Nincaluicolflastine en es it fr

Nincaluicolflastine Brand names, Nincaluicolflastine Analogs

Nincaluicolflastine Brand Names Mixture

  • No information avaliable

Nincaluicolflastine Chemical_Formula

C46H58N4O9

Nincaluicolflastine RX_link

http://www.rxlist.com/cgi/generic3/vinblastine.htm

Nincaluicolflastine fda sheet

http://www.accessdata.fda.gov/scripts/cder/onctools/summary.cfm?ID=29

Nincaluicolflastine msds (material safety sheet)

Nincaluicolflastine MSDS

Nincaluicolflastine Synthesis Reference

No information avaliable

Nincaluicolflastine Molecular Weight

810.974 g/mol

Nincaluicolflastine Melting Point

267 oC

Nincaluicolflastine H2O Solubility

Negligible

Nincaluicolflastine State

Solid

Nincaluicolflastine LogP

5.587

Nincaluicolflastine Dosage Forms

Liquid; Powder for solution; Solution

Nincaluicolflastine Indication

For treatment of breast cancer, testicular cancer, lymphomas, neuroblastoma, Hodgkin's and non-Hodgkin's lymphomas, mycosis fungoides, histiocytosis, and Kaposi's sarcoma.

Nincaluicolflastine Pharmacology

Vinblastine is a vinca alkaloid antineoplastic agent. The vinca alkaloids are structurally similar compounds comprised of 2 multiringed units: vindoline and catharanthine. The vinca alkaloids have become clinically useful since the discovery of their antitumour properties in 1959. Initially, extracts of the periwinkle plant (Catharanthus roseus) were investigated because of putative hypoglycemic properties, but were noted to cause marrow suppression in rats and antileukemic effects in vitro. Vinblastine has some immunosuppressant effect. The vinca alkaloids are considered to be cell cycle phase-specific.

Nincaluicolflastine Absorption

No information avaliable

Nincaluicolflastine side effects and Toxicity

Oral, mouse: LD50 = 423 mg/kg; Oral, rat: LD50 = 305 mg/kg.

Nincaluicolflastine Patient Information

Nincaluicolflastine Organisms Affected

Humans and other mammals