KR101710732B1 - 디아자카르바졸 및 사용 방법 - Google Patents
디아자카르바졸 및 사용 방법 Download PDFInfo
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- KR101710732B1 KR101710732B1 KR1020117000563A KR20117000563A KR101710732B1 KR 101710732 B1 KR101710732 B1 KR 101710732B1 KR 1020117000563 A KR1020117000563 A KR 1020117000563A KR 20117000563 A KR20117000563 A KR 20117000563A KR 101710732 B1 KR101710732 B1 KR 101710732B1
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- 0 *c(nc1)cc2c1[n]c(nc1)c2cc1-c1ccccc1 Chemical compound *c(nc1)cc2c1[n]c(nc1)c2cc1-c1ccccc1 0.000 description 10
- CJRRLCPMBQMCRO-UHFFFAOYSA-N Brc1cc(CCCC2)c2[s]1 Chemical compound Brc1cc(CCCC2)c2[s]1 CJRRLCPMBQMCRO-UHFFFAOYSA-N 0.000 description 1
- JLVSQPNCKCZXBK-UHFFFAOYSA-N Brc1ccc(CN2CCC2)cc1 Chemical compound Brc1ccc(CN2CCC2)cc1 JLVSQPNCKCZXBK-UHFFFAOYSA-N 0.000 description 1
- HFRNGSUSVIONOS-UHFFFAOYSA-N C(c(cc1)ccc1-c(cc1c2c3)cnc1[nH]c2cnc3-c1cnc[o]1)N1CCCCC1 Chemical compound C(c(cc1)ccc1-c(cc1c2c3)cnc1[nH]c2cnc3-c1cnc[o]1)N1CCCCC1 HFRNGSUSVIONOS-UHFFFAOYSA-N 0.000 description 1
- JPTYMEKKOCZXOG-UHFFFAOYSA-N C(c1ccccc1)[n]1nnc(-c(nc2)cc(c3c4)c2[nH]c3ncc4-c2ccc(CN3CCCCC3)cc2)c1 Chemical compound C(c1ccccc1)[n]1nnc(-c(nc2)cc(c3c4)c2[nH]c3ncc4-c2ccc(CN3CCCCC3)cc2)c1 JPTYMEKKOCZXOG-UHFFFAOYSA-N 0.000 description 1
- YNVXGINRVWCEMF-UHFFFAOYSA-N CC(C)(C#Cc(cc1c2c3)cnc1[n](COCC[Si](C)(C)C)c2cnc3C#N)O Chemical compound CC(C)(C#Cc(cc1c2c3)cnc1[n](COCC[Si](C)(C)C)c2cnc3C#N)O YNVXGINRVWCEMF-UHFFFAOYSA-N 0.000 description 1
- PUAHNRDGJCXNPC-AUTUFYTCSA-N CC(C)(C)OC(N(CC1)CC1Oc1c(c2cc(/C(/C=N)=C/NC)cnc2[nH]2)c2cnc1C#N)=O Chemical compound CC(C)(C)OC(N(CC1)CC1Oc1c(c2cc(/C(/C=N)=C/NC)cnc2[nH]2)c2cnc1C#N)=O PUAHNRDGJCXNPC-AUTUFYTCSA-N 0.000 description 1
- OCTXRKJVRKTLIS-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CC1Oc1c(c2cc(Br)cnc2[n]2S(c3ccccc3)(=O)=O)c2cnc1C#N)=O Chemical compound CC(C)(C)OC(N(CC1)CC1Oc1c(c2cc(Br)cnc2[n]2S(c3ccccc3)(=O)=O)c2cnc1C#N)=O OCTXRKJVRKTLIS-UHFFFAOYSA-N 0.000 description 1
- CRUYHUVCSYCUCU-UHFFFAOYSA-N CC(C)(c1ncc2[nH]c(ncc(-c(cc3)ccc3N3CCN(C)CC3)c3)c3c2c1)O Chemical compound CC(C)(c1ncc2[nH]c(ncc(-c(cc3)ccc3N3CCN(C)CC3)c3)c3c2c1)O CRUYHUVCSYCUCU-UHFFFAOYSA-N 0.000 description 1
- HSRTUQOWWNQALG-UHFFFAOYSA-N CC1(C)OB(c2cc(OC)c(CN3CCCCC3)cc2)OC1(C)C Chemical compound CC1(C)OB(c2cc(OC)c(CN3CCCCC3)cc2)OC1(C)C HSRTUQOWWNQALG-UHFFFAOYSA-N 0.000 description 1
- IOCXTXOMGLBRGD-UHFFFAOYSA-N CCN(CC1)CCC1Oc1ccncc1-c1ncc2[nH]c(ncc(-c3c[n](C)nc3)c3)c3c2c1 Chemical compound CCN(CC1)CCC1Oc1ccncc1-c1ncc2[nH]c(ncc(-c3c[n](C)nc3)c3)c3c2c1 IOCXTXOMGLBRGD-UHFFFAOYSA-N 0.000 description 1
