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产品目录

编号化学名称Cas号纯度化学结构
161227116Afuresertib HCl1047645-82-898% 
Afuresertib, also known as GSK2110183, is an orally bioavailable inhibitor of the ser
161227114ACY-7381375465-91-098% 
ACY-738 is a potent and selective HDAC6 inhibitor with improved brain bioavailability
161227113Acolbifene182167-02-898% 
Acolbifene, also known as EM-652, or SCH-57068, is a selective estrogen receptor modu
161227111Abametapir1762-34-198% 
Abametapir is the active ingredient of Xeglyze Lotion. Abametapir inhibits metallopro
161227107Alantolactone546-43-098% 
Alantolactone, a naturally occurring eudesmane-type sesquiterpene lactone (SL), could
161227106AS101106566-58-998% 
AS101, a potent in vitro and in vivo immunomodulator, is a novel inhibitor of IL-1bet
16122783ACP-1961420477-60-698% 
Acalabrutinib is a selective second-generation Brutons tyrosine kinase (BTK) inhibito
16122775APS-2-792002381-31-798% 
APS-2-79 is a MAPK antagonist that modulating KSR-dependent MAPK signalling by antago
16122761Aprotinin9087-70-198% 
Aprotinin is a small protein serine protease inhibitor, used to reduce perioperative
16122743A-3661527503-11-298% 
A-366 is a potent and selective G9a/GLP histone lysine methyltransferase inhibitor wi
16122713AZD01561821428-35-698% 
AZD0156 is a potent and selective inhibitors of ATM kinase, with potential chemo-/rad
16122704APTSTAT3-9R98% 
APTSTAT3-9R is a specific STAT3-binding peptide with addition of a cell-penetrating m
6111520AGN 205728859498-05-898% 
AGN 205728 is a potent and selective RAR antagonist with Ki/IC95 values of 3 nM/ 0.6
6111519AGN 20532798% 
AGN 205327 is a potent synthetic RARs agonist with EC50 of 3766/734/32 nM for RAR// r
6111517AGN 195183367273-07-298% 
AGN 195183 is a potent and selective agonist of RAR(Kd=3 nM) with improved binding se
6111516AGN 194310229961-45-998% 
AGN 194310(VTP-194310) is a potent and selective pan-RARs agonist with Kd values of 3
6111513Acetazolamide D31189904-01-598% 
Acetazolamide D3 is deuterium labeled Acetazolamide, which is a potent carbonic anhyd
6111501APS-2-792002381-25-998% 
APS-2-79 is an antagonist of MEK phosphorylation by RAF through direct binding of the
61125(+)-Apogossypol66389-74-098% 
(+)-Apogossypol(Apogossypol; NSC736630) is a potent inhibitor of Bcl-2 family protein
6111107A-836339959746-77-198% 
A-836339 is a cannabinoid CB2 receptor-selective agonist; exhibits high potencies at
6111105AB-MECA152918-26-898% 
AB-MECA is a high affinity A3 adenosine receptor agonist, has high affinity for recom
6111104Amitifadine hydrochloride410074-74-798% 
Amitifadine hydrochloride is a triple reuptake inhibitor (TRI) or serotonin-norepinep
6111101ATI-23411337878-62-298% 
ATI-2341, pepducin targeting the C-X-C chemokine receptor type 4 (CXCR4), is an allos
6111022Auristatin F163768-50-198% 
Auristatin F is a cytotoxic tubulin modifier with potent and selective antitumor acti
6111021Auristatin E160800-57-798% 
Auristatin E is a cytotoxic tubulin modifier with potent and selective antitumor acti
6111011ABT-6391235560-28-798% 
ABT-639 is a novel, peripherally acting, selective T-type Ca2+ channel blocker. ABT-6
61110013-aMino-1-Methyl-1H-pyrazole-4-carbonitrile21230-50-298% 
3-aMino-1-Methyl-1H-pyrazole-4-carbonitrile 21230-50-2
611935360A794458-56-398% 
360A is a strong affinity and selectivity inhibitor of G-quadruplex structures.
611916AT7519 trifluoroacetate1431697-85-698%
AT7519 trifluoroacetate is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of
611810Ampkinone1233082-79-598% 
Ampkinone is a small molecule activator of AMPK; stimulate functional activation of A