A0451
芦荟素
from Curacao aloe, ~50%
别名:
1,8-二羟基-10-（β- D -吡喃葡萄糖基）-3-（羟甲基）-9 (10H)-蒽酮, 10-β- D -吡喃葡萄糖基-1,8-二羟基-3-（羟甲基）-9 (10H)-蒽酮, 芦荟苷, 芦荟苷 A
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关于此项目
经验公式（希尔记法）:
C21H22O9
化学文摘社编号:
分子量:
418.39
UNSPSC Code:
41116107
NACRES:
NA.79
PubChem Substance ID:
EC Number:
215-808-0
Beilstein/REAXYS Number:
6077558
MDL number:
产品名称
芦荟素, from Curacao aloe, ~50%
InChI key
AFHJQYHRLPMKHU-OSYMLPPYSA-N
InChI
1S/C21H22O9/c22-6-8-4-10-14(21-20(29)19(28)17(26)13(7-23)30-21)9-2-1-3-11(24)15(9)18(27)16(10)12(25)5-8/h1-5,13-14,17,19-26,28-29H,6-7H2/t13-,14+,17-,19+,20-,21+/m1/s1
SMILES string
OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)[C@H]2c3cccc(O)c3C(=O)c4c(O)cc(CO)cc24
biological source
Curacao aloe
form
powder
concentration
~50%
color
yellow to brown
mp
418.39 °C ((785.10 °F ))
solubility
pyridine: 50 mg/mL, clear, dark red to very dark red and red purple
storage temp.
room temp
Quality Level
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Biochem/physiol Actions
大鼠的泻下活性需要真杆菌菌株条或类似肠道厌氧菌激活，推测是通过转化为芦荟大黄素蒽酮。
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
K Shimpo et al.
Phytotherapy research : PTR, 15(8), 705-711 (2001-12-18)
We examined the modifying effect of whole-leaf Aloe arborescens Miller var. natalensis Berger (designated as 'ALOE') on azoxymethane (AOM)-induced aberrant crypt foci (ACF), putative preneoplastic lesions, in the rat colorectum. Male F344 rats (4 weeks old) were fed the basal
Hong-Xing Wang et al.
Ying yong sheng tai xue bao = The journal of applied ecology, 21(1), 260-264 (2010-04-15)
By using transmission electron microscopy and high performance liquid chromatography, this paper studied the effects of enhanced UV-B radiation on the leaf anthraquinones content and cell ultrastructure of Aloe vera L. After treated with enhanced UV-B radiation 6 hours per
Jianniao Tian et al.
Chemical & pharmaceutical bulletin, 51(5), 579-582 (2003-05-09)
The fluorescence quenching reactions of barbaloin with bovine serum albumin (BSA) in pH 7.20 Tris-HCl buffer solution were studied. The quenching mechanism of BSA by barbaloin was interpreted using the Stern-Volmer (S-V) mechanism. The binding constant K values were 2.78
M Hattori et al.
Pharmacology, 47 Suppl 1, 125-133 (1993-10-01)
A strictly anaerobic bacterium, Bifidobacterium sp. SEN, capable of hydrolyzing the O-glucosyl of sennosides was isolated from human feces. The bacterium stepwisely hydrolyzed sennoside B to sennidin B through sennidin-8-monoglucoside in PYF medium but not in GAM broth. Addition of
[Studies of aloe. II. Mechanism of cathartic effect].
Y Ishii et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 108(9), 904-910 (1988-09-01)
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