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Chemical Structure Cat. No. Product Name CAS No.
Flomoxef Chemical Structure
BCP20920 Flomoxef 99665-00-6
Flomoxef is a cephamycin antibiotic with a difluoromethylthio-acetamido group at the 7-beta position of the cephem nucleus, commonly used for postoperative prophylaxis. Flomoxef has activity against epidermides, streptococci, propionibacteria, and both methicillin-resistant and -susceptible Staphylococcus aureus.
BN-2629 Chemical Structure
BCP20924 BN-2629 232931-57-6
BN-2629 is a DNA-intercalating agent potentially for the treatment of ovarian cancer and leukemia.
Fluensulfone Chemical Structure
BCP16864 Fluensulfone 318290-98-1
Fluensulfone is a new nematicide for chemical control of plant parasitic nematodes.
Cridanimod Chemical Structure
BCP25847 Cridanimod 38609-97-1
Cridanimod is a potent type I interferon (IFN) inducer that directly binds to STING and triggers a strong antiviral response through the TBK1/IRF3 route.
c-GpAp Chemical Structure
BCP25099 c-GpAp 849214-04-6
c-GpAp is a potent STING ligand.
2’2’-cGAMP Chemical Structure
BCP25471 2’2’-cGAMP 1465774-27-9
2’2’-cGAMP is a synthetic STING agonist.
ML RR-S2 CDA Chemical Structure
BCP29476 ML RR-S2 CDA 1638241-89-0
ML RR-S2 CDA (STING-Inducer-1) is a highly active cyclic-di-nucleotide immune stimulators that activate DCs via the cytoplamtic receptor STING (Stimulator of Interferon Genes).
ML RR-S2 CDA ammonium salt Chemical Structure
BCP29660 ML RR-S2 CDA ammonium salt 1638750-96-5
ML RR-S2 CDA ammonium salt is a synthetic cyclic dinucleotide derivative that functions as a highly potent agonist of STING, enhances binding affinity to STING and activates all known human STING alleles.
2'3'-cGAMP Chemical Structure
BCP25157 2'3'-cGAMP 1441190-66-4
2′3′-cGAMP is a potent STING activator that binds to STING with Kd of 1.61 uM.
MRT 68921 dihydrochloride Chemical Structure
BCP29697 MRT 68921 dihydrochloride 2080306-21-2
MRT 68921 dihydrochloride is a potent ULK inhibitor (IC50 values are 1.1 and 2.9 nM for ULK2 and ULK1, respectively). Inhibits autophagy in mouse embryonic fibroblasts.
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