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γ-Carboline

From Wikipedia, the free encyclopedia
γ-Carboline
Names
Preferred IUPAC name
5H-Pyrido[4,3-b]indole
Other names
5H-γ-Carboline
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard100.383.422Edit this at Wikidata
UNII
  • InChI=1S/C11H8N2/c1-2-4-10-8(3-1)9-7-12-6-5-11(9)13-10/h1-7,13H
    Key: RDMFHRSPDKWERA-UHFFFAOYSA-N
  • C1=CC=C2C(=C1)C3=C(N2)C=CN=C3
Properties
C11H8N2
Molar mass168.20 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

γ-Carboline, orgamma-carboline, also known as5H-pyrido[4,3-b]indole is anitrogen-containingtricyclicheterocycle. A large number of derivatives are known with varying pharmacological properties.[1][2][3][4]

See also

[edit]

References

[edit]
  1. ^Alekseyev RS, Kurki AV, Yurovskaya MA (2009). "γ-Carbolines and their hydrogenated derivatives. 1. Aromatic γ-carbolines: methods of synthesis, chemical and biological properties (review)".Chem Heterocycl Comp.45 (8):889–925.doi:10.1007/s10593-009-0373-9.S2CID 97096571.
  2. ^Alekseyev RS, Kurkin AV, Yurovskaya MA (2011). "γ-Carbolines and their hydrogenated derivatives 3. Hydrogenated derivatives of γ-carbolines: chemical and biological properties (Review)".Chem Heterocycl Comp.46 (10):1169–1198.doi:10.1007/s10593-011-0652-0.S2CID 95229099.
  3. ^Smirnova OB, Golovko TV, Granik VG (2011). "Carbolines. Part I: Comparison of some methods for the synthesis of α-, γ-, and δ-carbolines (a review)".Pharm Chem J.44 (12):654–678.doi:10.1007/s11094-011-0540-z.S2CID 7100718.
  4. ^Smirnova OB, Golovko TV, Granik VG (2011). "Carbolines. Part 2: Comparison of some of the properties of α-, γ-, and δ-carbolines (Review)".Pharm Chem J.45 (7):389–400.doi:10.1007/s11094-011-0641-8.S2CID 26600701.


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