Abstract
QSAR analyses of rifamycin B amides and hydrazides were carried out, and the following equations containing the substituent entropy constant, σs°, were obtained (the subscripts 1, 2 and 3 denote the substituent groups on the nitrogen atom). © 1983, The Pharmaceutical Society of Japan. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
APA
Kawaki, H., Takagi, T., & Sasaki, Y. (1983). Studies on Quantitative Structure-Activity Relationships. V. QSAR Investigations of Rifamycin B Amides and Hydrazides by Utilization of the Substituent Entropy Constant σ s°. Chemical and Pharmaceutical Bulletin, 31(1), 144–148. https://doi.org/10.1248/cpb.31.144
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free