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10338-51-9 分子结构
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(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol

ChemBase编号:73016
分子式:C14H20O7
平均质量:300.3044
单一同位素质量:300.12090298
SMILES和InChIs

SMILES:
[C@H]1([C@H]([C@@H]([C@H]([C@@H](O1)OCCc1ccc(cc1)O)O)O)O)CO
Canonical SMILES:
OC[C@H]1O[C@@H](OCCc2ccc(cc2)O)[C@@H]([C@H]([C@@H]1O)O)O
InChI:
InChI=1S/C14H20O7/c15-7-10-11(17)12(18)13(19)14(21-10)20-6-5-8-1-3-9(16)4-2-8/h1-4,10-19H,5-7H2/t10-,11-,12+,13-,14-/m1/s1
InChIKey:
ILRCGYURZSFMEG-RKQHYHRCSA-N

引用这个纪录

CBID:73016 http://www.chembase.cn/molecule-73016.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol
IUPAC传统名
salidroside
别名
Rhodioloside
Salidroside(Rhodioloside)
CAS号
10338-51-9
PubChem SID
162037936
PubChem CID
159278

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID 价格
Selleck Chemicals
S2396 external link 加入购物车 请登录
数据来源 数据ID
PubChem 159278 external link

理论计算性质

理论计算性质

JChem
Acid pKa 10.198019  质子受体
质子供体 LogD (pH = 5.5) -0.57985234 
LogD (pH = 7.4) -0.5805308  Log P -0.5798437 
摩尔折射率 72.0231 cm3 极化性 28.860756 Å3
极化表面积 119.61 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

安全信息 产品相关信息 生物活性(PubChem)
保存条件
-20°C expand 查看数据来源
成盐信息
Free Base expand 查看数据来源

详细说明

详细说明

Selleck Chemicals Selleck Chemicals
Selleck Chemicals -  S2396 external link
Research Area: Cancer
Biological Activity:
Salidroside (Rhodioloside; Rhodosin) is a glucoside compound with an IC50 of 4.99 ± 0.23 μg/mL for the proliferation of SACC-2. Salidroside (Rhodioloside; Rhodosin) could inhibit the proliferation of SACC-2 cells and induce SACC-2 cell apoptosis in vitro, which could be a kind of antitumor medicine in the future. Growing curve showed that SACC-2 cells of salidroside groups decreased with extending cell culture time. Immunohistochemistry staining showed that Caspase 3 and Caspase 8 were both strong positive expression in SACC-2 cells of salidroside groups, and poor positive expression in SACC-2 cells of control group, the difference was significant (P<0.01).Salidroside (Rhodioloside; Rhodosin) induces cell-cycle arrest and apoptosis in human breast cancer cells and may be a promising candidate for breast cancer treatment. [1][2][3]

参考文献

参考文献

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  • Hu X et al. Biochem Biophys Res Commun. 2010 Jul 16;398(1):62-7.
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专利

专利

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