MXPA06001819A - Derivados ciclicos como moduladores de la actividad del receptor de quimiocina. - Google Patents
Derivados ciclicos como moduladores de la actividad del receptor de quimiocina.Info
- Publication number
- MXPA06001819A MXPA06001819A MXPA06001819A MXPA06001819A MXPA06001819A MX PA06001819 A MXPA06001819 A MX PA06001819A MX PA06001819 A MXPA06001819 A MX PA06001819A MX PA06001819 A MXPA06001819 A MX PA06001819A MX PA06001819 A MXPA06001819 A MX PA06001819A
- Authority
- MX
- Mexico
- Prior art keywords
- substituted
- crr
- alkyl
- butyl
- alkynyl
- Prior art date
Links
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- 239000011343 solid material Substances 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- HGNXRTOUUOHZEO-OAGGEKHMSA-N tert-butyl (1r,4s,5r)-6-oxo-4-(phenylmethoxycarbonylamino)-7-azabicyclo[3.2.1]octane-7-carboxylate Chemical compound N([C@@H]1[C@]2(C[C@@](CC1)(N(C2=O)C(=O)OC(C)(C)C)[H])[H])C(=O)OCC1=CC=CC=C1 HGNXRTOUUOHZEO-OAGGEKHMSA-N 0.000 description 1
- VDVDCDBZFLIRLQ-FOIQADDNSA-N tert-butyl (1s,6r)-6-carbamoyl-6-(phenylmethoxycarbonylamino)cyclohex-3-ene-1-carboxylate Chemical compound CC(C)(C)OC(=O)[C@H]1CC=CC[C@@]1(C(N)=O)NC(=O)OCC1=CC=CC=C1 VDVDCDBZFLIRLQ-FOIQADDNSA-N 0.000 description 1
- NWYVGIOXHOXWNY-UHFFFAOYSA-N tert-butyl 6-oxo-5-(phenylmethoxycarbonylamino)-7-azabicyclo[3.2.1]octane-7-carboxylate Chemical compound O=C1N(C(=O)OC(C)(C)C)C(CCC2)CC21NC(=O)OCC1=CC=CC=C1 NWYVGIOXHOXWNY-UHFFFAOYSA-N 0.000 description 1
- NBRKLOOSMBRFMH-UHFFFAOYSA-N tert-butyl chloride Chemical compound CC(C)(C)Cl NBRKLOOSMBRFMH-UHFFFAOYSA-N 0.000 description 1
- NFYIFHKKXHUGPJ-UHFFFAOYSA-N tert-butyl n-[2-(trifluoromethoxy)phenyl]carbamate Chemical compound CC(C)(C)OC(=O)NC1=CC=CC=C1OC(F)(F)F NFYIFHKKXHUGPJ-UHFFFAOYSA-N 0.000 description 1
- FQFILJKFZCVHNH-UHFFFAOYSA-N tert-butyl n-[3-[(5-bromo-2-chloropyrimidin-4-yl)amino]propyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCCNC1=NC(Cl)=NC=C1Br FQFILJKFZCVHNH-UHFFFAOYSA-N 0.000 description 1
- SDHZUDDBCMQPPK-UHFFFAOYSA-N tert-butyl n-[4-(trifluoromethoxy)phenyl]carbamate Chemical compound CC(C)(C)OC(=O)NC1=CC=C(OC(F)(F)F)C=C1 SDHZUDDBCMQPPK-UHFFFAOYSA-N 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000004627 thianthrenyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3SC12)* 0.000 description 1
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- LEIMLDGFXIOXMT-UHFFFAOYSA-N trimethylsilyl cyanide Chemical compound C[Si](C)(C)C#N LEIMLDGFXIOXMT-UHFFFAOYSA-N 0.000 description 1
- 241001529453 unidentified herpesvirus Species 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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Classifications
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| PCT/US2004/027196 WO2005021500A1 (en) | 2003-08-21 | 2004-08-20 | Cyclic derivatives as modulators of chemokine receptor activity |
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| CA2432908A1 (en) | 2000-12-20 | 2002-06-27 | Bristol-Myers Squibb Pharma Company | Diamines as modulators of chemokine receptor activity |
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| AU2003218028A1 (en) * | 2002-03-08 | 2003-09-22 | Bristol-Myers Squibb Company | Cyclic derivatives as modulators of chemokine receptor activity |
| US7291615B2 (en) | 2003-05-01 | 2007-11-06 | Bristol-Myers Squibb Company | Cyclic derivatives as modulators of chemokine receptor activity |
| US7317019B2 (en) * | 2003-08-21 | 2008-01-08 | Bristol Myers Squibb Co. | N-alkylated diaminopropane derivatives as modulators of chemokine receptor activity |
| US7163937B2 (en) * | 2003-08-21 | 2007-01-16 | Bristol-Myers Squibb Company | Cyclic derivatives as modulators of chemokine receptor activity |
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| US10745701B2 (en) | 2007-06-28 | 2020-08-18 | The Trustees Of Princeton University | Methods of identifying and treating poor-prognosis cancers |
| MX2010002904A (es) | 2007-09-17 | 2010-06-02 | Abbott Lab | N-fenil-dioxo-hidropirimidinas utiles como inhibidores de virus de hepatitis c (hcv). |
| RU2543620C2 (ru) | 2007-09-17 | 2015-03-10 | Эббви Бахамаз Лтд. | Производные урацила или тимина для лечения гепатита с |
| PL2203431T3 (pl) | 2007-09-17 | 2012-01-31 | Abbvie Bahamas Ltd | Pirymidyny o działaniu przeciw zakaźnym oraz ich zastosowania |
| JP2010540527A (ja) * | 2007-09-25 | 2010-12-24 | アボット・ラボラトリーズ | ケモカイン受容体拮抗薬としてのオクタヒドロペンタレン化合物 |
| TW201035100A (en) | 2008-12-19 | 2010-10-01 | Cephalon Inc | Pyrrolotriazines as ALK and JAK2 inhibitors |
