CN102762208A - 作为ck2抑制剂的吡唑嘧啶和相关杂环 - Google Patents
作为ck2抑制剂的吡唑嘧啶和相关杂环 Download PDFInfo
- Publication number
- CN102762208A CN102762208A CN2010800630542A CN201080063054A CN102762208A CN 102762208 A CN102762208 A CN 102762208A CN 2010800630542 A CN2010800630542 A CN 2010800630542A CN 201080063054 A CN201080063054 A CN 201080063054A CN 102762208 A CN102762208 A CN 102762208A
- Authority
- CN
- China
- Prior art keywords
- optionally substituted
- compound
- alkyl
- compounds
- heterocyclyl
- Prior art date
- 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.)
- Pending
Links
- 0 CC*C(C(C(*)=**1C(*(C)*)=C)=C1*=C(CCC=C)N)=C(*C(*1C)=*)C1=O Chemical compound CC*C(C(C(*)=**1C(*(C)*)=C)=C1*=C(CCC=C)N)=C(*C(*1C)=*)C1=O 0.000 description 21
- DNKCWCSIJWZWCD-UHFFFAOYSA-N Nc1nc2c(C=O)cn[n]2c(NC2CC2)c1 Chemical compound Nc1nc2c(C=O)cn[n]2c(NC2CC2)c1 DNKCWCSIJWZWCD-UHFFFAOYSA-N 0.000 description 3
- ZBIARYMSEFBDPZ-PXNMLYILSA-N O=C(/C(/N1)=C/c(cn[n]2c(NC3CCNCC3)c3)c2nc3Nc2cccc(Cl)c2)NC1=O Chemical compound O=C(/C(/N1)=C/c(cn[n]2c(NC3CCNCC3)c3)c2nc3Nc2cccc(Cl)c2)NC1=O ZBIARYMSEFBDPZ-PXNMLYILSA-N 0.000 description 3
- VICKFLHKIOKFBP-UHFFFAOYSA-N CC(C)(C)OC(N(C1CC1)c1cc(Cl)nc2c(C=O)cn[n]12)=O Chemical compound CC(C)(C)OC(N(C1CC1)c1cc(Cl)nc2c(C=O)cn[n]12)=O VICKFLHKIOKFBP-UHFFFAOYSA-N 0.000 description 2
- IDMQTYIRKCOHHQ-NVMNQCDNSA-N O=C(/C(/N1)=C/c(cn[n]2c(S(Cc3ccccc3)=O)c3)c2nc3Nc2cccc(Cl)c2)NC1=O Chemical compound O=C(/C(/N1)=C/c(cn[n]2c(S(Cc3ccccc3)=O)c3)c2nc3Nc2cccc(Cl)c2)NC1=O IDMQTYIRKCOHHQ-NVMNQCDNSA-N 0.000 description 2
- CTYLPKJAZADEPP-ODLFYWEKSA-N CC(C)(C)C(N(CC1)CCC1Nc1cc(Nc2cccc(Cl)c2)nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]12)=O Chemical compound CC(C)(C)C(N(CC1)CCC1Nc1cc(Nc2cccc(Cl)c2)nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]12)=O CTYLPKJAZADEPP-ODLFYWEKSA-N 0.000 description 1
- WTOQHJPXRRZFPB-UHFFFAOYSA-N CC(C)(C)OC(N(C1CC1)c1cc(Cl)nc2c(C=N)cn[n]12)=O Chemical compound CC(C)(C)OC(N(C1CC1)c1cc(Cl)nc2c(C=N)cn[n]12)=O WTOQHJPXRRZFPB-UHFFFAOYSA-N 0.000 description 1
- YRIQYYJBLVENTH-UHFFFAOYSA-N CC(C)(C)OC(c1cccc(Nc2cc(Cl)nc3ccn[n]23)c1)=O Chemical compound CC(C)(C)OC(c1cccc(Nc2cc(Cl)nc3ccn[n]23)c1)=O YRIQYYJBLVENTH-UHFFFAOYSA-N 0.000 description 1
- DKWPWGZYBJQPPB-UHFFFAOYSA-N CC(C)(C)OC(c1cccc(Nc2cc(Nc3cc(Cl)ccc3)nc3ccn[n]23)c1)=O Chemical compound CC(C)(C)OC(c1cccc(Nc2cc(Nc3cc(Cl)ccc3)nc3ccn[n]23)c1)=O DKWPWGZYBJQPPB-UHFFFAOYSA-N 0.000 description 1
- NLZSZFAAMRITOP-UHFFFAOYSA-N CC(CNc1cc(Nc2cc(Cl)ccc2F)nc2c(C=O)cn[n]12)N1CCOCC1 Chemical compound CC(CNc1cc(Nc2cc(Cl)ccc2F)nc2c(C=O)cn[n]12)N1CCOCC1 NLZSZFAAMRITOP-UHFFFAOYSA-N 0.000 description 1
- CUJJCLBPCZZSNT-UHFFFAOYSA-N CC(CNc1cc(Nc2cc(Cl)ccc2F)nc2ccn[n]12)N1CCOCC1 Chemical compound CC(CNc1cc(Nc2cc(Cl)ccc2F)nc2ccn[n]12)N1CCOCC1 CUJJCLBPCZZSNT-UHFFFAOYSA-N 0.000 description 1
- YNPGQPNTJAFVMY-UHFFFAOYSA-N CCC(C)(C)OC(c1cccc(Nc2cc(Nc3cccc(Cl)c3)nc3c(CC(C(N4)=O)NC4=O)cn[n]23)c1)=O Chemical compound CCC(C)(C)OC(c1cccc(Nc2cc(Nc3cccc(Cl)c3)nc3c(CC(C(N4)=O)NC4=O)cn[n]23)c1)=O YNPGQPNTJAFVMY-UHFFFAOYSA-N 0.000 description 1