- NKLXXQYOXMZSNI-UHFFFAOYSA-N CCN(CCc1cc(O[SH+](C(F)(F)F)(O)[OH2+])c2)Cc1c2OC Chemical compound CCN(CCc1cc(O[SH+](C(F)(F)F)(O)[OH2+])c2)Cc1c2OC NKLXXQYOXMZSNI-UHFFFAOYSA-N 0.000 description 1
- WGVBYXAJSWOZQX-UHFFFAOYSA-N CCN1CCC(Cc2c(C#N)ncc([nH]3)c2c2c3nccc2)CC1 Chemical compound CCN1CCC(Cc2c(C#N)ncc([nH]3)c2c2c3nccc2)CC1 WGVBYXAJSWOZQX-UHFFFAOYSA-N 0.000 description 1
- GMDMSUICZYNPKZ-UHFFFAOYSA-N CCOc1c(CN2CCCCC2)ccc(Br)c1 Chemical compound CCOc1c(CN2CCCCC2)ccc(Br)c1 GMDMSUICZYNPKZ-UHFFFAOYSA-N 0.000 description 1
- GOBQXMMCSXITNA-UHFFFAOYSA-N CCc1cc(Br)cc(CC)c1CN Chemical compound CCc1cc(Br)cc(CC)c1CN GOBQXMMCSXITNA-UHFFFAOYSA-N 0.000 description 1
- LXBYWVMXZHOWGM-DXPMMOLWSA-O CN/C=C(\C=[NH2+])/c(cc1c2c3)ncc1[nH]c2ncc3-c1cc(OC)c(CN2CCCCC2)cc1 Chemical compound CN/C=C(\C=[NH2+])/c(cc1c2c3)ncc1[nH]c2ncc3-c1cc(OC)c(CN2CCCCC2)cc1 LXBYWVMXZHOWGM-DXPMMOLWSA-O 0.000 description 1
- DWVIJAFBCFPVOU-BUFUBBIOSA-O CN/C=C(\C=[NH2+])/c(nc1)cc2c1[nH]c(nc1)c2cc1-c1c[n](C)nc1 Chemical compound CN/C=C(\C=[NH2+])/c(nc1)cc2c1[nH]c(nc1)c2cc1-c1c[n](C)nc1 DWVIJAFBCFPVOU-BUFUBBIOSA-O 0.000 description 1
- UEBGVCNOFXEPEL-UHFFFAOYSA-N CN1CCC(Cc(cc2)ccc2Br)CC1 Chemical compound CN1CCC(Cc(cc2)ccc2Br)CC1 UEBGVCNOFXEPEL-UHFFFAOYSA-N 0.000 description 1
- HBEIHPSICGGZIF-UHFFFAOYSA-N COc1c(CO)ccc(Br)c1 Chemical compound COc1c(CO)ccc(Br)c1 HBEIHPSICGGZIF-UHFFFAOYSA-N 0.000 description 1
- YMANDCYDGJUYIB-UHFFFAOYSA-N C[n]1ncc(-c(cc2c3c4)cnc2[nH]c3cnc4Cl)c1 Chemical compound C[n]1ncc(-c(cc2c3c4)cnc2[nH]c3cnc4Cl)c1 YMANDCYDGJUYIB-UHFFFAOYSA-N 0.000 description 1
- CRKDVRWYLJCABF-UHFFFAOYSA-O Cc1cc(O[SH+]C(F)(F)F)cc(OC)c1CN1CCCCC1 Chemical compound Cc1cc(O[SH+]C(F)(F)F)cc(OC)c1CN1CCCCC1 CRKDVRWYLJCABF-UHFFFAOYSA-O 0.000 description 1
- MXFQHMVRYCFZEZ-UHFFFAOYSA-N Clc(cc1c2c3)ncc1[nH]c2ncc3Br Chemical compound Clc(cc1c2c3)ncc1[nH]c2ncc3Br MXFQHMVRYCFZEZ-UHFFFAOYSA-N 0.000 description 1
- FKQGBUOGZWGUOU-UHFFFAOYSA-N Fc(cc1c2c3)ncc1[nH]c2ncc3Br Chemical compound Fc(cc1c2c3)ncc1[nH]c2ncc3Br FKQGBUOGZWGUOU-UHFFFAOYSA-N 0.000 description 1
- NQFSLNFYSRONPJ-UHFFFAOYSA-N Fc1ncc2[nH]c(ncc(-c3ccc(CN4CCCCC4)cc3)c3)c3c2c1 Chemical compound Fc1ncc2[nH]c(ncc(-c3ccc(CN4CCCCC4)cc3)c3)c3c2c1 NQFSLNFYSRONPJ-UHFFFAOYSA-N 0.000 description 1
- GBMLHAJYZHFQQN-UHFFFAOYSA-N N#Cc(c(N1CCN(CC(F)(F)F)CC1)c1c2c3)ncc1[nH]c2ncc3Br Chemical compound N#Cc(c(N1CCN(CC(F)(F)F)CC1)c1c2c3)ncc1[nH]c2ncc3Br GBMLHAJYZHFQQN-UHFFFAOYSA-N 0.000 description 1
- DTGBXECCBCNBEE-UHFFFAOYSA-N N#Cc(cc1c2c3)ncc1[nH]c2ncc3O Chemical compound N#Cc(cc1c2c3)ncc1[nH]c2ncc3O DTGBXECCBCNBEE-UHFFFAOYSA-N 0.000 description 1
