109555-87-5|3-Naphthoylindole|(1H-indol-3-yl)(naphthalen-1-yl)methanone|-范德生物科技公司

3-Naphthoylindole

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names：
(1H-indol-3-yl)(naphthalen-1-yl)methanone
CAS号：
109555-87-5
MDL Number：
MF(分子式)： C19H13NO MW(分子量)： 271.32
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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询价

中文别名	3-Naphthoylindole
英文别名	3-Naphthoylindole; 3 Naphthoylindole; 3Naphthoylindole; 1'-Naphthoyl Indole; 3-(1-Naphthoyl)indole;
CAS号	109555-87-5
Inchi	InChI=1S/C19H13NO/c21-19(17-12-20-18-11-4-3-9-15(17)18)16-10-5-7-13-6-1-2-8-14(13)16/h1-12,20H
InchiKey	InChI=1S/C19H13NO/c21-19(17-12-20-18-11-4-3-9-15(17)18)16-10-5-7-13-6-1-2-8-14(13)16/h1-12,20H
分子式 Formula	C19H13NO
分子量 Molecular Weight	271.32
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	3-Naphthoylindole(CAS:109555-87-5):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	3-Naphthoylindole is discontinued (DEA controlled substance). It is a synthetic cannabinoid with differing affinities for the two primary CB receptors, that represents the simplest form of this group of cannabimimetics.
Application1
Application2
Application3

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危险性	Warning
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[1]Kim J, Park Y, Park M, Kim E, Yang W, Baeck S, Lee S, Han S. Simultaneous determination of five naphthoylindole-based synthetic cannabinoids and metabolites and their deposition in human and rat hair. J Pharm Biomed Anal. 2015 Jan;10

2:162-75. doi: 10.1016/j.jpba.2014.09.013. Epub 2014 Sep 21. PubMed PMID: 25282599.

[3]Uchiyama N, Kikura-Hanajiri R, Hakamatsuka T. [Evaluation of an on-site drug-testing device for the detection of synthetic cannabinoids in illegal herbal products]. Yakugaku Zasshi. 2015;135(3):535-41. doi: 10.1248/yakushi.14-00247. Epub 2015 Jan 19. Japanese. PubMed PMID: 25759062.

[4]Lovett DP, Yanes EG, Herbelin TW, Knoerzer TA, Levisky JA. Structure elucidation and identification of a common metabolite for naphthoylindole-based synthetic cannabinoids using LC-TOF and comparison to a synthetic reference standard. Forensic Sci Int. 2013 Mar 10;226(1-3):81-7. doi: 10.1016/j.forsciint.2012.12.012. Epub 2013 Jan 10. PubMed PMID: 23313601.

[5] Huffman JW, Zengin G, Wu MJ, Lu J, Hynd G, Bushell K, Thompson AL, Bushell S, Tartal C, Hurst DP, Reggio PH, Selley DE, Cassidy MP, Wiley JL, Martin BR. Structure-activity relationships for 1-alkyl-3-(1-naphthoyl)indoles at the cannabinoid CB(1) and CB(2) receptors: steric and electronic effects of naphthoyl substituents. New highly selective CB(2) receptor agonists. Bioorg Med Chem. 2005 Jan 3;13(1):89-112. PubMed PMID: 15582455.

5: Huffman JW, Mabon R, Wu MJ, Lu J, Hart R, Hurst DP, Reggio PH, Wiley JL, Martin BR. 3-Indolyl-1-naphthylmethanes: new cannabimimetic indoles provide evidence for aromatic stacking interactions with the CB(1) cannabinoid receptor. Bioorg Med Chem. 2003 Feb 20;11(4):539-49. PubMed PMID: 12538019.

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