CP-944629

CP-944629 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:CP-944629;CP 944629;CP944629
CAS:668990-94-1
Package:10 mg;25 mg;5 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Sigma-Aldrich  
Tel: 021-61415566 800-8193336
Email: orderCN@merckgroup.com
Products Intro: Product Name:CP-944629
CAS:668990-94-1
Purity:>=98% (HPLC) Package:25MG Remarks:PZ0238-25MG
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Email: marketing@energy-chemical.com
Products Intro: Product Name:CP-944629 >=98% (HPLC)
CAS:668990-94-1
Purity:NULL Package:25mg;5mg Remarks:NULL
Company Name: Beijing Biocreative Technology Co., Ltd.  
Tel: 15522676233
Email: 3007606172@qq.com
Products Intro: Product Name:CP-944629
CAS:668990-94-1
Purity:>98% Package:mg
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Products Intro: Product Name:CP-944629
CAS:668990-94-1
Purity:0 Package:25mg/RMB 10600;100mg/RMB 17500;50mg/RMB 13800
CP-944629 Basic information
Product Name:CP-944629
Synonyms:CP-944629;1,2,4-Triazolo[4,3-a]pyridine, 3-(1,1-dimethylethyl)-6-[4-(2,4,5-trifluorophenyl)-5-oxazolyl]-;CP-944629 >=98% (HPLC)
CAS:668990-94-1
MF:C19H15F3N4O
MW:372.34
EINECS:
Product Categories:
Mol File:668990-94-1.mol
CP-944629 Structure
CP-944629 Chemical Properties
density 1.39±0.1 g/cm3(Predicted)
storage temp. room temp
pka2.70±0.50(Predicted)
form powder
color white to beige
Safety Information
MSDS Information
CP-944629 Usage And Synthesis
Biochem/physiol ActionsCP-9446219 is a potent p38alpha (p38α) inhibitor (IC50 = 1.8 nM) with no inhibitory potency against a panel of 26 other knases (IC50 >10 μM), including p38gamma (p38γ) and p38delta (p38δ), MKK1, MAPK2/ERK2, JNK, MAPKAP-K1a, and MAPKAP-K2. CP-944629 effectively inhibits LPS-stimulated cellular TNF-α production in vitro (IC50 = 63 and 8.3 nM, using human whole blood and isolated mononuclear cells, respectively) and in rats in vivo (ED50 = 0.1 mg/kg p.o.) with good pharmacokinetic profile and oral availability (F = 66%/monkey, 54%/rat).
CP-944629 Preparation Products And Raw materials
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