Escape from Flatland 2: complexity and promiscuity
1
Pfizer - World Wide Medicinal Chemistry, 200 Cambridge park Dr., Cambridge, Massachusetts 02140, USA
|
Publication type: Journal Article
Publication date: 2013-01-01
SJR: —
CiteScore: —
Impact factor: —
ISSN: 20402503, 20402511
Organic Chemistry
Drug Discovery
Biochemistry
Pharmacology
Pharmaceutical Science
Molecular Medicine
Abstract
Toxicity plays a major role in attrition in the clinic and promiscuity has been linked to toxicity. A number of molecular descriptors have been identified that contribute to promiscuity including ionization and logP. In this study we report on the relationship between complexity, as measured by two descriptors [fraction sp3 (Fsp3) where Fsp3 = (number of sp3 hybridized carbons/total carbon count) and chiral carbon count], and promiscuity as well as Cyp450 inhibition. We find that increasing complexity reduces promiscuity and Cyp450 inhibition. As an understanding of key property descriptors has helped the pharmaceutical industry to address some of the deficiencies of compounds as pertains to bioavailability, awareness of the descriptors that impact promiscuity should allow us to better address toxicity in the clinic.
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Total citations:
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RIS
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TY - JOUR
DO - 10.1039/c2md20347b
UR - https://doi.org/10.1039/c2md20347b
TI - Escape from Flatland 2: complexity and promiscuity
T2 - MedChemComm
AU - Lovering, Frank
PY - 2013
DA - 2013/01/01
PB - Royal Society of Chemistry (RSC)
SP - 515
IS - 3
VL - 4
SN - 2040-2503
SN - 2040-2511
ER -
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@article{2013_Lovering,
author = {Frank Lovering},
title = {Escape from Flatland 2: complexity and promiscuity},
journal = {MedChemComm},
year = {2013},
volume = {4},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c2md20347b},
number = {3},
pages = {515},
doi = {10.1039/c2md20347b}
}
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Lovering, Frank. “Escape from Flatland 2: complexity and promiscuity.” MedChemComm, vol. 4, no. 3, Jan. 2013, p. 515. https://doi.org/10.1039/c2md20347b.