vinca

Vindoline is an indole alkaloid that exhibits antimitotic activity by inhibiting microtubule assembly.

Vincamine (Perval) is a major alkaloid of Vinca minor L., Apocynaceae. It has been used therapeutically as a vasodilator and antihypertensive agent, particularly in cerebrovascular disorders.

Apovincamine is a vinca alkaloid and a chemical precursor of Vinpocetine, which is a derivative of Vincamine with vasodilating activity.

19-Hydroxypseudovincadifformine is a useful organic compound for research related to life sciences and the catalog number is T125260.

14,15-Didehydrovincamenine is a natural product for research related to life sciences. The catalog number is TN2620 and the CAS number is 112219-48-4.

16,17-Dihydroapovincamine is a natural product for research related to life sciences. The catalog number is TN2642 and the CAS number is 57130-30-0.

16-O-Methyl-14,15-didehydroisovincanol is a natural product for research related to life sciences. The catalog number is TN2649 and the CAS number is 112237-71-5.

Vinburnine (Eburnalritardo) is a vasodilator. Vinburnine is a vinca alkaloid and a metabolite of vincamine.

Fluorocurarine chloride (Metvine; Vincanine methyl chloride) is a plant metabolite that can be isolated from the Vinca plant.

Vincristine sulfate is an alkaloidal natural product that binds to microtubule proteins and inhibits the formation of microtubules, thereby inhibiting mitosis in tumor cells. Vincristine sulfate is used as a microtubule destabilizing agent in research studies for the treatment of hematologic neoplasms such as leukemias and lymphomas, as well as in studies related to sarcomas in children.

Vinblastine sulfate (Vincaleukoblastine sulfate salt) can inhibit the formation of microtubule, it also inhibits nAChR(IC50=8.9 uM).

Vincristine binds to tubulin and inhibits the formation of microtubules, thereby inhibiting mitosis of the cancer cell. Vincristine can be used as a microtubule-destabilizing agent for research on the treatment of hematologic cancers, such as leukemia and

Rescinnamine is an inhibitor of angiotensin-converting enzyme. It also is a vinca alkaloid obtained from Rauwolfia serpentina and other species of Rauwolfia. It used as an antihypertensive drug.

Kopsinine, an indole alkaloid, is derived from the flowers of the periwinkle plant (Vinca spp.) [1].

Halichondrin B, sourced from the sponge Halichondria okadai, serves as a noncompetitive inhibitor of Vinca-alkaloid binding to tubulin, with an IC 50 for tubulin polymerization ranging from 1.2-1.4 μM, and exhibits anti-tumor activity [1].

Rescinnamine (Standard) is a reference standard for research and analysis in studies involving Rescinnamine. Rescinnamine is an inhibitor of angiotensin-converting enzyme. It also is a vinca alkaloid obtained from Rauwolfia serpentina and other species of Rauwolfia. It used as an antihypertensive drug.