MX9705309A - Analogos de n-acetilardeemina, metodo de preparacion y sus usos. - Google Patents
Analogos de n-acetilardeemina, metodo de preparacion y sus usos.Info
- Publication number
- MX9705309A MX9705309A MX9705309A MX9705309A MX9705309A MX 9705309 A MX9705309 A MX 9705309A MX 9705309 A MX9705309 A MX 9705309A MX 9705309 A MX9705309 A MX 9705309A MX 9705309 A MX9705309 A MX 9705309A
- Authority
- MX
- Mexico
- Prior art keywords
- cr3r3
- hydrogen
- linear
- branched chain
- chr4
- Prior art date
Links
- XTLQWSBGQKPGCF-YWDSKPHESA-N 5-n-acetylardeemin Chemical class C1=CC=C2C(=O)N3[C@H](C)C(=O)N4[C@H](N(C(C)=O)C=5C6=CC=CC=5)[C@@]6(C(C)(C)C=C)C[C@H]4C3=NC2=C1 XTLQWSBGQKPGCF-YWDSKPHESA-N 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 150000002431 hydrogen Chemical class 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000035945 sensitivity Effects 0.000 abstract 1
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
- C07D487/22—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 four or more hetero rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La presente invencion proporciona un compuesto que tiene la estructura (I), en donde R1, R6 y R7 son independientemente hidrogeno, OH, NH2, SH, halogeno, alquilo de 1 a 9 átomos de carbono, de cadena lineal o ramificada, alquilmercapto, alquilamino, dialquilamino, alcoxi, fenilo, etc.; en donde R0 y R2 son independientemente hidrogeno, OH, alquilo de cadena lineal o ramificada, -CR3R3-CH(O)CH2, -CR3R3-CH2CH3, -CR3R3-CH2CH2OH, -CR3R3-CH(OH)R4 o -CR3R3-CH(OH)R4 o -CR3R3-CH=CHR4, en donde R3 y R4 son independientemente hidrogeno, halogeno, alquilo de 1 a 9 átomos de carbono de cadena lineal o ramificada, fenilo, etc., en donde R5 es hidrogeno, alquilo de 1 a 9 átomos de carbono, de cadena lineal o ramificada, fenilo, etc.; en donde R8 es hidrogeno, acilo de 1 a 9 átomos de carbono, de cadena lineal o ramificada, benzoilo, etc.; con la condicion que (a) cuando R 2 es -CR3R3-CH(O)CH2, -CR3R3-CH2CH3, -CR3R3- CH2CH2OH, -CR3R3-CH(OH)R4 o -CR3R3-CH=CHR4, entonces R0 es hidrogeno; (b) cuando R0 es -CR3R3-CH(O)CH2, -CR3R3-CH2CH3, -CR3R3-CH2CH2OH, -CR3R3-CH(OH)R4 o -CR3R3-CH=CHR4, entonces R2 es OH; y (c) cuando (i) R0 o R2 es CR3R3-CH=CHR4, (ii) R3 y R5 son CH3 y (iii) R4 es hidrogeno, entonces R1, R6 y R7 no son todos hidrogeno. También se proporcionan compuestos relacionados y composiciones, y métodos para inhibir el crecimiento de células resistentes a varios fármacos por medio de la inversion MDR, sensibilidad colateral y sinergismo cuantitativo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US675095P | 1995-11-15 | 1995-11-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX9705309A true MX9705309A (es) | 1998-06-30 |
Family
ID=21722393
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX9705309A MX9705309A (es) | 1995-11-15 | 1997-07-14 | Analogos de n-acetilardeemina, metodo de preparacion y sus usos. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6147076A (es) |
| EP (1) | EP0815111B1 (es) |
| JP (1) | JPH10512899A (es) |
| AT (1) | ATE375348T1 (es) |
| AU (1) | AU729877B2 (es) |
| CA (1) | CA2209775C (es) |
| DE (1) | DE69637283D1 (es) |
| MX (1) | MX9705309A (es) |
| WO (1) | WO1997018215A1 (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999015174A1 (en) * | 1997-09-22 | 1999-04-01 | Sloan-Kettering Institute For Cancer Research | Reverse prenyl compounds as immunosuppressants |
| CN100352805C (zh) | 2000-11-08 | 2007-12-05 | 鲁汶天主教大学研究开发部 | 用作造影剂的取代的联吲哚衍生物、包含它们的药物组合物以及制造它们的中间体 |
