IL271761B - (12as)-8-methoxy-9-benzyloxy-11,12,12a,13-tetrahydro-6h-indolo[2,1-c][1,4]benzodiazepin-6-one, 4-benzyloxy-5-methoxy-2-nitrobenzoic acid and processes for preparing the same - Google Patents
(12as)-8-methoxy-9-benzyloxy-11,12,12a,13-tetrahydro-6h-indolo[2,1-c][1,4]benzodiazepin-6-one, 4-benzyloxy-5-methoxy-2-nitrobenzoic acid and processes for preparing the sameInfo
- Publication number
- IL271761B IL271761B IL271761A IL27176119A IL271761B IL 271761 B IL271761 B IL 271761B IL 271761 A IL271761 A IL 271761A IL 27176119 A IL27176119 A IL 27176119A IL 271761 B IL271761 B IL 271761B
- Authority
- IL
- Israel
- Prior art keywords
- benzyloxy
- methoxy
- formula
- sor
- carbon atoms
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 6
- ATZMTXLRQVTBIA-SFHVURJKSA-N (12as)-8-methoxy-9-phenylmethoxy-11,12,12a,13-tetrahydroindolo[2,1-c][1,4]benzodiazepin-6-one Chemical compound COC1=CC(C(N2C3=CC=CC=C3C[C@H]2CN2)=O)=C2C=C1OCC1=CC=CC=C1 ATZMTXLRQVTBIA-SFHVURJKSA-N 0.000 title description 2
- VTHHRADLOLKTLD-UHFFFAOYSA-N 4-(benzyloxy)-5-methoxy-2-nitrobenzoic acid Chemical compound COC1=CC(C(O)=O)=C([N+]([O-])=O)C=C1OCC1=CC=CC=C1 VTHHRADLOLKTLD-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 15
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 238000006722 reduction reaction Methods 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 description 22
- 229910052760 oxygen Inorganic materials 0.000 description 22
- 229910052717 sulfur Chemical group 0.000 description 22
- 125000005842 heteroatom Chemical group 0.000 description 20
- 125000004432 carbon atom Chemical group C* 0.000 description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 125000003118 aryl group Chemical group 0.000 description 13
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 12
- 239000001301 oxygen Chemical group 0.000 description 12
- 239000011593 sulfur Chemical group 0.000 description 12
- 125000003342 alkenyl group Chemical group 0.000 description 11
- 125000000304 alkynyl group Chemical group 0.000 description 11
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 description 10
- 125000004093 cyano group Chemical group *C#N 0.000 description 10
- 229910052736 halogen Inorganic materials 0.000 description 10
- 150000002367 halogens Chemical class 0.000 description 10
- 125000005647 linker group Chemical group 0.000 description 10
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 10
- 125000000623 heterocyclic group Chemical group 0.000 description 9
- 229910052698 phosphorus Inorganic materials 0.000 description 8
- 125000001424 substituent group Chemical group 0.000 description 8
- 239000002202 Polyethylene glycol Substances 0.000 description 7
- 125000003827 glycol group Chemical group 0.000 description 7
- 229920001223 polyethylene glycol Polymers 0.000 description 7
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 description 6
- 150000001557 benzodiazepines Chemical class 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 5
- 206010028980 Neoplasm Diseases 0.000 description 4
- 229940053197 benzodiazepine derivative antiepileptics Drugs 0.000 description 4
- 201000011510 cancer Diseases 0.000 description 3
- 231100000433 cytotoxic Toxicity 0.000 description 3
- 230000001472 cytotoxic effect Effects 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 125000003275 alpha amino acid group Chemical group 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000001028 anti-proliverative effect Effects 0.000 description 2
- 229940088710 antibiotic agent Drugs 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920001184 polypeptide Polymers 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- UQVNRKBFAXNOGA-LWTNMJDUSA-N (E)-tomaymycin Chemical class CO[C@H]1NC2=CC(O)=C(OC)C=C2C(=O)N2C\C(=C\C)C[C@@H]12 UQVNRKBFAXNOGA-LWTNMJDUSA-N 0.000 description 1
- KAOYLRLQZXRRBD-UHFFFAOYSA-N 1,2,3-benzothiadiazepine Chemical compound S1N=NC=CC2=CC=CC=C12 KAOYLRLQZXRRBD-UHFFFAOYSA-N 0.000 description 1
- VGGWNGWXGFWLRK-UHFFFAOYSA-N 8,9-dihydro-1H-[1,3]oxazolo[4,5-i][1,2]benzodiazepine Chemical class C1=CC=NNC2=C(OCN3)C3=CC=C21 VGGWNGWXGFWLRK-UHFFFAOYSA-N 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- 208000001132 Osteoporosis Diseases 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000001430 anti-depressive effect Effects 0.000 description 1
- 230000003556 anti-epileptic effect Effects 0.000 description 1
- 239000001961 anticonvulsive agent Substances 0.000 description 1
- 239000000935 antidepressant agent Substances 0.000 description 1
- 229940005513 antidepressants Drugs 0.000 description 1
- 229960003965 antiepileptics Drugs 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 229940049706 benzodiazepine Drugs 0.000 description 1
