異鳥嘌呤
化合物
異鳥嘌呤或2-羥基腺嘌呤(簡寫:B)屬於嘌呤類鹼基,它是鳥嘌呤的異構體。它是DNA的氧化損傷產物,已被證明會導致突變。[2]它和異胞嘧啶結合,用於非天然和酸類似物的研究中。[3][4]它可以2,6-二氨基嘌呤為原料通過化學法合成。[1]
異鳥嘌呤 | |
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IUPAC名 6-Amino-1,7-dihydropurin-2-one | |
別名 | 2-Hydroxyadenine |
識別 | |
CAS號 | 3373-53-3 ![]() |
PubChem | 76900 |
ChemSpider | 69351 |
SMILES |
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EINECS | 222-157-6 |
性質 | |
化學式 | C5H5N5O |
莫耳質量 | 151.1261 g·mol⁻¹ |
熔點 | >360°C[1] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
參考文獻
- ^ 1.0 1.1 Joseph W. Arico, Amy K. Calhoun, Larry W. McLaughlin. Preparation of the 2′-Deoxynucleosides of 2,6-Diaminopurine and Isoguanine by Direct Glycosylation. The Journal of Organic Chemistry. 2010-03-05, 75 (5): 1360–1365 [2019-03-18]. ISSN 0022-3263. doi:10.1021/jo902616s (英語).
- ^ Yang XL, Sugiyama H, Ikeda S, Saito I, Wang AH. Structural studies of a stable parallel-stranded DNA duplex incorporating isoguanine:cytosine and isocytosine:guanine basepairs by nuclear magnetic resonance spectroscopy. Biophys. J. 1998, 75 (3): 1163–1171. PMC 1299791 . PMID 9726918. doi:10.1016/S0006-3495(98)74035-4.
- ^ Andrzej Jaworski, Józef S. Kwiatkowski, Bogdan Lesyng: „Why isoguanine and isocytosine are not the components of the genetic code", International Journal of Quantum Chemistry, Supplement: Proceedings of the International Symposium on Quantum Biology and Quantum Pharmacology, 1985, 28 (Supplement S12), pp. 209–216 (doi:10.1002/qua.560280720).
- ^ Christopher Roberts, Rajanikanth Bandaru, Christopher Switzer: „Theoretical and Experimental Study of Isoguanine and Isocytosine: Base Pairing in an Expanded Genetic System", J. Am. Chem. Soc., 1997, 119 (20), pp. 4640–4649 (doi:10.1021/ja970123s).