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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
2071626Apcin300815-04-798% Min.
Apcin is an inhibitor of the anaphase-promoting complex/cyclosome (APC/C). It acts by
2071552Astemizole68844-77-998% Min.
Astemizole is a histamine H1-receptor antagonist. Astemizole competitively binds to h
2071539ARV-7711949837-12-098% Min.
ARV-771 is a small-molecule pan-BET degrader. ARV-771 demonstrates dramatically impro
2071531AZD-76482230820-11-698% Min.
AZD-7648 is a potent and selective DNA-PK inhibitor.
2071530AWZ1066S239272-16-198% Min.
AWZ1066S is a highly specific anti-Wolbachia drug candidate for a short-course treatm
2071523AER-271634913-39-698% Min.
AER-271 is a potent aquaporin-4 (AQP4) inhibitor. AER-271 blocks acute cerebral edema
2071517ABX-14311446817-84-098% Min.
ABX-1431 is a covalent, irreversible MGLL inhibitor. ABX-1431 is currently entering c
2071508AZ312088113-98-698% Min.
AZ31 is a potent and highly selective ATM inhibitor.
2071503AB-4231572510-80-598% Min.
AB-423 is a novel inhibitor of hepatitis b virus pregenomic rna encapsidation
2023232-aminopyrazolo[1,5-a]pyridine-3-carboxylic acid1542020-25-698% Min.
2062319 1-acetyl-5-nitro-3H-indol-2-one114985-63-698% Min.
2061313 1-acetyl-5-amino-2-indolinone422518-10-398% Min.
2062312(4aS,9bR)-Ethyl 6-bromo-5-(2-(methylamino)-2-oxoethyl)-3,4,4a,5-tetrahydro-1H-pyrido[4,3-b]indole-2(9bH)-carboxylate2098497-32-498% Min.
20623118-Acetyl-5-(benzyloxy)-2H-benzo[b][1,4]oxazin-3(4H)-one1035299-32-398% Min.
20623072-Amino-5-cyanopyrazine113305-94-598% Min.
20620255-amino-3,4-dimethylthieno[2,3-c]pyridazine-6-carboxylic acid1452226-14-096% Min.
2062009AT13148 intermediate(N1)1056901-64-496% Min.
2061701Anacetrapib875446-37-098% Min.
Anacetrapib, also known as MK-0859, is a CETP inhibitor being developed to treat hype
2061308Ambrisentan177036-94-198% Min.
Ambrisentan, also known as BSF-208075 and LU-208075, is a drug indicated for use in t
206101AZD03642097416-76-598% Min.
AZD-0364 is a potent and selectiveERK2inhibitor extracted from patent WO2017080979A1,
2051515Asapiprant932372-01-598% Min.
Asapiprant is a potent and selective DP1 receptor antagonist, with a Ki of 0.44 nM. A
2051513AKOS B0183046308-22-198% Min.
AKOS B018304 is a potent inhibitor of chikungunya virus with low micro molar activity.
23178AC-90179 HCl359878-19-698% Min.
AC-90179 is a high selective 5-hydroxytryptamine2A receptor inverse agonist. It is an
S-2030436-AMINOISOQUINOLINE23687-26-596% Min.
204605A134974186141-75-398% Min.
A134974 is a bioactive chemical.
204604A-12932011375557-33-798% Min.
A-1293201 is a potent and selective NAMPT inhibitor.
204603A-119637255713-47-498% Min.
A-119637 is a novel, selective and potent alpha1D antagonist.
204602A-10484001219624-62-098% Min.
A-1048400 is a potent and selective N-type and T-type calcium channel blocker.
204601 A-10621821-13-298% Min.
A-1062 is a resolvase-binding inhibitor. A1062 inhibits resolvase binding to the res
112193AMG-5102296729-00-398% Min.
AMG-510 is a potent KRAS G12C covalent inhibitor. AMG-510 selectively targets the KRA