JP2005531563A5 - - Google Patents
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- Publication number
- JP2005531563A5 JP2005531563A5 JP2004505374A JP2004505374A JP2005531563A5 JP 2005531563 A5 JP2005531563 A5 JP 2005531563A5 JP 2004505374 A JP2004505374 A JP 2004505374A JP 2004505374 A JP2004505374 A JP 2004505374A JP 2005531563 A5 JP2005531563 A5 JP 2005531563A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- optionally substituted
- group
- iii
- 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
- 150000001875 compounds Chemical class 0.000 claims 28
- 239000008194 pharmaceutical composition Substances 0.000 claims 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 229910052757 nitrogen Inorganic materials 0.000 claims 6
- 229910052760 oxygen Inorganic materials 0.000 claims 6
- 230000002062 proliferating effect Effects 0.000 claims 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 5
- 206010028980 Neoplasm Diseases 0.000 claims 5
- 239000002246 antineoplastic agent Substances 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 claims 4
- 229920006395 saturated elastomer Polymers 0.000 claims 4
- 150000001408 amides Chemical class 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 3
- 125000005647 linker group Chemical group 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 230000002265 prevention Effects 0.000 claims 3
- 229940002612 prodrug Drugs 0.000 claims 3
- 239000000651 prodrug Substances 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 150000001204 N-oxides Chemical class 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 125000002431 aminoalkoxy group Chemical group 0.000 claims 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims 2
- 229940034982 antineoplastic agent Drugs 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 210000000481 breast Anatomy 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 125000002837 carbocyclic group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 125000000524 functional group Chemical group 0.000 claims 2
- 210000004072 lung Anatomy 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 239000012453 solvate Substances 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 208000003174 Brain Neoplasms Diseases 0.000 claims 1
- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 230000004568 DNA-binding Effects 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 206010025323 Lymphomas Diseases 0.000 claims 1
- 208000034578 Multiple myelomas Diseases 0.000 claims 1
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 1
- 241000277331 Salmonidae Species 0.000 claims 1
- 206010039491 Sarcoma Diseases 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 230000003213 activating effect Effects 0.000 claims 1
- 125000004450 alkenylene group Chemical group 0.000 claims 1
- 125000004419 alkynylene group Chemical group 0.000 claims 1
- 230000000118 anti-neoplastic effect Effects 0.000 claims 1
- 230000000259 anti-tumor effect Effects 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 208000035269 cancer or benign tumor Diseases 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 230000004663 cell proliferation Effects 0.000 claims 1
- 230000001413 cellular effect Effects 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 208000029742 colonic neoplasm Diseases 0.000 claims 1
- 231100000433 cytotoxic Toxicity 0.000 claims 1
- 239000002254 cytotoxic agent Substances 0.000 claims 1
- 230000001472 cytotoxic effect Effects 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 230000002124 endocrine Effects 0.000 claims 1
- 230000002496 gastric effect Effects 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 210000000777 hematopoietic system Anatomy 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- JBFYUZGYRGXSFL-UHFFFAOYSA-N imidazolide Chemical compound C1=C[N-]C=N1 JBFYUZGYRGXSFL-UHFFFAOYSA-N 0.000 claims 1
- 230000000968 intestinal effect Effects 0.000 claims 1
- 210000003734 kidney Anatomy 0.000 claims 1
- 208000032839 leukemia Diseases 0.000 claims 1
- 210000004185 liver Anatomy 0.000 claims 1
- 230000001926 lymphatic effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- -1 methoxy-substituted phenyl Chemical group 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- CSMRPIFORJZYCJ-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-2,6-dimethyl-1-oxobenzo[b][1,6]naphthyridine-4-carboxamide Chemical compound C1=CC(C)=C2N=C3C(C(=O)NCCN(C)C)=CN(C)C(=O)C3=CC2=C1 CSMRPIFORJZYCJ-UHFFFAOYSA-N 0.000 claims 1
