Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 193285 | BMS-986104 | 1622180-31-7 | >98% |  |
| BMS-986104 is a potent and selective S1P1 receptor modulator, which demonstrates liga | ||||
| 193263 | BAY-1316957 | 1613264-40-6 | >98% |  |
| BAY-1316957 is a highly potent, selective, orally available human prostaglandin E2 re | ||||
| 193255 | BMS-986158 | 1800340-40-2 | >98% |  |
| BMS-986158 is a potent and selective BET inhibitor. BMS-986158 binds to the acetyl-ly | ||||
| 193207 | BMS-986163 | 1801151-09-6 | >98% |  |
| BMS-986163 a Negative Allosteric Modulator of GluN2B with Potential Utility in Major | ||||
| 193121 | BAY-293 | 2244904-70-7 | >98% |  |
| BAY-293 is a potent SOS1 inhibitors that block RAS activation via disruption of the R | ||||
| 19351 | BMS-816336 | 1009583-20-3 | >98% |  |
| BMS-816336 is an orally active, potent and selective 11β-HSD1 inhibitor. BMS-816336 | ||||
| 19341 | Belvarafenib | 1446113-23-0 | >98% |  |
| Belvarafenib, also known as GDC-5573, HM95573, RG6185, is a selective inhibitor of th | ||||
| 192221 | Burixafor HBr | 1191450-19-7 | >98% |  |
| Burixafor, also known as TG-0054, is an orally bioavailable inhibitor of CXC chemokin | ||||
| 191284 | BMS-986142 | 1643368-58-4 | >98% |  |
| BMS-986142 is a potent, selective, reversible BTK inhibitor. | ||||
| 191282 | Blu667 | 2097132-94-8 | >98% |  |
| Blu667 is a highly potent and selective RET inhibitor with an IC50 of 0.4 nM for wild | ||||
| 191257 | BAY1238097 | 1564268-08-1 | >98% |  |
| BAY1238097 is a potent and selective BET inhibitor. BAY1238097 binds to the acetylate | ||||
| 191253 | BMS-189453 | 166977-43-1 | >98% |  |
| BMS-189453, also known as BMS453, is a potent and selective RARβ agonist and a poten | ||||
| 191213 | BI-671800 | 1093108-50-9 | >98% |  |
| BI-671800 is a CRTH2 antagonist that treats patients with asthma. BI 671800 is associ | ||||
| 19124 | BI-3812 | 2166387-64-8 | >98% |  |
| BI-3812 is a potent inhibitor of the interaction of the BTB/POZ domain of BCL6 with s | ||||
| 1812286 | BAY 678 | 675103-36-3 | >98% |  |
| BAY 678 is a potent and selective cell-permeable human neutrophil elastase (HNE) inhi | ||||
| 1812261 | BN-82002 | 396073-89-5 | >98% |  |
| BN-82002, also known as CDC25 Phosphatase Inhibitor I, is a cell-permeable ortho-hydr | ||||
| 1811291 | BMS-509744 | 439575-02-7 | >98% |  |
| BMS-509744 is a potent interleukin-2 inducible T cell kinase (ITK) inhibitor (IC50 = | ||||
| 1811281 | BMS-688521 | 893397-44-9 | >98% |  |
| BMS-688521 is a small molecule antagonist of leukocyte function associated antigen-1 | ||||
| 1811264 | BMS-986195 | 1912445-55-6 | >98% |  |
| BMS-986195 is a potent, covalent, irreversible inhibitor of Bruton’s tyrosine kinas | ||||
| 1811262 | BAY-299 | 2080306-23-4 | >98% |  |
| BAY-299 is a potent and selective BRD1 and TAF1 inhibitor (IC50 values are 6 and 13 n | ||||
| 1810163 | BMS-986165 | 1609392-27-9 | >99% |  |
| BMS-986165 potently binds to the Tyk2 pseudokinase domain (Ki = 0.02 nM). BMS-986165 | ||||
| 187181 | Bictegravir | 1611493-60-7 | >98% |  |
| Bictegravir, also known as GS-9883, is a potent, unboosted, once-Daily HIV-1 Integras | ||||
| 187121 | Basimglurant | 1034442-21-1 | >98% |  |
| Basimglurant, also known as RO 4917523 and RG-7090, is a novel mGlu5 negative alloste | ||||
| 186232 | 3BDO | 890405-51-3 | >98% |  |
| 3BDO, a butyrolactone derivative, could target FKBP1A and activate the mTOR signaling | ||||
| 185314 | BMS-986205 | 1923833-60-6 | >98% |  |
| BMS-986205 is an anticancer drug candidate. | ||||
| 185182 | Birinapant | 1260251-31-7 | >98% |  |
| Birinapant, also known as TL32711, is a synthetic small molecule and peptido mimetic | ||||
| 18573 | Bryostatin 1 | 83314-01-6 | >98% |  |
| Bryostatin 1 is a potent Protein Kinase C modulator isolated from the bryozoan Bugula | ||||
| 1842812 | BMS-813160 | 1286279-29-5 | >98% |  |
| BMS-813160 is a potent and selective CCR2/CCR5 antagonist with potential immunomodula | ||||
| 184282 | BRD7116 | 329059-55-4 | >98% |  |
| BRD7116 is a potent and selective Inhibitor of leukemia stem cell (LSC) activity (EC5 | ||||
| 18496 | Bazedoxifene acetate | 198480-56-7 | >98% |  |
| Bazedoxifene, also known as WAY-140424, is a third generation selective estrogen rece | ||||