| Cat.No. | Name | Information |
|---|---|---|
| M9075 | Etomoxir sodium salt | Etomoxir((R)-(+)-Etomoxir) sodium salt is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig. |
| M10566 | Valepotriate | Valepotriate has anti-epileptic and anti-cancer activities, it isolated from Valeriana jatamansi Jones. |
| M41312 | Zalypsis | Zalypsis (PM00104) has anti-tumor activity. |
| M41311 | RTA 744 | RTA 744 (WP 744) is a Doxorubicin analogue. |
| M41310 | Ganoderic acid R | Ganoderic acid R is a potent anticancer agent. |
| M41309 | Ganoderic acid Mf | Ganoderic acid Mf is an antitumor triterpenoid. |
| M41308 | Secalonic acid D | Secalonic acid D is a toxic compound against tumor cells. |
| M41307 | Ganoderic acid T1 | Ganoderic acid T1 is a deacetylated derivative of Ganoderic acid T. |
| M41306 | Ara-SH | Ara-SH is a Cytarabine mercaptopropionic acid-substituted derivative. |
| M41305 | Tubulin inhibitor 32 | Tubulin inhibitor 32 is a potent and orally active tubulin inhibitor. |
| M41304 | Apoptosis inducer 11 | Apoptosis inducer 11 induces apoptosis through the mitochondrial pathway. |
| M41303 | Hydroxy-PP-Me | Hydroxy-PP-Me is a potent and specific CBR1 inhibitor with an IC50 of 759 nM. |
| M41302 | SLC7A11-IN-1 | SLC7A11-IN-1 is a potent solute carrier family 7 member 11 (SLC7A11, xCT) inhibitor. |
| M41301 | Vallesiachotamine | Vallesiachotamine, a known monoterpene indole alkaloid, possesses anti-tumor activity. |
| M41300 | CDK8-IN-13 | CDK8-IN-13 is a potent, selective and orally active CDK8 inhibitor with an IC50 value of 51.9 nM. |
| M41299 | Apoptosis inducer 12 | Apoptosis inducer 12 is an apoptosis inducer that induces apoptosis through the mitochondrial pathway. |
| M41298 | ASR-488 | ASR-488 activates the mRNA-binding protein CPEB1, induces apoptosis and inhibits bladder cancer growth. |
| M41297 | Antimycin A2c | Anticancer agent 141 is an antimycin alkaloid, with inhibitory pottential in HPV infected-cervical cancer. |
| M41296 | TAT-NEP1-40 acetate | TAT-NEP1-40 acetate is a therapeutic candidate for axonal regeneration and functional recovery after stroke. |
| M41295 | GSPT1 degrader-1 | GSPT1 degrader-1 is a potent degrader of G1 to S phase transition 1 (GSPT1) via ubiquitin-proteasome system. |
| M41294 | Ganoderic acid Mk | Ganoderic acid Mk (GA-Mk) is a triterpenoid acid, that can be isolated from the mycelia of Ganoderma lucidum. |
| M41293 | RUNX-IN-2 | RUNX-IN-2 covalently binds to the RUNX-binding sequences, and inhibits the binding of RUNX proteins to their target sites. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