| CN102276615B (zh) * | 2011-08-26 | 2013-10-23 | 四川大学 | 一种制备甲酰阿地咪的方法 |
| WO2014089177A2 (en) * | 2012-12-04 | 2014-06-12 | Massachusetts Institute Of Technology | Compounds, conjugates and compositions of epipolythiodiketopiperazines and polythiodiketopiperazines |
| CN103113376B (zh) * | 2013-02-04 | 2015-03-04 | 浙江工业大学 | 一种生物碱及制备方法和应用 |
| WO2017197045A1 (en) | 2016-05-11 | 2017-11-16 | Movassaghi Mohammad | Convergent and enantioselective total synthesis of communesin analogs |
| WO2018209239A1 (en) | 2017-05-11 | 2018-11-15 | Massachusetts Institute Of Technology | Potent agelastatin derivatives as modulators for cancer invasion and metastasis |
| US10640508B2 (en) | 2017-10-13 | 2020-05-05 | Massachusetts Institute Of Technology | Diazene directed modular synthesis of compounds with quaternary carbon centers |
| US11535634B2 (en) | 2019-06-05 | 2022-12-27 | Massachusetts Institute Of Technology | Compounds, conjugates, and compositions of epipolythiodiketopiperazines and polythiodiketopiperazines and uses thereof |
| CN110724149B (zh) * | 2019-10-17 | 2022-04-05 | 中山大学 | 一种海洋真菌来源的吲哚生物碱二聚体化合物及制备方法与抗海洋污损生物防除剂中的应用 |
| WO2022006145A1 (en) * | 2020-06-29 | 2022-01-06 | Zymergen Inc. | Modulus modifiers and films thereof |
| WO2022182415A1 (en) | 2021-02-24 | 2022-09-01 | Massachusetts Institute Of Technology | Himastatin derivatives, and processes of preparation thereof, and uses thereof |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58152487A (ja) * | 1982-03-05 | 1983-09-10 | Fujisawa Pharmaceut Co Ltd | Ｆｒ−９００２２０物質およびその製造法 |
| JPS6041678A (ja) * | 1983-08-16 | 1985-03-05 | Fujisawa Pharmaceut Co Ltd | インド−ル誘導体 |
| JPH06505474A (ja) * | 1991-01-31 | 1994-06-23 | アボツト・ラボラトリーズ | エンドセリン転換酵素阻害剤 |
| US5196420A (en) * | 1991-07-19 | 1993-03-23 | The United States Of America As Represented By The Secretary Of Agriculture | Cycloechinulin antiinsectan metabolite |
| US5284947A (en) * | 1992-09-15 | 1994-02-08 | Abbott Laboratories | Multiple drug resistance-attenuating compounds |
| US5338845A (en) * | 1992-12-02 | 1994-08-16 | Sterling Winthrop Inc. | Aspergillus species, cyclic dimeric dipeptide derivative substance P antagonist biosynthetic products thereof, and process for preparation thereof |
-
1996
- 1996-11-15 AU AU11425/97A patent/AU729877B2/en not_active Ceased
- 1996-11-15 CA CA002209775A patent/CA2209775C/en not_active Expired - Fee Related
- 1996-11-15 DE DE69637283T patent/DE69637283D1/de not_active Expired - Lifetime
- 1996-11-15 EP EP96942827A patent/EP0815111B1/en not_active Expired - Lifetime
- 1996-11-15 US US08/749,908 patent/US6147076A/en not_active Expired - Fee Related
- 1996-11-15 JP JP9519179A patent/JPH10512899A/ja not_active Ceased
- 1996-11-15 AT AT96942827T patent/ATE375348T1/de not_active IP Right Cessation
- 1996-11-15 WO PCT/US1996/019086 patent/WO1997018215A1/en not_active Ceased
-
1997
- 1997-07-14 MX MX9705309A patent/MX9705309A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0815111B1 (en) | 2007-10-10 |
| WO1997018215A1 (en) | 1997-05-22 |
| EP0815111A4 (en) | 1998-05-06 |
| EP0815111A1 (en) | 1998-01-07 |
| US6147076A (en) | 2000-11-14 |
| DE69637283D1 (de) | 2007-11-22 |
| AU729877B2 (en) | 2001-02-15 |
| CA2209775A1 (en) | 1997-05-22 |
| CA2209775C (en) | 2006-01-24 |
| AU1142597A (en) | 1997-06-05 |
| ATE375348T1 (de) | 2007-10-15 |
| JPH10512899A (ja) | 1998-12-08 |
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