γ-咔啉
γ-Carboline | |
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IUPAC名 5H-Pyrido[4,3-b]indole | |
别名 | 5H-γ-Carboline |
识别 | |
CAS号 | 244-69-9 |
PubChem | 130802 |
ChemSpider | 115684 |
SMILES |
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InChI |
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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
- ^ 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.
- ^ 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.
- ^ 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.
- ^ 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.
外部链接
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