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Home > Products
| Cat.No. | Product name | Product Description |
| R10841 | Mycophenolic acid | Mycophenolic acid is a potent IMPDH inhibitor and the active metabolite of an im |
| R10844 | 273206-92-1 | |
| R10846 | CTP-518 | |
| R10849 | Am095 | AM095 is a potent LPA1 receptor antagonist with IC50 values of 0.98 and 0.73 μM |
| R10854 | Ansamitocin P 3' (Antibiotic C 15003P3'; Maytansinol butyrate) | Ansamitocin P 3' exhibits antitumour activity, is an antibody drug conjugate cyt |
| R10855 | Moxidectin;CL301423 | Moxidectin(ProHeart 6; CL301423; Cydectin) is an anthelmintic drug which kills p |
| R10856 | Actinomycin D | Actinomycin D inhibits DNA repair with an IC50 of 0.42 μM. |
| R10858 | N10-(Trifluoroacetyl)pteroicacid | Product Name：4-(N-((2-Amino-4-oxo-3,4-dihydropteridin-6-yl)methyl)-2,2,2-trifluo |
| R10860 | Levomilnacipran | |
| R10861 | Prasugrel Hydrochloride | |
| R10862 | Mertansine (DM1) | Mertansine (DM1) is a microtubulin inhibitor and is an antibody-conjug |
| R10863 | Calicheamicin gamma1 | |
| R10865 | Nemorubicin；Methoxymorpholinyldoxorubicin; PNU 152243; PNU-152243A | Nemorubicin is a derivative of doxorubicin, and has antitumor activity. |
| R10866 | Levomefolate calcium | |
| R10874 | Homoharringtonine (Omacetaxine mepesuccinate; HHT) | Homoharringtonine (Omacetaxine mepesuccinate;HHT) is a cytotoxic alkaloid with a |
| R10877 | Arotinolol hydrochloride | |
| R10879 | Miriplatin;SM-11355 | Miriplatin (SM-11355) is a chemotherapy agent which belongs to the class of alky |
| R10885 | KP-103;Efinaconazole | Efinaconazole (KP-103) is a triazole antifungal agent and againsts T. mentagroph |
| R10889 | Pimavanserin;ACP-103 | Pimavanserin is a selective inverse agonist of the 5-HT2A receptor with pIC50 an |
| R10890 | NVP-ACC789 (ACC-789; ZK202650) | NVP-ACC789 is an inhibitor of human VEGFR-1, VEGFR-2 (mouse VEGFR-2), VEGFR-3 an |
| R10840 | Orlistat | Orlistat is a general lipase inhibitor with IC50 of 122 ng/ml for PL from human |
| R10881 | Sorafenib (Synonyms: Bay 43-9006) | Sorafenib (Bay 43-9006) is a potent, orally active multikinase inhibitor with IC |
| R10882 | Sunitinib (Synonyms: SU 11248) | Sunitinib Malate is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and |
| R10859 | Tacrolimus; FK506 | Tacrolimus (FK506) is a 23-membered macrolide lactone, it reduces peptidyl-proly |
| R10891 | Vatalanib | Vatalanib (PTK787) 2HCl is an inhibitor of VEGFR2/KDR with IC50 of 37 nM in a ce |
