S-methyl-methylparathion

structure given in first source; RN given refers to cpd without isomeric designation

Also Known As:

O-(4-nitrophenyl) O-methyl-S-methylphosphorothioate; S-methyl-methylparathion, (+-)-isomer; S-methyl-methylparathion, (R)-isomer; S-methyl-methylparathion, (S)-isomer; isoparathion methyl; methyl isoparathion; Phosphorothioic acid, O,S-dimethyl O-(4-nitrophenyl) ester

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Organic Chemicals: 133
- Organophosphorus Compounds: 300
  - Organophosphates: 1942
    - Organothiophosphates: 1
      - Parathion: 431
        Methyl Parathion: 86
        S-methyl-methylparathion: 1
  - Organothiophosphorus Compounds
    - Organothiophosphates: 1
      - Parathion: 431
        Methyl Parathion: 86
        S-methyl-methylparathion: 1
- Sulfur Compounds: 278
  - Organothiophosphorus Compounds
    - Organothiophosphates: 1
      - Parathion: 431
        Methyl Parathion: 86
        S-methyl-methylparathion: 1

Related Diseases

Pain (Aches)

02/15/1999 - "If this assumption is correct, AChE inhibited by (1R)- or (1S)-isomalathions should reactivate at the same rate as AChE inhibited by configurationally equivalent (S)- or (R)-isoparathion methyl, respectively, which are expected to inhibit AChE by loss of 4-nitrophenoxyl to yield O,S-dimethyl phosphorylated AChEs. "
02/15/1999 - "However, spontaneous and oxime-mediated k+3 values comparable to those of (R)-isoparathion methyl could not be obtained for AChEs inhibited by (1S,3R)- and (1S,3S)-isomalathion. "
02/15/1999 - "Both AChEs inhibited by either (1R,3R)- or (1R,3S)-isomalathion had comparable corresponding k+3 values (spontaneous and oxime-mediated) to those of AChEs inhibited with (S)-isoparathion methyl. "

Related Drugs and Biologics

1.	Oximes