CC1=CC=CC=C1 SJZKULRDWHPHGG-UHFFFAOYSA-N 0.000 description 1
• PPTXHISAVZQIPE-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C=1C=C(C=2N=C3N(C4CCC5(CC4)OCCO5)N=CC3=C(N3CC4CCC(O4)C3)N=2)C=CC=1NC(=O)NC1CC1 PPTXHISAVZQIPE-UHFFFAOYSA-N 0.000 description 1
• RIWKUMGHZXCSPC-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-(4-methoxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1CC(OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 RIWKUMGHZXCSPC-UHFFFAOYSA-N 0.000 description 1
• RTVWGFBQAKFHOF-UHFFFAOYSA-N 1-cyclopropyl-3-[4-[1-[2-(dimethylamino)ethyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound N1=C2N(CCN(C)C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)NC1CC1 RTVWGFBQAKFHOF-UHFFFAOYSA-N 0.000 description 1
• BMNJFVMKTJUWFA-UHFFFAOYSA-N 1-ethyl-3-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-[1-(pyridin-3-ylmethyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC=4C=NC=CC=4)CC3)C2=N1 BMNJFVMKTJUWFA-UHFFFAOYSA-N 0.000 description 1
• GBTSKWANNRXPIL-ZIAGYGMSSA-N 1-methyl-3-[4-[4-[(1r,4r)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C([C@@]1(OC[C@@]2([H])C1)[H])N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C1=CC=C(NC(=O)NC)C=C1 GBTSKWANNRXPIL-ZIAGYGMSSA-N 0.000 description 1
• GBTSKWANNRXPIL-KBPBESRZSA-N 1-methyl-3-[4-[4-[(1s,4s)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl]-1-(2,2,2-trifluoroethyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]urea Chemical compound C([C@]1(OC[C@]2([H])C1)[H])N2C(C=1C=NN(CC(F)(F)F)C=1N=1)=NC=1C1=CC=C(NC(=O)NC)C=C1 GBTSKWANNRXPIL-KBPBESRZSA-N 0.000 description 1
• IBXNCJKFFQIKKY-UHFFFAOYSA-N 1-pentyne Chemical compound CCCC#C IBXNCJKFFQIKKY-UHFFFAOYSA-N 0.000 description 1
• 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 1
• LOBCDKRMIJAOBY-UHFFFAOYSA-N 2,2,2-trifluoroethyl n-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCC(F)(F)F)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCCO4)C2=N1 LOBCDKRMIJAOBY-UHFFFAOYSA-N 0.000 description 1
• QDKGOMZIPXGDDJ-UHFFFAOYSA-N 2,3-dihydro-1h-indazole Chemical compound C1=CC=C2CNNC2=C1 QDKGOMZIPXGDDJ-UHFFFAOYSA-N 0.000 description 1
• OTTZHAVKAVGASB-HYXAFXHYSA-N 2-Heptene Chemical compound CCCC\C=C/C OTTZHAVKAVGASB-HYXAFXHYSA-N 0.000 description 1
• UNBCXQQDKMJLJR-UHFFFAOYSA-N 2-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]anilino]ethanol Chemical compound C1=CC(NCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCCO4)C2=N1 UNBCXQQDKMJLJR-UHFFFAOYSA-N 0.000 description 1
• SPNBEJKSCORJPL-UHFFFAOYSA-N 2-[6-chloro-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]-n,n-dimethylethanamine Chemical compound C1C(O2)CCC2CN1C1=C2C=NN(CCN(C)C)C2=NC(Cl)=N1 SPNBEJKSCORJPL-UHFFFAOYSA-N 0.000 description 1
• GGDYAKVUZMZKRV-UHFFFAOYSA-N 2-fluoroethanol Chemical compound OCCF GGDYAKVUZMZKRV-UHFFFAOYSA-N 0.000 description 1
• FGMZJCUDMPVZPL-UHFFFAOYSA-N 2-fluoroethyl n-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCF)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCCO4)C2=N1 FGMZJCUDMPVZPL-UHFFFAOYSA-N 0.000 description 1
• OTTZHAVKAVGASB-UHFFFAOYSA-N 2-heptene Natural products CCCCC=CC OTTZHAVKAVGASB-UHFFFAOYSA-N 0.000 description 1
• BIBLKMQGSUWADG-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[1-(1-benzylpiperidin-4-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC=4C=CC=CC=4)CC3)C2=N1 BIBLKMQGSUWADG-UHFFFAOYSA-N 0.000 description 1
• XGCLUDDBWNFUPM-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[1-(4-hydroxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(O)CC3)C2=N1 XGCLUDDBWNFUPM-UHFFFAOYSA-N 0.000 description 1
• XGYLDGYIGFBGEE-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[1-(4-methoxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1CC(OC)CCC1N1C2=NC(C=3C=CC(NC(=O)OCCO)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 XGYLDGYIGFBGEE-UHFFFAOYSA-N 0.000 description 1
• JZAUHELMZKOQPL-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[1-[2-(dimethylamino)ethyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound N1=C2N(CCN(C)C)N=CC2=C(N2CC3CCC(O3)C2)N=C1C1=CC=C(NC(=O)OCCO)C=C1 JZAUHELMZKOQPL-UHFFFAOYSA-N 0.000 description 1
• LRGZQRPDPGROLN-UHFFFAOYSA-N 2-hydroxyethyl n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-oxocyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(=O)CC3)C2=N1 LRGZQRPDPGROLN-UHFFFAOYSA-N 0.000 description 1
• BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 1
• ILPBINAXDRFYPL-UHFFFAOYSA-N 2-octene Chemical compound CCCCCC=CC ILPBINAXDRFYPL-UHFFFAOYSA-N 0.000 description 1
• 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 1
• 125000006479 2-pyridyl methyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
• AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
• IICQZTQZQSBHBY-UHFFFAOYSA-N 2t-nonene Natural products CCCCCCC=CC IICQZTQZQSBHBY-UHFFFAOYSA-N 0.000 description 1
• OWHVATIGFHITHY-UHFFFAOYSA-N 3-(6-chloro-1-ethylpyrazolo[3,4-d]pyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C1C(O2)CCC2CN1C1=C2C=NN(CC)C2=NC(Cl)=N1 OWHVATIGFHITHY-UHFFFAOYSA-N 0.000 description 1
• WWNBSHZOGSBGRJ-UHFFFAOYSA-N 3-(6-chloro-1-phenylpyrazolo[3,4-d]pyrimidin-4-yl)-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C12=NC(Cl)=NC(N3CC4CCC(O4)C3)=C2C=NN1C1=CC=CC=C1 WWNBSHZOGSBGRJ-UHFFFAOYSA-N 0.000 description 1
• ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 1
• UMCMPZBLKLEWAF-BCTGSCMUSA-N 3-[(3-cholamidopropyl)dimethylammonio]propane-1-sulfonate Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCC[N+](C)(C)CCCS([O-])(=O)=O)C)[C@@]2(C)[C@@H](O)C1 UMCMPZBLKLEWAF-BCTGSCMUSA-N 0.000 description 1
• NBCYBRMEUCHHLV-UHFFFAOYSA-N 3-[6-chloro-1-(1,4-dioxaspiro[4.5]decan-8-yl)pyrazolo[3,4-d]pyrimidin-4-yl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C12=NC(Cl)=NC(N3CC4CCC(O4)C3)=C2C=NN1C(CC1)CCC21OCCO2 NBCYBRMEUCHHLV-UHFFFAOYSA-N 0.000 description 1
• DQGQKSCDTHITNB-UHFFFAOYSA-N 3-[6-chloro-1-(2-fluoroethyl)pyrazolo[3,4-d]pyrimidin-4-yl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C1C(O2)CCC2CN1C1=C2C=NN(CCF)C2=NC(Cl)=N1 DQGQKSCDTHITNB-UHFFFAOYSA-N 0.000 description 1
• HGWUUOXXAIISDB-UHFFFAOYSA-N 3-azabicyclo[3.1.0]hexane Chemical compound C1NCC2CC21 HGWUUOXXAIISDB-UHFFFAOYSA-N 0.000 description 1
• FEWJPZIEWOKRBE-UHFFFAOYSA-M 3-carboxy-2,3-dihydroxypropanoate Chemical compound OC(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-M 0.000 description 1
• ALKYHXVLJMQRLQ-UHFFFAOYSA-M 3-carboxynaphthalen-2-olate Chemical compound C1=CC=C2C=C(C([O-])=O)C(O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-M 0.000 description 1
