65733-16-6
Chemical Structure
S-Methoprene
Synonym(s): (+)-Methoprene; (7S)-Methoprene
- CAS No.: 65733-16-6
- Formula:C19H34O3
- Molecular Weight:310.47
IUPAC Name: isopropyl (S,2E,4E)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienoate
InChIKey: NFGXHKASABOEEW-GYMWBFJFSA-N
SMILES: CC(C)(OC)CCC[C@H](C)C/C=C/C(C)=C/C(OC(C)C)=O
Biological Activity: S-Methoprene is an insect juvenile hormone analog and effective insecticide that blocks the transition from pupa to adult. S-Methoprene is also a CB(1) receptor ligand and inhibits the binding of the CB1 receptor antagonist [3H]CP-55940 to the CB1 receptor (IC50: 19.31 μM)[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
S-Methoprene | 98.58% | S-Methoprene is an insect juvenile hormone analog and effective insecticide that blocks the transition from pupa to adult. S-Methoprene is also a CB(1) receptor ligand and inhibits the binding of the CB1 receptor antagonist [3H]CP-55940 to the CB1 receptor (IC50: 19.31 μM). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
S-Methoprene (Standard) | ≥98% | 2-Methyl-3-(trifluoromethyl)aniline (Standard) is the analytical standard of 2-Methyl-3-(trifluoromethyl)aniline. This product is intended for research and analytical applications. 2-Methyl-3-(trifluoromethyl)aniline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Adnan SM, et al. Accelerated Sexual Maturation in Methoprene-Treated Sterile and Fertile Male Queensland Fruit Flies (Diptera: Tephritidae), and Mosquito Larvicide as an Economical and Effective Source of Methoprene. J Econ Entomol. 2019 Dec 9;112(6):2842-2849. [Content Brief]
- [2]. Dhopeshwarkar AS, et al. The actions of benzophenanthridine alkaloids, piperonyl butoxide and (S)-methoprene at the G-protein coupled cannabinoid CB₁ receptor in vitro. Eur J Pharmacol. 2011 Mar 1;654(1):26-32. [Content Brief]
Keywords
