Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
208191 | OATD-01 (GLPG-4716) | 2088453-21-6 | ≧98.0% | ![]() |
OATD-01 (GLPG-4716), a dual inhibitor of acidic mammalian chitinase (AMCase) and chit | ||||
2091501 | AB-680 | 2105904-82-1 | 98% Min. | ![]() |
AB-680 is highly potent, reversible and selective CD73 inhibitor. AB680 to be a rever | ||||
2091502 | 5-(chloromethyl)-1-propyl-1H-imidazole hydrochloride | 497223-15-1 | ≧95.0% | ![]() |
5-(chloromethyl)-1-propyl-1H-imidazole hydrochloride is an important intermediate of | ||||
2091906 | BAY-2416964 | 2242464-44-2 | 98% Min. | ![]() |
BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist | ||||
20103001 | ASN007 | 2055597-12-9 | ≧98.0% | ![]() |
ASN007 , a novel oral ERK inhibitor , has shown anti-tumor activity in both solid tum | ||||
20103002 | Senaparib | 1401682-78-7 | ≧98.0% | ![]() |
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with | ||||
20103004 | 2,6-difluoro-3,5-dimethoxybenzeneamine | 651734-54-2 | ≧98.0% | ![]() |
2,6-difluoro-3,5-dimethoxybenzeneamine is a key intermeidate ofPemigatinib.1Kg~10Kg s | ||||
201221 | Razuprotafib sodium | 1809275-69-1 | ≧98.0% | ![]() |
Razuprotafib, also known as AKB-9778, is a small molecule inhibitor of vascular endot | ||||
20123101 | Samelisant | 1415792-84-5 | ≧98.0% | ![]() |
Samelisant is a novel, highly selective and potent small molecule oral inhibitor targ | ||||
26188 | Firibastat ( QGC-001 ) | 648927-86-0 | ≧98.0% | ![]() |
Firibastat, (originally named QGC001) is the first drug candidate of a new class of c | ||||
21224 | BI-187004 | 1303515-32-3 | ≧98.0% | ![]() |
BI-187004, also known as VTP-34072, is an 11β-hydroxysteroid dehydrogenase 1 inhibit | ||||
21236 | Centanafadine HCl | 923981-14-0 | ≧98.0% | ![]() |
Centanafadine, also known as EB-1020, is an adrenergic uptake inhibitor and dopamine |
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