• ZQDPJFUHLCOCRG-UHFFFAOYSA-N 3-hexene Chemical compound CCC=CCC ZQDPJFUHLCOCRG-UHFFFAOYSA-N 0.000 description 1
• DQQNMIPXXNPGCV-UHFFFAOYSA-N 3-hexyne Chemical compound CCC#CCC DQQNMIPXXNPGCV-UHFFFAOYSA-N 0.000 description 1
• LTPYZOHXYRDBPG-UHFFFAOYSA-N 3-hydroxypropyl n-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OCCCO)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCCO4)C2=N1 LTPYZOHXYRDBPG-UHFFFAOYSA-N 0.000 description 1
• USCSRAJGJYMJFZ-UHFFFAOYSA-N 3-methyl-1-butyne Chemical compound CC(C)C#C USCSRAJGJYMJFZ-UHFFFAOYSA-N 0.000 description 1
• YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
• LQVCUGATZFCLAS-UHFFFAOYSA-N 3-oxa-7,9-diazabicyclo[3.3.1]nonane Chemical compound C1OCC2CNCC1N2 LQVCUGATZFCLAS-UHFFFAOYSA-N 0.000 description 1
• 125000006201 3-phenylpropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• VMIPTJUFAWNUEU-UHFFFAOYSA-N 4,6-dichloro-1-(oxan-2-yl)pyrazolo[3,4-d]pyrimidine Chemical compound C12=NC(Cl)=NC(Cl)=C2C=NN1C1CCCCO1 VMIPTJUFAWNUEU-UHFFFAOYSA-N 0.000 description 1
• TYMWHTJGWKSXRY-UHFFFAOYSA-N 4,6-dichloro-1-methylpyrazolo[3,4-d]pyrimidine Chemical compound N1=C(Cl)N=C2N(C)N=CC2=C1Cl TYMWHTJGWKSXRY-UHFFFAOYSA-N 0.000 description 1
• CTYPROOLWJDUTA-UHFFFAOYSA-N 4,6-dichloro-1h-pyrazolo[3,4-d]pyrimidine Chemical compound ClC1=NC(Cl)=C2C=NNC2=N1 CTYPROOLWJDUTA-UHFFFAOYSA-N 0.000 description 1
• HWVGNHHLGUIAOC-UHFFFAOYSA-N 4-[1-(2-fluoroethyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]aniline Chemical compound C1=CC(N)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2CCF)C2=N1 HWVGNHHLGUIAOC-UHFFFAOYSA-N 0.000 description 1
• CKNHHTRURFNJKG-UHFFFAOYSA-N 4-[2-(dimethylamino)ethoxy]-n,n-dimethylaniline Chemical compound CN(C)CCOC1=CC=C(N(C)C)C=C1 CKNHHTRURFNJKG-UHFFFAOYSA-N 0.000 description 1
• XWRHARWOHHFQQA-UHFFFAOYSA-N 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-phenylpyrazolo[3,4-d]pyrimidin-6-yl]aniline Chemical compound C1=CC(N)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C=3C=CC=CC=3)C2=N1 XWRHARWOHHFQQA-UHFFFAOYSA-N 0.000 description 1
• NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 description 1
• HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
• WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
• OXRWICUICBZVAE-UHFFFAOYSA-N 4-methylpent-1-yne Chemical compound CC(C)CC#C OXRWICUICBZVAE-UHFFFAOYSA-N 0.000 description 1
• PHNDZBFLOPIMSM-UHFFFAOYSA-N 4-morpholin-4-ylaniline Chemical compound C1=CC(N)=CC=C1N1CCOCC1 PHNDZBFLOPIMSM-UHFFFAOYSA-N 0.000 description 1
• 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 1
• VERUFXOALATMPS-UHFFFAOYSA-N 5,5-diamino-2-(2-phenylethenyl)cyclohex-3-ene-1,1-disulfonic acid Chemical compound C1=CC(N)(N)CC(S(O)(=O)=O)(S(O)(=O)=O)C1C=CC1=CC=CC=C1 VERUFXOALATMPS-UHFFFAOYSA-N 0.000 description 1
• FATPQDPUKVVCLT-UHFFFAOYSA-N 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indole Chemical compound O1C(C)(C)C(C)(C)OB1C1=CC=C(NC=C2)C2=C1 FATPQDPUKVVCLT-UHFFFAOYSA-N 0.000 description 1
• WYVFAIDIZFAWMI-UHFFFAOYSA-N 5-azabicyclo[2.1.1]hexane Chemical compound C1CC2CC1N2 WYVFAIDIZFAWMI-UHFFFAOYSA-N 0.000 description 1
• KIWWEIOFOPULSX-UHFFFAOYSA-N 6-oxa-3-azabicyclo[3.1.0]hexane Chemical compound C1NCC2OC12 KIWWEIOFOPULSX-UHFFFAOYSA-N 0.000 description 1
• SNZSSCZJMVIOCR-UHFFFAOYSA-N 7-azabicyclo[2.2.1]heptane Chemical compound C1CC2CCC1N2 SNZSSCZJMVIOCR-UHFFFAOYSA-N 0.000 description 1
• YPWFNLSXQIGJCK-UHFFFAOYSA-N 7-oxabicyclo[2.2.1]heptane Chemical compound C1CC2CCC1O2 YPWFNLSXQIGJCK-UHFFFAOYSA-N 0.000 description 1
• POOPWPIOIMBTOH-UHFFFAOYSA-N 8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C1NCC2CCC1O2 POOPWPIOIMBTOH-UHFFFAOYSA-N 0.000 description 1
• XADOTNAXKKFKDY-UHFFFAOYSA-N 8-oxa-3-azabicyclo[3.2.1]octane;hydrochloride Chemical compound Cl.C1NCC2CCC1O2 XADOTNAXKKFKDY-UHFFFAOYSA-N 0.000 description 1
• ZKHQWZAMYRWXGA-KQYNXXCUSA-J ATP(4-) Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-J 0.000 description 1
• 244000215068 Acacia senegal Species 0.000 description 1
• 235000006491 Acacia senegal Nutrition 0.000 description 1
• QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
• 208000024893 Acute lymphoblastic leukemia Diseases 0.000 description 1
• 208000014697 Acute lymphocytic leukaemia Diseases 0.000 description 1
• 239000005995 Aluminium silicate Substances 0.000 description 1
• 101100006523 Arabidopsis thaliana CHC2 gene Proteins 0.000 description 1
• 235000003911 Arachis Nutrition 0.000 description 1
• 244000105624 Arachis hypogaea Species 0.000 description 1
• 108010011485 Aspartame Proteins 0.000 description 1
• 229910015845 BBr3 Inorganic materials 0.000 description 1
• 239000005711 Benzoic acid Substances 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
• BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
• 241000167854 Bourreria succulenta Species 0.000 description 1
• CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
• FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
• FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
• QRFAFGCAVNGXKY-FDRBHKFBSA-N C1C[C@@H](O)CC[C@H]1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 Chemical compound C1C[C@@H](O)CC[C@H]1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 QRFAFGCAVNGXKY-FDRBHKFBSA-N 0.000 description 1
• 102000002110 C2 domains Human genes 0.000 description 1
• 108050009459 C2 domains Proteins 0.000 description 1
• 101100037762 Caenorhabditis elegans rnh-2 gene Proteins 0.000 description 1
• BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
• 241000700199 Cavia porcellus Species 0.000 description 1
• PTHCMJGKKRQCBF-UHFFFAOYSA-N Cellulose, microcrystalline Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC)C(CO)O1 PTHCMJGKKRQCBF-UHFFFAOYSA-N 0.000 description 1
• 102100035673 Centrosomal protein of 290 kDa Human genes 0.000 description 1
• 241000282693 Cercopithecidae Species 0.000 description 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
• KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
• 108091007958 Class I PI3Ks Proteins 0.000 description 1
• 208000035473 Communicable disease Diseases 0.000 description 1
• HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 description 1
• FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
• FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
• RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
• 229920001353 Dextrin Polymers 0.000 description 1
• 239000004375 Dextrin Substances 0.000 description 1
• FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
