Vernomycin B

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: Vernomycin B
• 英文别名: 4-methoxy-7-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]furo[3,2-g]chromen-5-one
• 化学式: C₁₉H₂₀O₁₀
• 分子量: 408.4
• InChiKey: SJRACCTZSAUMGO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.6
• 重原子数：
  29
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  148
• 氢给体数：
  4
• 氢受体数：
  10

文献信息

• Herbicidal composition comprising chromone derivatives and a method for weed control
  申请人：INVESTIGACIONES BIOLÓGICAS EN AGROQUÍMICOS ROSARIO S.A.

  公开号：US11083197B2

  公开（公告）日：2021-08-10

  An herbicidal composition comprising one or more compounds of Formula I: where R1 and R2 are H or taken together with the carbon atoms to which the are attached form a furane ring; R3 and R4 each independently represent H, —OH or —O—(C1-C4) alkyl; and R5 is H, (C1-C4) alkyl, —(C1-C2) alkylene-O-glucoside or —COOH; and an agriculturally acceptable vehicle. There is also disclosed a method for weed control by application of compounds of Formula I and the use of the composition for controlling weeds.

  一种除草组合物，包含一种或多种式 I 的化合物： 其中 R1 和 R2 是 H 或与所连接的碳原子一起形成呋喃环；R3 和 R4 各自独立地代表 H、-OH 或 -O-(C1-C4)烷基；R5 是 H、(C1-C4)烷基、-(C1-C2)亚烷基-O-葡萄糖苷或 -COOH；以及农业上可接受的载体。本发明还公开了一种通过施用式 I 化合物控制杂草的方法，以及该组合物控制杂草的用途。
• HERBICIDAL COMPOSITION COMPRISING CHROMONE DERIVATIVES AND A METHOD FOR WEED CONTROL
  申请人：ORTEGA FEDERICO

  公开号：US20190021328A1

  公开（公告）日：2019-01-24

  An herbicidal composition comprising one or more compounds of Formula I: where R 1 and R 2 are H or taken together with the carbon atoms to which the are attached form a furane ring; R 3 and R 4 each independently represent H, —OH or —O—(C 1 -C 4 ) alkyl; and R 5 is H, (C 1 -C 4 ) alkyl, —(C 1 -C 2 ) alkylene-O-glucoside or —COOH; and an agriculturally acceptable vehicle. There is also disclosed a method for weed control by application of compounds of Formula I and the use of the composition for controlling weeds.
• [EN] THERAPEUTIC RELEASE AGENTS<br/>[FR] AGENTS DE LIBÉRATION THÉRAPEUTIQUES
  申请人：ORGANON NV

  公开号：WO2008100977A2

  公开（公告）日：2008-08-21

  [EN] Pharmacological inhibition of fatty acid amide hydrolase (FAAH) activity leads to increased levels of fatty acid amides. Esters of alkylcarbamic acids are disclosed that are inhibitors of FAAH activity. Compounds disclosed herein inhibit FAAH activity. Described herein are processes for the preparation of esters of alkylcarbamic acid compounds, compositions that include them, and methods of use thereof.
  [FR] L'inhibition pharmacologique de l'activité de l'amide hydrolase d'acides gras (FAAH) entraîne une augmentation des taux d'amides d'acides gras. L'invention concerne des esters d'acides alkylcarbamiques qui constituent des inhibiteurs de l'activité de la FAAH. Les composés décrits inhibent l'activité de la FAAH. L'invention concerne aussi des procédés de préparation d'esters de composés d'acides alkylcarbamiques, des compositions renfermant ceux-ci et des procédés d'utilisation de celles-ci.