- YBHGPBZYGJHEJI-UHFFFAOYSA-N CCCCNc1cc(Nc(cc2)ccc2-[n]2nccc2)nc2c(C=O)c(C)n[n]12 Chemical compound CCCCNc1cc(Nc(cc2)ccc2-[n]2nccc2)nc2c(C=O)c(C)n[n]12 YBHGPBZYGJHEJI-UHFFFAOYSA-N 0.000 description 1
- FYVUMRWLVSWAKZ-PXNMLYILSA-N CN(C(/C(/N1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3Nc(cc2)ccc2C#N)=O)C1=O Chemical compound CN(C(/C(/N1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3Nc(cc2)ccc2C#N)=O)C1=O FYVUMRWLVSWAKZ-PXNMLYILSA-N 0.000 description 1
- MZQQHYDUINOMDG-UHFFFAOYSA-N CN(C(CN1)=O)C1=O Chemical compound CN(C(CN1)=O)C1=O MZQQHYDUINOMDG-UHFFFAOYSA-N 0.000 description 1
- KUWKEKARVSYKEP-ZDLGFXPLSA-N CN(C)CCCOc(c(Cl)c1)ccc1Nc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)c1 Chemical compound CN(C)CCCOc(c(Cl)c1)ccc1Nc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)c1 KUWKEKARVSYKEP-ZDLGFXPLSA-N 0.000 description 1
- PMSNUDCDNMXHIH-LSCVHKIXSA-N CNC1CN(Cc2ccc(-c3nc4c(/C=C(/C(N5)=O)\NC5=O)cn[n]4c(NC4CC4)c3)[s]2)CC1 Chemical compound CNC1CN(Cc2ccc(-c3nc4c(/C=C(/C(N5)=O)\NC5=O)cn[n]4c(NC4CC4)c3)[s]2)CC1 PMSNUDCDNMXHIH-LSCVHKIXSA-N 0.000 description 1
- MHGYXMSVSFEOPY-WTKPLQERSA-N COC(Nc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)c1)=O Chemical compound COC(Nc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)c1)=O MHGYXMSVSFEOPY-WTKPLQERSA-N 0.000 description 1
- LZSYIMUFBKNGJK-UHFFFAOYSA-N COC(Nc1nc2c(C=C)cn[n]2c(NC2CC2)c1)=O Chemical compound COC(Nc1nc2c(C=C)cn[n]2c(NC2CC2)c1)=O LZSYIMUFBKNGJK-UHFFFAOYSA-N 0.000 description 1
- SOVFPGABDVIXHQ-YWEYNIOJSA-N CS(c1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)n1)=O Chemical compound CS(c1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)n1)=O SOVFPGABDVIXHQ-YWEYNIOJSA-N 0.000 description 1
- DOBWRWWGRZTEHG-UHFFFAOYSA-N CSC(N1)=Nc2ccn[n]2C1=O Chemical compound CSC(N1)=Nc2ccn[n]2C1=O DOBWRWWGRZTEHG-UHFFFAOYSA-N 0.000 description 1
- YYYJAQABQGZRDC-YWEYNIOJSA-N CSc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)n1 Chemical compound CSc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)n1 YYYJAQABQGZRDC-YWEYNIOJSA-N 0.000 description 1
- CHTBQYPYDLREEG-UHFFFAOYSA-N CSc1nc2c(C=O)cn[n]2c(NC2CC2)n1 Chemical compound CSc1nc2c(C=O)cn[n]2c(NC2CC2)n1 CHTBQYPYDLREEG-UHFFFAOYSA-N 0.000 description 1
- PDFYLKPBYWPEDQ-UHFFFAOYSA-N CSc1nc2ccn[n]2c(Cl)n1 Chemical compound CSc1nc2ccn[n]2c(Cl)n1 PDFYLKPBYWPEDQ-UHFFFAOYSA-N 0.000 description 1
- BPBMPOTUWJXBFC-UHFFFAOYSA-N Clc1cccc(Nc2nc3ccn[n]3c(SCc3ccccc3)c2)c1 Chemical compound Clc1cccc(Nc2nc3ccn[n]3c(SCc3ccccc3)c2)c1 BPBMPOTUWJXBFC-UHFFFAOYSA-N 0.000 description 1
- ZGKQPERSCWXCEE-UHFFFAOYSA-N Clc1nc2ccn[n]2c(SCc2ccccc2)c1 Chemical compound Clc1nc2ccn[n]2c(SCc2ccccc2)c1 ZGKQPERSCWXCEE-UHFFFAOYSA-N 0.000 description 1
- QVUSNIRLKPWERW-UHFFFAOYSA-N N#Cc(cc1)ccc1Nc1nc2c(C=O)cn[n]2c(NC2CC2)c1 Chemical compound N#Cc(cc1)ccc1Nc1nc2c(C=O)cn[n]2c(NC2CC2)c1 QVUSNIRLKPWERW-UHFFFAOYSA-N 0.000 description 1
- YCUXOAQEJMTBOY-UHFFFAOYSA-N N#Cc1cc(-c2nc3c(C=O)cn[n]3c(NC3CC3)c2)ccc1 Chemical compound N#Cc1cc(-c2nc3c(C=O)cn[n]3c(NC3CC3)c2)ccc1 YCUXOAQEJMTBOY-UHFFFAOYSA-N 0.000 description 1
- ZDDJUFMUPQETHV-APSNUPSMSA-N N#Cc1cccc(-c2nc3c(/C=C(/C(N4)=O)\NC4=O)cn[n]3c(NC3CC3)c2)c1 Chemical compound N#Cc1cccc(-c2nc3c(/C=C(/C(N4)=O)\NC4=O)cn[n]3c(NC3CC3)c2)c1 ZDDJUFMUPQETHV-APSNUPSMSA-N 0.000 description 1
