HRP20221279T1 - Modulatori somatostatina i njihove uporabe - Google Patents
Modulatori somatostatina i njihove uporabe Download PDFInfo
- Publication number
- HRP20221279T1 HRP20221279T1 HRP20221279TT HRP20221279T HRP20221279T1 HR P20221279 T1 HRP20221279 T1 HR P20221279T1 HR P20221279T T HRP20221279T T HR P20221279TT HR P20221279 T HRP20221279 T HR P20221279T HR P20221279 T1 HRP20221279 T1 HR P20221279T1
- Authority
- HR
- Croatia
- Prior art keywords
- quinolin
- difluorophenyl
- fluoro
- pyrido
- octahydro
- Prior art date
Links
- 102000005157 Somatostatin Human genes 0.000 title 1
- 108010056088 Somatostatin Proteins 0.000 title 1
- NHXLMOGPVYXJNR-ATOGVRKGSA-N somatostatin Chemical compound C([C@H]1C(=O)N[C@H](C(N[C@@H](CO)C(=O)N[C@@H](CSSC[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2C3=CC=CC=C3NC=2)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N1)[C@@H](C)O)NC(=O)CNC(=O)[C@H](C)N)C(O)=O)=O)[C@H](O)C)C1=CC=CC=C1 NHXLMOGPVYXJNR-ATOGVRKGSA-N 0.000 title 1
- 229960000553 somatostatin Drugs 0.000 title 1
- 125000004550 quinolin-6-yl group Chemical group N1=CC=CC2=CC(=CC=C12)* 0.000 claims 61
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 56
- 229910052739 hydrogen Inorganic materials 0.000 claims 49
- 239000001257 hydrogen Substances 0.000 claims 49
- -1 -OH Chemical group 0.000 claims 37
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 36
- 150000002431 hydrogen Chemical group 0.000 claims 35
- 125000004093 cyano group Chemical group *C#N 0.000 claims 32
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 32
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 32
- 150000001875 compounds Chemical class 0.000 claims 28
- 150000003839 salts Chemical class 0.000 claims 21
- 239000012453 solvate Substances 0.000 claims 21
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 16
- 239000000203 mixture Substances 0.000 claims 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 12
- 125000004429 atom Chemical group 0.000 claims 10
- 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 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 8
- CUYKNJBYIJFRCU-UHFFFAOYSA-N 3-aminopyridine Chemical compound NC1=CC=CN=C1 CUYKNJBYIJFRCU-UHFFFAOYSA-N 0.000 claims 7
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 6
- 206010000599 Acromegaly Diseases 0.000 claims 6
- 206010052399 Neuroendocrine tumour Diseases 0.000 claims 6
- 125000002393 azetidinyl group Chemical group 0.000 claims 6
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 6
- 125000002757 morpholinyl group Chemical group 0.000 claims 6
- 208000016065 neuroendocrine neoplasm Diseases 0.000 claims 6
- 201000011519 neuroendocrine tumor Diseases 0.000 claims 6
- 239000000825 pharmaceutical preparation Substances 0.000 claims 6
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 5
- 125000004549 quinolin-4-yl group Chemical group N1=CC=C(C2=CC=CC=C12)* 0.000 claims 5
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 4
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 4
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 4
- 125000006299 oxetan-3-yl group Chemical group [H]C1([H])OC([H])([H])C1([H])* 0.000 claims 4
- 125000004193 piperazinyl group Chemical group 0.000 claims 4
- 125000003386 piperidinyl group Chemical group 0.000 claims 4
