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Cat.No. Product name Product Description
R10761 5-Chloro-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole CAS NO.:318290-98-1 Product Name:5-Chloro-; 5-chloro-; 5-Chloro-2-[(3,4,4-triflu
R10763 Kevetrin hydrochloride; NSC525990 Kevetrin hydrochloride is a small molecule and activator of the tumor suppressor
R10764 BMH-21 BMH-21 is a DNA intercalator, which binds ribosomal DNA and inhibits RNA polymer
R10766 SC-202671 JNK inhibitor IX is a selective and potent JNK inhibitor with pIC50 of 6.5 and 6
R10767 MPEP hydrochloride MPEP is a potent, highly selective non-competitive antagonist at the mGlu5a rece
R10768 KU-60019 KU-60019 is an improved analogue of KU-55933, with IC50 of 6.3 nM for ATM in cel
R10769 O4I2 O4I2 is a potent Oct3/4 inducer in various human cell lines including human fibr
R10770 1016535-83-3
R10771 O4I1 O4I1 is as a potent Oct3/4 inducer.Target: Oct3/4
R10773 220904-99-4
R10774 TG6-10-1 TG6-10-1 is an EP2 antagonist, shows low-nanomolar antagonist activity against o
R10775 B7/CD28 interaction inhibitor 1 B7/CD28 interaction inhibitor 1 (copmound 6b) is a potent B7.1-CD28 interaction
R10776 4-Keto13-cis-Retinoic Acid CAS NO.:71748-57-7Product Name:4-Keto 13-cis-Retinoic Acid Methyl EsterSynonyms:
R10777 bml-210 BML-210 is the novel HDAC inhibitor, and its mechanism of action has not been ch
R10778 Pimelic diphenylamide 106; TC-H106 Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I HDAC (HD
R10779 UF010 UF010 is a potent and selective HADC inhibitor with IC50 ~0.06 μM, 0.1 μM, 0.5 μ
R10780 KC7F2 KC7F2 is a potent HIF-1 pathway inhibitor and that its potential as a cancer the
R10781 WDR50103 WDR5-0103 is a potent and selective WD repeat-containing protein 5 (WDR5) antago
R10782 EXP-3174 Losartan Carboxylic Acid (E-3174), an active carboxylic acid metabolite of Losar
R10783 vorapaxar intermediate 1
R10784 vorapaxar intermediate 2
R10785 Savolitinib (Volitinib; HMPL-504; AZD-6094) Savolitinib(Volitinib; AZD-6094; Volitinib) is an orally bioavailable inhibitor
R10786 FMK FMK is a RSK2 kinase inhibitor.
R10789 CPI-203 CPI203 is a novel potent, selective and cell permeable inhibitor of the bromodom
R10790 2-(2,6-dimethylphenylamino)-N-(7-(hydroxyamino)-7-oxoheptyl)pyrimidine-5-carboxamide
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