Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
112194 | AMG-510 racemate | 2252403-56-6 | 98% Min. | |
AMG-510 is a potent KRAS G12C covalent inhibitor. AMG-510 selectively targets the KRA | ||||
112191 | Aprocitentan | 1103522-45-7 | 98% Min. | |
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed | ||||
6111903 | Aramchol | 246529-22-6 | 98% Min. | |
Galmed Pharmaceuticals Announces Successful Completion of End of Phase 2 Meeting With | ||||
513191 | Acibenzolar acid | 35272-27-6 | 96% Min. | |
benzo[d][1,2,3]thiadiazole-7-carboxylic acid,Acibenzolar acid,CGA 210 007 | ||||
193291 | AR-C155858 | 496791-37-8 | >98% | |
AR-C155858 is a potent inhibitor of monocarboxylate transporters MCT1 and MCT2 that b | ||||
193288 | ACT-709478 | 1838651-58-3 | >98% | |
ACT-709478 is a Potent, Selective T-type Calcium Channel Blocker as a Drug Candidate | ||||
193287 | A1874 | 2064292-12-0 | >98% | |
A1874 is a nutlin-based and BRD4-degrading PROTAC which induces BRD4 degradation in c | ||||
193254 | AZD9567 | 1893415-00-3 | >98% | |
AZD9567 is an oral differentiated non-steroidal selective glucocorticoid receptor mod | ||||
193222 | AZ1495 | 2196204-23-4 | >98% | |
AZ1495 is a potent and selective IRAK4 inhibitor. | ||||
193208 | ATR-101 HCl | 133825-81-7 | >98% | |
ATR-101, also known as PD-132301 (a free base) or PD-132301-2 (a HCl salt), is in cli | ||||
193192 | ARN-3236 | 1613710-01-2 | >98% | |
ARN-3236 is potent, orally active and selective SIK2 inhibitor. ARN-3236 inhibited th | ||||
193134 | ARN 077 | 1373625-34-3 | >98% | |
ARN 077 is a potent and selective N-acylethanolamine acid amidase (NAAA) inhibitor wi | ||||
193125 | Aleglitazar | 475479-34-6 | >98% | |
Aleglitazar, also known as RG-1439 or RO-0728804, is a peroxisome proliferator-activa | ||||
19382 | Alvimopan | 156053-89-3 | >98% | |
Alvimopan, also known as HSDB-7704 and LY246736, is a drug which behaves as a periphe | ||||
19381 | Abrocitinib | 1622902-68-4 | >98% | |
Abrocitinib, Bulk in stock, contact us by email for the quotation. Kg scale intermedi | ||||
19372 | AA26-9 | 1312782-34-5 | >98% | |
AA26-9 is a potent and broad-spectrum serine hydrolase inhibitor. AA26-9-inhibited en | ||||
19365 | AZD-0284 | 2101291-07-8 | >98% | |
AZD-0284 is a potent, selective, inverse agonist of the nuclear receptor RORγ for th | ||||
19363 | AZ304 | 942507-42-8 | >98% | |
AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits wild type B | ||||
19356 | AZ876 | 898800-26-5 | >98% | |
AZ876, also known as AZ-876, is a liver X receptor agonist. AZ876 protects against pa | ||||
19316 | AGN-190299 | 118292-41-4 | >98% | |
Tazarotene is a retinoid prodrug which is converted to its active form, the cognate c | ||||
19315 | AM281 | 202463-68-1 | >98% | |
AM281 is a synthetic cannabinoid CB1 receptor antagonist. | ||||
19312 | ASP9521 | 1126084-37-4 | >98% | |
ASP9521 is a novel, selective, orally bioavailable inhibitor of 17β-hydroxysteroid d | ||||
192275 | AZD0364 | 2097416-76-5 | >98% | |
AZD0364 is an ERK1 and/or ERK2 kinase for the treatment of cancer. ERK1 and ERK2 kina | ||||
192212 | ATF6-activator-147 | 393121-74-9 | >98% | |
ATF6-activator-147 is an ATF6 simulator which acts as a prodrug that preferentially t | ||||
192156 | AZD1152 | 722543-31-9 | >98% | |
AZD1152 is a pro-drug of Barasertib-hQPA, which is a highly selective Aurora B inhibi | ||||
191287 | AZD3229 | 2248003-60-1 | >98% | |
AZD3229 is a potent pan-KIT mutant inhibitor for the treatment of gastrointestinal st | ||||
191251 | AM095 sodium | 1345614-59-6 | >98% | |
AM095 is a potent LPA1 receptor antagonist because it inhibited GTPγS binding to Chi | ||||
191212 | AZD4573 free base | 2057509-72-3 | >98% | |
AZD-4573 is a selective, short-acting inhibitor of the serine/threonine cyclin-depend | ||||
191146 | AR-9281 | 913548-29-5 | >98% | |
AR-9281 is a soluble epoxide hydrolase (s-EH) inhibitor potentially for the treatment | ||||
191112 | ARRY-797 (ARRY-371797) | 1036404-17-7 | 99% Min. | |
ARRY-797 is an oral, selective p38 mitogen-activated protein kinase inhibitor. ARRY-7 |
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