dock suite of accelrys discovery studio 2.0 software (Accelrys)
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Accelrys
dock suite of accelrys discovery studio 2.0 software
Dock Suite Of Accelrys Discovery Studio 2.0 Software, supplied by Accelrys, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dock+suite+of+accelrys+discovery+studio+2%2E0+software/dock+suite+of+accelrys+discovery+studio+2+0+software/10__1016_slash_j__molstruc__2018__01__020-72-22-25
Average 90 stars, based on 1 article reviews
Dock Suite Of Accelrys Discovery Studio 2.0 Software, supplied by Accelrys, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dock+suite+of+accelrys+discovery+studio+2%2E0+software/dock+suite+of+accelrys+discovery+studio+2+0+software/10__1016_slash_j__molstruc__2018__01__020-72-22-25
Average 90 stars, based on 1 article reviews
dock suite of accelrys discovery studio 2.0 software - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: Investigation of the interaction between benzaldehyde thiosemicarbazone compounds and xanthine oxidase Article Snippet: A series of substituted benzaldehyde thiosemicarbazide compounds (1e7) were synthesized as xanthine oxidase (XO) inhibitors, and the interactions between substituted benzaldehyde thiosemicarbazide compounds (1e7) and XO were studied by ultraviolet spectroscopy, fluorescence spectroscopy, and molecular docking.. It was found that the hydrogen bond and hydrophobicity were the main interactions between substituted benzaldehyde thiosemicarbazide compounds and XO, and introducing eOH at the para position of the benzene ring and a Phor Me-group at the amino terminal of compound 4 increased the modifier's inhibitory activity.. The results suggest that the newly introduced benzene ring interacted with the hydrophobic cavity of XO by means of the p-p stacking force between the newly introduced benzene ring and the aromatic amino acid residues, such as the Phe residue, which greatly increased the modifier's inhibitory activity. Article Title: (-)-N-Formylanonaine from Michelia alba as a human tyrosinase inhibitor and antioxidant. Article Snippet: a Department of Fragrance and Cosmetic Science, Kaohsiung Medical University, Kaohsiung 807, Taiwan, ROC b School of Medicine and Health Sciences, Fooyin University, Kaohsiung County 831, Taiwan c Department of Chemical Engineering, National Cheng Kung University, Tainan 701, Taiwan d Department of Physiology, Kaohsiung Medical University, Orthopaedic Research Center, and the Department of Orthopaedics, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan e Department of Chemical Engineering, National Chung Hsing University, Taichung 402, Taiwan f Department of Dermatology, Kaohsiung Medical University College of Medicine and Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung 807, Taiwan g Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300, Taiwan |