• 235000019739 Dicalciumphosphate Nutrition 0.000 description 1
• 101100022323 Drosophila melanogaster Marf gene Proteins 0.000 description 1
• LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
• 241000792859 Enema Species 0.000 description 1
• VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
• 239000005977 Ethylene Substances 0.000 description 1
• CTKXFMQHOOWWEB-UHFFFAOYSA-N Ethylene oxide/propylene oxide copolymer Chemical compound CCCOC(C)COCCO CTKXFMQHOOWWEB-UHFFFAOYSA-N 0.000 description 1
• 229930091371 Fructose Natural products 0.000 description 1
• 239000005715 Fructose Substances 0.000 description 1
• RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
• VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
• 102000003688 G-Protein-Coupled Receptors Human genes 0.000 description 1
• 108090000045 G-Protein-Coupled Receptors Proteins 0.000 description 1
• 239000004471 Glycine Substances 0.000 description 1
• 102000009465 Growth Factor Receptors Human genes 0.000 description 1
• 108010009202 Growth Factor Receptors Proteins 0.000 description 1
• 239000007995 HEPES buffer Substances 0.000 description 1
• SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 1
• 101000715664 Homo sapiens Centrosomal protein of 290 kDa Proteins 0.000 description 1
• CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
• SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
• VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
• KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
• 108010076876 Keratins Proteins 0.000 description 1
• 102000011782 Keratins Human genes 0.000 description 1
• WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
• JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
• 241000080284 Lectrides Species 0.000 description 1
• NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 description 1
• 206010025323 Lymphomas Diseases 0.000 description 1
• 240000003183 Manihot esculenta Species 0.000 description 1
• 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
• 244000246386 Mentha pulegium Species 0.000 description 1
• 235000016257 Mentha pulegium Nutrition 0.000 description 1
• 235000004357 Mentha x piperita Nutrition 0.000 description 1
• AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
• MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 1
• GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
• FAUNBOBDFJICCL-SNXBXODESA-N N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)N[C@H]1CC[C@H](N)CC1 Chemical compound N1=C2N(CC)N=CC2=C(N2CC3CCC(O3)C2)N=C1C(C=C1)=CC=C1NC(=O)N[C@H]1CC[C@H](N)CC1 FAUNBOBDFJICCL-SNXBXODESA-N 0.000 description 1
• 229910002651 NO3 Inorganic materials 0.000 description 1
• NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
• OSFPHMZQBQZLAY-UHFFFAOYSA-N OBO.NC1=CC=CC=C1 Chemical compound OBO.NC1=CC=CC=C1 OSFPHMZQBQZLAY-UHFFFAOYSA-N 0.000 description 1
• 206010030113 Oedema Diseases 0.000 description 1
• 108700020796 Oncogene Proteins 0.000 description 1
• 102000043276 Oncogene Human genes 0.000 description 1
• 240000007594 Oryza sativa Species 0.000 description 1
• 235000007164 Oryza sativa Nutrition 0.000 description 1
• MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
• 101150073900 PTEN gene Proteins 0.000 description 1
• 241000282577 Pan troglodytes Species 0.000 description 1
• 241001504519 Papio ursinus Species 0.000 description 1
• 235000019483 Peanut oil Nutrition 0.000 description 1
• 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 description 1
• 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 description 1
• XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
• 108090000315 Protein Kinase C Proteins 0.000 description 1
• 102000003923 Protein Kinase C Human genes 0.000 description 1
• CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
• 239000012980 RPMI-1640 medium Substances 0.000 description 1
• 102000014400 SH2 domains Human genes 0.000 description 1
• 108050003452 SH2 domains Proteins 0.000 description 1
• 206010039491 Sarcoma Diseases 0.000 description 1
• 244000061456 Solanum tuberosum Species 0.000 description 1
• 235000002595 Solanum tuberosum Nutrition 0.000 description 1
• 235000021355 Stearic acid Nutrition 0.000 description 1
• 241000862969 Stella Species 0.000 description 1
• QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
• 229920002253 Tannate Polymers 0.000 description 1
• 229940123237 Taxane Drugs 0.000 description 1
• BPEGJWRSRHCHSN-UHFFFAOYSA-N Temozolomide Chemical compound O=C1N(C)N=NC2=C(C(N)=O)N=CN21 BPEGJWRSRHCHSN-UHFFFAOYSA-N 0.000 description 1
• DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
• GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
• 239000007983 Tris buffer Substances 0.000 description 1
• 102000014384 Type C Phospholipases Human genes 0.000 description 1
• 108010079194 Type C Phospholipases Proteins 0.000 description 1
• 108010073929 Vascular Endothelial Growth Factor A Proteins 0.000 description 1
• 229940122803 Vinca alkaloid Drugs 0.000 description 1
• 240000008042 Zea mays Species 0.000 description 1
• 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
• 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
• BOGSOFADOWIECK-UHFFFAOYSA-N [N].C=1C=NNC=1 Chemical compound [N].C=1C=NNC=1 BOGSOFADOWIECK-UHFFFAOYSA-N 0.000 description 1
• 239000000205 acacia gum Substances 0.000 description 1
• 125000004062 acenaphthenyl group Chemical group C1(CC2=CC=CC3=CC=CC1=C23)* 0.000 description 1
• DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
• 150000001241 acetals Chemical class 0.000 description 1
• 239000013543 active substance Substances 0.000 description 1
• 230000010933 acylation Effects 0.000 description 1
• 238000005917 acylation reaction Methods 0.000 description 1
• 239000000654 additive Substances 0.000 description 1
• 238000005377 adsorption chromatography Methods 0.000 description 1
• 230000002411 adverse Effects 0.000 description 1
• 239000000443 aerosol Substances 0.000 description 1
• 235000010443 alginic acid Nutrition 0.000 description 1
• 239000000783 alginic acid Substances 0.000 description 1
• 229920000615 alginic acid Polymers 0.000 description 1
• 229960001126 alginic acid Drugs 0.000 description 1
• 150000004781 alginic acids Chemical class 0.000 description 1
• HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
• 235000012211 aluminium silicate Nutrition 0.000 description 1
• SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 1
• 125000004103 aminoalkyl group Chemical group 0.000 description 1
