Calculation of hydrophobic constant (log P) from. pi. and f constants
A Leo, PYC Jow, C Silipo, C Hansch - Journal of medicinal …, 1975 - ACS Publications
The highest level of confidence can be placed in calculatedlog P values when (1) the log P
of a parent solute is known,(2) constants for the required substituent (s) are available, and (3) …
of a parent solute is known,(2) constants for the required substituent (s) are available, and (3) …
Toward a quantitative comparative toxicology of organic compounds
…, D Kim, AJ Leo, E Novellino, C Silipo… - CRC critical reviews …, 1989 - Taylor & Francis
… the most generally obtainable parameter for relative biological activity is log 1/C, where C
is the molar concentration of an organic compound producing a standard biological response …
is the molar concentration of an organic compound producing a standard biological response …
Structure-activity relationships of dihydrofolated reductase inhibitors
JM Blaney, C Hansch, C Silipo, A Vittoria - Chemical Reviews, 1984 - ACS Publications
… In attempting to simplify the presentation of test results in the appendix, we have listed a
single figure which is either log 1/C or log 1/Kicxpp. … Replacing N by C in the 3-deazo …
single figure which is either log 1/C or log 1/Kicxpp. … Replacing N by C in the 3-deazo …
Correlation analysis. Its application to the structure-activity relation of triazines inhibiting dihydrofolate reductase
C Silipo, C Hansch - Journal of the American Chemical Society, 1975 - ACS Publications
… C in log 1 ¡C in Table I represents the molar concentration which produces50% reversible
inhibition of dihydrofolate reductase obtained from either L1210/DF8 mouse leukemia or …
inhibition of dihydrofolate reductase obtained from either L1210/DF8 mouse leukemia or …
Partition coefficients and the structure-activity relation of the anesthetic gases
C Hansch, A Vittoria, C Silipo… - Journal of medicinal …, 1975 - ACS Publications
… Corwin Hansch,* Antonio Vittoria,1 Carlo Silipo,s and Priscilla Y. C. Jow … We have
assumed that the C=C function is electronegative enough to conferpolar character on …
assumed that the C=C function is electronegative enough to conferpolar character on …
Quantitative structure-activity relationship of chymotrypsin-ligand interactions
C Hansch, C Grieco, C Silipo… - Journal of Medicinal …, 1977 - ACS Publications
… In this equation, MR-1, MR-2, and MR-3 refer to the molar refractivities of -NHCORi (or -NHS02Ri),
R2, and OR3 falling in p space as shown in structures in 2a-c. is an indicator variable …
R2, and OR3 falling in p space as shown in structures in 2a-c. is an indicator variable …
Study of Benzodiazepines Receptor Sites Using a Combined QSAR‐CoMFA Approach
G Greco, E Novellino, C Silipo… - Quantitative Structure …, 1992 - Wiley Online Library
… The substitution at the 2’-position of the C phenyl ring was modelled with an indicator
variable (12,); in fact, the few structural modifications at this position did not allow the use of …
variable (12,); in fact, the few structural modifications at this position did not allow the use of …
Quantitative structure-activity relation of reversible dihydrofolate reductase inhibitors. Diaminotriazines
C Hansch, C Silipo - Journal of Medicinal Chemistry, 1974 - ACS Publications
… The QSAR for 83 inhibitors is described by log 1 ¡C = … the variance in log 1/C of the 83
complex modifications of I; hence, 18% of the information in log 1/C cannot be accounted for. This …
complex modifications of I; hence, 18% of the information in log 1/C cannot be accounted for. This …
Synthesis and trazodone-like pharmacological profile of 1-and 2-[3-[4-(X)-1-piperazinyl]-propyl]-benzotriazoles
…, R Meli, E Perissutti, V Santagada, C Silipo… - European journal of …, 1993 - Elsevier
A series of 1- and 2-[3-[4-(X)-1-piperazinyl]-propyl]benzotriazoles were prepared and
evaluated for their trazodone-like pharmacological profile; as preliminary pharmacological …
evaluated for their trazodone-like pharmacological profile; as preliminary pharmacological …
Correlation analysis of Baker's studies on enzyme inhibition. 1. Guanine deaminase, xanthine oxidase, dihydrofolate reductase, and complement
C Silipo, C Hansch - Journal of Medicinal Chemistry, 1976 - ACS Publications
… Thedependent variables (log 1/C) in the equations reported in this paper are all in terms of
the molar concentration causing50% inhibition of enzyme activity. The constants for v and MR …
the molar concentration causing50% inhibition of enzyme activity. The constants for v and MR …