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Cat.No. Product name Product Description
R10736 OAC-1 OAC1 (Oct4-activating compound 1) can enhance the efficiency of reprogramming.
R10737 OAC2 OAC2 is an Oct4-activating compound which activates expression through the Oct4
R10740 Dihydroethidium Dihydroethidium(Hydroethidine; PD-MY 003) is a superoxide indicator; exhibits bl
R10741 Apilimod(STA 5326) Apilimod(STA 5326) is a potent IL-12/IL-23 inhibitor, IL-12 production in cultur
R10742 Apilimod mesylate (STA 5326 mesylate) Apilimod(STA 5326) mesylate is a potent IL-12/IL-23 inhibitor, IL-12 production
R10748 C7280948 C7280948 is an inhibitor of histone arginine methyltransferase PRMT1 with IC50 v
R10756 trans-Tranilast Trans-Tranilast is an antiallergic drug, used to treat bronchial asthma, allergi
R10757 Bimiralisib (Synonyms: PQR309) Bimiralisib (PQR309) is a potent, brain-penetrant, orally bioavailable, pan-clas
R10758 Tizoxanide Tizoxanide is the active metabolite of Nitazoxanide, which is a thiazolide anti-
R10760 BQU57 BQU57, a derivative of RBC8, is a selective GTPase Ral inhibitor relative to the
R10769 O4I2 O4I2 is a potent Oct3/4 inducer in various human cell lines including human fibr
R10771 O4I1 O4I1 is as a potent Oct3/4 inducer.Target: Oct3/4
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:
R10789 CPI-203 CPI203 is a novel potent, selective and cell permeable inhibitor of the bromodom
R10808 PTZ-343; phenothiazine sodium salt PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi
R10809 Golotimod; SCV 07 Golotimod is an orally bioavailable synthetic peptide containing the amino acids
R10810 Uramustine Uramustine is a chemotherapy drug which belongs to the class of alkylating agent
R10822 PTZ-343 PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi
R10833 Lesinurad;RDEA594 Lesinurad is a selective uric acid re-absorption inhibitor (SURI) and is also a
R10836 MS417
R10265 ID8;ID-8 ID-8 is a DYRK inhibitor, and sustains embryonic stem cell self-renewal in long-
R10161 GW4064 GW4064 is an agonist of farnesoid X receptor (FXR) with EC50 of 65 nM in CV1 cel
R10263 Fexaramine Fexaramine is a small molecule farnesoid X receptor (FXR) agonist with 100-fold
R10546 Obeticholic acid; INT747 Obeticholic Acid is a potent and selective farnesoid X receptor (FXR) agonist wi
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