- 230000001537 neural effect Effects 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 230000002611 ovarian Effects 0.000 claims 1
- 210000001672 ovary Anatomy 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 210000000496 pancreas Anatomy 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 210000002307 prostate Anatomy 0.000 claims 1
- 210000003491 skin Anatomy 0.000 claims 1
- 210000001550 testis Anatomy 0.000 claims 1
- 229940124597 therapeutic agent Drugs 0.000 claims 1
- 210000001519 tissue Anatomy 0.000 claims 1
- 210000004291 uterus Anatomy 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPS2344A AUPS234402A0 (en) | 2002-05-15 | 2002-05-15 | Anti-tumour polycyclic carboxamides |
| PCT/AU2003/000569 WO2003097642A1 (en) | 2002-05-15 | 2003-05-12 | Anti-tumour polycyclic carboxamides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005531563A JP2005531563A (ja) | 2005-10-20 |
| JP2005531563A5 true JP2005531563A5 (enExample) | 2006-06-29 |
Family
ID=3835914
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004505374A Pending JP2005531563A (ja) | 2002-05-15 | 2003-05-12 | 抗腫瘍性多環式カルボキサミド |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US7504507B2 (enExample) |
| EP (1) | EP1507778B1 (enExample) |
| JP (1) | JP2005531563A (enExample) |
| AT (1) | ATE546447T1 (enExample) |
| AU (1) | AUPS234402A0 (enExample) |
| CA (1) | CA2485494C (enExample) |
| NZ (1) | NZ537015A (enExample) |
| WO (1) | WO2003097642A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AUPS234402A0 (en) * | 2002-05-15 | 2002-06-13 | Auckland Uniservices Limited | Anti-tumour polycyclic carboxamides |
| CA2554775A1 (en) * | 2004-01-30 | 2005-08-18 | Chemgenex Pharmaceuticals, Inc. | Naphthalimide dosing by n-acetyl transferase genotyping |
| US20080248134A1 (en) * | 2005-05-04 | 2008-10-09 | Auckland Uniservices Limited | Oral compositions, use and combinations of N-[2-(dimethylamino)ethyl]-2,6 dimethyl-1-oxo-1,2-dihydrobenzo[b]-1,6-naphthyridine-4-carboxamide and closely related analogues thereof |
| CZ304996B6 (cs) | 2013-01-17 | 2015-03-18 | Ústav Organické Chemie A Biochemie Akademie Věd Čr, V.V.I. | Deriváty helquatů, jejich příprava a použití jako léčiva |
| CZ307163B6 (cs) | 2014-05-29 | 2018-02-14 | Ăšstav organickĂ© chemie a biochemie AV ÄŚR, v.v.i. | Helquaty s heteroaromatickými substituenty, jejich příprava a použití jako stabilizátory G-kvadruplexů |
| WO2017097928A1 (en) * | 2015-12-08 | 2017-06-15 | Universität Zu Köln | Cpap-tubulin module |
| CN109265396A (zh) * | 2018-09-12 | 2019-01-25 | 李玮 | 多环酰胺化合物的合成新方法与抗癌活性 |
| CN115677691B (zh) * | 2022-08-24 | 2023-08-29 | 潍坊富邦药业有限公司 | 一种苯并萘啶酰胺抗癌药sn28049及其类似物的制备方法 |
| CN118852160A (zh) * | 2024-09-24 | 2024-10-29 | 世华合创生物技术开发(山东)有限公司 | 一种三环酰胺化合物、制备方法及应用 |
| CN119350329B (zh) * | 2024-12-23 | 2025-03-21 | 世华合创生物技术开发(山东)有限公司 | 一种二氮杂三环胺化合物、制备方法及应用 |
| CN119350330B (zh) * | 2024-12-23 | 2025-03-21 | 世华合创生物技术开发(山东)有限公司 | 一种二氮杂三环胺化合物、制备方法及其应用 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4160452A (en) * | 1977-04-07 | 1979-07-10 | Alza Corporation | Osmotic system having laminated wall comprising semipermeable lamina and microporous lamina |
| US4256108A (en) * | 1977-04-07 | 1981-03-17 | Alza Corporation | Microporous-semipermeable laminated osmotic system |
| US4265874A (en) * | 1980-04-25 | 1981-05-05 | Alza Corporation | Method of delivering drug with aid of effervescent activity generated in environment of use |
| NZ201084A (en) * | 1982-06-25 | 1985-10-11 | New Zealand Dev Finance | 4-carboxamidoacridine derivatives and pharmaceutical compositions containing such |
| AUPS234402A0 (en) * | 2002-05-15 | 2002-06-13 | Auckland Uniservices Limited | Anti-tumour polycyclic carboxamides |
-
2002
- 2002-05-15 AU AUPS2344A patent/AUPS234402A0/en not_active Abandoned
-
2003
- 2003-05-12 US US10/514,523 patent/US7504507B2/en not_active Expired - Fee Related
- 2003-05-12 WO PCT/AU2003/000569 patent/WO2003097642A1/en not_active Ceased
- 2003-05-12 CA CA2485494A patent/CA2485494C/en not_active Expired - Fee Related
- 2003-05-12 JP JP2004505374A patent/JP2005531563A/ja active Pending
- 2003-05-12 NZ NZ537015A patent/NZ537015A/en not_active IP Right Cessation
- 2003-05-12 EP EP03717051A patent/EP1507778B1/en not_active Expired - Lifetime
- 2003-05-12 AT AT03717051T patent/ATE546447T1/de active
-
2009
- 2009-02-17 US US12/372,416 patent/US20090156630A1/en not_active Abandoned
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