- 230000024245 cell differentiation Effects 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000002934 diuretic Substances 0.000 description 1
- 229940030606 diuretics Drugs 0.000 description 1
- ZRALSGWEFCBTJO-UHFFFAOYSA-O guanidinium Chemical compound NC(N)=[NH2+] ZRALSGWEFCBTJO-UHFFFAOYSA-O 0.000 description 1
- 230000000055 hyoplipidemic effect Effects 0.000 description 1
- 208000021822 hypotensive Diseases 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- UVNXNSUKKOLFBM-UHFFFAOYSA-N imidazo[2,1-b][1,3,4]thiadiazole Chemical compound N1=CSC2=NC=CN21 UVNXNSUKKOLFBM-UHFFFAOYSA-N 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 230000002062 proliferating effect Effects 0.000 description 1
- RYHNOTGTYWODPH-UHFFFAOYSA-N pyrrolo[1,2-b][1,2,5]benzothiadiazepine Chemical class N1=CC2=CC=CN2SC2=CC=CC=C21 RYHNOTGTYWODPH-UHFFFAOYSA-N 0.000 description 1
- YUOCYTRGANSSRY-UHFFFAOYSA-N pyrrolo[2,3-i][1,2]benzodiazepine Chemical class C1=CN=NC2=C3C=CN=C3C=CC2=C1 YUOCYTRGANSSRY-UHFFFAOYSA-N 0.000 description 1
- -1 pyrrolo[l Chemical class 0.000 description 1
- BXVYJQULAWJPSR-UHFFFAOYSA-N thiadiazepine Chemical compound S1C=CC=CN=N1 BXVYJQULAWJPSR-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07K5/1005—Tetrapeptides with the first amino acid being neutral and aliphatic
- C07K5/1008—Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15020109P | 2009-02-05 | 2009-02-05 | |
| PCT/US2010/023150 WO2010091150A1 (en) | 2009-02-05 | 2010-02-04 | Novel benzodiazepine derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL271761A IL271761A (en) | 2020-02-27 |
| IL271761B true IL271761B (en) | 2022-09-01 |
Family
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Family Applications (6)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL271761A IL271761B (en) | 2009-02-05 | 2010-02-04 | (12as)-8-methoxy-9-benzyloxy-11,12,12a,13-tetrahydro-6h-indolo[2,1-c][1,4]benzodiazepin-6-one, 4-benzyloxy-5-methoxy-2-nitrobenzoic acid and processes for preparing the same |
| IL295601A IL295601B2 (en) | 2009-02-05 | 2010-02-04 | Benzodiazepine Derivatives and Processes for Producing the Same |
| IL214475A IL214475A (en) | 2009-02-05 | 2011-08-04 | History of benzodiazepine, preparations containing them and their uses |
| IL241633A IL241633A0 (en) | 2009-02-05 | 2015-09-16 | History of benzodiazepines, preparations containing them and their uses |
| IL241634A IL241634B (en) | 2009-02-05 | 2015-09-16 | History of new benzodiazepines, preparations containing them and their uses |
| IL241632A IL241632B (en) | 2009-02-05 | 2015-09-16 | History of benzodiazepines, preparations containing them and their uses |
Family Applications After (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL295601A IL295601B2 (en) | 2009-02-05 | 2010-02-04 | Benzodiazepine Derivatives and Processes for Producing the Same |
| IL214475A IL214475A (en) | 2009-02-05 | 2011-08-04 | History of benzodiazepine, preparations containing them and their uses |
| IL241633A IL241633A0 (en) | 2009-02-05 | 2015-09-16 | History of benzodiazepines, preparations containing them and their uses |
| IL241634A IL241634B (en) | 2009-02-05 | 2015-09-16 | History of new benzodiazepines, preparations containing them and their uses |
| IL241632A IL241632B (en) | 2009-02-05 | 2015-09-16 | History of benzodiazepines, preparations containing them and their uses |
Country Status (16)
| Country | Link |
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| US (10) | US8426402B2 (OSRAM) |
| EP (3) | EP3100745B1 (OSRAM) |
| JP (4) | JP5977522B2 (OSRAM) |
| KR (3) | KR102021728B1 (OSRAM) |
| CN (4) | CN102365021B (OSRAM) |
| AU (1) | AU2010210646B2 (OSRAM) |
| BR (1) | BRPI1008749B8 (OSRAM) |
| CA (2) | CA3014224C (OSRAM) |
| ES (1) | ES2604668T3 (OSRAM) |
| IL (6) | IL271761B (OSRAM) |
| MX (2) | MX368362B (OSRAM) |
| NZ (2) | NZ594177A (OSRAM) |
| RU (2) | RU2683325C2 (OSRAM) |
| SG (3) | SG173152A1 (OSRAM) |
| WO (1) | WO2010091150A1 (OSRAM) |
| ZA (1) | ZA201105352B (OSRAM) |
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| BRPI0510883B8 (pt) | 2004-06-01 | 2021-05-25 | Genentech Inc | composto conjugado de droga e anticorpo, composição farmacêutica, método de fabricação de composto conjugado de droga e anticorpo e usos de uma formulação, de um conjugado de droga e anticorpo e um agente quimioterapêutico e de uma combinação |
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| ATE427949T1 (de) * | 2005-10-05 | 2009-04-15 | Spirogen Ltd | 4-a4-(5-oxo-2,3,5,11a-tetrahydro-5h-pyrrolo a2, 1-cua1,4ubenzodiazepin-8-yloxy)-butyrylaminou-1 - pyrrol-2-carbonsaurealkylesterderivate und verwandte verbindung zur behandlung einer proliferativen erkrankung |
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