- BHRWKKAURRAIEP-WZUFQYTHSA-N NC(c1ccc(-c2nc3c(/C=C(/C(N4)=O)\NC4=O)cn[n]3c(NC3CC3)c2)[s]1)=O Chemical compound NC(c1ccc(-c2nc3c(/C=C(/C(N4)=O)\NC4=O)cn[n]3c(NC3CC3)c2)[s]1)=O BHRWKKAURRAIEP-WZUFQYTHSA-N 0.000 description 1
- IYIWNHKDTDVOPK-UHFFFAOYSA-N NC(c1ccc(-c2nc3c(C=O)cn[n]3c(NC3CC3)c2)[s]1)=O Chemical compound NC(c1ccc(-c2nc3c(C=O)cn[n]3c(NC3CC3)c2)[s]1)=O IYIWNHKDTDVOPK-UHFFFAOYSA-N 0.000 description 1
- YFTFNILDLUMMRL-MFOYZWKCSA-N O=C(/C(/N1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3-c2ccc(CN3CCNCC3)[s]2)NC1=O Chemical compound O=C(/C(/N1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3-c2ccc(CN3CCNCC3)[s]2)NC1=O YFTFNILDLUMMRL-MFOYZWKCSA-N 0.000 description 1
- OYOCDZLFPKERPX-MFOYZWKCSA-N O=C(/C(/N1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3-c2ccc(CN3CCOCC3)[s]2)NC1=O Chemical compound O=C(/C(/N1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3-c2ccc(CN3CCOCC3)[s]2)NC1=O OYOCDZLFPKERPX-MFOYZWKCSA-N 0.000 description 1
- WYQRMIAXGHCXIP-CGYDICSFSA-N O=C(/C(/N1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3N(CC2)C[C@@H]2F)NC1=O Chemical compound O=C(/C(/N1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3N(CC2)C[C@@H]2F)NC1=O WYQRMIAXGHCXIP-CGYDICSFSA-N 0.000 description 1
- RPCMXNFXSNSLCR-MLPAPPSSSA-N O=C(/C(/N1)=C/c(cn[n]2c(NC3CC3)n3)c2nc3Oc2cccc(Cl)c2)NC1=O Chemical compound O=C(/C(/N1)=C/c(cn[n]2c(NC3CC3)n3)c2nc3Oc2cccc(Cl)c2)NC1=O RPCMXNFXSNSLCR-MLPAPPSSSA-N 0.000 description 1
- OWPDNCRGIFXISG-UUASQNMZSA-N O=C(/C(/N1)=C/c(cn[n]2c(NC3CNCC3)c3)c2nc3Nc2cccc(Cl)c2)NC1=O Chemical compound O=C(/C(/N1)=C/c(cn[n]2c(NC3CNCC3)c3)c2nc3Nc2cccc(Cl)c2)NC1=O OWPDNCRGIFXISG-UUASQNMZSA-N 0.000 description 1
- QLFHLWNGLSVQLL-MLPAPPSSSA-N O=C(/C(/N1)=C/c(cn[n]2c(Nc3n[nH]cc3)c3)c2nc3Nc2cccc(Cl)c2)NC1=O Chemical compound O=C(/C(/N1)=C/c(cn[n]2c(Nc3n[nH]cc3)c3)c2nc3Nc2cccc(Cl)c2)NC1=O QLFHLWNGLSVQLL-MLPAPPSSSA-N 0.000 description 1
- GOCSFUSQHIBANS-WZUFQYTHSA-N O=C(/C(/N1)=C/c2c3nc(NCC4CC4)nc(NC4CC4)[n]3nc2)NC1=O Chemical compound O=C(/C(/N1)=C/c2c3nc(NCC4CC4)nc(NC4CC4)[n]3nc2)NC1=O GOCSFUSQHIBANS-WZUFQYTHSA-N 0.000 description 1
- XAOCMDKIMLJEMO-ODLFYWEKSA-N O=C(/C(/N1)=C/c2cnc3[n]2cc(-c2cc(CN4CCOCC4)ccc2)nc3NC2CC2)NC1=O Chemical compound O=C(/C(/N1)=C/c2cnc3[n]2cc(-c2cc(CN4CCOCC4)ccc2)nc3NC2CC2)NC1=O XAOCMDKIMLJEMO-ODLFYWEKSA-N 0.000 description 1
- QLUQVWUYSTXMKN-AUWJEWJLSA-N O=C(/C(/N1)=C/c2cnc3[n]2cc(-c2cc(OC(F)(F)F)ccc2)nc3NC2CC2)NC1=O Chemical compound O=C(/C(/N1)=C/c2cnc3[n]2cc(-c2cc(OC(F)(F)F)ccc2)nc3NC2CC2)NC1=O QLUQVWUYSTXMKN-AUWJEWJLSA-N 0.000 description 1
- BTRQSBOYOIKTSH-ACAGNQJTSA-N O=C(/C(/S1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3-c2cc(F)ncc2)NC1=S Chemical compound O=C(/C(/S1)=C/c(cn[n]2c(NC3CC3)c3)c2nc3-c2cc(F)ncc2)NC1=S BTRQSBOYOIKTSH-ACAGNQJTSA-N 0.000 description 1
- UBYVOQDIVWWYHS-WZUFQYTHSA-N O=C(C1CC1)Nc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)c1 Chemical compound O=C(C1CC1)Nc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)c1 UBYVOQDIVWWYHS-WZUFQYTHSA-N 0.000 description 1