• 229950003153 amsonate Drugs 0.000 description 1
• 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
• 238000010171 animal model Methods 0.000 description 1
• 125000000129 anionic group Chemical group 0.000 description 1
• 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
• 230000003527 anti-angiogenesis Effects 0.000 description 1
• 239000012062 aqueous buffer Substances 0.000 description 1
• 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
• 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
• 239000008122 artificial sweetener Substances 0.000 description 1
• 150000001543 aryl boronic acids Chemical class 0.000 description 1
• 239000000605 aspartame Substances 0.000 description 1
• 235000010357 aspartame Nutrition 0.000 description 1
• IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
• 229960003438 aspartame Drugs 0.000 description 1
• 239000012752 auxiliary agent Substances 0.000 description 1
• OISFUZRUIGGTSD-LJTMIZJLSA-N azane;(2r,3r,4r,5s)-6-(methylamino)hexane-1,2,3,4,5-pentol Chemical compound N.CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO OISFUZRUIGGTSD-LJTMIZJLSA-N 0.000 description 1
• 125000004069 aziridinyl group Chemical group 0.000 description 1
• HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 description 1
• 230000006399 behavior Effects 0.000 description 1
• 230000008901 benefit Effects 0.000 description 1
• 229960000686 benzalkonium chloride Drugs 0.000 description 1
• 229940077388 benzenesulfonate Drugs 0.000 description 1
• SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
• 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
• 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 description 1
• WARCRYXKINZHGQ-UHFFFAOYSA-N benzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1 WARCRYXKINZHGQ-UHFFFAOYSA-N 0.000 description 1
• 235000010233 benzoic acid Nutrition 0.000 description 1
• 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
• 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 description 1
• 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
• CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
• MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical compound C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 1
• 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 1
• 125000005340 bisphosphate group Chemical group 0.000 description 1
• 230000000903 blocking effect Effects 0.000 description 1
• 230000036765 blood level Effects 0.000 description 1
• 230000036770 blood supply Effects 0.000 description 1
• 206010006007 bone sarcoma Diseases 0.000 description 1
• IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 229910000019 calcium carbonate Inorganic materials 0.000 description 1
• 229910001424 calcium ion Inorganic materials 0.000 description 1
• 239000001506 calcium phosphate Substances 0.000 description 1
• CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
• 235000013539 calcium stearate Nutrition 0.000 description 1
• 239000008116 calcium stearate Substances 0.000 description 1
• 229940078456 calcium stearate Drugs 0.000 description 1
• MIOPJNTWMNEORI-UHFFFAOYSA-N camphorsulfonic acid Chemical compound C1CC2(CS(O)(=O)=O)C(=O)CC1C2(C)C MIOPJNTWMNEORI-UHFFFAOYSA-N 0.000 description 1
• 208000035269 cancer or benign tumor Diseases 0.000 description 1
• 230000003327 cancerostatic effect Effects 0.000 description 1
• 239000007894 caplet Substances 0.000 description 1
• 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 1
• 229940084030 carboxymethylcellulose calcium Drugs 0.000 description 1
• 210000000170 cell membrane Anatomy 0.000 description 1
• 230000004663 cell proliferation Effects 0.000 description 1
• 230000005754 cellular signaling Effects 0.000 description 1
• 210000003169 central nervous system Anatomy 0.000 description 1
• 239000012829 chemotherapy agent Substances 0.000 description 1
• 235000019693 cherries Nutrition 0.000 description 1
• FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
• 238000013375 chromatographic separation Methods 0.000 description 1
• 238000004587 chromatography analysis Methods 0.000 description 1
• 101150005988 cin2 gene Proteins 0.000 description 1
• 238000000576 coating method Methods 0.000 description 1
• 229940110456 cocoa butter Drugs 0.000 description 1
• 235000019868 cocoa butter Nutrition 0.000 description 1
• 239000003240 coconut oil Substances 0.000 description 1
• 235000019864 coconut oil Nutrition 0.000 description 1
• 239000008119 colloidal silica Substances 0.000 description 1
• 229940075614 colloidal silicon dioxide Drugs 0.000 description 1
• 239000000599 controlled substance Substances 0.000 description 1
• 230000001276 controlling effect Effects 0.000 description 1
• 235000005822 corn Nutrition 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• 208000035250 cutaneous malignant susceptibility to 1 melanoma Diseases 0.000 description 1
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
• 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
• 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
• ILLHQJIJCRNRCJ-UHFFFAOYSA-N dec-1-yne Chemical compound CCCCCCCCC#C ILLHQJIJCRNRCJ-UHFFFAOYSA-N 0.000 description 1
• YKNMBTZOEVIJCM-UHFFFAOYSA-N dec-2-ene Chemical compound CCCCCCCC=CC YKNMBTZOEVIJCM-UHFFFAOYSA-N 0.000 description 1
• RWDDSTHSVISBEA-UHFFFAOYSA-N dec-2-yne Chemical compound CCCCCCCC#CC RWDDSTHSVISBEA-UHFFFAOYSA-N 0.000 description 1
• JUWXVJKQNKKRLD-UHFFFAOYSA-N dec-3-yne Chemical compound CCCCCCC#CCC JUWXVJKQNKKRLD-UHFFFAOYSA-N 0.000 description 1
• KVUNBQMRRNMQIZ-UHFFFAOYSA-N dec-4-yne Chemical compound CCCCCC#CCCC KVUNBQMRRNMQIZ-UHFFFAOYSA-N 0.000 description 1
• UURSXESKOOOTOV-UHFFFAOYSA-N dec-5-ene Chemical compound CCCCC=CCCCC UURSXESKOOOTOV-UHFFFAOYSA-N 0.000 description 1
• JWBQJUFCNOLNNC-UHFFFAOYSA-N dec-5-yne Chemical compound CCCCC#CCCCC JWBQJUFCNOLNNC-UHFFFAOYSA-N 0.000 description 1
• 230000003247 decreasing effect Effects 0.000 description 1
• 238000010511 deprotection reaction Methods 0.000 description 1
• 235000019425 dextrin Nutrition 0.000 description 1
• 239000008121 dextrose Substances 0.000 description 1
• 150000001982 diacylglycerols Chemical class 0.000 description 1
• 125000005331 diazinyl group Chemical group N1=NC(=CC=C1)* 0.000 description 1
• NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 description 1
• 229940038472 dicalcium phosphate Drugs 0.000 description 1
• 229910000390 dicalcium phosphate Inorganic materials 0.000 description 1
