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γ-咔啉

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γ-Carboline
IUPAC名
5H-Pyrido[4,3-b]indole
别名 5H-γ-Carboline
识别
CAS号 244-69-9  checkY
PubChem 130802
ChemSpider 115684
SMILES
 
  • C1=CC=C2C(=C1)C3=C(N2)C=CN=C3
InChI
 
  • 1S/C11H8N2/c1-2-4-10-8(3-1)9-7-12-6-5-11(9)13-10/h1-7,13H
InChIKey RDMFHRSPDKWERA-UHFFFAOYSA-N
性质
化学式 C11H8N2
摩尔质量 168.20 g/mol g·mol⁻¹
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

γ-咔啉(英语:γ-Carboline)是一种含氮杂环有机化合物,分子式C11H8N2[1][2][3][4]

参考文献

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

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