✦ LIBER ✦

Mode of action of oxathiin systemic fungicides: III. Effect on mitochondrial activities

✍ Scribed by D.E. Mathre

Book ID: 119026520
Publisher: Elsevier Science
Year: 1971
Tongue: English
Weight: 712 KB
Volume: 1
Category: Article
ISSN: 0048-3575
DOI: 10.1016/0048-3575(71)90198-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mode of action of oxathiin systemic fung

Mode of action of oxathiin systemic fungicides. Structure-activity relations

✍ Mathre, Donald E. 📂 Article 📅 1971 🏛 American Chemical Society 🌐 English ⚖ 377 KB

Effects of oxathiin systemic fungicides

Effects of oxathiin systemic fungicides on various biological systems

✍ D. E. Mathre 📂 Article 📅 1972 🏛 Springer 🌐 English ⚖ 253 KB

A potent effect of 1,4-oxathiin systemic

A potent effect of 1,4-oxathiin systemic fungicides on succinate oxidation by a particulate preparation from Ustilago maydis

✍ G.A. White 📂 Article 📅 1971 🏛 Elsevier Science 🌐 English ⚖ 361 KB

The Biochemical Mode of Action of the No

The Biochemical Mode of Action of the Novel Selective Fungicide Cyazofamid: Specific Inhibition of Mitochondrial Complex III in Phythium spinosum

✍ Shigeru Mitani; Satoshi Araki; Yasuko Takii; Takeshi Ohshima; Norifusa Matsuo; H 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 146 KB

Inhibitory effect of the class III antia

Inhibitory effect of the class III antiarrhythmic drug nifekalant on HERG channels: mode of action

✍ Shunichi Kushida; Takehiko Ogura; Issei Komuro; Haruaki Nakaya 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 253 KB

Acidic derivatives of the fungicide fenp

Acidic derivatives of the fungicide fenpiclonil: effect of adding a methyl group to the N-substituted chain on systemicity and fungicidal activity

✍ Jean-François Chollet; Françoise Rocher; Cyril Jousse; Céline Delétage-Grandon; 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 174 KB

## Abstract A new acidic derivative of the fungicide fenpiclonil was synthesized containing a methyl group on the alpha‐position of the carboxyl function of __N__‐carboxymethyl‐3‐cyano‐4‐(2,3‐dichlorophenyl)pyrrole. The phloem mobility of the resulting __N__‐(1‐carboxyethyl)‐3‐cyano‐4‐(2,3‐dichloro