• ACYGYJFTZSAZKR-UHFFFAOYSA-J dicalcium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Ca+2].[Ca+2].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O ACYGYJFTZSAZKR-UHFFFAOYSA-J 0.000 description 1
• 150000004683 dihydrates Chemical class 0.000 description 1
• 238000010790 dilution Methods 0.000 description 1
• 239000012895 dilution Substances 0.000 description 1
• FSBVERYRVPGNGG-UHFFFAOYSA-N dimagnesium dioxido-bis[[oxido(oxo)silyl]oxy]silane hydrate Chemical compound O.[Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O FSBVERYRVPGNGG-UHFFFAOYSA-N 0.000 description 1
• SPCNPOWOBZQWJK-UHFFFAOYSA-N dimethoxy-(2-propan-2-ylsulfanylethylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)SCCSC(C)C SPCNPOWOBZQWJK-UHFFFAOYSA-N 0.000 description 1
• 239000001177 diphosphate Substances 0.000 description 1
• XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
• 235000011180 diphosphates Nutrition 0.000 description 1
• LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 1
• 239000007884 disintegrant Substances 0.000 description 1
• BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
• 229910000397 disodium phosphate Inorganic materials 0.000 description 1
• 235000019800 disodium phosphate Nutrition 0.000 description 1
• 238000004090 dissolution Methods 0.000 description 1
• LOZWAPSEEHRYPG-UHFFFAOYSA-N dithiane Natural products C1CSCCS1 LOZWAPSEEHRYPG-UHFFFAOYSA-N 0.000 description 1
• POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
• MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
• 229940043264 dodecyl sulfate Drugs 0.000 description 1
• 238000009510 drug design Methods 0.000 description 1
• 238000009509 drug development Methods 0.000 description 1
• 229940126534 drug product Drugs 0.000 description 1
• 238000007908 dry granulation Methods 0.000 description 1
• 210000005069 ears Anatomy 0.000 description 1
• 229940009662 edetate Drugs 0.000 description 1
• 229960001484 edetic acid Drugs 0.000 description 1
• 238000000132 electrospray ionisation Methods 0.000 description 1
• 238000010828 elution Methods 0.000 description 1
• 229950005627 embonate Drugs 0.000 description 1
• 239000008387 emulsifying waxe Substances 0.000 description 1
• 238000005538 encapsulation Methods 0.000 description 1
• 239000007920 enema Substances 0.000 description 1
• 229940095399 enema Drugs 0.000 description 1
• 210000000981 epithelium Anatomy 0.000 description 1
• 229950000206 estolate Drugs 0.000 description 1
• CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 description 1
• 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 1
• GPEMEWBIHVXARA-UHFFFAOYSA-N ethyl 4-[6-[4-(ethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)NCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OCC)C2=N1 GPEMEWBIHVXARA-UHFFFAOYSA-N 0.000 description 1
• FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 1
• LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
• 229940093471 ethyl oleate Drugs 0.000 description 1
• 238000001704 evaporation Methods 0.000 description 1
• 230000008020 evaporation Effects 0.000 description 1
• 229960004979 fampridine Drugs 0.000 description 1
• 235000019197 fats Nutrition 0.000 description 1
• 239000000835 fiber Substances 0.000 description 1
• 239000000945 filler Substances 0.000 description 1
• 239000000706 filtrate Substances 0.000 description 1
• 238000003818 flash chromatography Methods 0.000 description 1
• 239000012530 fluid Substances 0.000 description 1
• 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
• 125000001153 fluoro group Chemical group F* 0.000 description 1
• NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
• 238000001640 fractional crystallisation Methods 0.000 description 1
• 238000005194 fractionation Methods 0.000 description 1
• 229960002737 fructose Drugs 0.000 description 1
• 229940050411 fumarate Drugs 0.000 description 1
• 230000006870 function Effects 0.000 description 1
• 125000003838 furazanyl group Chemical group 0.000 description 1
• 125000002541 furyl group Chemical group 0.000 description 1
• 239000007897 gelcap Substances 0.000 description 1
• 239000011521 glass Substances 0.000 description 1
• 229960001731 gluceptate Drugs 0.000 description 1
• KWMLJOLKUYYJFJ-VFUOTHLCSA-N glucoheptonic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O)C(O)=O KWMLJOLKUYYJFJ-VFUOTHLCSA-N 0.000 description 1
• 229940050410 gluconate Drugs 0.000 description 1
• 239000008103 glucose Substances 0.000 description 1
• 229930195712 glutamate Natural products 0.000 description 1
• 229940049906 glutamate Drugs 0.000 description 1
• 150000002334 glycols Chemical class 0.000 description 1
• 239000003102 growth factor Substances 0.000 description 1
• 150000008282 halocarbons Chemical class 0.000 description 1
• YVXHZKKCZYLQOP-UHFFFAOYSA-N hept-1-yne Chemical compound CCCCCC#C YVXHZKKCZYLQOP-UHFFFAOYSA-N 0.000 description 1
• AMSFEMSYKQQCHL-UHFFFAOYSA-N hept-2-yne Chemical compound CCCCC#CC AMSFEMSYKQQCHL-UHFFFAOYSA-N 0.000 description 1
• WZHKDGJSXCTSCK-UHFFFAOYSA-N hept-3-ene Chemical compound CCCC=CCC WZHKDGJSXCTSCK-UHFFFAOYSA-N 0.000 description 1
• KLYHSJRCIZOUHE-UHFFFAOYSA-N hept-3-yne Chemical compound CCCC#CCC KLYHSJRCIZOUHE-UHFFFAOYSA-N 0.000 description 1
• 101150008896 hetR gene Proteins 0.000 description 1
• IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
• 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 235000001050 hortel pimenta Nutrition 0.000 description 1
• XGIHQYAWBCFNPY-AZOCGYLKSA-N hydrabamine Chemical compound C([C@@H]12)CC3=CC(C(C)C)=CC=C3[C@@]2(C)CCC[C@@]1(C)CNCCNC[C@@]1(C)[C@@H]2CCC3=CC(C(C)C)=CC=C3[C@@]2(C)CCC1 XGIHQYAWBCFNPY-AZOCGYLKSA-N 0.000 description 1
• 150000003840 hydrochlorides Chemical class 0.000 description 1
• XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
• QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
• WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
• 239000005457 ice water Substances 0.000 description 1
• 125000002883 imidazolyl group Chemical group 0.000 description 1
• 239000012729 immediate-release (IR) formulation Substances 0.000 description 1
• 238000000099 in vitro assay Methods 0.000 description 1
• 238000001727 in vivo Methods 0.000 description 1
• 238000005462 in vivo assay Methods 0.000 description 1
• 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
• 230000001939 inductive effect Effects 0.000 description 1
• 208000015181 infectious disease Diseases 0.000 description 1
• 229910052500 inorganic mineral Inorganic materials 0.000 description 1
• 229960000367 inositol Drugs 0.000 description 1