| US8383812B2 (en) | 2009-10-13 | 2013-02-26 | Bristol-Myers Squibb Company | N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-3-(7-tert-butylpyrazolo[1,5-A][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin-1-yl)cyclohexyl)acetamide, a dual modulator of chemokine receptor activity, crystalline forms and processes |
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| WO2011100227A1 (en) * | 2010-02-09 | 2011-08-18 | Bristol-Myers Squibb Company | Benzylpyrrolidinone derivatives as modulators of chemokine receptor activity |
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| US8703768B2 (en) | 2010-06-09 | 2014-04-22 | Hoffmann-La Roche Inc. | Nitrogen containing heteroaryl compounds |
| BR112013001138A2 (pt) | 2010-07-16 | 2016-07-05 | Abbvie Inc | ligantes de fosfina para reações catalíticas |
| US8975443B2 (en) | 2010-07-16 | 2015-03-10 | Abbvie Inc. | Phosphine ligands for catalytic reactions |
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| US8927533B2 (en) * | 2011-09-19 | 2015-01-06 | Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. | Thio derivatives bearing lactams as potent HDAC inhibitors and their uses as medicaments |
| WO2013149376A1 (en) | 2012-04-02 | 2013-10-10 | Abbott Laboratories | Chemokine receptor antagonists |
| WO2014151953A1 (en) | 2013-03-15 | 2014-09-25 | The California Institute For Biomedical Research | Compounds and methods for inducing chondrogenesis |
| WO2017004134A1 (en) * | 2015-06-29 | 2017-01-05 | Nimbus Iris, Inc. | Irak inhibitors and uses thereof |
| PL3448848T3 (pl) | 2016-04-29 | 2024-03-11 | Bayer Pharma Aktiengesellschaft | Postać polimorficzna N-{6-(2-hydroksypropan-2-ylo)-2-[2-(metylosulfonylo)etylo]-2H-indazol-5-ilo}-6-(trifluorometylo)pirydyno-2-karboksyamidu |
| PT3448849T (pt) | 2016-04-29 | 2020-06-30 | Bayer Pharma AG | Síntese de indazóis |
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| EA202092094A1 (ru) * | 2018-03-05 | 2020-12-10 | Бристол-Маерс Сквибб Компани | Фенилпирролидиноновые агонисты формилпептидного рецептора 2 |
| WO2022032187A1 (en) | 2020-08-07 | 2022-02-10 | Bristol-Myers Squibb Company | Fgf21 combined with ccr2/5 antagonists for the treatment of fibrosis |
| CN112778109B (zh) * | 2021-01-15 | 2022-09-06 | 台州臻挚生物科技有限公司 | 1-[3-氯-5-(三氟甲基)苯基]-2,2,2-三氟乙酮及其衍生物的制备方法 |
| US20240390337A1 (en) * | 2021-09-22 | 2024-11-28 | Drexel University | Rela/rsh inhibitors for the treatment or prevention of medical biofilms |
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-
2004
- 2004-08-19 US US10/923,619 patent/US7163937B2/en not_active Expired - Lifetime
- 2004-08-20 SI SI200432117T patent/SI1656345T1/sl unknown
- 2004-08-20 JP JP2006524092A patent/JP4795238B2/ja not_active Expired - Fee Related
- 2004-08-20 BR BRPI0413713-2A patent/BRPI0413713A/pt not_active IP Right Cessation
- 2004-08-20 CA CA2536384A patent/CA2536384C/en not_active Expired - Fee Related
- 2004-08-20 MX MXPA06001819A patent/MXPA06001819A/es active IP Right Grant
- 2004-08-20 RS YUP-2006/0116A patent/RS20060116A/sr unknown
- 2004-08-20 NZ NZ545317A patent/NZ545317A/en not_active IP Right Cessation
- 2004-08-20 ES ES04781806.7T patent/ES2437104T3/es not_active Expired - Lifetime
- 2004-08-20 EP EP04781806.7A patent/EP1656345B1/en not_active Expired - Lifetime
- 2004-08-20 PL PL04781806T patent/PL1656345T3/pl unknown
- 2004-08-20 RU RU2006108867/04A patent/RU2006108867A/ru not_active Application Discontinuation
- 2004-08-20 HR HRP20131048TT patent/HRP20131048T1/hr unknown
- 2004-08-20 KR KR1020067003442A patent/KR101120338B1/ko not_active Expired - Fee Related
- 2004-08-20 PT PT47818067T patent/PT1656345E/pt unknown
- 2004-08-20 DK DK04781806.7T patent/DK1656345T3/da active
- 2004-08-20 AU AU2004268968A patent/AU2004268968B2/en not_active Ceased
- 2004-08-20 WO PCT/US2004/027196 patent/WO2005021500A1/en not_active Ceased
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2006
- 2006-02-14 NO NO20060717A patent/NO335946B1/no not_active IP Right Cessation
- 2006-02-20 IS IS8313A patent/IS8313A/is unknown
- 2006-02-20 IL IL173824A patent/IL173824A/en not_active IP Right Cessation
- 2006-10-10 US US11/545,415 patent/US7482335B2/en not_active Expired - Lifetime
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2009
- 2009-01-15 US US12/354,258 patent/US7829571B2/en not_active Expired - Lifetime
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- 2013-10-08 IL IL228794A patent/IL228794A0/en unknown
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