Home

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

Signaling Pathways

Chemical Structure Cat. No. Product Name CAS No.
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.
Ancitabine hydrochloride Chemical Structure
BCP12373 Ancitabine hydrochloride 10212-25-6
Ancitabine hydrochloride is a hydrochloride salt resulting from the reaction of equimolar amounts of ancitabine and hydrogen chloride. It has a role as an antimetabolite and an antineoplastic agent. It contains an ancitabine(1+).
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.
Rezafungin acetate Chemical Structure
BCP49640 Rezafungin acetate 1631754-41-0
Rezafungin acetate is a novel echinocandin-based antifungal agent with potent antifungal activity against Candida, Aspergillus and Pneumocystis. Rezafungin has higher stability and greater solubility in plasma, aqueous and buffered solutions.
H-Gly-hyp-ala-OH Chemical Structure
BCP49639 H-Gly-hyp-ala-OH 62147-09-5
Cyanine 7 maleimide Chemical Structure
BCP49636 Cyanine 7 maleimide 2120392-49-4
Sunitinib Chemical Structure
BCP02336 Sunitinib 557795-19-4
Sunitinib is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFRβ with IC50 of 80 nM and 2 nM, and also inhibits c-Kit.
SN-011 Chemical Structure
BCP41129 SN-011 2249435-90-1
SN-011 is a potent and selective mouse and human STING inhibitor, with an IC50 of 76 nM for STING signaling.
123下一页末页共 11313 条记录 1 / 1132 页 
0086-13720134139