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| IUPAC Name: | N-[9-[(2R,3R,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide |
| Description: | N6-Benzoyl-2'-deoxy-2'-fluoroadenosine is a nucleoside analog where a benzoyl group is attached to the N6 position of the adenine base and a fluorine atom is substituted at the 2' position of the deoxyribose sugar. This modification is typically explored in medicinal chemistry to alter the nucleoside's interaction with enzymes involved in nucleic acid synthesis or to improve its pharmacokinetic properties. Such modifications are aimed at developing compounds with potential therapeutic applications, including antiviral or anticancer activities, by enhancing potency, selectivity, or stability. |
| Molecular Weight: | 373.34 |
| Molecular Formula: | C17H16FN5O4 |
| Canonical SMILES: | C1=CC=C(C=C1)C(=O)NC2=NC=NC3=C2N=CN3C4C(C(C(O4)CO)O)F |
| InChI: | InChI=1S/C17H16FN5O4/c18-11-13(25)10(6-24)27-17(11)23-8-21-12-14(19-7-20-15(12)23)22-16(26)9-4-2-1-3-5-9/h1-5,7-8,10-11,13,17,24-25H,6H2,(H,19,20,22,26)/t10-,11-,13-,17-/m1/s1 |
| InChI Key: | HLJZTLWDAQVZBU-YAMOITTJSA-N |
| Purity: | ≥98% by HPLC |
| Density: | 1.67±0.1 g/cm3(Predicted) |
| Storage: | Store at 2-8 °C |
| LogP: | 0.74030 |
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Carbonyl Compounds
(S)-Hexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one hydrochloride
1-(5-Methoxy-1,3-benzoxazol-2-yl)piperidine-3-carboxylic acid
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