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| Cat.No. | Product name | Product Description |
| R2032130 | Tipiracil hydrochloride | Tipiracil (hydrochloride) is a thymidine phosphorylase inhibitor (TPI), used for |
| R2032131 | Valrubicin | Valrubicin is a chemotherapy agent, inhibits TPA- and PDBu-induced PKC activatio |
| R2032132 | PP1;AGL 1872;EI 275 | PP1 is a potent, and Src family-selective tyrosine kinase inhibitor with IC50 of |
| R2032133 | Elagolix sodium;NBI-56418 sodium | Elagolix sodium is a human GnRH receptor (GnRHR) antagonist with an IC50 and Ki |
| R2032134 | Coelenterazine | Coelenterazine is a luminescent enzyme substrate for apoaequorin and Renilla luc |
| R2032135 | Anidulafungin;LY303366 | Anidulafungin is a new semisynthetic echinocandin with antifungal potency. |
| R2032136 | Setipiprant;ACT-129968;KYTH-105 | Setipiprant is an orally available, selective CRTH2 antagonist.CRTH2 is a G prot |
| R2032137 | Tosedostat;CHR-2797 | Tosedostat is an aminopeptidase inhibitor. |
| R2032138 | Azeliragon;TTP488;PF-04494700 | Azeliragon (TTP488) is an orally bioavailable inhibitor of the receptor for adva |
| R2032139 | (-)-Huperzine A(HupA) | (-)-Huperzine A (Huperzine A), an active Lycopodium alkaloid extracted from trad |
| R2032140 | Crisaborole;AN-2728;PF-06930164 | Crisaborole (AN-2728) is a potent inhibitor of PDE4 and cytokine release; inhibi |
| R2032141 | Ascomycin;Immunomycin;FR-900520;FK520) | Ascomycin(Immunomycin, FR-900520, FK520) is an ethyl analog of tacrolimus (FK506 |
| R2032142 | Balicatib(AAE-581) | Balicatib(AAE-581) is a potent and selective inhibitor of cathepsin K; 10-100 fo |
| R2032143 | Dovitinib(TKI-258, CHIR-258) | Dovitinib (TKI258; CHIR-258) is a multi-targeted tyrosine kinase inhibitor with |
| R2032144 | E-3810(Lucitanib) | Lucitanib (E-3810) is a novel dual inhibitor of VEGFR and FGFR, potently and sel |
| R2032145 | Ellipticine(NSC71795) | Ellipticine (NSC 71795) is a potent antineoplastic agent; inhibits DNA topoisome |
| R2032146 | Enocitabine | Enocitabine is a nucleoside analog, and is a potent DNA replication inhibitor, a |
| R2032147 | Entinostat(MS-275, SNDX-275) | Entinostat is an oral and selective class I HDAC inhibitor, with IC50s of 243 nM |
| R2032148 | Epothilone A | Epothilone A is a competitive inhibitor of the binding of [3H] paclitaxel to tub |
| R2032149 | FK866 | (E)-Daporinad (FK866) is an effective inhibitor of nicotinamide phosphoribosyltr |
| R2032150 | Flavopiridol Hydrochloride;Alvocidib Hydrochloride;L86-8275 Hydrochloride;HMR-1275 Hydrochloride) | Flavopiridol Hydrochloride (Alvocidib Hydrochloride) is a broad inhibitor of CDK |
| R2032151 | 甲磺酸氟马替尼/氟马替尼;FluMatinib Mesylate | Flumatinib mesylate (HH-GV-678 mesylate), a derivative of imatinib, is a multi-k |
| R2032152 | Fulvestrant(ICI182780;ZD9238;ZM182780) | Fulvestrant (ICI 182780; ZD 9238; ZM 182780) is a potent estrogen receptor antag |
| R2032153 | Icotinib(Hydrochloride) | Icotinib Hydrochloride (BPI-2009) is a potent and specific EGFR inhibitor with a |
| R2032154 | Ispinesib(SB-715992) | Ispinesib is a specific inhibitor of kinesin spindle protein (KSP), with a Ki ap |