- RZQANKISADRBCX-UHFFFAOYSA-N N#Cc(ncc1c2c3cccnc3[nH]1)c2OC1C(CC2)CCN2C1 Chemical compound N#Cc(ncc1c2c3cccnc3[nH]1)c2OC1C(CC2)CCN2C1 RZQANKISADRBCX-UHFFFAOYSA-N 0.000 description 1
- SWAGZEYGJLWAGQ-UHFFFAOYSA-N N#Cc1ncc2[nH]c3ncccc3c2c1 Chemical compound N#Cc1ncc2[nH]c3ncccc3c2c1 SWAGZEYGJLWAGQ-UHFFFAOYSA-N 0.000 description 1
- UOICMMKVFPTQMX-UHFFFAOYSA-N Nc(c(I)c1)cnc1Cl Chemical compound Nc(c(I)c1)cnc1Cl UOICMMKVFPTQMX-UHFFFAOYSA-N 0.000 description 1
- PMBMWAUXJPACJZ-UHFFFAOYSA-N Nc(cc1c2c3)ncc1[nH]c2ncc3-c1ccc(CN2CCCCC2)cc1 Chemical compound Nc(cc1c2c3)ncc1[nH]c2ncc3-c1ccc(CN2CCCCC2)cc1 PMBMWAUXJPACJZ-UHFFFAOYSA-N 0.000 description 1
- NFUNIIAPEARQDU-UHFFFAOYSA-N Nc(nc1)cc2c1[nH]c(nc1)c2cc1NC(N1CCCC1)=O Chemical compound Nc(nc1)cc2c1[nH]c(nc1)c2cc1NC(N1CCCC1)=O NFUNIIAPEARQDU-UHFFFAOYSA-N 0.000 description 1
- YCNXGPMGMAKDPM-UHFFFAOYSA-N OC(c1c[s]c(Br)c1)=O Chemical compound OC(c1c[s]c(Br)c1)=O YCNXGPMGMAKDPM-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- 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
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- A61K31/54—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 sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
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- 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
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
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- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- 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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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Oncology (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)
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Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102746336B (zh) | 2005-06-29 | 2015-08-19 | 施瑞修德制药公司 | 氨基磷酸酯烷化剂前体药物 |
| CA2725754C (en) * | 2008-06-11 | 2017-05-23 | Hazel Joan Dyke | Diazacarbazoles and methods of use |
| AR072084A1 (es) * | 2008-06-12 | 2010-08-04 | Sanofi Aventis | Derivados de azacarbolinas, su preparacion y su utilizacion terapeutica como inhibidores de las quinasas pim |
| BRPI0924844A2 (pt) * | 2009-03-24 | 2016-01-26 | Sanofi Sa | derivados de azacarbolinas 9h-pirrol[2,3-b:5,4-c']dipiridina, sua preparação e sua utilização terapêutica. |
| FR2950891B1 (fr) * | 2009-10-06 | 2012-11-09 | Sanofi Aventis | Derives d'azacarbolines 9h-pyrrolo[2,3-b:5,4-c']dipyridine, leur preparation et leur utilisation therapeutique |
| US20110183938A1 (en) * | 2009-12-16 | 2011-07-28 | Genentech, Inc. | 1,7-diazacarbazoles and methods of use |
