|
|
| | JWH 210 N-pentanoic acid metabolite Basic information |
| Product Name: | JWH 210 N-pentanoic acid metabolite | | Synonyms: | JWH 210 N-pentanoic acid metabolite;PKGSQKIUCYVUDF-UHFFFAOYSA-N;3-[(4-ethyl-1-naphthalenyl)carbonyl]-1H-indole-1-pentanoicacid;1H-Indole-1-pentanoic acid, 3-[(4-ethyl-1-naphthalenyl)carbonyl]- | | CAS: | 1427521-36-5 | | MF: | C26H25NO3 | | MW: | 399.48 | | EINECS: | | | Product Categories: | | | Mol File: | 1427521-36-5.mol |  |
| | JWH 210 N-pentanoic acid metabolite Chemical Properties |
| Boiling point | 647.5±45.0 °C(Predicted) | | density | 1.17±0.1 g/cm3(Predicted) | | solubility | DMF: 50 mg/ml; DMSO: 20 mg/ml; Ethanol: 0.5 mg/ml | | form | A crystalline solid | | pka | 4.73±0.10(Predicted) |
| | JWH 210 N-pentanoic acid metabolite Usage And Synthesis |
| Description | JWH 210 is a potent cannabimimetic alkylindole that has been identified in extracts from herbal blends. Structurally and functionally similar alkylindoles are rapidly metabolized by the liver and secreted in the urine, with 5-carboxypentyl metabolites detected in the urine.1,2,3 JWH 210 N-pentanoic acid metabolite is an expected metabolite of JWH 210, detectable primarily in the urine. Its biological activities have yet to be determined. | | References | 1. Teske, J., Weller, J.P., Fieguth, A., et al. Sensitive and rapid quantification of the cannabinoid receptor agonist naphthalen-1-yl-(1-pentylindol-3-yl)methanone (JWH-018) in human serum by liquid chromatography-tandem mass spectrometry J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 878(27),2659-2663(2010).
2. Sobolevsky, T., Prasolov, I., and Rodchenkov, G. Detection of JWH-018 metabolites in smoking mixture post-administration urine Forensic Sci. Int. 200(1-3),141-147(2010).
3. Wintermeyer, A., Mller, I., Thevis, M., et al. In vitro phase I metabolism of the synthetic cannabimimetic JWH-018 Anal. Bioanal. Chem. 398(5),2141-2153(2010). |
| | JWH 210 N-pentanoic acid metabolite Preparation Products And Raw materials |
|