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Cat.No. Product name Product Description
R2202001 Naringetol Naringenin is the predominant flavanone in grapefruit; displays strong anti-infl
R2203201 NF-κΒ activator 2 NF-κΒ activator 2 is a potent and orally active NF-ҡB activator, with
R2203202 Src Inhibitor 3 Src Inhibitor 3 is a potent, orally active c-terminal Src kinase (CSK) 
R2203181 I-BET567 I-BET567 is a potent and orally active inhibitor of pan-BET candidate
R2203222 Afn-1252 AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reducta
R2203212 MAX-40279 hydrochloride MAX-40279 hydrochloride is a dual and potent inhibitor of FLT3 kinase
R2202111 GSK-2018682 GSK2018682 is an agonist for S1P1 and S1P5 receptor with pEC50s of 7.7 and 7.2,
R2202112 PF3644022 PF-3644022 is a potent, selective, orally active and ATP-competitive MAPKAPK2 (M
R2202113 SGC-SMARCA-BRDVIII SGC-SMARCA-BRDVIII is a potent and selective inhibitor of SMARCA2/4 and PB1(5),
R2202114 BVT948 BVT948 is a protein tyrosine phosphatase (PTP) inhibitor which can also inhibit
R2202115 PFI-90 PFI-90 is a selective inhibitor of histone demethylase (KDM3B) that inhibits PAX
R2202116 TBAP-001 TBAP-001 (Synthesis 13), extracted from patent WO2015075483A1, is a pan-RAF kina
R2202117 Robinetin Robinetin (3,3',4',5',7-Pentahydroxyflavone), a naturally occurring flavonoid wi
R2202118 MRTX1133 MRTX1133 is a noncovalent, potent, and selective KRAS G12D inhibitor. MRTX1133 o
R2202119 HLY78 HLY78 is an activator of the Wnt/β-catenin signaling pathway, which targets the
R2202120 SB-265610 SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonis
R2202121 GSK2033 GSK2033 is a LXR antagonist with pIC50s of 7 and 7.4 for LXRα or LXRβ, respectiv
R2202122 KL-11743 KL-11743 is a potent, orally active, and glucose-competitive inhibitor of the cl
R2202123 Ch55 Ch55 is a potent synthetic retinoid. Ch55 binds to RAR-α and RAR-β receptors wit
R2103226 Polyphyllin I Polyphyllin I is a bioactive constituent extracted from Paris polyphylla, h
R2001291 Coti-2 COTI-2, an anti-cancer drug with low toxicity, is an orally available third gene
R2204121 Lisavanbulin (S)-2,6-diamino-N-(4-(2-(2-(4-((2-cyanoethyl)amino)-1,2,5-oxadiazol-3-yl)-1H-ben
R2204201 MRTX-1719 MRTX-1719 is a potent first-in-class selective inhibitor of the PRMT5/MTA&n
R2202125 Remibrutinib(LOU064) Remibrutinib, is a potent and orally active bruton tyrosine kinase (BTK) inhibit
R2202126 AZD9056 hydrochloride AZD9056 hydrochloride is a selective orally active inhibitor of P2X7 which plays
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