| ES2621857T3 (es) | 2010-11-16 | 2017-07-05 | Array Biopharma, Inc. | Combinación de inhibidores de la cinasa 1 de punto de control e inhibidores de la cinasa WEE1 |
| CN102503959B (zh) * | 2011-10-25 | 2015-04-08 | 南方医科大学 | 一种稠三环类化合物及其制备方法、以及含该类化合物的药物组合物及其应用 |
| RU2641693C2 (ru) * | 2011-11-09 | 2018-01-22 | Кансер Ресёрч Текнолоджи Лимитед | Соединения 5-(пиридин-2-иламино)-пиразин-2-карбонитрила и их терапевтическое применение |
| WO2013096687A1 (en) * | 2011-12-22 | 2013-06-27 | Threshold Pharmaceuticals, Inc. | Administration of hypoxia activated prodrugs in combination with chk1 inhibitors for treating cancer |
| AU2013250726B2 (en) | 2012-04-20 | 2017-01-05 | Advinus Therapeutics Limited | Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof |
| EP2671881A1 (en) | 2012-06-07 | 2013-12-11 | Syngenta Participations AG. | Pesticidally active pyridyl- and pyrimidyl- substituted thiazole derivatives |
| ES2704744T3 (es) | 2012-06-13 | 2019-03-19 | Incyte Holdings Corp | Compuestos tricíclicos sustituidos como inhibidores de FGFR |
| CN105764501A (zh) | 2013-07-26 | 2016-07-13 | 现代化制药公司 | 改善比生群治疗效益的组合物 |
| US10071109B2 (en) | 2013-11-06 | 2018-09-11 | Molecular Templates, Inc. | Predictive biomarker for hypoxia-activated prodrug therapy |
| KR102359214B1 (ko) | 2014-04-04 | 2022-02-07 | 델 마 파마슈티컬스 | 폐의 비소세포 암종 및 난소암을 치료하기 위한 디안하이드로갈락티톨 및 이의 유사체 또는 유도체 |
| CN107118207B (zh) * | 2017-05-22 | 2020-10-02 | 苏州东南药业股份有限公司 | 一类cdk抑制剂的制备方法 |
| CR20200590A (es) | 2018-05-04 | 2021-04-26 | Incyte Corp | Formas sólidas de un inhibidor de fgfr y procesos para prepararlas |
| MA52493A (fr) | 2018-05-04 | 2021-03-10 | Incyte Corp | Sels d'un inhibiteur de fgfr |
| WO2020061377A1 (en) * | 2018-09-19 | 2020-03-26 | Genentech, Inc. | Spirocyclic 2,3-dihydro-7-azaindole compounds and uses thereof |
| US11485734B2 (en) | 2018-10-02 | 2022-11-01 | Northwestern University | Beta-carbolines as positive allosteric modulators of the human serotonin receptor 2C (5-HT2C) |
| CN119350306A (zh) | 2018-12-13 | 2025-01-24 | 英特维特国际股份有限公司 | 1-[(3r,4s)-4-氰基四氢吡喃-3-基]-3-[(2-氟-6-甲氧基-4-吡啶基)氨基]吡唑-4-甲酰胺制备方法 |
| BR112022010664A2 (pt) | 2019-12-04 | 2022-08-16 | Incyte Corp | Derivados de um inibidor de fgfr |
| US12168662B1 (en) | 2023-12-15 | 2024-12-17 | King Faisal University | Pyrido[4′,3′:4,5]pyrrolo[2,3-c][2,7]naphthyridines compounds as CK2 inhibitors |
| US12129252B1 (en) | 2024-02-15 | 2024-10-29 | King Faisal University | Pyrrolo[2,3-c][2,6]naphthyridine-8-carboxylic acids as CK2 inhibitors |
Family Cites Families (18)
