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Cat.No. Product name Product Description
R2053300 FM19G11 Synonyms:[2-(4-methylphenyl)-2-oxoethyl] 3-[(2,4-dinitrobenzoyl)amino]benzoate
R2053301 FG7142;ZK39106;LSU-65 FG 7142 (ZK 39106; LSU-65), a non-selectively benzodiazepine inverse agonist, ha
R2053302 ZG-10 Density:1.301±0.06g/cm3 at temp:20℃.Synonyms: 4-​[[4-​(Dimethylamino)​-​1-​oxo-​
R2053303 JNJ-10198409;JNJ10198409 JNJ-10198409 is a relatively selective, orally active, and ATP competitive PDGF-
R2053304 Piromidic acid Piromidic acid is a quinolone antibiotic.
R2053305 4'-Hydroxy TorseMide Synonyms:1-[4-(4-hydroxy-3-methylanilino)pyridin-3-yl]sulfonyl-3-propan-2-ylurea
R2053306 WST-5 Synonyms:disodium,2-[[4-[2-(1,3-benzothiazol-2-yl)-3-[4-[4-[3-(1,3-benzothiazol-
R2053307 PHTPP PHTPP is a selective ERβ antagonist.
R2053308 O151 Synonyms:N-cyclohexylidene-4-bromobenzohydrazide
R2053309 AB-005 AB-005 or [1-[(1-methyl-2-piperidinyl)methyl]-1H-indol-3-yl](2,2,3,3-tetramethyl
R2053310 LF3 LF3 is an antagonist of the β-Catenin/TCF4 interaction with antitumor activity;
R2053311 ODQ Synonyms:[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one
R2053312 Valiglurax;VU0652957;VU2957 References 1. Panarese JD, et al. Bioorg Med Chem Lett. 2018 Nov 1. pii: S0960-8
R2053313 BRD3308 BRD3308 is a highly selective HDAC3 inhibitor with an IC50 of 54 nM. BRD3308 is
R2053314 PNU-120596;NSC216666 PNU-120596 (NSC 216666 ) is a potent and selective positive allosteric α7 nAChR
R2053315 Metarrestin;ML246 Metarrestin (ML246) disrupts the nucleolar structure and inhibits RNA polymerase
R2053316 Biotin Diacid Synonyms:2-[3-[(3aS,4S,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4
R2053317 DREADD Agonist 21 DREADD agonist 21 is a potent human muscarinic acetylcholine M3 receptors (hM3Dq
R2053318 Flucindole Synonyms:6,8-difluoro-N,N-dimethyl-2,3,4,9-tetrahydro-1H-carbazol-3-amine
R2053319 VU6010608 Synonyms:Benzamide, 3,4-dimethoxy-N-[2-(1H-1,2,4-triazol-1-yl)-5-(trifluorometho
R2053320 RCM-1 RCM-1 is a FOXM1 inhibitor.
R2053321 Squarunkin A hydrochloride Potent inhibitor of UNC119 chaperone protein-cargo interaction (IC50 = 10 nM for
R2053322 ML-210 ML-210 is a selective and covalent glutathione peroxidase 4 (GPX4) inhibitor wit
R2053323 Aldox Synonyms:N-[3-(dimethylamino)propyl]tetradecanamide
R2053324 FEMA 4774 Synonyms:4-amino-5-(3-(isopropylamino)-2,2-dimethyl-3-oxopropoxy)-2-methylquinol
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