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 4
- 206010028980 Neoplasm Diseases 0.000 claims 3
- 208000002193 Pain Diseases 0.000 claims 3
- 201000011510 cancer Diseases 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- 208000027866 inflammatory disease Diseases 0.000 claims 3
- 208000017169 kidney disease Diseases 0.000 claims 3
- 230000004770 neurodegeneration Effects 0.000 claims 3
- 208000015122 neurodegenerative disease Diseases 0.000 claims 3
- 201000001119 neuropathy Diseases 0.000 claims 3
- 230000007823 neuropathy Effects 0.000 claims 3
- 208000033808 peripheral neuropathy Diseases 0.000 claims 3
- 208000020016 psychiatric disease Diseases 0.000 claims 3
- 208000023504 respiratory system disease Diseases 0.000 claims 3
- HNEGJTWNOOWEMH-UHFFFAOYSA-N 1-fluoropropane Chemical group [CH2]CCF HNEGJTWNOOWEMH-UHFFFAOYSA-N 0.000 claims 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 2
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 2
- 125000003725 azepanyl group Chemical group 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- KTIBWQBSHBKIHC-JWQCQUIFSA-N methyl (3R,4R)-4-amino-1-[6-(3-cyano-2-hydroxyphenyl)-3-(3,5-difluorophenyl)quinolin-4-yl]piperidine-3-carboxylate Chemical compound N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C1=C(C(=CC=C1)C#N)O)C1=CC(=CC(=C1)F)F)C(=O)OC KTIBWQBSHBKIHC-JWQCQUIFSA-N 0.000 claims 2
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 2
- 125000003566 oxetanyl group Chemical group 0.000 claims 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- BIWOSRSKDCZIFM-UHFFFAOYSA-N piperidin-3-ol Chemical compound OC1CCCNC1 BIWOSRSKDCZIFM-UHFFFAOYSA-N 0.000 claims 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- CRKQQBZNEFOMCY-JWQCQUIFSA-N (3R,4R)-4-amino-1-[6-(3-cyano-2-hydroxyphenyl)-3-(3,5-difluorophenyl)quinolin-4-yl]-N-methylpiperidine-3-carboxamide Chemical compound N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C1=C(C(=CC=C1)C#N)O)C1=CC(=CC(=C1)F)F)C(=O)NC CRKQQBZNEFOMCY-JWQCQUIFSA-N 0.000 claims 1
- WGNUJHPFOBIXCZ-DNQXCXABSA-N (3R,4R)-4-amino-1-[6-(3-cyano-2-hydroxyphenyl)-3-(3,5-difluorophenyl)quinolin-4-yl]piperidine-3-carboxamide Chemical compound N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C1=C(C(=CC=C1)C#N)O)C1=CC(=CC(=C1)F)F)C(=O)N WGNUJHPFOBIXCZ-DNQXCXABSA-N 0.000 claims 1
- IOLPVDHOVAVWTN-UHFFFAOYSA-N 1-[2-[4-(4-aminopiperidin-1-yl)-3-(3,5-difluorophenyl)quinolin-6-yl]-4,6-difluorophenyl]-3-methoxyurea Chemical compound NC1CCN(CC1)C1=C(C=NC2=CC=C(C=C12)C1=C(C(=CC(=C1)F)F)NC(=O)NOC)C1=CC(=CC(=C1)F)F IOLPVDHOVAVWTN-UHFFFAOYSA-N 0.000 claims 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N 2-hydroxy-pyridine Natural products OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 claims 1
- BJQZVISGHDIVCW-UHFFFAOYSA-N 3-[4-(4-aminopiperidin-1-yl)-3-(3,5-difluorophenyl)quinolin-6-yl]-2-(2-hydroxyethoxy)benzonitrile Chemical compound NC1CCN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)OCCO)C1=CC(=CC(=C1)F)F BJQZVISGHDIVCW-UHFFFAOYSA-N 0.000 claims 1
- ULUQRQOMEBQOIC-UHFFFAOYSA-N 3-[4-(4-aminopiperidin-1-yl)-3-(3,5-difluorophenyl)quinolin-6-yl]-2-(methoxymethoxy)benzonitrile Chemical compound NC1CCN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)OCOC)C1=CC(=CC(=C1)F)F ULUQRQOMEBQOIC-UHFFFAOYSA-N 0.000 claims 1
