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芦荟苦素 | 30861-27-9

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中文名称:芦荟苦素
英文名称:Aloesin
CAS No.:30861-27-9 分子式:C19H22O9 分子量:394.3726
植物源: 芦荟   
如需查看该化合物的详细结构式,mol文件,smile, InChi 请点击:芦荟苦素结构式
价格行情:芦荟苦素价格
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芦荟苦素的其他展现形式
  • 相关化合物
双花母草素 4H-1-Benzopyran-4-one,6-b-D-glucopyranosyl-5,7-dihydroxy-2-methyl- CAS No.:89701-85-9
丁香3 4H-1-Benzopyran-4-one,8-b-D-glucopyranosyl-5,7-dihydroxy-2-methyl- CAS No.:152041-16-2
4H-1-Benzopyran-4-one,6-b-D-glucopyranosyl-7-hydroxy-5-methyl-2-(2-oxopropyl)- CAS No.:119256-74-5
简介
Aloesin (Aloeresin) 是一种 tyrosinase 抑制剂,并显示出抗炎活性、紫外线保护和抗细菌作用。Aloesin 能诱导细胞凋亡,可用于卵巢癌研究。
名称和标识符
InChIKey HKIKAXXIWJHWLY-ZIIYPAMZSA-N
Inchi 1S/C19H22O9/c1-7-3-10(22)14(19-17(26)16(25)15(24)12(6-20)28-19)18-13(7)11(23)5-9(27-18)4-8(2)21/h3,5,12,15-17,19-20,22,24-26H,4,6H2,1-2H3/t12-,15-,16+,17-,19+/m1/s1
SMILES O1[C@]([H])(C([H])([H])O[H])[C@]([H])([C@@]([H])([C@]([H])([C@]1([H])C1=C(C([H])=C(C([H])([H])[H])C2C(C([H])=C(C([H])([H])C(C([H])([H])[H])=O)OC1=2)=O)O[H])O[H])O[H])O[H]
别名信息
- 中文别名 -
芦荟苦素 苦素 芦荟酯B
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- 英文别名 -
4H-1-Benzopyran-4-one,8-b-D-glucopyranosyl-7-hydroxy-5-methyl-2-(2-oxopropyl)- Aloeresin 4H-1-Benzopyran-4-one,8-b-D-glucopyranosyl-7 ALOESIN (1R)-1,5-anhydro-1-[7-hydroxy-5-methyl-4-oxo-2-(2-oxopropyl)-4H-chromen-8-yl]glucitol D-glucitol, 1,5-anhydro-1-C-[7-hydroxy-5-methyl-4-oxo-2-(2-oxopropyl)-4H-1-benzopyran-8-yl]-, (1R)- Aloe resin B Y27M69Y8ES Aloeresin B 4H-1-Benzopyran-4-one, 8-beta-D-glucopyranosyl-7-hydroxy-5-methyl-2-(2-oxopropyl)- Aloersin B NSC631262 2-acetonyl-7-hydroxy-5-methyl-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]chromen-4-one 7-hydroxy-5-methyl-2-(2-oxopropyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one s9284 4H-
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物化性质
 实验特性
LogP -0.54660
PSA 157.66000
折射率 1.636
沸点 628.0±55.0℃ at 760 mmHg
闪点 224.2°C
密度 1.5
 计算特性
精确分子量 394.126
氢键供体数量 5
氢键受体数量 9
可旋转化学键数量 4
同位素质量 394.126
重原子数量 28
复杂度 647
同位素原子数量 0
确定原子立构中心数量 5
不确定原子立构中心数量 0
确定化学键立构中心数量 0
不确定化学键立构中心数量 0
共价键单元数量 1
疏水参数计算参考值(XlogP) -1.3
拓扑分子极性表面积 154
分子量 394.4
国际标准相关数据
EINECS 631262
相关文献

1. C-Glycosyl compounds. Part VI. Aloesin, a C-glucosylchromone from Aloe sp.
L. J. Haynes,D. K. Holdsworth,R. Russell J. Chem. Soc. C 1970 2581

2. A material-basis study of Aloe vera on the wnt/β-catenin signaling pathway using a knockin/knockout method with high-speed countercurrent chromatography
Cong Dai,Meng-ping Liu,Wei-jia Zhang,Christopher Wai Kei Lam,Jian-ru Guo,Wa Li,Juan Wu,Jie-feng Chen,Zuan-guang Chen,Wei Zhang,Mei-cun Yao RSC Adv. 2017 7 38819

3. Simultaneous HPLC quantification of seven chromones in Aloe barbadensis Miller using a single reference standard
Jia-Sheng Zhong,Jin-Zhi Wan,Yu-Peng Liu,Wen-Jing Ding,Xiao-Fang Wu,Zhi-Yong Xie Anal. Methods 2014 6 4388

4. Structure and function of the chalcone synthase superfamily of plant type III polyketide synthases
Ikuro Abe,Hiroyuki Morita Nat. Prod. Rep. 2010 27 809

5. The chemistry and bioactivity of Southern African flora II: flavonoids, quinones and minor compound classes
Smith B. Babiaka,Fidele Ntie-Kang,Bakoh Ndingkokhar,James A. Mbah,Wolfgang Sippl,Joseph N. Yong RSC Adv. 2015 5 57704

6. A review of past promises, present realities and a vibrant future for wound dressing from naturally occurring to sustainable materials
Supriya H.,Sandeep Tripathi,Suryasarathi Bose RSC Sustain. 2023 1 763

7. Preparation, antibacterial activity, and electrocatalytic detection of hydrazine based on biogenic CuFeO2/PANI nanocomposites synthesized using Aloe barbadensis miller
Pooja Singh,Kshitij RB Singh,Rahul Verma,Priyanka Prasad,Ranjana Verma,Subha Narayan Das,Jay Singh,Ravindra Pratap Singh New J. Chem. 2022 46 8805

8. Natural product C-glycosyltransferases – a scarcely characterised enzymatic activity with biotechnological potential
Natalia Putkaradze,David Teze,Folmer Fredslund,Ditte Hededam Welner Nat. Prod. Rep. 2021 38 432

9. Simultaneous determination of aloin A and aloe emodin in products containing Aloe vera by ultra-performance liquid chromatography with tandem mass spectrometry
Perry G. Wang,Wanlong Zhou,Wayne G. Wamer,Alexander J. Krynitsky,Jeanne I. Rader Anal. Methods 2012 4 3612

10. Thiosemicarbazones with tyrosinase inhibitory activity
Katarzyna Ha?dys,Rafa? Latajka Med. Chem. Commun. 2019 10 378

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