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Cat.No. Product name Product Description
R2030429 4-[4-(1-Hydroxyethyl)-2-Methoxy-5-nitrophenoxy]butanoic Acid
R2030430 Cyanine3 carboxylic acid
R2030431 Cy3.5-COOH
R2030432 Cyanine5.5 carboxylic acid
R2030433 Cyanine5 carboxylic acid
R2030434 Tegafur Impurity
R2030435 4-((2,4-dichloro-5-methoxyphenyl)amino)-6-methoxy-7-(3-(piperazin-1-yl)propoxy)quinoline-3-carbonitrile
R2030436 2-(4-benzoyl-3-hydroxyphenoxy)acetic acid
R2030437 2-amino-6-bromo-5,6-dihydrobenzothiazol-7(4H)-one
R2030438 3,3',5,5'-TETRA(TERT-BUTYL)[1,1'-BIPHENYL]-4,4'-DIOL
R2030439 Benzonitrile,4,4',4''-[1,3,5-benzenetriyltris(oxy)]tris-(9CI)
R2030440 tert-butyl N-[2-[[5-methoxy-4-[[4-(1-methylindol-3-yl)pyrimidin-2-yl]amino]-2-nitrophenyl](methyl)amino]ethyl]-N-methylcarbamate
R2031168 (R)-N-(pyrrolidin-3-ylmethyl)methanesulfonamide 该产品曾做过需定制
R2003041 LIT-001 TFA LIT-001 is the first nonpeptide oxytocin receptor (OT-R) agonist (EC50=55 nM; Ki
R2003051 Cefminox sodium (MT-141) Cefminox sodium (MT-141) is a semisynthetic cephamycin, which exhibits a broad s
R2003081 SRT3025 HCl;Sirtuin modulator 1 Sirtuin modulator 1 is a modulator of SIRTl, a homolog of SIRT3, with EC1.5 of &
R00391 Safinamide (FCE 26743) Safinamide (FCE 26743) selectively and reversibly inhibits MAO-B with IC50 of 98
R00310 Nilotinib Impurity 9 Nilotinib is an orally available Bcr-Abl tyrosine kinase inhibitor with antineop
R00311 Cardiogenol C, Hydrochloride Cardiogenol C hydrochloride is a cell-permeable pyrimidine compound which potent
R00313 Cisplatin (CDDP; cis-Diaminodichloroplatinum) Cisplatin is a antineoplastic chemotherapy drug which works by cross-linking wit
R00314 Defactinib Defactinib (VS-6063; PF-04554878) is a novel FAK inhibitor with potential antian
R00315 Defactinib hydrochloride;VS-6063 hydrochloride; PF 04554878 hydrochloride Defactinib hydrochloride (VS-6063 hydrochloride; PF 04554878 hydrochloride) is a
R00318 Donepezil;E2020 free base Donepezil (E2020 free base) is a specific and potent AChE inhibitor with IC50s o
R00320 olodaterol hydrochloride Olodaterol hydrochloride is the hydrochloride salt form of Olodaterol, which is
R00321 RET-IN-1 RET-IN-1 is a RET kinase inhibitor extracted from patent WO2018071447A
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