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Catalog NoChemical NameCAS NumberPurityChemical Structure
17982BAY-5981906919-67-298.0%
BAY-598 is a potent, peptide-competitive chemical probe for SMYD2. BAY-598 has a uniq
17981BAY-598 R-isomer1906920-28-298.0%
BAY-598 R-isomer is the R-isomer of BAY589. BAY-598 R-isomer may be used as a referen
17916Brasofensine171655-91-798.0%
Brasofensine is a monoamine reuptake blocker is a phenyltropane that had been under d
1783013B021290541-46-698.0%
B02, also known as RAD51-IN-02, is a RAD51 inhibitor. B02 can enhance DOX sensitivity
1781003BLU-2851703793-34-398.0% 
BLU-285 is a potent and selective inhibitor of PDGFR D842V and KIT Exon 17 mutants an
1781002BAY-18953441876467-74-198.0% 
BAY-1895344 is developed for the treatment of patients with advanced solid tumors and
178813BIBR1532321674-73-198.0% 
BIBR1132 is highly selective for inhibition of telomerase, resulting in delayed growt
2017877BMS-9324811263871-36-898.0% 
BMS-932481 modulates A Peptides in the Plasma and Cerebrospinal Fluid of Healthy Volu
20178216B-1613214066-78-198.0% 
(2S,4S)-1-tert-butyl 2-Methyl 4-(aMinoMethyl)pyrrolidine-1,2-dicarboxylate 
2017822Balamapimod863029-99-698.0% 
Balamapimod, also known as MKI-822, is a Ras/Raf/MEK inhibitor. Balamapimod, may be p
17030606BP-1-1021334493-07-098% 
BP-1-102 is a potent, orally bioavailable and selective STAT3 inhibitor. BP-1-102 bin
17030604BAY-8761799753-84-698% 
BAY-876 is a potent and Selective GLUT1 Inhibitor. BAY-876 showed good metabolic stab
17030312BRD-75521137359-47-798% 
BRD-7552 is a PDX1 transcription factor inducer. It up regulates PDX1 expression in b
17030305BDA-3661821496-27-898% 
BDA-366 is a BCL2-BH4 antagonist. BDA-366 suppresses human myeloma growth. BDA-366 in
17030116Bimiralisib1225037-39-798% 
Bimiralisib, also known as PQR309, is an orally bioavailable pan inhibitor of phospho
17030110BEC HCl222638-67-798% 
BEC, also known as S-(2-boronoethyl)-L-cysteine, is an a slow-binding and competitive
17109003BGP-1566611-37-898% 
BGP-15, is a nicotinic amidoxime derivative with PARP inhibitory activity. It has bee
16122908Butylphthalide6066-49-598% 
Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of
16122907Buthionine Sulphoximine5072-26-498%
Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe
16122906Brivaracetam357336-20-098% 
Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra
16122905Brigatinib (AP-26113)1197953-54-098% 
Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL
16122904Brevianamide F38136-70-898% 
Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally o
16122903Bohemine189232-42-698% 
Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh
16122902BMS-6874531000998-59-398% 
BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR
16122901BML-210537034-17-698% 
BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition
16122868BIIB021848695-25-098% 
BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule
16122867BI605906960293-88-398% 
BI605906 is a IKK inhibitor. BI605906 inhibits TNF-dependent IB degradation and expre
16122866Benzbromarone3562-84-398% 
Benzbromarone is a uricosuric agent and non-competitive inhibitor of xanthine oxidase
16122805BAY-59-3074406205-74-198% 
BAY-59-3074 is a novel cannabinoid CB1/CB2 receptor partial agonist with analgesic pr
16122804Batimastat130370-60-498% 
Batimastat (also known as BB-94) is a synthetic matrix metalloproteinase inhibitor th