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Catalog No CAS NO Product name
CR3630
1034297-58-9
CRT5
CRT5 (CRT0066051), a pyrazine benzamide, is a potent and selective PKD inhibitor with IC50 of 1 nM, 2 nM, and 1.5 nM for PKD1, PKD..
CR3629
1449747-00-5
CYM5520
CYM-5520 is a pyrrolyl ketone derivative that acts as a potent, selective, allosteric agonist of sphingosine-1-phosphate receptor ..
CR3628
1229652-22-5
HA-155
HA155 (Autotaxin Inhibitor IV), a boronic acid-based compound, inhibits autotaxin with IC50 of 5.7 nM by selectively binding to it..
CR3627
957513-35-8
ASN03576800
ASN03576800 is an inhibitor of the VP40 matrix protein. Synonyms: ASN03576800;2-[2-(1,3-benzodioxol-5-ylamino)-2-oxoethyl]sulfin..
CR3626
57754-86-6
Nisoxetine hydrochloride
Nisoxetine hydrochloride is a potent and selective noradrenaline transporter (NET) inhibitor with Kd of 0.76 nM. Nisoxetine hydroc..
CR3625
1638211-04-7
ML303 
ML303 is a pyrazolopyridine influenza virus nonstructural protein 1 (NS1) antagonist (IC90 = 155 nM), with an EC50 of 0.7 μM for ..
CR3624
1454619-13-6
PU-H54
Synonyms: 3H-Purin-6-amine, 8-[(2,4-dimethylphenyl)thio]-3-(4-pentyn-1-yl)-;8-[(2,4-Dimethylphenyl)thio]-3-(4-pentyn-1-yl)-3H-puri..
CR3623
4382-63-2
PFK-015
PFK-015 is an effective inhibitor of PFKFB3 with IC50 of 110 nM (recombinant PFKFB3) and inhibits PFKFB3 activity in cancer cells ..
CR3622
1428630-86-7
ML254
ML254 is shown to competitively interact with the MPEP allosteric binding site. ML254 can serve as a significant pure-PAM tool com..
CR3621
902589-96-2
YMU1
YMU1 is an inhibitor of human thymidylate kinase (hTMPK). YMU1 stabilizes the conformation of ligand-induced degradation (LID) reg..
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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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