021-51111890
购物车（）
sales@molnova.cn
Liquidambaric lactone
CAS No. 185051-75-6
Liquidambaric lactone ( —— )
产品货号. M22856 CAS No. 185051-75-6
枫香内酯是从大花卫矛 (Euonymus grandiflorus Wall) 中分离出来的化合物。枫香内酯可能具有抑制 HIV-1 逆转录酶活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ￥2673 | 有现货 |
|
| 100MG | 获取报价 | 有现货 |
|
| 200MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Liquidambaric lactone
-
注意事项本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断
-
产品简述枫香内酯是从大花卫矛 (Euonymus grandiflorus Wall) 中分离出来的化合物。枫香内酯可能具有抑制 HIV-1 逆转录酶活性。
-
产品描述Liquidambaric lactone is a compound isolated from Euonymus grandiflorus Wall.Liquidambaric lactone may have inhibitory HIV-1 reverse transcriptase activity.Among the 25 fractions obtained from the alcohol extractive of the roots of Lantana camara L.(Verbenaceae) by silica gel column chromatography,three fractions demonstrated inhibitory HIV-1 reverse transcriptase activity.Furthermore,six pentacyclic triterpenes were isolated by reduced pressure column chromatography and identified as oleanonic acid(1),Liquidambaric lactone(2),lantadene A(3),lantadene B(4),oleanolic acid(5),and 25-hydroxy-oleanolic acid(6) by spectral analysis. Compounds 2 and 6 were reported firstly in the plants of Verbenaceae family,and the structure of 6 was confirmed firstly by X-ray crystallography.
-
体外实验——
-
体内实验——
-
同义词——
-
通路Microbiology/Virology
-
靶点HIV
-
受体HIV-1
-
研究领域——
-
适应症——
化学信息
-
CAS Number185051-75-6
-
分子量468.67
-
分子式C30H44O4
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESC[C@]1([C@@]2(CC[C@@]3([H])C4(C)C)C)[C@@]([C@@H](O5)[C@@H]5[C@]2([H])[C@]3(CCC4=O)C)(OC6=O)[C@@](CC(C)(C)CC7)([H])[C@]67CC1
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Roots of Lantana camara:Chemical Constituents and HIV-1 Reverse Transcriptase Inhibitory Activity. Natural Product Research & Development, 2011 , 23 (1) :25-29.
产品手册
关联产品
-
Kaempferol 3-O-(6-ga...
Kaempferol-3-O-(6′′-galloyl)-β-glucopyranoside 是一种吡喃葡萄糖苷。Kaempferol-3-O-(6′′-galloyl)-β-glucopyranoside 抑制 HIV-2 RNase H 的 IC50 为 5.19 μM。
-
Saquinavir mesylate
HIV-1 蛋白酶的有效选择性抑制剂，在细胞测定中 IC50 为 0.5-6 nM。
-
TAT 48-57
TAT (48-57) is a cell-permeable peptide, derived from HIV-1 transactivator of transcription (Tat) protein residue 48-57.This peptide is amino acid residues 48 to 57 fragment of the basic domain of HIV Tat.