- WRGFDQAWYGKLPG-UHFFFAOYSA-N O=Cc(cn[n]1c(NC2CC2)c2)c1nc2-c1cc(F)ncc1 Chemical compound O=Cc(cn[n]1c(NC2CC2)c2)c1nc2-c1cc(F)ncc1 WRGFDQAWYGKLPG-UHFFFAOYSA-N 0.000 description 1
- YSOZCUCGNNFPOR-UHFFFAOYSA-N O=Cc(cn[n]1c(NC2CC2)c2)c1nc2Cl Chemical compound O=Cc(cn[n]1c(NC2CC2)c2)c1nc2Cl YSOZCUCGNNFPOR-UHFFFAOYSA-N 0.000 description 1
- PEWIEYBFORJOLN-QPEQYQDCSA-N OC(C(CC1)CC=C1Nc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)n1)=O Chemical compound OC(C(CC1)CC=C1Nc1nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]2c(NC2CC2)n1)=O PEWIEYBFORJOLN-QPEQYQDCSA-N 0.000 description 1
- WYQDQFWVPFBFQQ-IUXPMGMMSA-N OC(c1cccc(Nc2cc(Nc3cccc(Cl)c3)nc3c(/C=C(/C(N4)=O)\NC4=O)cn[n]23)c1)=O Chemical compound OC(c1cccc(Nc2cc(Nc3cccc(Cl)c3)nc3c(/C=C(/C(N4)=O)\NC4=O)cn[n]23)c1)=O WYQDQFWVPFBFQQ-IUXPMGMMSA-N 0.000 description 1
- HPPUSHYQBOAMHB-ZDLGFXPLSA-N OCCN(CC1)CCC1Nc1cc(Nc2cccc(Cl)c2)nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]12 Chemical compound OCCN(CC1)CCC1Nc1cc(Nc2cccc(Cl)c2)nc2c(/C=C(/C(N3)=O)\NC3=O)cn[n]12 HPPUSHYQBOAMHB-ZDLGFXPLSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Communicable Diseases (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26680109P | 2009-12-04 | 2009-12-04 | |
| US61/266,801 | 2009-12-04 | ||
| US35416510P | 2010-06-11 | 2010-06-11 | |
| US61/354,165 | 2010-06-11 | ||
| PCT/US2010/056712 WO2011068667A1 (en) | 2009-12-04 | 2010-11-15 | Pyrazolopyrimidines and related heterocycles as ck2 inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102762208A true CN102762208A (zh) | 2012-10-31 |
Family
ID=44115232
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2010800630542A Pending CN102762208A (zh) | 2009-12-04 | 2010-11-15 | 作为ck2抑制剂的吡唑嘧啶和相关杂环 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US8575177B2 (enExample) |
| EP (1) | EP2509602B9 (enExample) |
| JP (1) | JP5802676B2 (enExample) |
| KR (1) | KR101851130B1 (enExample) |
| CN (1) | CN102762208A (enExample) |
| AU (1) | AU2010326268B2 (enExample) |
| BR (1) | BR112012013508A2 (enExample) |
| CA (1) | CA2782684C (enExample) |
| ES (1) | ES2629170T3 (enExample) |
| IL (1) | IL220086B (enExample) |
| PL (1) | PL2509602T3 (enExample) |
| RU (1) | RU2607453C2 (enExample) |
| SG (1) | SG181507A1 (enExample) |
| WO (1) | WO2011068667A1 (enExample) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103360399A (zh) * | 2013-08-02 | 2013-10-23 | 北京大学 | 6-芳基取代-咪唑-[1,2-b]哒嗪类衍生物,其制备方法及用途 |
| CN104844605A (zh) * | 2014-02-13 | 2015-08-19 | 生华生物科技股份有限公司 | 吡唑并嘧啶前药及其制备方法和应用 |
| CN105457029A (zh) * | 2014-09-29 | 2016-04-06 | 中国科学院上海巴斯德研究所 | 抑制酪蛋白激酶2活性在促进i型干扰素表达的应用 |
| CN105992768A (zh) * | 2013-12-10 | 2016-10-05 | 百时美施贵宝公司 | 用作IL-12、IL-23和/或IFNα响应的调节剂的咪唑并哒嗪化合物 |
| CN106103445A (zh) * | 2014-02-21 | 2016-11-09 | 癌症研究技术有限公司 | 作为cdk抑制剂的吡唑并[1,5‑a]嘧啶‑5,7‑二胺化合物和它们的治疗用途 |
| CN106170489A (zh) * | 2014-05-28 | 2016-11-30 | 诺华股份有限公司 | 新的吡唑并嘧啶衍生物及其作为malt1抑制剂的用途 |
| CN107188901A (zh) * | 2017-05-27 | 2017-09-22 | 无锡捷化医药科技有限公司 | 一种(3‑(3‑(二甲氨基)丙氧基)苯基)硼酸的制备方法 |
| CN116075502A (zh) * | 2020-03-30 | 2023-05-05 | 生华生物科技股份有限公司 | 用于治疗rna病毒(特别是covid-19)感染的抗病毒化合物及方法 |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2555261T3 (es) * | 2010-06-01 | 2015-12-30 | Bayer Intellectual Property Gmbh | Imidazopirazinas sustituidas |
