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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 |  Featured Products
Cat.No. Product Name / Activity Added
HY-100815B (RS)-AMPA March 2017
 
HY-101276 AZD-1236 March 2017
 
HY-101277 Vadadustat March 2017
 
HY-101278 Thiomyristoyl March 2017
Thiomyristoyl is a potent and specific <b>SIRT2</b> inhibitor with an <b>IC<sub>50</sub></b> of 28 nM.
 
HY-101279 ST034307 March 2017
 
HY-10128 ZM-447439 March 2017
ZM 447439 is a selective and ATP-competitive inhibitor for Aurora A and Aurora B with IC50 of 110 nM, 130 nM respectively, > 8 fold selectivity than Aurora C, MEK1, Src.
 
HY-101280 LB-60-OF61 March 2017
 
HY-101281 VU6008667 March 2017
 
HY-101283 HCH6-1 March 2017
 
HY-10161 Tozasertib March 2017
Tozasertib (MK-0457; VX-680) is the inhibitor of Aurora-A, -B, -C kinases with Ki values of 0.
 
HY-10180 MLN8054 March 2017
MLN8054 is a potent and selective inhibitor of Aurora A with IC50 of 4 nM; exhibits more than 40-fold selective for Aurora A than Aurora B.
 
HY-10192 NVP-TAE 684 March 2017
NVP-TAE684(TAE684) is a highly potent and selective small-molecule ALK inhibitor, which blocked the growth of ALCL-derived and ALK-dependent cell lines with IC50 values between 2 and 10 nM.
 
HY-10249 GSK-690693 March 2017
GSK690693 is a pan-Akt inhibitor targeting Akt1/2/3 with IC50 of 2 nM/13 nM/9 nM, also sensitive to the AGC kinase family: PKA, PrkX and PKC isozymes.
 
HY-10355 AKT inhibitor VIII March 2017
Akt Inhibitor VIII is a cell-permeable quinoxaline compound that has been shown to potently, selectively, allosterically, and reversibly inhibit Akt1, Akt2, and Akt3 activity (IC50 = 58 nM, 210 nM, and 2.
 
HY-10358 MK 2206 (dihydrochloride) March 2017
MK-2206 2Hcl is a highly selective inhibitor of Akt1/2/3 with IC50 of 8 nM/12 nM/65 nM, respectively; no inhibitory activities against 250 other protein kinases observed.
 
 
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