R10864 |
MMAE |
Monomethyl auristatin E (MMAE) is a synthetic antineoplastic agent, which is lin
|
R10842 |
Mycophenolate mofetil; Linfonex |
Mycophenolate Mofetil is a non-competitive, selective and reversible inhibitor o
|
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.
|
R10857 |
Pteroic Acid |
Pteroic Acid is a constituent as well as a degradation product of Folic Acid for
|
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
|