JP2009544758A5 - - Google Patents

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Publication number
JP2009544758A5
JP2009544758A5 JP2009522956A JP2009522956A JP2009544758A5 JP 2009544758 A5 JP2009544758 A5 JP 2009544758A5 JP 2009522956 A JP2009522956 A JP 2009522956A JP 2009522956 A JP2009522956 A JP 2009522956A JP 2009544758 A5 JP2009544758 A5 JP 2009544758A5
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JP
Japan
Prior art keywords
compound
formula
disease
salt
temperature
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Withdrawn
Application number
JP2009522956A
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English (en)
Japanese (ja)
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JP2009544758A (ja
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Priority claimed from US11/782,704 external-priority patent/US7671062B2/en
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Publication of JP2009544758A publication Critical patent/JP2009544758A/ja
Publication of JP2009544758A5 publication Critical patent/JP2009544758A5/ja
Withdrawn legal-status Critical Current

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JP2009522956A 2006-07-28 2007-07-26 ケモカイン受容体活性のモジュレーター、結晶形および方法 Withdrawn JP2009544758A (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US83423506P 2006-07-28 2006-07-28
US89602607P 2007-03-21 2007-03-21
US11/782,704 US7671062B2 (en) 2006-07-28 2007-07-25 Modulators of chemokine receptor activity, crystalline forms and process
PCT/US2007/074438 WO2008014381A2 (en) 2006-07-28 2007-07-26 Modulators of chemokine receptor activity, crystalline forms and process

Publications (2)

Publication Number Publication Date
JP2009544758A JP2009544758A (ja) 2009-12-17
JP2009544758A5 true JP2009544758A5 (cg-RX-API-DMAC7.html) 2010-08-12

Family

ID=38823540

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009522956A Withdrawn JP2009544758A (ja) 2006-07-28 2007-07-26 ケモカイン受容体活性のモジュレーター、結晶形および方法

Country Status (29)

Country Link
US (1) US7671062B2 (cg-RX-API-DMAC7.html)
EP (2) EP2184283A1 (cg-RX-API-DMAC7.html)
JP (1) JP2009544758A (cg-RX-API-DMAC7.html)
KR (1) KR20090035036A (cg-RX-API-DMAC7.html)
CN (1) CN101511822A (cg-RX-API-DMAC7.html)
AR (1) AR062114A1 (cg-RX-API-DMAC7.html)
AT (1) ATE471928T1 (cg-RX-API-DMAC7.html)
AU (1) AU2007279256A1 (cg-RX-API-DMAC7.html)
BR (1) BRPI0715066A2 (cg-RX-API-DMAC7.html)
CA (1) CA2659259A1 (cg-RX-API-DMAC7.html)
CL (3) CL2007002194A1 (cg-RX-API-DMAC7.html)
CO (1) CO6190527A2 (cg-RX-API-DMAC7.html)
CY (1) CY1110785T1 (cg-RX-API-DMAC7.html)
DE (1) DE602007007335D1 (cg-RX-API-DMAC7.html)
DK (1) DK2049477T3 (cg-RX-API-DMAC7.html)
EA (1) EA014960B1 (cg-RX-API-DMAC7.html)
ES (1) ES2346591T3 (cg-RX-API-DMAC7.html)
HR (1) HRP20100371T1 (cg-RX-API-DMAC7.html)
IL (1) IL196518A0 (cg-RX-API-DMAC7.html)
MX (1) MX2009000803A (cg-RX-API-DMAC7.html)
NO (1) NO20090256L (cg-RX-API-DMAC7.html)
NZ (1) NZ574656A (cg-RX-API-DMAC7.html)
PE (1) PE20080838A1 (cg-RX-API-DMAC7.html)
PL (1) PL2049477T3 (cg-RX-API-DMAC7.html)
PT (1) PT2049477E (cg-RX-API-DMAC7.html)
SG (1) SG158925A1 (cg-RX-API-DMAC7.html)
SI (1) SI2049477T1 (cg-RX-API-DMAC7.html)
TW (1) TW200823203A (cg-RX-API-DMAC7.html)
WO (1) WO2008014381A2 (cg-RX-API-DMAC7.html)

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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
EP2567959B1 (en) 2011-09-12 2014-04-16 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
MA42133A (fr) * 2015-05-21 2021-06-02 Chemocentryx Inc Modulateurs du ccr2
DK3655395T3 (da) * 2017-07-20 2022-03-07 Bristol Myers Squibb Co Fremgangsmåde til fremstilling af n-((1r,2s,sr)-5-(tert-butylamino)-2-((s)-3-(7- tert-butylpyrazolo[1,5-a][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin-1- yl)cyclohexyl)acetamid
CA3075638A1 (en) 2017-09-25 2019-03-28 Chemocentryx, Inc. Combination therapy using a chemokine receptor 2 (ccr2) antagonist and a pd-1/pd-l1 inhibitor
US20190269664A1 (en) 2018-01-08 2019-09-05 Chemocentryx, Inc. Methods of treating solid tumors with ccr2 antagonists
ES2991280T3 (es) 2018-01-08 2024-12-03 Chemocentryx Inc Antagonistas de CCR2 para el tratamiento del linfoma cutáneo de linfocitos T
CN115494184B (zh) * 2022-05-09 2023-07-28 浙江海正药业股份有限公司 一种同时检测药物中异丙苯磺酸甲酯、异丙苯磺酸乙酯的方法

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