中文名 | IAXO-102 |
英文名 | IAXO-102 |
别名 | 化合物IAXO-102 (2R,3R,4S,5R,6S)-2-(氨基甲基)-6-甲氧基-4,5-双(十四烷氧基)四氢-2H-吡喃-3-醇 |
英文别名 | IAXO-102 Methyl 6-amino-6-deoxy-2,3-di-O-tetradecyl-α-D-glucopyranoside α-D-Glucopyranoside, methyl 6-amino-6-deoxy-2,3-di-O-tetradecyl- |
CAS | 1115270-63-7 |
化学式 | C35H71NO5 |
分子量 | 585.96 |
密度 | 0.96±0.1 g/cm3(Predicted) |
沸点 | 650.2±55.0 °C(Predicted) |
酸度系数 | 13.00±0.70(Predicted) |
存储条件 | under inert gas (nitrogen or Argon) at 2–8 °C |
体外研究 | IAXO-102 (1-10 µM, for 2 hours) inhibits MAPK and p65 NF-κB phosphorylation in human umbilical vein endothelial (HUVEC) cells. IAXO-102 (10 µM, for 17 hours) suppresses LPS induced proinflammatory proteins MCP-1 and IL-8 production in HUVEC. Western Blot Analysis Cell Line: Human umbilical vein endothelial (HUVEC) cells Concentration: 1-10 µM Incubation Time: Pretreatment for 1 hour and then exposed to LPS (100 ng/mL) for additional 1 hour Result: Significantly inhibited LPS-stimulated MAPK/p65nF-ΚB phosphorylation. |
体内研究 | IAXO-102 (3 mg/kg/day, s.c. for 28 days) significantly retards Angiotensin II induced increase in aortic diameter in mice. Animal Model: Six-monthold ApoE −/− /C57Bl6 Dosage: 3 mg/kg/day Administration: S.C. for 28 days Result: Significantly retarded Angiotensin II-induced increase in aortic diameter. |
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