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Inhibitors & Agonists

CATALOG NOPRODUCT NAMECASPURITYSTRUCTURE
179302PF-562271 HCl 939791-41-0>98%
PF-562271, also known as PF-562,271 and PF-271, is an orally bioavailable small molec
52775NVP-BKM120 Hydrochloride1312445-63-898%
Also see <a href="http://www.sun-shinechem.com/Details/BKM120(NVP-BKM120,%20B
121429Omipalisib(GSK2126458,GSK458)1086062-66-998%
GSK2126458 is a highly selective and potent inhibitor of PI3K with Ki of 0.019 nM/0.1
160926001Voxtalisib ( XL-765)934493-76-298% by HPLC
PI3K/mTOR dual kinase inhibitor XL765 inhibits both PI3K kinase and mTOR kinase, whic
179155Ipatasertib HCl1489263-16-298.0%
Ipatasertib, also known as GDC0068, is an orally active, potent and selective Akt inh
17918SF25231174428-47-798.0%
SF2523 is a highly selective and potent dual pan-PI3K/BRD4 inhibitor. SF2523 exhibits
17101617Autophinib1644443-47-9>98%
Autophinib is a novel potent autophagy inhibitor, inhibiting autophagy induced by sta
18423TPX-0005 1802220-02-5>98%
TPX-0005 is a Src/FAK/Janus kinase 2 (JAK2) inhibitor. TPX-0005 plus EGFR TKI suppres
184218BQR6951513879-21-4>98%
BQR695,也被称为NVP-BQR695, 是一种有效且具有选择性的PI4K抑制剂。
18433IPI-3063 1425043-73-7>98%
IPI-3063 is a Selective Phosphoinoside-3-Kinase p110δ Inhibitor. IPI-3063 Potently S
184321Ensartinib ( X396 )1370651-20-9>98%
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
18595GNE-79151351761-44-8>98%
GNE-7915 is a potent LRRK2 kinase inhibitor.