Comprehensive data on a 2D-QSAR model for Heme Oxygenase isoform 1 inhibitors.

Comprehensive data on a 2D-QSAR model for Heme Oxygenase isoform 1 inhibitors.
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DOI:
10.1016/j.dib.2017.09.036
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发表时间:
2017-12
期刊:
影响因子:
1.2
通讯作者:
Pittalà V
Pittalà V
中科院分区:
其他
文献类型:
--
作者:
Amata E;Marrazzo A;Dichiara M;Modica MN;Salerno L;Prezzavento O;Nastasi G;Rescifina A;Romeo G;Pittalà V

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数据来自血红素加氧酶数据库(HemeOxDB),并根据2D-QSAR要求进行了优化。这些数据提供了关于一组超过380种血红素加氧酶-1(HO-1)抑制剂的信息。2D-QSAR模型的开发已经进行了使用CORAL软件使用SMILES,分子图和混合描述符(SMILES和图形一起)。此处包括HO-1半数最大抑制浓度(IC 50)的2D-QSAR模型回归,表示为pIC 50(pIC 50 =− LogIC 50)。2D-QSAR模型也被用于预测本文报道的FDA批准的药物的HO-1 pIC 50值。
The data have been obtained from the Heme Oxygenase Database (HemeOxDB) and refined according to the 2D-QSAR requirements. These data provide information about a set of more than 380 Heme Oxygenase-1 (HO-1) inhibitors. The development of the 2D-QSAR model has been undertaken with the use of CORAL software using SMILES, molecular graphs and hybrid descriptors (SMILES and graph together). The 2D-QSAR model regressions for HO-1 half maximal inhibitory concentration (IC50) expressed as pIC50 (pIC50=−LogIC50) are here included. The 2D-QSAR model was also employed to predict the HO-1 pIC50values of the FDA approved drugs that are herewith reported.
S2RSLDB:Sigma-2受体选择性配体的全面手动策划的,可访问的Internet可访问数据库。
DOI: 10.1186/s13321-017-0191-5
发表时间: 2017
影响因子: 8.6
作者:
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