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Catalog No CAS NO Product name
CR3732
688352-84-3
R243
R243 is a potent and selective CCR8 antagonist. R243 inhibits CCL1/CCR8 interaction and inhibits CCR8 signaling and chemotaxis. R2..
CR3731
1776115-10-6
BMS-986188
BMS-986188 is a positive allosteric modulator (PAM) of δ-opioid receptors with EC50 of 0.05 μM in a β-arrestin recruitment assa..
CR3730
684238-37-7
BMS-986187
BMS-986187 is a potent and selective positive allosteric modulator (PAM) of the δ-opioid receptor and a G-protein-biased alloster..
CR3729
1462267-08-8
ML266
ML266 (CID-46943215) is a activator of glucocerebrosidase (GCase) that does not inhibit the enzyme’s action but can still facilit..
CR3728
1462267-07-7
NCGC607
NCGC607 is a a noninhibitory chaperone of glucocerebrosidase (GCase).
CR3727
847555-75-3
(S)-SHA 68
Synonyms: (9S)-3-oxo-1,1-diphenyltetrahydrooxazolo[3,4-a]pyrazine-7-carboxylic acid 4-fluorobenzylamide;(3aS)-N-(4-fluorobenzyl)-3..
CR3726
1821370-71-1
pythiDC
PythiDC is a selective inhibitor of collagen prolyl 4-hydroxylase, neither causing general toxicity nor disrupting iron homeostasi..
CR3725
404828-08-6
GSK3 Inhibitor XIII
GSK3 Inhibitor XIII is an aminopyrazole ATP-competitive inhibitor of glycogen synthase kinase 3 (GSK3), with 34% inhibition when u..
CR3724
1443414-10-5
Metarrestin (ML246)
Metarrestin (ML246) is an orally active, specific perinucleolar compartment inhibitor that disrupts the nucleolar structure and in..
CR3723
1083162-61-1
FIN56
FIN56 is a specific inducer of ferroptosis. The mechanism involves two distinct pathways: one pathway is degradation of GPX4, whic..
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Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
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