| CA3007787C (en) | 2010-06-03 | 2020-03-10 | Pharmacyclics Llc | The use of inhibitors of bruton's tyrosine kinase (btk) |
| WO2012170827A2 (en) * | 2011-06-08 | 2012-12-13 | Cylene Pharmaceuticals, Inc. | Pyrazolopyrimidines and related heterocycles as ck2 inhibitors |
| US9309250B2 (en) | 2011-06-22 | 2016-04-12 | Vertex Pharmaceuticals Incorporated | Substituted pyrrolo[2,3-b]pyrazines as ATR kinase inhibitors |
| EP2843072B1 (en) * | 2012-04-27 | 2017-06-14 | Nippon Steel & Sumitomo Metal Corporation | Seamless steel pipe and method for manufacturing same |
| CA2880896C (en) | 2012-06-26 | 2021-11-16 | Del Mar Pharmaceuticals | Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or ahi1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof |
| TW201414737A (zh) * | 2012-07-13 | 2014-04-16 | 必治妥美雅史谷比公司 | 作爲激酶抑制劑之咪唑并三□甲腈 |
| CA2879570A1 (en) | 2012-07-24 | 2014-01-30 | Pharmacyclics, Inc. | Mutations associated with resistance to inhibitors of bruton's tyrosine kinase (btk) |
| WO2014089379A1 (en) | 2012-12-07 | 2014-06-12 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| CA2897200C (en) | 2013-01-14 | 2021-07-06 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors |
| PE20191245A1 (es) | 2013-01-15 | 2019-09-18 | Incyte Holdings Corp | Compuestos de tiazolcarboxamidas y piridinacarboxamida utiles como inhibidores de quinasa pim |
| EP2970289A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Inc. | Compounds useful as inhibitors of atr kinase |
| US9663519B2 (en) | 2013-03-15 | 2017-05-30 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| EP2970288A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| CN105492011A (zh) | 2013-04-08 | 2016-04-13 | 丹尼斯·M·布朗 | 不理想给药化学化合物的治疗增效 |
| CN105658653A (zh) | 2013-08-23 | 2016-06-08 | 因赛特公司 | 可用作pim激酶抑制剂的呋喃并-和噻吩并-吡啶甲酰胺化合物 |
| CN103570728B (zh) * | 2013-11-12 | 2015-12-30 | 山东大学 | 一种取代吡唑并[1,5-a]嘧啶类衍生物及其制备方法与应用 |
| WO2015085132A1 (en) | 2013-12-06 | 2015-06-11 | Vertex Pharmaceuticals Incorporated | 2-amino-6-fluoro-n-[5-fluoro-pyridin-3-yl]pyrazolo[1,5-a]pyrimidin-3-carboxamide compound useful as atr kinase inhibitor, its preparation, different solid forms and radiolabelled derivatives thereof |
| HRP20200186T1 (hr) | 2014-06-05 | 2020-05-29 | Vertex Pharmaceuticals Inc. | Radioaktivno obilježeni derivati 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]-pirazolo[1,5-a]pirimidin-3-karboksamid spojeva koji se koriste kao inhibitori atr kinaze, priprava navedenih spojeva i njihovi različiti čvrsti oblici |
| JP6936007B2 (ja) | 2014-06-17 | 2021-09-15 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Chk1阻害剤とatr阻害剤との組み合わせを使用してがんを処置する方法 |
| US9822124B2 (en) | 2014-07-14 | 2017-11-21 | Incyte Corporation | Bicyclic heteroaromatic carboxamide compounds useful as Pim kinase inhibitors |
| US9580418B2 (en) | 2014-07-14 | 2017-02-28 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors |
| CA2968884A1 (en) * | 2014-12-10 | 2016-06-16 | Massachusetts Institute Of Technology | Fused 1,3-azole derivatives useful for the treatment of proliferative diseases |
