| Identification | More | [Name]
9H-PYRIDO[3,4-B]INDOLE | [CAS]
244-63-3 | [Synonyms]
2,9-DIAZAFLUORENE
9H-BETA-CARBOLINE
9H-PYRIDO[3,4-B]INDOLE
B-CARBOLINE
BETA-CARBOLINE
CARBAZOLINE
NORHARMAN
NORHARMANE
2-azacarbazole
9H-β-Carboline
Pyridoindole
NORHARMANE FREE BASE
NORHARMAN 98%
NSC 8441
PYRIDO(3,4-B)INDOLE
NSC 84417 | [EINECS(EC#)]
205-959-0 | [Molecular Formula]
C11H8N2 | [MDL Number]
MFCD00004956 | [Molecular Weight]
168.19 | [MOL File]
244-63-3.mol |
| Chemical Properties | Back Directory | [Appearance]
Off-White Solid | [Melting point ]
199-201 °C
| [Boiling point ]
287.13°C (rough estimate) | [density ]
1.1722 (rough estimate) | [refractive index ]
1.5200 (estimate) | [storage temp. ]
2-8°C
| [solubility ]
DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) | [form ]
crystalline
| [pka]
15.44±0.30(Predicted) | [color ]
light yellow
| [Water Solubility ]
2693g/L(17 ºC) | [Usage]
The compund has cytotoxic effects | [InChI]
InChI=1S/C11H8N2/c1-2-4-10-8(3-1)9-5-6-12-7-11(9)13-10/h1-7,13H | [InChIKey]
AIFRHYZBTHREPW-UHFFFAOYSA-N | [SMILES]
N1C2=C(C=CC=C2)C2C=CN=CC1=2 | [LogP]
3.170 | [CAS DataBase Reference]
244-63-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed. | [Safety Statements ]
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S22:Do not breathe dust . | [RIDADR ]
3261 | [WGK Germany ]
3
| [RTECS ]
UU9350000
| [HS Code ]
29339900 | [Storage Class]
11 - Combustible Solids | [Toxicity]
dnd-hmn:hla 50 mmol/L MUREAV 89,95,81 |
| Hazard Information | Back Directory | [Hazard]
Toxic; nervous system effects.
| [Chemical Properties]
Off-White Solid | [Uses]
The compund has cytotoxic effects | [Definition]
ChEBI: The parent compound of the beta-carbolines, a tricyclic structure comprising an indole ring system ortho- fused to C-3 and C-4 of a pyridine ring. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 72, p. 2962, 1950 DOI: 10.1021/ja01163a041
Tetrahedron, 49, p. 49, 1993 DOI: 10.1016/S0040-4020(01)80505-6 | [Biological Activity]
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]. | [Biochem/physiol Actions]
Inhibitor of indoleamine 2,3-dioxygenase (IDO). | [Safety Profile]
Poison by intravenous route.Experimental reproductive effects. Human mutation datareported. When heated to decomposition it emits toxicfumes of NOx. | [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. |
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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https://www.jkchemical.com |
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Energy Chemical
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400-0056266 |
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www.energy-chemical.com |
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Maya High Purity Chemicals
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+86 (573) 82222445 (0)18006601000 452520369 |
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