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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
611918Ca2+ channel agonist 11402821-24-298%
Ca2+ channel agonist 1 is a N-type Ca2+ channel activity agonist, with EC50 of 14.23
611912CX-4945 sodium salt1309357-15-098%
CX-4945 (Silmitasertib) sodium salt is a potent and selective ATP-competitive small m
611824CAL-130 Racemate474012-90-398% 
CAL-130 racemate is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reporte
611823CAL-130 Hydrochloride1431697-78-798% 
CAL-130 Hcl is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported tha
611822CAL-1301431697-74-398% 
CAL-130 is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that co
611816Compound 401168425-64-798% 
Compound 401 is a synthetic inhibitor of DNA-PK (IC50 = 0.28 M) that also targets mTO
611815CC-115 hydrochloride1300118-55-198% 
CC-115 hydrochloride is a inhibitor of mTOR/DNA-PK (IC50= 21/ 13 nM). CC-115 shows go
6118013 CAI28755-03-598% 
3CAI is a potent allosteric and specific AKT inhibitor, which exerts efficacy in vitr
161009017Chrysophanic acid481-74-398% by HPLC 
Chrysophanic acid preferentially blocked proliferation in SNU-C5 cells but not in oth
160926016CAY105051218777-13-998% by HPLC 
CAY10505 is a phosphatidylinositol 3-kinase- inhibitor , was found to significantly i
160926015CH5132799 (PA-799)1007207-67-198% by HPLC 
CH5132799, also known as PA-799, is a novel class I PI3K inhibitor, which exhibited a
16090101CCT2457371489389-18-598%
CCT245737(CCT-245737, CAS 1489389-18-5) is the first orally active, clinical developm
16071407CWHM-121564286-55-098% by HPLC 
vitro ligand-binding assays, with somewhat less potency against v5 than against the o
16071401CMK821794-90-598% by HPLC 
CMK
16070917Copanlisib1032568-63-0≧98.0% 
Copanlisib, also known as BAY 80-6946, is a phosphoinositide 3-kinase (PI3K) inhibito
16070913CCT2447471404095-34-698% by HPLC 
CCT244747 is a novel potent, highly selective, orally active ATP-competitive CHK1 inh
16070704CP-673451343787-29-198% by HPLC 
CP-673451 is a selective inhibitor of PDGFR/ with IC50 of 10 nM/1 nM in cell-free ass
16062904CHIR-99021252917-06-998% by HPLC 
CHIR-99021, also known as CT99021, is a glycogen synthase kinase 3 (GSK3) inhibitor t
16062115CA-074134448-10-598% by HPLC 
CA-074
16053104CF-102163042-96-498% by HPLC 
CF-102, also known as 2-Cl-IB-MECA, is an orally bioavailable, synthetic, highly sele
SSC65304CHIR-090728865-23-498% by HPLC 
CHIR-090 is a potent LpxC inhibitor, displays two-step time-dependent inhibition and
0325094-cyclopropylphenylacetic acid40641-90-598% 
Coming soon!
0325062-Chloro-3-fluoro-4-(trifluoromethyl)pyridine628692-22-898% 
Coming soon!
032402CEP-1347156177-65-098% 
Coming soon!
030201CPI-2031446144-04-298% 
CPI 203 is a novel potent, selective and cell permeable inhibitor of the bromodomain
022202CL-387785194423-06-898% 
CL-387785 is an irreversible inhibitor of EGFR with IC50 of 370+/-120 pM; is able to
021802CC-2231228013-30-698% 
CC-223 is a potent mTOR kinase inhibitor (IC50=16 nM), with >150-fold sensitivity
012601CJ-023423415903-37-698% 
CJ-023423 is a novel, potent and selective prostaglandin EP4 receptor antagonist with
012004CC-1151228013-15-798% 
CC-115 is a dual inhibitor of DNA-dependent protein kinase and mammalian target of ra
012002CB-50831542705-92-998% 
CB-5083 is a novel first in class, potent orally bio-available p97 inhibitor that dis