| EP3247713B1 (en) * | 2015-01-23 | 2019-08-28 | GlaxoSmithKline Intellectual Property Development Limited | Pyrazolo[3,4-d]pyrimidin derivative and its use for the treatment of leishmaniasis |
| WO2016196244A1 (en) | 2015-05-29 | 2016-12-08 | Incyte Corporation | Pyridineamine compounds useful as pim kinase inhibitors |
| AR105967A1 (es) | 2015-09-09 | 2017-11-29 | Incyte Corp | Sales de un inhibidor de pim quinasa |
| EP3355926B1 (en) | 2015-09-30 | 2025-12-24 | Vertex Pharmaceuticals Inc. | Combination of dna damaging agents and atr inhibitors for use in a method for treating cancer using |
| WO2017059251A1 (en) | 2015-10-02 | 2017-04-06 | Incyte Corporation | Heterocyclic compounds useful as pim kinase inhibitors |
| CN109071456A (zh) | 2016-02-16 | 2018-12-21 | 麻省理工学院 | 作为myc调节剂的max结合剂及其用途 |
| EP3474855B1 (en) | 2016-06-24 | 2022-01-26 | Polaris Pharmaceuticals, Inc. | Ck2 inhibitors, compositions and methods thereof |
| TWI778050B (zh) | 2017-04-21 | 2022-09-21 | 美商醫肯納腫瘤學公司 | 吲哚ahr抑制劑及其用途 |
| MX393995B (es) | 2017-07-28 | 2025-03-24 | Yuhan Corp | Proceso mejorado para preparar derivados de aminopirimidina |
| JP7216705B2 (ja) | 2017-07-28 | 2023-02-02 | ニンバス ラクシュミ, インコーポレイテッド | Tyk2阻害剤およびその使用方法 |
| GB201715194D0 (en) | 2017-09-20 | 2017-11-01 | Carrick Therapeutics Ltd | Compounds and their therapeutic use |
| WO2019113487A1 (en) | 2017-12-08 | 2019-06-13 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
| US11071727B2 (en) | 2018-01-26 | 2021-07-27 | Northwestern University | Therapeutic targeting of proteolytic cleavage of the mixed lineage leukemia gene product (MLL1) by taspase1 using kinase inhibitors |
| MY210039A (en) | 2018-10-30 | 2025-08-22 | Kronos Bio Inc | Compounds, compositions, and methods for modulating cdk9 activity |
| CN112608316B (zh) * | 2019-07-30 | 2022-10-21 | 厦门宝太生物科技股份有限公司 | 一种吡唑并三嗪类腺苷受体拮抗剂 |
| PL4065582T3 (pl) | 2019-11-26 | 2025-08-18 | Ikena Oncology, Inc. | Polimorficzne pochodne karbazolu i ich zastosowania |
| GB201918541D0 (en) | 2019-12-16 | 2020-01-29 | Carrick Therapeutics Ltd | Therapeutic compounds and their use |
| KR102337404B1 (ko) * | 2020-01-03 | 2021-12-10 | 연세대학교 산학협력단 | 조직 재생용 조성물 |
| CN116323569A (zh) * | 2020-09-15 | 2023-06-23 | 田边三菱制药株式会社 | 三嗪化合物的盐、其晶型及制造方法 |
| CN115867553B (zh) * | 2021-01-09 | 2026-03-06 | 巴格沃克斯研究有限公司 | 作为腺苷2A受体和腺苷2B受体拮抗剂的二氨基吡唑[1, 5-a]并嘧啶-6-腈化合物 |
| US12343421B2 (en) * | 2021-11-01 | 2025-07-01 | Solaana MD LLC | Vitamin D base layer |
| JP2026509368A (ja) * | 2023-03-09 | 2026-03-18 | アクイナ ファーマシューティカルズ, インコーポレイテッド | Tdp-43及びタウ凝集の阻害剤 |
| US12269826B1 (en) * | 2023-11-16 | 2025-04-08 | King Faisal University | 7H-pyrido[4′,3′:4,5]pyrrolo[2,3-c][1,7]naphthyridine compounds as CK2 inhibitors |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5624677A (en) | 1995-06-13 | 1997-04-29 | Pentech Pharmaceuticals, Inc. | Controlled release of drugs delivered by sublingual or buccal administration |
| TWI238064B (en) * | 1995-06-20 | 2005-08-21 | Takeda Chemical Industries Ltd | A pharmaceutical composition for prophylaxis and treatment of diabetes |
| JP2005513026A (ja) * | 2001-11-15 | 2005-05-12 | インサイト サン ディエゴ インコーポレイテッド | 高コレステロール血症、異脂肪血症および他の代謝障害;癌、および他の疾患を治療するn−置換複素環 |
