Products

Catalog No	Chemical Name	CAS Number	Purity
16122910	Capromorelin tartrate	193273-69-7	98%
Capromorelin, also known as CP-424,391, is a growth hormone secretagogue and ghrelin
16122909	Canertinib	289499-45-2	98%
Canertinib dihydrochloride is the hydrochloride salt of an orally bio-available quina
16122806	Camostat Mesilate	59721-29-8	98%
Camostat Mesilate, also known as FOY 305, is a serine protease inhibitor. Serine prot
16122738	CPI-0610	1380087-89-7	98%
CPI-0610 is a potent and selective benzoisoxazoloazepine BET bromodomain inhibitor an
16122737	CPI-637	1884712-47-3	98%
CPI-637 is a selective and cell-active benzodiazepinone CBP/EP300 bromodomain inhibit
6111701	CeMMEC13	1790895-25-8	98%
CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF
6111108	CB1-IN-1	1429239-98-4	98%
CB1-IN-1 is a peripherally restricted CB1R antagonist, with Ki of 0.3 nM and 21 nM fo
6111016	Coelenterazine	55779-48-1	98%
Coelenterazine
61110004	1-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazine	1228780-72-0	98%
1-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazine
611933	CC0651	1319207-44-7	98%
CC0651 is an allosteric inhibitor of the human cdc34 ubiquitin-conjugating enzyme tha
611920	CDKI-73	1421693-22-2	98%
CDKI-73 is a potent CDK9 inhibitor with Ki of 4 nM; shows selective toxicity to CLL c
611919	CDK9-IN-6	1391855-95-0	98%
CDK9-IN-6 is a CDK9 inhibitor, refers to Example 399 in WO 2012101062 A1
611918	Ca2+ channel agonist 1	1402821-24-2	98%
Ca2+ channel agonist 1 is a N-type Ca2+ channel activity agonist, with EC50 of 14.23
611912	CX-4945 sodium salt	1309357-15-0	98%
CX-4945 (Silmitasertib) sodium salt is a potent and selective ATP-competitive small m
611824	CAL-130 Racemate	474012-90-3	98%
CAL-130 racemate is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reporte
611823	CAL-130 Hydrochloride	1431697-78-7	98%
CAL-130 Hcl is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported tha
611822	CAL-130	1431697-74-3	98%
CAL-130 is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that co
611816	Compound 401	168425-64-7	98%
Compound 401 is a synthetic inhibitor of DNA-PK (IC50 = 0.28 M) that also targets mTO
611815	CC-115 hydrochloride	1300118-55-1	98%
CC-115 hydrochloride is a inhibitor of mTOR/DNA-PK (IC50= 21/ 13 nM). CC-115 shows go
611801	3 CAI	28755-03-5	98%
3CAI is a potent allosteric and specific AKT inhibitor, which exerts efficacy in vitr
161009017	Chrysophanic acid	481-74-3	98% by HPLC
Chrysophanic acid preferentially blocked proliferation in SNU-C5 cells but not in oth
160926016	CAY10505	1218777-13-9	98% by HPLC
CAY10505 is a phosphatidylinositol 3-kinase- inhibitor , was found to significantly i
160926015	CH5132799 (PA-799)	1007207-67-1	98% by HPLC
CH5132799, also known as PA-799, is a novel class I PI3K inhibitor, which exhibited a
16090101	CCT245737	1489389-18-5	98%
CCT245737(CCT-245737, CAS 1489389-18-5) is the first orally active, clinical developm
16071407	CWHM-12	1564286-55-0	98% by HPLC
vitro ligand-binding assays, with somewhat less potency against v5 than against the o
16071401	CMK	821794-90-5	98% by HPLC
CMK
16070917	Copanlisib	1032568-63-0	≧98.0%
Copanlisib, also known as BAY 80-6946, is a phosphoinositide 3-kinase (PI3K) inhibito
16070913	CCT244747	1404095-34-6	98% by HPLC
CCT244747 is a novel potent, highly selective, orally active ATP-competitive CHK1 inh
16070704	CP-673451	343787-29-1	98% by HPLC
CP-673451 is a selective inhibitor of PDGFR/ with IC50 of 10 nM/1 nM in cell-free ass
16062904	CHIR-99021	252917-06-9	98% by HPLC
CHIR-99021, also known as CT99021, is a glycogen synthase kinase 3 (GSK3) inhibitor t