- GHILNKWBALQPDP-UHFFFAOYSA-N 3-[4-(4-aminopiperidin-1-yl)-3-(3,5-difluorophenyl)quinolin-6-yl]-2-hydroxybenzonitrile Chemical compound NC1CCN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)O)C1=CC(=CC(=C1)F)F GHILNKWBALQPDP-UHFFFAOYSA-N 0.000 claims 1
- MCEDWFWPINMPTJ-UHFFFAOYSA-N 3-[4-(4-aminopiperidin-1-yl)-3-(3,5-difluorophenyl)quinolin-6-yl]-5-chloro-4-fluoro-2-hydroxybenzonitrile Chemical compound NC1CCN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=C(C=1F)Cl)O)C1=CC(=CC(=C1)F)F MCEDWFWPINMPTJ-UHFFFAOYSA-N 0.000 claims 1
- HWLUDPGRVTYPHZ-DNQXCXABSA-N 3-[4-[(3R,4R)-4-amino-3-fluoropiperidin-1-yl]-3-(3,5-difluorophenyl)quinolin-6-yl]-2-hydroxybenzonitrile Chemical compound N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)O)C1=CC(=CC(=C1)F)F)F HWLUDPGRVTYPHZ-DNQXCXABSA-N 0.000 claims 1
- YZICXZWMZPMDCN-IXCJQBJRSA-N 3-[4-[(3R,4R)-4-amino-3-methoxypiperidin-1-yl]-3-(3,5-difluorophenyl)quinolin-6-yl]-2-(methoxymethoxy)benzonitrile Chemical compound N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)OCOC)C1=CC(=CC(=C1)F)F)OC YZICXZWMZPMDCN-IXCJQBJRSA-N 0.000 claims 1
- UCEROSLYAVYPKA-UHFFFAOYSA-N 3-[5-(4-aminopiperidin-1-yl)-6-(3,5-difluorophenyl)-1,8-naphthyridin-3-yl]-2-hydroxybenzonitrile Chemical compound NC1CCN(CC1)C1=C2C=C(C=NC2=NC=C1C1=CC(=CC(=C1)F)F)C=1C(=C(C#N)C=CC=1)O UCEROSLYAVYPKA-UHFFFAOYSA-N 0.000 claims 1
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
- JVSLFJAHSXCAAZ-UHFFFAOYSA-N ClC=1C(=C(C=CC=1)C=1C=C2C(=C(C=NC2=CC=1)C1=CC(=CC(=C1)F)F)N1CCC(CC1)N)C=NO Chemical compound ClC=1C(=C(C=CC=1)C=1C=C2C(=C(C=NC2=CC=1)C1=CC(=CC(=C1)F)F)N1CCC(CC1)N)C=NO JVSLFJAHSXCAAZ-UHFFFAOYSA-N 0.000 claims 1
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- IBYBYCAQCXHPOP-AOYPEHQESA-N N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)O)C1=CC(=CC(=C1)F)F)OC Chemical compound N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)O)C1=CC(=CC(=C1)F)F)OC IBYBYCAQCXHPOP-AOYPEHQESA-N 0.000 claims 1
- RXLMOBGRSJQZJL-XNMGPUDCSA-N N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C=C(C#N)C=CC=1)C1=CC(=CC(=C1)F)F)OC Chemical compound N[C@H]1[C@@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C=C(C#N)C=CC=1)C1=CC(=CC(=C1)F)F)OC RXLMOBGRSJQZJL-XNMGPUDCSA-N 0.000 claims 1
- IBYBYCAQCXHPOP-RSXGOPAZSA-N N[C@H]1[C@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)O)C1=CC(=CC(=C1)F)F)OC Chemical compound N[C@H]1[C@H](CN(CC1)C1=C(C=NC2=CC=C(C=C12)C=1C(=C(C#N)C=CC=1)O)C1=CC(=CC(=C1)F)F)OC IBYBYCAQCXHPOP-RSXGOPAZSA-N 0.000 claims 1
- 108020004566 Transfer RNA Proteins 0.000 claims 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims 1
- 239000002775 capsule Substances 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 229960004979 fampridine Drugs 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- VFQXVTODMYMSMJ-UHFFFAOYSA-N isonicotinamide Chemical compound NC(=O)C1=CC=NC=C1 VFQXVTODMYMSMJ-UHFFFAOYSA-N 0.000 claims 1
- PRSNYHONPORVAA-UHFFFAOYSA-N methyl N-[2-[4-(4-aminopiperidin-1-yl)-3-(3,5-difluorophenyl)quinolin-6-yl]-4,6-difluorophenyl]carbamate Chemical compound NC1CCN(CC1)C1=C(C=NC2=CC=C(C=C12)C1=C(C(=CC(=C1)F)F)NC(OC)=O)C1=CC(=CC(=C1)F)F PRSNYHONPORVAA-UHFFFAOYSA-N 0.000 claims 1