| US7206308B2 (en) * | 2001-12-22 | 2007-04-17 | International Business Machines Corporation | Method of providing a non-blocking routing network |
| JP2005530739A (ja) * | 2002-04-19 | 2005-10-13 | セルラー ジェノミクス,インコーポレーテッド | イミダゾ[1,2−a]ピラジン−8−イルアミン、生成方法、および使用方法 |
| AU2003255528B2 (en) | 2002-07-10 | 2009-07-16 | Merck Serono Sa | Azolidinone-vinyl fused-benzene derivatives |
| WO2004006916A1 (en) * | 2002-07-10 | 2004-01-22 | Applied Research Systems Ars Holding Nv | Use of compounds for increasing spermatozoa motility |
| CN1701073B (zh) * | 2002-09-04 | 2011-06-22 | 先灵公司 | 作为细胞周期蛋白依赖激酶抑制剂的吡唑并[1,5-a]嘧啶 |
| US7205308B2 (en) * | 2002-09-04 | 2007-04-17 | Schering Corporation | Trisubstituted 7-aminopyrazolopyrimidines as cyclin dependent kinase inhibitors |
| EP1551396A1 (en) | 2002-09-26 | 2005-07-13 | Pintex Pharmaceuticals, Inc. | Pin1-modulating compounds and methods of use thereof |
| EP1599482A4 (en) * | 2003-02-28 | 2008-10-01 | Teijin Pharma Ltd | PYRAZOLO1,5-A PYRIMIDINE DERIVATIVES |
| TW200536536A (en) * | 2004-02-25 | 2005-11-16 | Schering Corp | Pyrazolotriazines as kinase inhibitors |
| US7842698B2 (en) * | 2004-09-03 | 2010-11-30 | Merck Serono S.A. | Pyridine methylene azolidinones and use thereof phosphoinositide inhibitors |
| US20090215818A1 (en) * | 2006-07-24 | 2009-08-27 | Smithkline Beecham Corporation | Thiozolidinedione derivatives as pi3 kinase inhibitors |
| FR2907120B1 (fr) * | 2006-10-12 | 2013-01-11 | Sanofi Aventis | Nouveaux derives imidazolones,leur preparation a titre de medicaments,compositions pharmaceutiques,utilisation comme inhibiteurs de proteines kinases notamment cdc7 |
| WO2009100375A1 (en) * | 2008-02-06 | 2009-08-13 | Bristol-Myers Squibb Company | Substituted imidazopyridazines useful as kinase inhibitors |
| AU2010249493A1 (en) * | 2009-05-20 | 2011-12-08 | Cylene Pharmaceuticals, Inc. | Pyrazolopyrimidines and related heterocycles as kinase inhibitors |
-
2010
- 2010-11-15 KR KR1020127017450A patent/KR101851130B1/ko active Active
- 2010-11-15 BR BR112012013508A patent/BR112012013508A2/pt not_active IP Right Cessation
- 2010-11-15 WO PCT/US2010/056712 patent/WO2011068667A1/en not_active Ceased
- 2010-11-15 US US12/946,759 patent/US8575177B2/en active Active
- 2010-11-15 ES ES10834934.1T patent/ES2629170T3/es active Active
- 2010-11-15 SG SG2012041034A patent/SG181507A1/en unknown
- 2010-11-15 JP JP2012542060A patent/JP5802676B2/ja active Active
- 2010-11-15 RU RU2012127792A patent/RU2607453C2/ru active
- 2010-11-15 CN CN2010800630542A patent/CN102762208A/zh active Pending
- 2010-11-15 CA CA2782684A patent/CA2782684C/en active Active
- 2010-11-15 EP EP10834934.1A patent/EP2509602B9/en active Active
- 2010-11-15 AU AU2010326268A patent/AU2010326268B2/en active Active
- 2010-11-15 PL PL10834934T patent/PL2509602T3/pl unknown
-
2012
- 2012-05-31 IL IL220086A patent/IL220086B/en active IP Right Grant
-
2013
- 2013-09-13 US US14/026,591 patent/US9303033B2/en active Active
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103360399A (zh) * | 2013-08-02 | 2013-10-23 | 北京大学 | 6-芳基取代-咪唑-[1,2-b]哒嗪类衍生物,其制备方法及用途 |