• 210000004347 intestinal mucosa Anatomy 0.000 description 1
• 230000003834 intracellular effect Effects 0.000 description 1
• 230000031146 intracellular signal transduction Effects 0.000 description 1
• 238000007918 intramuscular administration Methods 0.000 description 1
• 238000007912 intraperitoneal administration Methods 0.000 description 1
• 238000007913 intrathecal administration Methods 0.000 description 1
• HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
• 239000003456 ion exchange resin Substances 0.000 description 1
• 229920003303 ion-exchange polymer Polymers 0.000 description 1
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
• KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
• 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
• 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
• 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 1
• 125000000842 isoxazolyl group Chemical group 0.000 description 1
• NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
• 229940043355 kinase inhibitor Drugs 0.000 description 1
• 238000009533 lab test Methods 0.000 description 1
• 229940001447 lactate Drugs 0.000 description 1
• 229940099584 lactobionate Drugs 0.000 description 1
• JYTUSYBCFIZPBE-AMTLMPIISA-N lactobionic acid Chemical compound OC(=O)[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O JYTUSYBCFIZPBE-AMTLMPIISA-N 0.000 description 1
• 229940070765 laurate Drugs 0.000 description 1
• 229960004194 lidocaine Drugs 0.000 description 1
• 238000001294 liquid chromatography-tandem mass spectrometry Methods 0.000 description 1
• 238000000622 liquid--liquid extraction Methods 0.000 description 1
• SXQCTESRRZBPHJ-UHFFFAOYSA-M lissamine rhodamine Chemical group [Na+].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=C(S([O-])(=O)=O)C=C1S([O-])(=O)=O SXQCTESRRZBPHJ-UHFFFAOYSA-M 0.000 description 1
• 239000003589 local anesthetic agent Substances 0.000 description 1
• 239000006210 lotion Substances 0.000 description 1
• 239000007937 lozenge Substances 0.000 description 1
• 230000001050 lubricating effect Effects 0.000 description 1
• 239000003580 lung surfactant Substances 0.000 description 1
• 239000008176 lyophilized powder Substances 0.000 description 1
• 239000003120 macrolide antibiotic agent Substances 0.000 description 1
• ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
• 239000001095 magnesium carbonate Substances 0.000 description 1
• 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
• 235000014380 magnesium carbonate Nutrition 0.000 description 1
• 239000000391 magnesium silicate Substances 0.000 description 1
• 229910052919 magnesium silicate Inorganic materials 0.000 description 1
• 235000019792 magnesium silicate Nutrition 0.000 description 1
• 229940049920 malate Drugs 0.000 description 1
• VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
• BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
• IWYDHOAUDWTVEP-UHFFFAOYSA-M mandelate Chemical compound [O-]C(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-M 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 238000004949 mass spectrometry Methods 0.000 description 1
• 239000011159 matrix material Substances 0.000 description 1
• 201000001441 melanoma Diseases 0.000 description 1
• QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-UHFFFAOYSA-N 0.000 description 1
• JDGXLFQOFXXWDD-UHFFFAOYSA-N methyl 4-[6-[4-(2-aminoethylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NCCN)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 JDGXLFQOFXXWDD-UHFFFAOYSA-N 0.000 description 1
• GHEPKBIXMUAVEZ-UHFFFAOYSA-N methyl 4-[6-[4-(ethoxycarbonylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1=CC(NC(=O)OCC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCN(CC3)C(=O)OC)C2=N1 GHEPKBIXMUAVEZ-UHFFFAOYSA-N 0.000 description 1
• ZWPWQGBCRAPVJN-UHFFFAOYSA-N methyl 4-[6-[4-[2-(dimethylamino)ethoxycarbonylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)OCCN(C)C)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 ZWPWQGBCRAPVJN-UHFFFAOYSA-N 0.000 description 1
• AEOBKUSSBOEXPK-UHFFFAOYSA-N methyl 4-[6-[4-[[2-(hydroxymethyl)phenyl]carbamoylamino]phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C(=CC=CC=4)CO)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 AEOBKUSSBOEXPK-UHFFFAOYSA-N 0.000 description 1
• 229940102396 methyl bromide Drugs 0.000 description 1
• 229920000609 methyl cellulose Polymers 0.000 description 1
• FCHXJPIEIHNGJM-UHFFFAOYSA-N methyl n-[4-[1-(1,4-dioxaspiro[4.5]decan-8-yl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC4(CC3)OCCO4)C2=N1 FCHXJPIEIHNGJM-UHFFFAOYSA-N 0.000 description 1
• PGBGLLBAOIBVRC-UHFFFAOYSA-N methyl n-[4-[1-(4-hydroxycyclohexyl)-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(O)CC3)C2=N1 PGBGLLBAOIBVRC-UHFFFAOYSA-N 0.000 description 1
• XHGGQKRROBXJKS-UHFFFAOYSA-N methyl n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(4-oxocyclohexyl)pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C3CCC(=O)CC3)C2=N1 XHGGQKRROBXJKS-UHFFFAOYSA-N 0.000 description 1
• SQJNNLMDYFXTSS-UHFFFAOYSA-N methyl n-[4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-propan-2-ylpyrazolo[3,4-d]pyrimidin-6-yl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OC)=CC=C1C1=NC(N2CC3CCC(O3)C2)=C(C=NN2C(C)C)C2=N1 SQJNNLMDYFXTSS-UHFFFAOYSA-N 0.000 description 1
• LRMHVVPPGGOAJQ-UHFFFAOYSA-N methyl nitrate Chemical compound CO[N+]([O-])=O LRMHVVPPGGOAJQ-UHFFFAOYSA-N 0.000 description 1
• OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
• JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
• 239000001923 methylcellulose Substances 0.000 description 1
• 235000010981 methylcellulose Nutrition 0.000 description 1
• 244000005700 microbiome Species 0.000 description 1
• 239000003094 microcapsule Substances 0.000 description 1
• 239000008108 microcrystalline cellulose Substances 0.000 description 1
• 229940016286 microcrystalline cellulose Drugs 0.000 description 1
• 230000003228 microsomal effect Effects 0.000 description 1
• 239000004005 microsphere Substances 0.000 description 1
• 235000010755 mineral Nutrition 0.000 description 1
• 239000011707 mineral Substances 0.000 description 1
• 239000002480 mineral oil Substances 0.000 description 1
• 235000010446 mineral oil Nutrition 0.000 description 1
• 150000004682 monohydrates Chemical class 0.000 description 1
• HDZGCSFEDULWCS-UHFFFAOYSA-N monomethylhydrazine Chemical compound CNN HDZGCSFEDULWCS-UHFFFAOYSA-N 0.000 description 1
• 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
