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Norharmane (Synonyms: 2-Azacarbazole,β-Carboline,2,9-Diazafluorene,NSC 84417)

رقم الكتالوجGC15833 Copy One-Click Copy Product Info

نورهارمان (نورهارمان) ، وهو قلويد بيتا-كاربولين ، هو مثبط أوكسيديز أحادي الأمين قوي وقابل للانعكاس ، بقيم IC50 تبلغ 6.5 و 4.7 ميكرومتر لـ MAO-A و MAO-B ، على التوالي

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Norharmane التركيب الكيميائي

Cas No.: 244-63-3

الحجم السعر المخزون الكميّة
500mg
40٫00
متوفر
1g
75٫00
متوفر
5g
352٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.



Description of Norharmane

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].

References:
[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.

Chemical Properties of Norharmane

Cas No. 244-63-3 SDF
المرادفات 2-Azacarbazole,β-Carboline,2,9-Diazafluorene,NSC 84417
Chemical Name 9H-Pyrido[3,4-b]indole
Canonical SMILES C1(C=CC=C2)=C2C(C=CN=C3)=C3N1
Formula C11H8N2 M.Wt 168.2
الذوبان ≤1mg/ml in ethanol;1mg/ml in DMSO;1mg/ml in dimethyl formamide Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Norharmane

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 5.9453 mL 29.7265 mL 59.453 mL
5 mM 1.1891 mL 5.9453 mL 11.8906 mL
10 mM 594.5 μL 2.9727 mL 5.9453 mL
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3. All of the above co-solvents are available for purchase on the GlpBio website.

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Review for Norharmane

Average Rating: 5 ★★★★★ (Based on Reviews and 37 reference(s) in Google Scholar.)

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