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Signaling Pathway

编号化学名称Cas号纯度化学结构
24003NVL-655 ( ALK-IN-27 )2739866-40-9≧98.0%
NVL-655是一种新型脑渗透性ALK选择性抑制剂,旨在解决目前可用的
20656IK-9302563892-44-2≧98.0%
IK-930 是一种新型选择性小分子 TEAD 抑制剂,可防止棕榈酸结合,
21238Seralutinib1619931-27-998% Min.
Seralutinib,也称为 PK-10571 和 GB002,是一种新型吸入性 Pdgfr 激酶抑
24001Bomedemstat1990504-34-1≧98.0%
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
20657Zilurgisertib2173389-57-4≧98.0%
Zilurgisertib(之前称为 INCB 00928)是一种激活素受体样激酶 2(ALK2,
52021Ganetespib(STA-9090)888216-25-998% 
Ganetespib blocked the ability of HSP90 to bind to biotinylated geldanamycin and disr
51803Semaxanib (SU5416)204005-46-998% 
Semaxanib (SU5416) is a potent and selectiveVEGFR(Flk-1/KDR) inhibitor withIC50of 1.2
122919Tenapanor1234423-95-098% 
Tenapanoris an inhibitor of the sodium-proton exchanger NHE3. Thisantiporter protein
16122810Elacestrant dihydrochloride1349723-93-8≧98.0%
Elacestrant dihydrochloride, also known as RAD1901, is an orally available, selective
512193ITI-214磷酸盐1642303-38-598% Min.
ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic
21248Giredestrant1953133-47-5≧98.0%
Giredestrant, also known as GDC-9545 and RG6171, is a SERD. GDC-9545 is an orally ava
20367Piflufolastat1423758-00-2≧96%
Piflufolastat, also known as DCFPYL is a PSMA-targeted PET imaging agent for prostate