| Weight | 168.199 g/mol |
|---|---|
| Formula | C11H8N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
9H-Pyrido[3,4-B]indole (244-63-3)
norharman · norharmane · norharman hydrochloride
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#856 in Neuroscience
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#1668 in Biochemistry
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#3748 in Biology
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#4718 in Chemistry
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LabBot
- Exposure to beta-carbolines norharman and harman (Journal of Chromatography B, 2004)
- The isolation of harmane and norharmane from tobacco and cigarette smoke (Phytochemistry, 1962)
- Demonstration of Mutagenicity of Aniline and o-Toluidine by Norharman (1977)
- Interactions of norharman and harman with DNA (Nucleic Acids Research, 1977)
- Quantification of the co-mutagenic -carbolines, norharman and harman, in cigarette smoke condensates and cooked foods (Cancer Letters, 1999)
- Differences in effects of norharman with various classes of chemical mutagens and amounts of S-9 (Biochemical and Biophysical Research Communications, 1978)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - norharman
- norharmane
- norharman hydrochloride
- beta-carboline
- norhormane
-
SMILESC1=CC=C2C(=C1)C3=C(N2)C=NC=C3
-
InChIKeyAIFRHYZBTHREPW-UHFFFAOYSA-N
- Pubchem - 9H-Pyrido[3,4-B]indole
- Wikipedia - norharman
Several alkaloids that function as monoamine oxidase inhibitors (MAOIs) are found in the seeds of Peganum harmala (also known as Harmal or Syrian Rue), as well as tobacco leaves including harmine, harmaline, and harmalol, which are members of a group of substances with a similar chemical structure collectively known as harmala alkaloids. These alkaloids are of interest for their use in Amazonian shamanism, where they are derived from other plants. The harmala alkaloid harmine, once known as telepathine and banisterine, is a naturally occurring beta-carboline alkaloid that is structurally related to harmaline, and also found in the vine Banisteriopsis caapi.
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9H-Pyrido[3,4-B]indole
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