雷特格韦钾盐
中文名称 | 雷特格韦钾盐 |
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中文同义词 | 拉替拉韦钾;雷特格韦钾盐;雷特格韦-13C-D3;拉替拉韦钾盐;雷特格韦钾;N-(2-(4-(4-氟苄基氨基甲酰基)-5-羟基-1-甲基-6-氧代-1,6-二氢嘧啶-2-基)丙-2-基)-5-甲基-1,3,4-恶二唑-2-甲酰胺钾盐;拉替拉韦钾中间体;N-(2-(4-(4-氟苄基氨基甲酰基)-5-羟基-1-甲基-6-氧代-1,6-二氢嘧啶-2-基)丙-2-基)-5-甲基-1,3,4-恶二唑-2-甲酰胺钾盐(拉替拉韦中间体) |
英文名称 | Raltegravir potassium |
英文同义词 | N-[(4-Fluorophenyl)methyl]-1,6-dihydro-5-hydroxy-1-methyl-2-[1-methyl-1-[[(5-methyl-1,3,4-oxadiazol-2-yl)carbonyl]amino]ethyl]-6-oxo-4-pyrimidinecarboxamide Potassium Salt;Raltegravir Potassium Salt;MK 0518;Raltegravir(MK-0518);Raltegravir K;Raltegravir-13C-d3;Raltegravir potassium;Raltegravir potassium, >=98% |
CAS号 | 871038-72-1 |
分子式 | C20H20FN6O5.K |
分子量 | 482.511 |
EINECS号 | 682-461-3 |
相关类别 | 医药中间体;抗生素;小分子抑制剂;小分子抑制剂,天然产物;医药原料;拉替拉韦中间体;化学试剂;API;All Inhibitors;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals;Inhibitor |
Mol文件 | 871038-72-1.mol |
结构式 |
雷特格韦钾盐 性质
熔点 | 155-157°C |
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储存条件 | -20°C Freezer |
溶解度 | DMSO(稍微加热)、甲醇(稍微加热)、水(稍微加热) |
形态 | 固体 |
颜色 | 白色至浅米色 |
CAS 数据库 | 871038-72-1 |
Target | Value |
HIV integrase
() |
PFV IN carrying the S217H substitution is 10-fold less susceptible to Raltegravir with IC 50 of 900 nM. PFV IN displays 10% of WT activity and is inhibited by Raltegravir with an IC 50 of 200 nM, indicating a appr twofold decrease in susceptibility to the IN strand transfer inhibitor (INSTI) compared with WT IN. S217Q PFV IN is as sensitive to Raltegravir as the WT enzyme. Raltegravir is metabolized by glucuronidation, not hepatically. Raltegravir has potent in vitro activity against HIV-1, with a 95% inhibitory concentration of 31±20 nM, in human T lymphoid cell cultures. Raltegravir is also active against HIV-2 when Raltegravir is tested in CEMx174 cells, with an IC 95 of 6 nM. Raltegravir metabolism occurs primarily through glucuronidation. Drugs that are strong inducers of the glucuronidation enzyme, UGT1A1, significantly reduce Raltegravir concentrations and should not be used. Raltegravir exhibits weak inhibitory effects on hepatic cytochrome P450 activity. Raltegravir does not induce CYP3A4 RNA expression or CYP3A4-dependent testosterone 6-β-hydroxylase activity. Raltegravir cellular permeativity is reduced in the presence of magnesium and calcium. Raltegravir and related HIV-1 integrase (IN) strand transfer inhibitors (INSTIs efficiently block viral replication. In acutely infected human lymphoid CD4 + T-cell lines MT-4 and CEMx174, SIVmac251 replication is efficiently inhibited by Raltegravir, which shows an EC 90 in the low nanomolar range.
Raltegravir induces viro-immunological improvement of nonhuman primates with progressing SIVmac251 infection. One non-human primate shows an undetectable viral load following Raltegravir monotherapy.
安全信息
海关编码 | 2934990002 |
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更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
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2024/08/19 | 46216 | 雷特格韦钾盐 Raltegravir potassium salt, Thermo Scientific Chemicals | 871038-72-1 | 250ml | 2414元 |
2024/08/19 | 46216 | 雷特格韦钾盐 Raltegravir potassium salt, Thermo Scientific Chemicals | 871038-72-1 | 1g | 6639元 |