• 235000019796 monopotassium phosphate Nutrition 0.000 description 1
• 210000004400 mucous membrane Anatomy 0.000 description 1
• 230000035772 mutation Effects 0.000 description 1
• PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
• SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
• 239000006199 nebulizer Substances 0.000 description 1
• 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
• 230000001537 neural effect Effects 0.000 description 1
• OSSQSXOTMIGBCF-UHFFFAOYSA-N non-1-yne Chemical compound CCCCCCCC#C OSSQSXOTMIGBCF-UHFFFAOYSA-N 0.000 description 1
• LXKRETAGISZJAD-UHFFFAOYSA-N non-2-yne Chemical compound CCCCCCC#CC LXKRETAGISZJAD-UHFFFAOYSA-N 0.000 description 1
• YCBSHDKATAPNIA-UHFFFAOYSA-N non-3-ene Chemical compound CCCCCC=CCC YCBSHDKATAPNIA-UHFFFAOYSA-N 0.000 description 1
• SRRDSRCWRHKEKU-UHFFFAOYSA-N non-3-yne Chemical compound CCCCCC#CCC SRRDSRCWRHKEKU-UHFFFAOYSA-N 0.000 description 1
• KPADFPAILITQBG-UHFFFAOYSA-N non-4-ene Chemical compound CCCCC=CCCC KPADFPAILITQBG-UHFFFAOYSA-N 0.000 description 1
• RAYTXPDVKZFUEI-UHFFFAOYSA-N non-4-yne Chemical compound CCCCC#CCCC RAYTXPDVKZFUEI-UHFFFAOYSA-N 0.000 description 1
• 231100000252 nontoxic Toxicity 0.000 description 1
• 230000003000 nontoxic effect Effects 0.000 description 1
• 235000015097 nutrients Nutrition 0.000 description 1
• UMIPWJGWASORKV-UHFFFAOYSA-N oct-1-yne Chemical compound CCCCCCC#C UMIPWJGWASORKV-UHFFFAOYSA-N 0.000 description 1
• QCQALVMFTWRCFI-UHFFFAOYSA-N oct-2-yne Chemical compound CCCCCC#CC QCQALVMFTWRCFI-UHFFFAOYSA-N 0.000 description 1
• UDEISTCPVNLKRJ-UHFFFAOYSA-N oct-3-yne Chemical compound CCCCC#CCC UDEISTCPVNLKRJ-UHFFFAOYSA-N 0.000 description 1
• IRUCBBFNLDIMIK-UHFFFAOYSA-N oct-4-ene Chemical compound CCCC=CCCC IRUCBBFNLDIMIK-UHFFFAOYSA-N 0.000 description 1
• GZTNBKQTTZSQNS-UHFFFAOYSA-N oct-4-yne Chemical compound CCCC#CCCC GZTNBKQTTZSQNS-UHFFFAOYSA-N 0.000 description 1
• OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
• ZHVULPDNOFUIML-UHFFFAOYSA-N octane;hydrochloride Chemical compound Cl.CCCCCCCC ZHVULPDNOFUIML-UHFFFAOYSA-N 0.000 description 1
• 229940049964 oleate Drugs 0.000 description 1
• ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
• 210000000056 organ Anatomy 0.000 description 1
• 239000012074 organic phase Substances 0.000 description 1
• 239000003960 organic solvent Substances 0.000 description 1
• 229940000673 orphan drug Drugs 0.000 description 1
• 239000002859 orphan drug Substances 0.000 description 1
• 230000003204 osmotic effect Effects 0.000 description 1
• 125000002971 oxazolyl group Chemical group 0.000 description 1
• KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 1
• 230000003647 oxidation Effects 0.000 description 1
• 238000007254 oxidation reaction Methods 0.000 description 1
• 125000000466 oxiranyl group Chemical group 0.000 description 1
• 239000006179 pH buffering agent Substances 0.000 description 1
• 229940014662 pantothenate Drugs 0.000 description 1
• 235000019161 pantothenic acid Nutrition 0.000 description 1
• 239000011713 pantothenic acid Substances 0.000 description 1
• 239000002245 particle Substances 0.000 description 1
• 239000006072 paste Substances 0.000 description 1
• 239000000312 peanut oil Substances 0.000 description 1
• 239000008188 pellet Substances 0.000 description 1
• RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
• 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
• 230000010412 perfusion Effects 0.000 description 1
• 210000000578 peripheral nerve Anatomy 0.000 description 1
• 239000000825 pharmaceutical preparation Substances 0.000 description 1
• NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
• 239000010452 phosphate Substances 0.000 description 1
• RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
• 150000003904 phospholipids Chemical class 0.000 description 1
• 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
• 239000003757 phosphotransferase inhibitor Substances 0.000 description 1
• 230000004962 physiological condition Effects 0.000 description 1
• 229940075930 picrate Drugs 0.000 description 1
• OXNIZHLAWKMVMX-UHFFFAOYSA-M picrate anion Chemical compound [O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-M 0.000 description 1
• 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 description 1
• 150000003057 platinum Chemical class 0.000 description 1
• 229920001993 poloxamer 188 Polymers 0.000 description 1
• 229940044519 poloxamer 188 Drugs 0.000 description 1
• 229920001223 polyethylene glycol Polymers 0.000 description 1
• 229920000642 polymer Polymers 0.000 description 1
• GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
• 239000008057 potassium phosphate buffer Substances 0.000 description 1
• 230000003389 potentiating effect Effects 0.000 description 1
• 235000019814 powdered cellulose Nutrition 0.000 description 1
• 229920003124 powdered cellulose Polymers 0.000 description 1
• 238000011533 pre-incubation Methods 0.000 description 1
• 239000002243 precursor Substances 0.000 description 1
• 238000002953 preparative HPLC Methods 0.000 description 1
• WLYMHDJDXWEETI-UHFFFAOYSA-N propan-2-yl 4-[4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-6-[4-(phenylcarbamoylamino)phenyl]pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC=4C=CC=CC=4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 WLYMHDJDXWEETI-UHFFFAOYSA-N 0.000 description 1
• VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 1
• 239000003380 propellant Substances 0.000 description 1
• 125000006410 propenylene group Chemical group 0.000 description 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
• 108090000623 proteins and genes Proteins 0.000 description 1
• 102000004169 proteins and genes Human genes 0.000 description 1
• 230000002685 pulmonary effect Effects 0.000 description 1
• 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
• 125000003226 pyrazolyl group Chemical group 0.000 description 1
• 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
• 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
• ZAHRKKWIAAJSAO-UHFFFAOYSA-N rapamycin Natural products COCC(O)C(=C/C(C)C(=O)CC(OC(=O)C1CCCCN1C(=O)C(=O)C2(O)OC(CC(OC)C(=CC=CC=CC(C)CC(C)C(=O)C)C)CCC2C)C(C)CC3CCC(O)C(C3)OC)C ZAHRKKWIAAJSAO-UHFFFAOYSA-N 0.000 description 1
• 238000006268 reductive amination reaction Methods 0.000 description 1
• 230000027425 release of sequestered calcium ion into cytosol Effects 0.000 description 1
• 230000001850 reproductive effect Effects 0.000 description 1
• 238000011160 research Methods 0.000 description 1
