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Featured Products
HY-100815B  |  (RS)-AMPA
HY-101276  |  AZD-1236
HY-101277  |  Vadadustat
HY-101278  |  Thiomyristoyl
HY-101279  |  ST034307
HY-101280  |  LB-60-OF61
HY-101281  |  VU6008667
HY-101283  |  HCH6-1
HY-21343  |  1-(5-Bromo-2-chloro-3-pyridinyl)ethanone
HY-21344  |  Methyl 4-(bromomethyl)-3-pyridinecarboxylate
HY-21345  |  Pyrazole-3-carboxylic acid, 4-methyl-, methyl ester
HY-10128  |  ZM-447439
HY-10161  |  Tozasertib
HY-10180  |  MLN8054
HY-10192  |  NVP-TAE 684
HY-10249  |  GSK-690693
HY-10355  |  AKT inhibitor VIII
HY-10358  |  MK 2206 (dihydrochloride)
HY-11002  |  CP-466722
HY-11007  |  GNF-2
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Products
Cat.No. Product Name / Activity Added
HY-100129 JNJ-17203212 March 2017
JNJ-17203212 is a novel and selective TRPV1 antagonist, with IC50 of 65 nM and 102 nM for human TRPV1 and rat TRPV1.
 
HY-100212 JE-2147 March 2017
 
HY-100407 JNJ16259685 March 2017
JNJ16259685 is a selective antagonist of <b>mGlu1 receptor</b>, and inhibits the synaptic activation of mGlu1 in a concentration-dependent manner with <b>IC<sub>50</sub></b> of 19 nM.
 
HY-100604 JNJ-40418677 March 2017
 
HY-100668 JYL 1421 March 2017
 
HY-100675 JTE 013 March 2017
 
HY-100770 JD-5006 March 2017
 
HY-100846 JQEZ5 March 2017
 
HY-100849 JAK3i March 2017
 
HY-100868 JPH203 March 2017
JPH203 is a potent and selective L-type amino acid transporter 1 inhibitor (<b>LAT1</b>), used for cancer research.
 
HY-101189 JNJ-39758979 March 2017
 
HY-10329 JNJ-7706621 March 2017
JNJ-7706621 is pan-CDK inhibitor with the highest potency on CDK1/2 with IC50 of 9 nM/4 nM and showing >6-fold selectivity for CDK1/2 than CDK3/4/6; also potently inhibits Aurora A/B and has no activity on Plk1 and Wee1.
 
HY-10383 J-104132 March 2017
 
HY-10486 JDTic March 2017
JDTic is a highly selective antagonist for the κ-opioid receptor; without affecting the μ- or δ-opioid receptors.
 
HY-10487 JDTic (dihydrochloride) March 2017
JDTic 2Hcl is a highly selective antagonist for the κ-opioid receptor; without affecting the μ- or δ-opioid receptors.
 
 
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