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Chemical Structure Cat. No. Product Name CAS No.
Conglobatin Chemical Structure
BCP38737 Conglobatin 72263-05-9
Conglobatin is produced by the strain of Streptomyces conglobatus.
HIF-2a Translation Inhibitor 76 Chemical Structure
BCP38668 HIF-2a Translation Inhibitor 76 882268-69-1
HIF-2a Translation Inhibitor 76 is a cell-permeable HIF-2a translation inhibitor (IC50 value 5 μM).
BIX 01294 trihydrochloride hydrate Chemical Structure
BCP38667 BIX 01294 trihydrochloride hydrate 1808255-64-2
BIX 01294 trihydrochloride hydrate, a diazepin-quinazolinamine derivative, is a histone-lysine methyltransferase (HMTase) inhibitor that modulates the epigenetic status of chromatin.
GSK2798745 Chemical Structure
BCP38659 GSK2798745 1419609-94-1
GSK2798745 is a potent and selective TRPV4 Ion Channel Inhibitor with IC50 = 1.8 nM.
Nemiralisib Chemical Structure
BCP38658 Nemiralisib 1254036-71-9
Nemiralisib, also known as GSK2269557, is a highly potent and selective inhaled PI3Kδ inhibitor for the treatment of COPD.
MIRA-1 Chemical Structure
BCP38613 MIRA-1 72835-26-8
MIRA-1 is a potent, selective Werner syndrome helicase (WRN helicase) with IC50 of 20 uM.
Dyclonine Chemical Structure
BCP38594 Dyclonine 586-60-7
Dyclonine is n-Ethylpiperidine in which one of the hydrogens attached to the methyl group is substituted by a 4-butoxybenzoyl group. It has a role as a topical anaesthetic. It is a member of piperidines and an aromatic ketone.
L-368,899 hydrochloride Chemical Structure
BCP38590 L-368,899 hydrochloride 160312-62-9
L-368,899 hydrochloride is the hydrochloride salt of L-368,899, which is a non-peptide, orally active and potent oxytocin receptor antagonist with IC50 value of 8.9 nM.
Fuzuopali Chemical Structure
BCP38585 Fuzuopali 1358715-18-0
Fluzoparib is a selective poly [ADP-ribose] polymerase 1 (PARP1) and poly [ADP-ribose] polymerase 2 inhibitor (PARP2).
ULK-101 Chemical Structure
BCP37780 ULK-101 2443816-45-1?
ULK-101 is a potent and selective ULK1 inhibitor with in vitro IC50 of 8.3 nM.
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