| Product Name | Andrographolide |
|---|---|
| CAS | 5508-58-7 |
| Formula | C20H30O5 |
| MW | 350.45 |
| Appearance | 白色粉末 |
| Melting point | 218 °C (decomp) |
| Boiling point | 557.3±50.0 °C | Condition: Press: 760 Torr |
| PKa | 12.36±0.20 | Condition: Most Acidic Temp: 25 °C |
| Product Name | Andrographolide |
|---|---|
| CAS | 5508-58-7 |
| Formula | C20H30O5 |
| MW | 350.45 |
| Appearance | 白色粉末 |
| Melting point | 218 °C (decomp) |
| Boiling point | 557.3±50.0 °C | Condition: Press: 760 Torr |
| PKa | 12.36±0.20 | Condition: Most Acidic Temp: 25 °C |
WKQ-0000135
中文名稱：穿心蓮內(nèi)酯
中文別名：穿心蓮乙素；雄茸內(nèi)酯
英文名稱：Andrographolide
英文別名：2(3H)-Furanone, 3-[2-[decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-1-naphthalenyl]ethylidene]dihydro-4-hydroxy-, [1R-[1α[E(S*)],4aβ,5α,6α,8aα]]-;5β,9βH,10α-Labda-8(20),12-dien-16-oic acid, 3α,14,15,18-tetrahydroxy-, γ-lactone (7CI);Andrographis (6CI);(3E,4S)-3-[2-[(1R,4aS,5R,6R,8aS)-Decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-1-naphthalenyl]ethylidene]dihydro-4-hydroxy-2(3H)-furanone;3-dehydroandrographolide or 19-dehydroandrographolide? p. 1388;Andrographiside aglycon;Andrographolid;Andrographolide;
分子式：C20H30O5
分子量：350.45
CAS號：5508-58-7
純度：HPLC≥98%
熔點(diǎn)：218 °C (decomp)
沸點(diǎn)：557.3±50.0 °C | Condition: Press: 760 Torr
密度：1.2317 g/cm3 | Condition: Temp: 21 °C
酸系度數(shù)：12.36±0.20 | Condition: Most Acidic Temp: 25 °C
儲(chǔ)存條件：-20℃，干燥、避光、密封
規(guī)格：5mg10mg20mg50mg100mg500mg1g2g等應(yīng)客戶需求包裝
供應(yīng)單位：四川省維克奇生物科技有限公司
供應(yīng)電話：028-81700200/4008005713
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| Molecular cloning and functional characterization of multiple NADPH-cytochrome P450 reductases from Andrographis paniculata | ||
| Source:SCI：INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES | Author:Huixin Lin | Notes：影響因子：3.671 |
| Reference description | ||
The reference standard of andrographolide (purity ≥ 95%) was purchased from Weikeqi Biological Technology Co., Ltd (Sichuan, China). Standard stock solutions (1 mg/ml) were obtained by dissolving the compounds and were serially diluted with methanol to obtain working standard solutions of various concentrations. | ||
| Amido surface-functionalized magnetic molecularly imprinted polymers for the efficient extraction of Sibiskoside from Sibiraea angustata | ||
| Source:SCI：JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | Author:YuLan Liang | Notes：影響因子：2.813 |
| Reference description | ||
extracted and purified by our laboratory from the aerial portion of Sibiraea angustata and structural identification was done by the spectroscopic analysis. Andrographolide (≥98%), Loganin (≥98%) and Gastrodin (≥ 98%) were purchased from Sichuan Weikeqi Biological Technology Co., Ltd. (Chengdu, China). Deionized ultrawater was used from a laboratory purification system. | ||
| Synergistic effects of tanshinone IIA and andrographolide on the apoptosis of cancer cells via crosstalk between p53 and reactive oxygen species pathways | ||
| Source:SCI：Pharmacological Reports | Author:Li, Yingxue | Notes：影響因子：2.754 |
| Reference description | ||
Tan IIA (purity?>?98%) and Andro (purity?>?98%) were purchased from Sichuan Weikeqi Biological Tech Co., Ltd (Chengdu, China). The compounds were dissolved in dimethyl sulfoxide (DMSO) as stock solutions, and further diluted with Dulbecco’s Modified Eagle Medium (DMEM) to desired concentrations. | ||
| Albumin Supplement Affects the Metabolism and Metabolism-Related Drug–Drug Interaction of Fenoprofen Enantiomers | ||
| Source:SCI：CHIRALITY | Author:Nan Wang | Notes：影響因子：1.886 |
| Reference description | ||
were purchased from BDGentest (Woburn, MA). (R)-fenoprofen and (S)- fenoprofen were pre-pared in-house. Andrographolide was purchased from Sichuan WeikeqiBiotechnology (Chengdu, Sichuan, China). All other reagents were ofhigh-performance liquid chromatography (HPLC) grade or of the highestgrade commercially available | ||