• 230000002441 reversible effect Effects 0.000 description 1
• 201000009410 rhabdomyosarcoma Diseases 0.000 description 1
• 235000009566 rice Nutrition 0.000 description 1
• 238000007363 ring formation reaction Methods 0.000 description 1
• 102220223285 rs1060502353 Human genes 0.000 description 1
• CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
• 235000019204 saccharin Nutrition 0.000 description 1
• 229940081974 saccharin Drugs 0.000 description 1
• 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
• YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
• 229960001860 salicylate Drugs 0.000 description 1
• 239000012047 saturated solution Substances 0.000 description 1
• CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 238000000926 separation method Methods 0.000 description 1
• 239000008159 sesame oil Substances 0.000 description 1
• 235000011803 sesame oil Nutrition 0.000 description 1
• 102000034285 signal transducing proteins Human genes 0.000 description 1
• 108091006024 signal transducing proteins Proteins 0.000 description 1
• 230000011664 signaling Effects 0.000 description 1
• 150000004760 silicates Chemical class 0.000 description 1
• QFJCIRLUMZQUOT-HPLJOQBZSA-N sirolimus Chemical compound C1C[C@@H](O)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 QFJCIRLUMZQUOT-HPLJOQBZSA-N 0.000 description 1
• 235000020183 skimmed milk Nutrition 0.000 description 1
• 239000002002 slurry Substances 0.000 description 1
• 229910000029 sodium carbonate Inorganic materials 0.000 description 1
• 235000017550 sodium carbonate Nutrition 0.000 description 1
• 239000001509 sodium citrate Substances 0.000 description 1
• NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
• 235000011083 sodium citrates Nutrition 0.000 description 1
• 229940083575 sodium dodecyl sulfate Drugs 0.000 description 1
• RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
• 159000000000 sodium salts Chemical class 0.000 description 1
• MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 1
• ILJOYZVVZZFIKA-UHFFFAOYSA-M sodium;1,1-dioxo-1,2-benzothiazol-3-olate;hydrate Chemical compound O.[Na+].C1=CC=C2C(=O)[N-]S(=O)(=O)C2=C1 ILJOYZVVZZFIKA-UHFFFAOYSA-M 0.000 description 1
• 210000004872 soft tissue Anatomy 0.000 description 1
• 238000000638 solvent extraction Methods 0.000 description 1
• 239000000600 sorbitol Substances 0.000 description 1
• 239000003549 soybean oil Substances 0.000 description 1
• 235000012424 soybean oil Nutrition 0.000 description 1
• 239000007921 spray Substances 0.000 description 1
• 230000000087 stabilizing effect Effects 0.000 description 1
• 239000007858 starting material Substances 0.000 description 1
• 239000008117 stearic acid Substances 0.000 description 1
• 239000008227 sterile water for injection Substances 0.000 description 1
• 238000003860 storage Methods 0.000 description 1
• 238000007920 subcutaneous administration Methods 0.000 description 1
• KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
• 150000005846 sugar alcohols Polymers 0.000 description 1
• 239000002511 suppository base Substances 0.000 description 1
• 239000004094 surface-active agent Substances 0.000 description 1
• 230000002459 sustained effect Effects 0.000 description 1
• 230000002195 synergetic effect Effects 0.000 description 1
• 239000007916 tablet composition Substances 0.000 description 1
• 229940095064 tartrate Drugs 0.000 description 1
• 229960004964 temozolomide Drugs 0.000 description 1
• QFJCIRLUMZQUOT-UHFFFAOYSA-N temsirolimus Natural products C1CC(O)C(OC)CC1CC(C)C1OC(=O)C2CCCCN2C(=O)C(=O)C(O)(O2)C(C)CCC2CC(OC)C(C)=CC=CC=CC(C)CC(C)C(=O)C(OC)C(O)C(C)=CC(C)C(=O)C1 QFJCIRLUMZQUOT-UHFFFAOYSA-N 0.000 description 1
• 229950002757 teoclate Drugs 0.000 description 1
• SWCSYMBZMXHFMG-UHFFFAOYSA-N tert-butyl 4-[6-[4-(cyclopropylcarbamoylamino)phenyl]-4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)pyrazolo[3,4-d]pyrimidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1N1C2=NC(C=3C=CC(NC(=O)NC4CC4)=CC=3)=NC(N3CC4CCC(O4)C3)=C2C=N1 SWCSYMBZMXHFMG-UHFFFAOYSA-N 0.000 description 1
• DKACXUFSLUYRFU-UHFFFAOYSA-N tert-butyl n-aminocarbamate Chemical compound CC(C)(C)OC(=O)NN DKACXUFSLUYRFU-UHFFFAOYSA-N 0.000 description 1
• 150000004685 tetrahydrates Chemical class 0.000 description 1
• 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
• 150000003527 tetrahydropyrans Chemical group 0.000 description 1
• 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
• 125000005247 tetrazinyl group Chemical group N1=NN=NC(=C1)* 0.000 description 1
• 125000003831 tetrazolyl group Chemical group 0.000 description 1
• 125000004305 thiazinyl group Chemical group S1NC(=CC=C1)* 0.000 description 1
• 125000000335 thiazolyl group Chemical group 0.000 description 1
• 230000008719 thickening Effects 0.000 description 1
• 125000001544 thienyl group Chemical group 0.000 description 1
• 238000011269 treatment regimen Methods 0.000 description 1
• 150000003626 triacylglycerols Chemical class 0.000 description 1
• 125000004306 triazinyl group Chemical group 0.000 description 1
• 125000001425 triazolyl group Chemical group 0.000 description 1
• 150000004684 trihydrates Chemical class 0.000 description 1
• 239000001226 triphosphate Substances 0.000 description 1
• 235000011178 triphosphate Nutrition 0.000 description 1
• UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
• LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
• 238000001665 trituration Methods 0.000 description 1
• 210000004881 tumor cell Anatomy 0.000 description 1
• 125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
• 238000011144 upstream manufacturing Methods 0.000 description 1
• 238000005292 vacuum distillation Methods 0.000 description 1
• NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical class CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
• 235000013311 vegetables Nutrition 0.000 description 1
• 239000003981 vehicle Substances 0.000 description 1
• 238000005406 washing Methods 0.000 description 1
• 238000005550 wet granulation Methods 0.000 description 1
• 238000009736 wetting Methods 0.000 description 1
• 239000000080 wetting agent Substances 0.000 description 1
• 239000009637 wintergreen oil Substances 0.000 description 1
• 239000000230 xanthan gum Substances 0.000 description 1
• 235000010493 xanthan gum Nutrition 0.000 description 1
• 229920001285 xanthan gum Polymers 0.000 description 1
• 229940082509 xanthan gum Drugs 0.000 description 1
• 238000012447 xenograft mouse model Methods 0.000 description 1