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Norharmane
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Norharmane图片
CAS NO:244-63-3
规格:98%
分子量:168.2
包装与价格:
包装价格(元)
500mg电议
1g电议
5g电议

产品介绍
inhibitor of indoleamine 2,3-dioxygenase
CAS:244-63-3
分子式:C11H8N2
分子量:168.2
纯度:98%
存储:Store at -20°C

Background:

Norharmane acts as a co-mutagen. Norharmane is a natural β-carboline first isolated from plants of the Zygophyllaceae family. It is a heterocyclic amine (HCA) that may also be found in fried meats, tobacco smoke, and coffee. Harman and norharmane are aminocarbolines known as “co-mutagens” because they do not show mutagenicity to Salmonella serovar typhimurium [1][2][3].


Norharmane acts as a co-mutagen. Norharmane is widely distributed in our environment. It was not mutagenic to Salmonella typhimurium TA98 and TA100 either with or without S9 mix, but became mutagenic to S.typhimurium TA98 with S9 mix when non-mutagenic aromatic amines like aniline or o- or m-toluidine are added. Also, Norharmane and aromatic amines induced the formation of DNA adduct in S.typhimurium TA98 [3].


Harman and norharmane with concentrations of 0.275 uM and 0.9 uM respectively might inhibited MAO-A and MAO-B. In adult male rats, a novel cocktail of cigarette smoke constituents, containing five minor alkaloids (nornicotine, cotinine, myosmine, anatabine, and anabasine), two β-carbolines (harman and norharmane), and acetaldehyde, did not significantly enhance nicotine self-administration [2].


参考文献:
[1].  Jamali MA, Zhang Y, Teng H, et al. Inhibitory Effect of Rosa rugosa Tea Extract on the Formation of Heterocyclic Amines in Meat Patties at Different Temperatures. Molecules. 2016 Jan 30;21(2):173.
[2].  Smith TT, Schaff MB, Rupprecht LE, et al. Effects of MAO inhibition and a combination of minor alkaloids, β-carbolines, and acetaldehyde on nicotine self-administration in adult male rats. Drug Alcohol Depend. 2015 Oct 1;155:243-52.
[3].  Mori M1, Totsuka Y, Fukutome K, et al. Formation of DNA adducts by the co-mutagen norharman with aromatic amines. Carcinogenesis. 1996 Jul;17(7):1499-503.