用户名: 密码: 验证码:
Descriptor collision and confusion: Toward the design of descriptors to mask chemical structures
详细信息    查看全文
文摘
We examined “descriptor collision” for several chemical fingerprint systems (MDL 320, Daylight, SMDL), and for a 2D-based descriptor set. For large databases (ChemNavigator and WOMBAT), the smallest collision rate remains around 5%. We systematically increase the “descriptor collision” rate (here termed “descriptor confusion”), in order to design a set of “descriptors to mask chemical structures”, DMCS. If effective, a DMCS system would not allow third parties to determine the original chemical structures used to derive the DMCS set (i.e., reverse engineering). Using SMDL keys, the “confusion” rate is increased to 45.6% by eliminating those keys that have a low frequency of occurrence in WOMBAT structures. We applied an automated PLS engine, WB-PLS [Olah et al., J. Comput. Aided Mol. Des., 18 (2004) 437], to 1277 series of structures from 948 targets in WOMBAT, in order to validate the biological relevance of the SMDL descriptors as a potential DMCS set. The “reduced set” of SMDL descriptors has a small loss of modeling power (around 20%) compared to the initial descriptor set, while the collision rate is significantly increased. These results indicate that the development of an effective DMCS is possible. If well documented, DMCS systems would encourage private sector data release (e.g., related to water solubility) and directly benefit public sector science.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700