- ABIQZCNTCJBBMH-UHFFFAOYSA-N methyl N-[2-[4-(4-aminopiperidin-1-yl)-3-(3,5-difluorophenyl)quinolin-6-yl]-6-cyanophenyl]carbamate Chemical compound NC1CCN(CC1)C1=C(C=NC2=CC=C(C=C12)C1=C(C(=CC=C1)C#N)NC(OC)=O)C1=CC(=CC(=C1)F)F ABIQZCNTCJBBMH-UHFFFAOYSA-N 0.000 claims 1
- GRFNBEZIAWKNCO-UHFFFAOYSA-N mhp Natural products OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 claims 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 claims 1
- 239000006187 pill Substances 0.000 claims 1
- ZGNXATVKGIJQGC-UHFFFAOYSA-N piperidine-3-carbonitrile Chemical compound N#CC1CCCNC1 ZGNXATVKGIJQGC-UHFFFAOYSA-N 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 239000003826 tablet Substances 0.000 claims 1
- 125000003831 tetrazolyl group Chemical group 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
Classifications
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- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/50—Pyridazines; Hydrogenated pyridazines
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- 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
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- C—CHEMISTRY; METALLURGY
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
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- C07D498/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pyridine Compounds (AREA)
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| PCT/US2017/041694 WO2018013676A1 (en) | 2016-07-14 | 2017-07-12 | Somatostatin modulators and uses thereof |
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| PL3484865T3 (pl) | 2016-07-14 | 2023-01-09 | Crinetics Pharmaceuticals, Inc. | Modulatory somatostatyny i ich zastosowania |
| WO2018170284A1 (en) | 2017-03-16 | 2018-09-20 | Crinetics Pharmaceuticals, Inc. | Somatostatin modulators and uses thereof |
| WO2019023278A1 (en) | 2017-07-25 | 2019-01-31 | Crinetics Pharmaceuticals, Inc. | MODULATORS OF SOMATOSTATIN AND USES THEREOF |
| CA3088658A1 (en) | 2018-01-17 | 2019-07-25 | Crinetics Pharmaceuticals, Inc. | Process of making somatostatin modulators |
| WO2019157458A1 (en) * | 2018-02-12 | 2019-08-15 | Crinetics Pharmaceuticals, Inc. | Somatostatin modulators and uses thereof |
| EP3807248A4 (en) * | 2018-05-29 | 2021-10-27 | Council of Scientific and Industrial Research | BICYCLIC TOPOISOMERASE I INHIBITOR COMPOUNDS, THEIR PREPARATION AND USE |
| JP7431813B2 (ja) | 2018-09-18 | 2024-02-15 | クリネティックス ファーマシューティカルズ,インク. | ソマトスタチンモジュレーターとその使用 |
| JP2022540922A (ja) * | 2019-07-17 | 2022-09-20 | クリネティックス ファーマシューティカルズ,インク. | ソマトスタチンモジュレーターの結晶形態 |
| TWI841768B (zh) * | 2019-08-14 | 2024-05-11 | 美商克林提克斯醫藥股份有限公司 | 非肽生長抑制素(somatostatin)5型受體激動劑及其用途 |
| SMT202500315T1 (it) * | 2020-09-09 | 2025-11-10 | Crinetics Pharmaceuticals Inc | Formulazioni di un modulatore della somatostatina |
| CN117043149A (zh) | 2021-02-17 | 2023-11-10 | 克林提克斯医药股份有限公司 | 促生长素抑制素调节剂的结晶形式 |
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| EP4378971A4 (en) | 2021-09-28 | 2024-11-20 | Denka Company Limited | CHLOROPRENE BLOCK COPOLYMER, LATEX, LATEX COMPOSITION AND RUBBER COMPOSITION |
| AU2023207068A1 (en) * | 2022-01-11 | 2024-07-11 | Crinetics Pharmaceuticals, Inc. | Uses of a somatostatin modulator for the treatment of carcinoid syndrome |
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