COA of Formula: C13H13N. Recently I am researching about SIMILARITY/DIVERSITY ANALYSIS; MOLECULAR DESCRIPTORS; GETAWAY DESCRIPTORS; PREDICTION; DOCKING; INDEXES; ASSAY; RICE, Saw an article supported by the Tarbiat Modares University. Published in SPRINGER in NEW YORK ,Authors: Gholivand, K; Abbod, M; Valmoozi, AAE; Barzegar, O; Tabar, HN; Yaghoubi, R; Hosseini, M; Safaie, N; Dashtaki, MR; Dusek, M; Mani-Varnosfaderani, A. The CAS is 91-00-9. Through research, I have a further understanding and discovery of Diphenylmethanamine
A series of phosphonic acid and bisphosphoramidate derivatives were synthesized and characterized. The bioactivities against the fungal pathogen Macrophomina phaseolina and human acetylcholinesterase AChE enzyme were studied using QSAR based on multiple linear regression. L17, with (p-Cl-C6H4-NH) (p-Cl-C6H4)C(H)P(O)(OC2H5)(2) skeleton, demonstrated a great mortality on the M. phaseolina mycelial growth by 83% inhibition at 150 mg/L; the other tested derivative showed moderate to weak antifungal activity against the fungus. QSAR model based on the GA-MLR method revealed the importance of 3D descriptors (De, Mor18e, H8m, and Mor30p) on the antifungal activity. It showed good capability in predicting the fungicidal activity of the studied molecules. Another derivative, L5, with (m-CH3-NC5H4-NH)(m-CH3-C6H4)C(H)P(O)(OCH3)(2) skeleton displays the most potent anti-AChE activity. The electronic parameters, Delta EL-H, and E-LUMO, have the highest contribution of human AChE. The authors suggest that these models could be usefully employed in designing more effective crop protection compounds without side effects on non-target organisms.
About Diphenylmethanamine, If you have any questions, you can contact Gholivand, K; Abbod, M; Valmoozi, AAE; Barzegar, O; Tabar, HN; Yaghoubi, R; Hosseini, M; Safaie, N; Dashtaki, MR; Dusek, M; Mani-Varnosfaderani, A or concate me.. COA of Formula: C13H13N
Reference:
Amide – Wikipedia,
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