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 About 11 results found for searched term "87-44-5" (0.051 seconds)

Cat.No.  Name Target
M1854 VX-770 (Ivacaftor) CFTR
Ivacaftor
VX-770 (Ivacaftor) is a first-in-class potentiator of CFTR, which targeting G551D-CFTR and F508del-CFTR with EC50 of 100 nM and 25 nM, respectively.
M3617 LY2874455 FGFR
LY2874455 is a novel and potent FGF/FGFR inhibitor.
M7668 BMS-646786 P2 Receptor
BPTU
BMS-646786 is a potent and specific inhibitor of P2Y1 purinergic receptor that inhibits ADP-mediated platelet aggregation in human blood samples.
M8810 Taprostene sodium salt Others
Highly selective IP1 prostanoid receptor agonist.
M13569 S29434 Autophagy
NMDPEF
S29434 (NMDPEF) is a potent, competitive, selective and cell-permeable inhibitor of quinone reductase 2 (QR2), with IC50s ranging from 5 to 16 nM for human QR2 at different organizational levels, and has good selectivity for QR2 over QR1.
M18555 (25RS)-Ruscogenin Others
(25RS)-Ruscogenin
M18711 β-Caryophyllene Cannabinoid
β-Caryophyllene is a CB2 receptor agonist.
M38680 Glepidotin B Antibiotic
Glepidotin B is a dihydroflavonol compound isolated from the extracts of American licorice, Glycyrrhiza lepidota (Leguminosae). Glepidotin B is an antimicrobial agent.
M40423 Viteralone Others
Viteralone (compound 5) is a natural product that can be isolated from Vitex negundo. Viteralone is cytotoxic to HL-60 cancer cells.
M43249 M65 Others
M65 is a specific antagonist of PAC1 receptor that inhibits ANP secretion.
M54825 SV 156 Dopamine Receptor
SV156; SV-156
SV 156 is a potent and selective D2 dopamine receptor antagonist, with a Ki of 2.5 nM for hD2. SV 156 has approximately 40-fold binding selectivity for D2 dopamine receptors compared to the D3 receptor subtype.



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