Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
17982 | BAY-598 | 1906919-67-2 | 98.0% | |
BAY-598 is a potent, peptide-competitive chemical probe for SMYD2. BAY-598 has a uniq | ||||
17981 | BAY-598 R-isomer | 1906920-28-2 | 98.0% | |
BAY-598 R-isomer is the R-isomer of BAY589. BAY-598 R-isomer may be used as a referen | ||||
17916 | Brasofensine | 171655-91-7 | 98.0% | |
Brasofensine is a monoamine reuptake blocker is a phenyltropane that had been under d | ||||
1783013 | B02 | 1290541-46-6 | 98.0% | |
B02, also known as RAD51-IN-02, is a RAD51 inhibitor. B02 can enhance DOX sensitivity | ||||
1781003 | BLU-285 | 1703793-34-3 | 98.0% | |
BLU-285 is a potent and selective inhibitor of PDGFR D842V and KIT Exon 17 mutants an | ||||
1781002 | BAY-1895344 | 1876467-74-1 | 98.0% | |
BAY-1895344 is developed for the treatment of patients with advanced solid tumors and | ||||
178813 | BIBR1532 | 321674-73-1 | 98.0% | |
BIBR1132 is highly selective for inhibition of telomerase, resulting in delayed growt | ||||
2017877 | BMS-932481 | 1263871-36-8 | 98.0% | |
BMS-932481 modulates A Peptides in the Plasma and Cerebrospinal Fluid of Healthy Volu | ||||
20178216 | B-1613 | 214066-78-1 | 98.0% | |
(2S,4S)-1-tert-butyl 2-Methyl 4-(aMinoMethyl)pyrrolidine-1,2-dicarboxylate | ||||
2017822 | Balamapimod | 863029-99-6 | 98.0% | |
Balamapimod, also known as MKI-822, is a Ras/Raf/MEK inhibitor. Balamapimod, may be p | ||||
17030606 | BP-1-102 | 1334493-07-0 | 98% | |
BP-1-102 is a potent, orally bioavailable and selective STAT3 inhibitor. BP-1-102 bin | ||||
17030604 | BAY-876 | 1799753-84-6 | 98% | |
BAY-876 is a potent and Selective GLUT1 Inhibitor. BAY-876 showed good metabolic stab | ||||
17030312 | BRD-7552 | 1137359-47-7 | 98% | |
BRD-7552 is a PDX1 transcription factor inducer. It up regulates PDX1 expression in b | ||||
17030305 | BDA-366 | 1821496-27-8 | 98% | |
BDA-366 is a BCL2-BH4 antagonist. BDA-366 suppresses human myeloma growth. BDA-366 in | ||||
17030116 | Bimiralisib | 1225037-39-7 | 98% | |
Bimiralisib, also known as PQR309, is an orally bioavailable pan inhibitor of phospho | ||||
17030110 | BEC HCl | 222638-67-7 | 98% | |
BEC, also known as S-(2-boronoethyl)-L-cysteine, is an a slow-binding and competitive | ||||
17109003 | BGP-15 | 66611-37-8 | 98% | |
BGP-15, is a nicotinic amidoxime derivative with PARP inhibitory activity. It has bee | ||||
16122908 | Butylphthalide | 6066-49-5 | 98% | |
Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of | ||||
16122907 | Buthionine Sulphoximine | 5072-26-4 | 98% | |
Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe | ||||
16122906 | Brivaracetam | 357336-20-0 | 98% | |
Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra | ||||
16122905 | Brigatinib (AP-26113) | 1197953-54-0 | 98% | |
Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL | ||||
16122904 | Brevianamide F | 38136-70-8 | 98% | |
Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally o | ||||
16122903 | Bohemine | 189232-42-6 | 98% | |
Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh | ||||
16122902 | BMS-687453 | 1000998-59-3 | 98% | |
BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR | ||||
16122901 | BML-210 | 537034-17-6 | 98% | |
BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition | ||||
16122868 | BIIB021 | 848695-25-0 | 98% | |
BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule | ||||
16122867 | BI605906 | 960293-88-3 | 98% | |
BI605906 is a IKK inhibitor. BI605906 inhibits TNF-dependent IB degradation and expre | ||||
16122866 | Benzbromarone | 3562-84-3 | 98% | |
Benzbromarone is a uricosuric agent and non-competitive inhibitor of xanthine oxidase | ||||
16122805 | BAY-59-3074 | 406205-74-1 | 98% | |
BAY-59-3074 is a novel cannabinoid CB1/CB2 receptor partial agonist with analgesic pr | ||||
16122804 | Batimastat | 130370-60-4 | 98% | |
Batimastat (also known as BB-94) is a synthetic matrix metalloproteinase inhibitor th |
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