| CN103360399B (zh) * | 2013-08-02 | 2016-03-02 | 北京大学 | 6-芳基取代-咪唑-[1,2-b]哒嗪类衍生物,其制备方法及用途 |
| CN105992768A (zh) * | 2013-12-10 | 2016-10-05 | 百时美施贵宝公司 | 用作IL-12、IL-23和/或IFNα响应的调节剂的咪唑并哒嗪化合物 |
| CN104844605A (zh) * | 2014-02-13 | 2015-08-19 | 生华生物科技股份有限公司 | 吡唑并嘧啶前药及其制备方法和应用 |
| CN106103445A (zh) * | 2014-02-21 | 2016-11-09 | 癌症研究技术有限公司 | 作为cdk抑制剂的吡唑并[1,5‑a]嘧啶‑5,7‑二胺化合物和它们的治疗用途 |
| CN106103445B (zh) * | 2014-02-21 | 2019-08-09 | 癌症研究技术有限公司 | 作为cdk抑制剂的吡唑并[1,5-a]嘧啶-5,7-二胺化合物和它们的治疗用途 |
| CN106170489A (zh) * | 2014-05-28 | 2016-11-30 | 诺华股份有限公司 | 新的吡唑并嘧啶衍生物及其作为malt1抑制剂的用途 |
| CN106170489B (zh) * | 2014-05-28 | 2019-05-03 | 诺华股份有限公司 | 新的吡唑并嘧啶衍生物及其作为malt1抑制剂的用途 |
| CN105457029A (zh) * | 2014-09-29 | 2016-04-06 | 中国科学院上海巴斯德研究所 | 抑制酪蛋白激酶2活性在促进i型干扰素表达的应用 |
| CN107188901A (zh) * | 2017-05-27 | 2017-09-22 | 无锡捷化医药科技有限公司 | 一种(3‑(3‑(二甲氨基)丙氧基)苯基)硼酸的制备方法 |
| CN116075502A (zh) * | 2020-03-30 | 2023-05-05 | 生华生物科技股份有限公司 | 用于治疗rna病毒(特别是covid-19)感染的抗病毒化合物及方法 |
| CN116075502B (zh) * | 2020-03-30 | 2024-04-12 | 生华生物科技股份有限公司 | 用于治疗rna病毒(特别是covid-19)感染的抗病毒化合物及方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5802676B2 (ja) | 2015-10-28 |
| KR20130067486A (ko) | 2013-06-25 |
| EP2509602B1 (en) | 2017-01-25 |
| AU2010326268B2 (en) | 2016-11-03 |
| RU2012127792A (ru) | 2014-08-10 |
| SG181507A1 (en) | 2012-07-30 |
| US20140094448A1 (en) | 2014-04-03 |
| WO2011068667A1 (en) | 2011-06-09 |
| JP2013512903A (ja) | 2013-04-18 |
| US20110152240A1 (en) | 2011-06-23 |
| US8575177B2 (en) | 2013-11-05 |
| EP2509602A4 (en) | 2013-10-09 |
| CA2782684C (en) | 2018-09-04 |
| EP2509602A1 (en) | 2012-10-17 |
| PL2509602T3 (pl) | 2017-08-31 |
| AU2010326268A1 (en) | 2012-07-26 |
| RU2607453C2 (ru) | 2017-01-10 |
| CA2782684A1 (en) | 2011-06-09 |
| IL220086B (en) | 2018-02-28 |
| BR112012013508A2 (pt) | 2019-09-24 |
| KR101851130B1 (ko) | 2018-04-23 |
| ES2629170T3 (es) | 2017-08-07 |
| EP2509602B9 (en) | 2017-11-01 |
| IL220086A0 (en) | 2012-09-24 |
| US9303033B2 (en) | 2016-04-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102762208A (zh) | 作为ck2抑制剂的吡唑嘧啶和相关杂环 | |
| US7531539B2 (en) | Pyrrolotriazine kinase inhibitors | |
| CN102625803A (zh) | 药学上有用的杂环-取代的内酰胺 | |
| KR101532256B1 (ko) | 키나제 억제제로서의 이미다조트리아진 및 이미다조피리미딘 | |
| US7834019B2 (en) | Substituted pyrazolo[3,4-d]pyrimidinone derivatives | |
| US8445676B2 (en) | Pyrrolotriazine kinase inhibitors | |
| CN102014914A (zh) | 3h-[1,2,3]三唑并[4,5-d]嘧啶化合物、其作为mtor激酶和pi3激酶抑制剂的用途、以及它们的合成 | |
| US20090062288A1 (en) | Pyrrolotriazine compounds useful as kinase inhibitors and methods of treating kinase-associated conditions therewith | |
| JP7093306B2 (ja) | PDE1阻害剤としての1,5-ジヒドロ-4H-ピラゾロ[3,4-d]ピリミジン-4-オン及び1,5-ジヒドロ-4H-ピラゾロ[4,3-c]ピリジン-4-オン | |
| CN102647904A (zh) | 新型三环蛋白激酶调节剂 | |
| CN101883774A (zh) | 噻吩并嘧啶和吡唑并嘧啶化合物及其用作mtor激酶和pi3激酶抑制剂的用途 | |
| IL301180A (en) | Use of pyrazolopyrimidine derivatives for the treatment of P13K-related disorders | |
| CN101917995A (zh) | Polo样激酶抑制剂 | |
| CN102647906A (zh) | 三环化合物及其药学用途 | |
| WO2012170827A2 (en) | Pyrazolopyrimidines and related heterocycles as ck2 inhibitors | |
| TW201602115A (zh) | 新穎二環性或三環性雜環化合物 | |
| TW201348240A (zh) | 噻吩并嘧啶 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20121031 |