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Cat.No. Product name Product Description
R2101095 PF-CBP1 hydrochloride PF-CBP1 hydrochloride is a highly selective inhibitor of the CREB binding protei
R2101096 TSPC TSPC is an inhibitor for GA perception by in vitro and in planta evaluations.
R2101097 SHA68 SHA 68 is a potent and selective antagonist of non-peptide neuropeptide S recept
R2101098 GSK963 GSK963 (Racemate), a structurally distinct, potent and selective inhibitor of RI
R2101099 GSK962 GSK962 is a GSK963 inactive enantiomer. It can be used to confirm the on-target
R2101100 NSC45586 A selective protein phosphatase PHLPP inhibitor with IC50 of 4 uM for PP2C domai
R2101101 ML198 ML198 is a novel activator and non-inhibitory chaperone of glucocerebrosidase. M
R2101102 Ribocil Ribocil is a highly selective chemical modulator of bacterial riboflavin riboswi
R2101103 Farampator (CX-691;Org24448) Farampator (CX691, Org24448) is a positive modulator of AMPA receptor.
R2101104 GSK3 Inhibitor XIII GSK3 Inhibitor XIII (GSK3i XIII) is an ATP-binding site inhibitor of GSK-3.
R2101105 pythiDC PythiDC is a selective inhibitor of collagen prolyl 4-hydroxylase.
R2101106 (S)SHA-68 SHA-68 is a selective neuropeptide S receptor (NPSR) antagonist that displays no
R2101107 NCGC607 NCGC607 is a a small-molecule noninhibitory chaperone of glucocerebrosidase.
R2101108 ML266 (CID-46943215) ML266 (CID-46943215) is a activator of glucocerebrosidase (GCase) that does not
R2101109 BMS986187 BMS-986187 is a novel potent, positive allosteric modulator of δ-opioid receptor
R2101110 BMS986188 BMS-986188 is a positive allosteric modulator (PAM) of δ-opioid receptors with E
R2101111 R243 R243 is a CCR8 signaling and chemotaxis inhibitor.
R2101112 BGC-20-1531 BGC-20-1531 is a EP4 antagonist for the treatment of acute migraine.
R2101113 Aka Lumine AkaLumine is a luciferin analogue. The bioluminescence produced by AkaLumine in
R2101114 SGC2085 hydrochloride SGC2085 is a potent and selective coactivator associated arginine methyltransfer
R2101115 TMP778 TMP778 is a selective RORγt inverse agonist. TMP778 can selectively block mouse
R2101116 TX1-85-1 TX1-85-1 is an irreversible inhibitor of Her3 (ErbB3) with IC50 of 23 nM. TX1-85
R2101117 Azaindole 1;TC-S 7001 Azaindole 1 (TC-S 7001) is a selective and ATP-competitive ROCK inhibitor with I
R2101118 Shield-1 Shield-1 is a specific, cell-permeant and high-affinity ligand of FK506-binding
R2101119 NCGC00262650 NCGC00262650 is a dual inhibitor of AMA1-RON2 interaction and c-Src tyrosine kin
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