Home

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

All Products

Chemical Structure Cat. No. Product Name CAS No.
L-alpha-palmitin Chemical Structure
BCP16096 L-alpha-palmitin 32899-41-5
(S)-Sunvozertinib Chemical Structure
BCP43185 (S)-Sunvozertinib 2370013-49-1
DZD9008 is an oral, potent, irreversible, wild type-selective EGFR inhibitor against EGFR or HER2 Exon20ins and other mutations with IC50 ranging from 0.4 nM to 2.1 nM for mutant EGFR.
AS2676293 Chemical Structure
BCP46977 AS2676293 1393999-79-5
AS2676293 is an orally active small-molecule receptor activator of nuclear factor-κB ligand (RANKL) inhibitor, inhibits RANKL-induced osteoclastogenesis using RAW264 cells with IC50 of 0.19 uM.
Intedanib Chemical Structure
BCP01744 Intedanib 656247-17-5
Nintedanib is an inhibitor of the receptor tyrosine kinases VEGFR/FGFR/PDGFR (IC50s: 13-34/37-610/59/65 nM for VEGFR1-3, FGFR1-4, and PDGFRα/β, respectively).
帕拉米韦杂质05 Chemical Structure
BCP49647 帕拉米韦杂质05 383910-22-3
BMS-502 Chemical Structure
BCP49646 BMS-502 2407854-18-4
BMS-502 is a potent dual inhibitor of diacylglycerol kinase (DGK) α and ζ with IC50 of 4.6 nM and 2.1 nM.
Tetrachlorocyclopropene Chemical Structure
BCP49645 Tetrachlorocyclopropene 6262-42-6
TL 12-186 Chemical Structure
BCP49644 TL 12-186 2250025-88-6
TL12-186 is a Cereblon-dependent kinase degrader that degrades CDK, BTK, FLT3, Aurora and other kinases.TL12-186 inhibits CDK2/cyclin A and CDK9/cyclin T1 with IC50s of 73 and 55 nM, respectively.
DCTP-N3 Chemical Structure
BCP49643 DCTP-N3 1048021-94-8
DCTP is a nucleoside triphosphate that can be used for DNA synthesis. Deoxycytidine triphosphate has many applications, such as real-time PCR, cDNA synthesis, and DNA sequencing.
Fospropofol Chemical Structure
BCP49641 Fospropofol 258516-89-1
Fospropofol is a water soluble prodrug and is converted to propofol in the liver.
123下一页末页共 32724 条记录 1 / 3273 页 
0086-13720134139