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| HUP0300894A3 (en) | 2000-03-15 | 2008-05-28 | Sanofi Aventis Deutschland | Substituted beta-carbolines, process for their preparation, pharmaceutical compositions containing them and their use |
| GB0116966D0 (en) * | 2001-07-11 | 2001-09-05 | Pharma Mar Sa | Anittumoral compounds |
| GB0121941D0 (en) * | 2001-09-11 | 2001-10-31 | Astrazeneca Ab | Chemical compounds |
| DE60217532T8 (de) * | 2001-11-07 | 2008-02-07 | Millennium Pharmaceuticals, Inc., Cambridge | Carboline derivate als ikb-inhibitoren zur behandlung des m ultiplen myelomas |
| BRPI0407544A (pt) * | 2003-02-17 | 2006-02-14 | Pharmacia Italia Spa | derivados de pirazol tetracìclicos como inibidores da cinase, processo para a sua preparação e composições farmacêuticas que os compreendem |
| SE0401655D0 (sv) | 2004-06-24 | 2004-06-24 | Astrazeneca Ab | New compounds |
| EP1896472A1 (de) * | 2005-06-09 | 2008-03-12 | Boehringer Ingelheim International GmbH | Alpha-carboline als cdk-1 inhibitoren |
| US8119655B2 (en) * | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
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| CA2666130A1 (en) | 2006-10-09 | 2008-04-17 | Takeda San Diego, Inc. | Kinase inhibitors |
| EP2170886A1 (en) * | 2007-07-02 | 2010-04-07 | Cancer Research Technology Limited | 9h-pyrimido[4,5-b]indoles, 9h-pyrido[4',3':4,5]pyrrolo[2,3-d]pyridines, and 9h-1,3,6,9-tetraaza-fluorenes as chk1 kinase function inhibitors |
| US8133506B2 (en) | 2008-03-12 | 2012-03-13 | Aptalis Pharmatech, Inc. | Drug delivery systems comprising weakly basic drugs and organic acids |
| WO2009129401A1 (en) | 2008-04-16 | 2009-10-22 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
| CA2725754C (en) * | 2008-06-11 | 2017-05-23 | Hazel Joan Dyke | Diazacarbazoles and methods of use |
| AR072084A1 (es) * | 2008-06-12 | 2010-08-04 | Sanofi Aventis | Derivados de azacarbolinas, su preparacion y su utilizacion terapeutica como inhibidores de las quinasas pim |
| WO2010015589A1 (en) | 2008-08-05 | 2010-02-11 | Nycomed Gmbh | Benzyl-substituted tetracyclic heterocyclic compounds as pde5 inhibitors |
| BRPI0924844A2 (pt) * | 2009-03-24 | 2016-01-26 | Sanofi Sa | derivados de azacarbolinas 9h-pirrol[2,3-b:5,4-c']dipiridina, sua preparação e sua utilização terapêutica. |
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Non-Patent Citations (2)
| Title |
|---|
| BIOORGANIC AND MEDICINAL CHEMISTRY, vol. 15, 2007, pages 950-5964 |
| JOURNAL OF THE CHEMICAL SOCIETY, vol. 1997, 1997, pages 581-3585 |
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