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Featured Products
HY-10372  |  PP121
HY-10005  |  Flavopiridol
HY-10008  |  SNS-032
HY-10087  |  Navitoclax
HY-10161  |  Tozasertib
HY-10162  |  Olaparib
HY-10180  |  MLN8054
HY-10192  |  NVP-TAE 684
HY-10193  |  AZD-1480
HY-10249  |  GSK-690693
HY-10254  |  PD0325901
HY-10355  |  AKT inhibitor VIII
HY-10358  |  MK 2206 (dihydrochloride)
HY-10997  |  PCI-32765
HY-11001  |  PHA-793887
HY-11002  |  CP-466722
HY-11007  |  GNF-2
HY-30237  |  Roscovitine
HY-50662  |  A-769662
HY-50767  |  Palbociclib
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Products
Cat.No. Product Name / Activity Added
HY-100001 SKF-96365 (hydrochloride) September 2017
SKF-96365 hydrochloride, an <b>SOCE</b> inhibitor, exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal cancer cells.
 
HY-100002 ML162 September 2017
 
HY-100003 ML210 September 2017
 
HY-100004 Fumarate hydratase-IN-1 September 2017
Fumarate hydratase-IN-1, an enzyme of the TCA cycle.
 
HY-100005 Fumarate hydratase-IN-2 September 2017
 
HY-100005A Fumarate hydratase-IN-2 (sodium salt) September 2017
.
 
HY-100006 MRT68921 September 2017
MRT68921 is the most potent inhibitor of <b>ULK1</b> and <b>ULK2</b>, with <b>IC<sub>50</sub></b> values of 2.
 
HY-100006A MRT68921 (hydrochloride) September 2017
MRT68921 hydrochloride is the most potent inhibitor of both ULK1 and ULK2, with greater than a 15-fold reduction in the IC50 for ULK1 (2.
 
HY-100007 TAK-438 (free base) September 2017
TAK-438 (free base) is a novel P-CAB (potassium-competitive acid blocker) that reversibly inhibits H+/K+ ATPase with IC50 of 19 nM (pH 6.
 
HY-100008 Peretinoin September 2017
Peretinoin is an oral acyclic retinoid, inhibits HCV RNA amplification and virus release by altering lipid metabolism.
 
HY-100009 Ufenamate September 2017
Ufenamate is a topical analgesic.
 
HY-10001 Calcipotriol September 2017
Calcipotriol is a synthetic VitD<sub>3</sub> analogue with a high affinity for the <b>vitamin D</b> receptor.
 
HY-100010 Sulfathiourea September 2017
 
HY-100011 SR-3029 September 2017
SR 3029 is a potent and highly specific CK1δ/CK1ε inhibitor with the IC50 of 97 nM.
 
HY-100012 CBR-5884 September 2017
CBR-5884 is a novel and noncompetitive 3-Phosphoglycerate dehydrogenase (PHGDH) inhibitor with IC50=33 μM).
 
 
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