Antineoplastic agents

General description This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate.

(&#8722)-Epigallocatechin gallate is a bioactive compound, which is an important constituent of green tea. It may serve as a potent candidate to prevent cancer.

Potent anticancer compound. Anti-angiogenic.

Potent anticancer compound. Anti-angiogenic.

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

Biochem/physiol Actions (-)-Epothilone A is a microtubule (MT) stabilizing drug and natural macrolide antitumor from myxobacteria Sorangium cellulosum . EpoA exhibits kinetics similar to paclitaxel by inducing tubulin polymerization in vitro and

(-)-Fenchone is a bridged bicyclic ketone found in fennel oil and thuja oil.(-)-Fenchone undergoes condensation with pyridinylalkylamines to form chiral iminopyridine ligands, which find applications in enantioselective copper-catalyzed Henry (nitro

(-)-Fenchone is a bridged bicyclic ketone found in fennel oil and thuja oil.(-)-Fenchone undergoes condensation with pyridinylalkylamines to form chiral iminopyridine ligands, which find applications in enantioselective copper-catalyzed Henry (nitro

(-)-Fenchone is a bridged bicyclic ketone found in fennel oil and thuja oil.(-)-Fenchone undergoes condensation with pyridinylalkylamines to form chiral iminopyridine ligands, which find applications in enantioselective copper-catalyzed Henry (nitro

A tumor-promoting teleocidin compound that activates PKC (Ki = 3.4 nM and 1 &muM for PKC&eta and PKC&gamma, respectively) induces differentiation of human embryonic stem cells into pancreatic progenitors.

Potently and irreversibly inactivates SAH hydrolase (Ki = 8.39 nM) has antitumor activity against mouse leukemia L1210 cells and broad-spectrum antiviral activity.

Potently and irreversibly inactivates SAH hydrolase (Ki = 8.39 nM) has antitumor activity against mouse leukemia L1210 cells and broad-spectrum antiviral activity.