Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
1811162 | PF-05231023 | 1037589-69-7 | >98% | |
PF-05231023 is a long-acting FGF21 mimetic. PF-05231023 decreases body weight and imp | ||||
1811211 | Anlotinib HCl ( AL-3818 ) | 1360460-82-7 | ≧98.0% | |
Anlotinib is a novel oral tyrosine kinase inhibitor (TKI) targeting c-kit, platelet-d | ||||
191122 | Tafenoquine ( WR 238605 ) | 106635-80-7 | ≧98.0% | |
Tafenoquine is being investigated as a potential treatment for malaria, as well as fo | ||||
S510901 | Cenicriviroc Mesylate | 497223-28-6 | 98% Min. | |
Cenicriviroc (CVC) is an oral, once-daily, potent immunomodulator that blocks two che | ||||
512193 | ITI-214(phosphate) | 1642303-38-5 | 98% Min. | |
ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic | ||||
6111901 | UNC2541 | 1612782-86-1 | 98% Min. | |
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit | ||||
112591 | U-73343 | 142878-12-4 | 98% Min. | |
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p | ||||
204302 | Lerociclib | 1628256-23-4 (free base) | 98% | |
Lerociclib , also known as G1T38, is an oral, potent and selective CDK4/6 inhibitor f | ||||
204504 | Zegocractin ( CM-4620 ) | 1713240-67-5 | ≧98.0% | |
Zegocractin (CM-4620, Auxora(TM)) is a small-molecule inhibitor of the calcium releas | ||||
S-203041 | [4-(2,2,2-trifluoroethoxy)phenyl]boronic acid | 886536-37-4 | 95% | |
g scale to Kg scale may be provided. | ||||
262324 | 2-(3-Fluoro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 1350426-06-0 | 98% Min. | |
52004 | Belnacasan | 273404-37-8 | 98% | |
Belnacasan is a prodrug ofVRT-043198, a caspase-1 inhibitor that was developed by Ver |
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