Authors Lv, P; Chen, YL; Wang, DW; Wu, XW; Li, QX; Hua, RM in ELSEVIER published article about FATTY-ACID SYNTHASE; POTENTIAL ANTIMALARIAL; HERBICIDAL ACTIVITY; CONDENSING ENZYMES; ANALOGS; RESISTANCE; HYBRIDS in [Lv, Pei; Chen, Yiliang; Wu, Xiangwei; Hua, Rimao] Anhui Agr Univ, Sch Resource & Environm, Key Lab Agri Food Safety Anhui Prov, Hefei 230036, Peoples R China; [Wang, Dawei; Li, Qing X.] Nankai Univ, Coll Chem, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China; [Li, Qing X.] Univ Hawaii Manoa, Dept Mol Biosci & Bioengn, Honolulu, HI 96822 USA in 2020, Cited 24. Product Details of 100-51-6. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6
5-Substituted benzylidene 3-acylthiotetronic acids are antifungal. A series of 3-acylthiotetronic acid derivatives with varying substitutions at the 5-position were designed, synthesized, and characterized, based on the binding pose of 3-acyl thiolactone with the protein C171Q KasA. Fungicidal activities of these compounds were screened against Valsa Mali, Curvularia lunata, Fusarium graminearum, and Fusarium oxysporum f. sp. lycopersici. Most target compounds exhibited excellent fungicidal activities against target fungi at the concentration of 50 mu g.mL(-1). Compounds 11c and 11i displayed the highest activity with a broad spectrum. The median effective concentration (EC50) values of 11c and 11i were 1.9-10.7 and 3.1-7.8 mu g.mL(-1), respectively, against the tested fungi, while the EC50 values of the fungicides azoxystrobin, carbendazim, and fluopyram were respectively 0.30, 4.22, and > 50 mu g.mL(-1) against V. Mali; 6.7, 41.7, and 0.18 mu g.mL(-1) against C. lunata; 22.4, 0.42, and 0.43 mu g.mL(-1) against F. graminearum; and 4.3, 0.12, and > 50 mu g.mL(-1) against F. oxysporum f. sp. lycopersici. The structures and activities of the target compounds against C. lunata were analyzed to obtain a statistically significant comparative molecular field analysis (CoMFA) model with high prediction abilities (q(2) = 0.9816, r(2) = 0.8060), and its reliability was verified. The different substituents on the benzylidene at the 5-position had significant effects on the activity, while the introduction of a halogen atom at the benzene ring of benzylidene was able to improve the activity against the tested fungi. (C) 2020 THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company.
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Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles