Syntheses of chlorpromazine undecahydrododecaborate and nonahydrodecaborate-promising agents for neutron capture therapy of malignant melanoma.
- 1 January 1976
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 24 (4) , 778-781
- https://doi.org/10.1248/cpb.24.778
Abstract
It was suggested by dermatologists that B compounds of chlorpromazine are promising agents for neutron capture therapy of malignant melanoma. The compounds should have a high B content, good stability and sufficient solubility in water. To fulfill these requirements, chlorpromazine undecahydrododecarborate and nonahydrodecaborate were synthesized from 2-chloro-10(3-bromopropyl)phenothiazine and ammonioundecahydrododecaborate or 2-ammoniononahydrodecaborate, respectively.This publication has 3 references indexed in Scilit:
- On Chlorpromazine Binding in vivo**From the Department of Dermatology, Stanford University School of Medicine, Stanford, California.Journal of Investigative Dermatology, 1965
- Electron-paramagnetic-resonance studies of the chlopromazine free radical formed during enzymic oxidation by peroxidase-hydrogen peroxideBiochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects, 1964
- FURTHER STUDIES CONCERNING THE ACCUMULATION OF POLYCYCLIC COMPOUNDS ON UVEAL MELANIN1964