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Postion:Product Catalog >N,N-dimethyl-5-[(4-phenylphenyl)methyl]tetrazole-1-carboxamide
N,N-dimethyl-5-[(4-phenylphenyl)methyl]tetrazole-1-carboxamide
  • N,N-dimethyl-5-[(4-phenylphenyl)methyl]tetrazole-1-carboxamide
  • N,N-dimethyl-5-[(4-phenylphenyl)methyl]tetrazole-1-carboxamide
  • N,N-dimethyl-5-[(4-phenylphenyl)methyl]tetrazole-1-carboxamide

N,N-dimethyl-5-[(4-phenylphenyl)methyl]tetrazole-1-carboxamide

Price $1
Package 1g
Min. Order: 1g
Supply Ability: 200kg
Update Time: 2020-01-10

Product Details

Product Name: N,N-dimethyl-5-[(4-phenylphenyl)methyl]tetrazole-1-carboxamide CAS No.: 874902-19-9
Min. Order: 1g Purity: 99%
Supply Ability: 200kg Release date: 2020/01/10

Mary

 

Name
N,N-dimethyl-5-[(4-phenylphenyl)methyl]tetrazole-1-carboxamide
Synonym
More Synonyms

 LY-2183240 Biological Activity

Description
LY2183240 is a novel and highly potent blocker of anandamide uptake (IC50 = 270 pM). LY2183240 inhibits fatty acid amide hydrolase (FAAH) activity (IC50 = 12.4 nM). IC50: 270 pM (anandamide uptake); 12.4 nM (FAAH)Target: FAAH; Anandamide uptakeFollowing i.p. administration in rats, LY2183240 increases brain anandamide concentration and exerts antinociceptive effects in formalin model of pain.
Related Catalog
Signaling Pathways >> Metabolic Enzyme/Protease >> FAAH
Signaling Pathways >> Neuronal Signaling >> FAAH
Research Areas >> Neurological Disease
References

[1]. Dickason-Chesterfield AK, et al. Pharmacological characterization of endocannabinoid transport and fatty acid amide hydrolase inhibitors. Cell Mol Neurobiol. 2006 Jul-Aug;26(4-6):407-23.

[2]. Alexander JP, Cravatt BF. The putative endocannabinoid transport blocker LY2183240 is a potent inhibitor of FAAH and several other brain serine hydrolases. J Am Chem Soc. 2006 Aug 2;128(30):9699-704.

[3]. Maione S, et al. Antinociceptive effects of tetrazole inhibitors of endocannabinoid inactivation: cannabinoid and non-cannabinoid receptor-mediated mechanisms. Br J Pharmacol. 2008 Nov;155(5):775-82.

[4]. Pelorosso FG, et al. The endocannabinoid anandamide inhibits kinin B1 receptor sensitization through cannabinoid CB1 receptor stimulation in human umbilical vein. Eur J Pharmacol. 2009 Jan 5;602(1):176-9.

[5]. Powers MS, et al. Effects of the novel endocannabinoid uptake inhibitor, LY2183240, on fear-potentiated startle and alcohol-seeking behaviors in mice selectively bred for high alcohol preference. Psychopharmacology (Berl). 2010 Dec;212(4):571-83.

[6]. Sun L, et al. Endocannabinoid activation of CB1 receptors contributes to long-lasting reversal of neuropathic pain by repetitive spinal cord stimulation. Eur J Pain. 2017 May;21(5):804-814.

 Chemical & Physical Properties

Density
1.2±0.1 g/cm3
Boiling Point
506.1±53.0 °C at 760 mmHg
Melting Point
87-88ºC
Molecular Formula
C17H17N5O
Molecular Weight
307.350
Flash Point
259.9±30.9 °C
Exact Mass
307.143311
PSA
63.91000
LogP
2.15
Vapour Pressure
0.0±1.3 mmHg at 25°C
Index of Refraction
1.640

 MSDS

LY-2183240 MSDS(Chinese)

 Safety Information

Risk Phrases
22

 Synonyms

5-(4-Biphenylylmethyl)-N,N-dimethyl-1H-tetrazole-1-carboxamide
LY-2183240
HMS3269E15
1H-Tetrazole-1-carboxamide
1H-Tetrazole-1-carboxamide, 5-([1,1'-biphenyl]-4-ylmethyl)-N,N-dimethyl-
5-(Biphenyl-4-ylmethyl)-N,N-dimethyl-1H-tetrazole-1-carboxamide
LY2183240
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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  • Address: Room 702, Floor 7, Building 10, National University Science Park, High-Tech Zone, Zhengzhou City, H
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