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Research in Pharmaceutical Sciences، جلد ۱۳، شماره ۳، صفحات ۱۹۲-۲۰۴
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
Probing the chemical interaction space governed by 4-amino-substituted benzenesulfonamides and carbonic anhydrase isoforms |
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| چکیده انگلیسی مقاله |
Isoform diversity, critical physiological roles and involvement in major diseases/disorders such as glaucoma, epilepsy, Alzheimer’s disease, obesity, and cancers have made carbonic anhydrase (CA), one of the most interesting case studies in the field of computer aided drug design. Since applying non-selective inhibitors can result in major side effects, there have been considerable efforts so far to achieve selective inhibitors for different isoforms of CA. Using proteochemometrics approach, the chemical interaction space governed by a group of 4-amino-substituted benzenesulfonamides and human CAs has been explored in the present study. Several validation methods have been utilized to assess the validity, robustness and predictivity power of the proposed proteochemometric model. Our model has offered major structural information that can be applied to design new selective inhibitors for distinct isoforms of CA. To prove the applicability of the proposed model, new compounds have been designed based on the offered discriminative structural features. |
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| کلیدواژه‌های انگلیسی مقاله |
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| نویسندگان مقاله |
| Behnam Rasti
2Department of Chemistry, Faculty of Science, University of Tehran, Tehran, I.R. Iran.
| Yeganeh Entezari Heravi
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| نشانی اینترنتی |
http://rps.mui.ac.ir/index.php/jrps/article/view/1824 |
| فایل مقاله |
اشکال در دسترسی به فایل - ./files/site1/rds_journals/115/article-115-628426.pdf |
| کد مقاله (doi) |
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| زبان مقاله منتشر شده |
en |
| موضوعات مقاله منتشر شده |
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| نوع مقاله منتشر شده |
Original Article |
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