Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
1810163 | BMS-986165 | 1609392-27-9 | >99% | ![]() |
BMS-986165 potently binds to the Tyk2 pseudokinase domain (Ki = 0.02 nM). BMS-986165 | ||||
90731 | GDC-0810 ( Brilanestrant , ARN-810 ) | 1365888-06-7 | ≧98.0% | ![]() |
GDC-0810 (Brilanestrant, ARN-810, RG6046) is a selective estrogen receptor degrader ( | ||||
51702 | AZD1208 | 1204144-28-4 | 98% | ![]() |
AZD1208 is a potent, highly selective, and orally available Pim kinase inhibitor that | ||||
19356 | AZ876 | 898800-26-5 | >98% | ![]() |
AZ876, also known as AZ-876, is a liver X receptor agonist. AZ876 protects against pa | ||||
6111904 | Lemborexant (E-2006) | 1369764-02-2 | 98% Min. | ![]() |
Lemborexant(CAS 1369764-02-2)is a novel investigational small molecule that inhib | ||||
52007 | SRT1720 | 1001645-58-4 | 98% | ![]() |
SRT1720 is a selectiveSIRT1activator withEC50of 0.16 M, but is >230-fold less pote | ||||
112101 | AV-412 | 451492-95-8 | 99.38% | ![]() |
AV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth fact | ||||
188281 | Arimoclomol maleate | 289893-26-1 | 98% | ![]() |
Arimoclomol, also known as BRX-220, is potentially useful for the treatment of Nieman | ||||
6111901 | UNC2541 | 1612782-86-1 | 98% Min. | ![]() |
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit | ||||
122919 | Tenapanor | 1234423-95-0 | 98% | ![]() |
Tenapanoris an inhibitor of the sodium-proton exchanger NHE3. Thisantiporter protein | ||||
52003 | Zosuquidar trihydrochloride | 167465-36-3 | 99% | ![]() |
zosuquidar trihydrochloride is adifluorocyclopropyl quinoline. Zosuquidar trihydrochl | ||||
6111110 | Nastorazepide | 209219-38-5 | 98% | ![]() |
Nastorazepide (Z-360) is a selective, orally available, 1,5-benzodiazepine-derivative |
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