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508-02-1 分子结构
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(4R,6aS,6bR,8aR,10S,12aR,12bR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4-carboxylic acid

ChemBase编号:72965
分子式:C30H48O3
平均质量:456.70032
单一同位素质量:456.3603454
SMILES和InChIs

SMILES:
C1[C@@H](C([C@H]2[C@](C1)([C@@H]1[C@@](CC2)([C@]2(C(=CC1)[C@H]1C(CC2)[C@@H](CC(C1)(C)C)C(=O)O)C)C)C)(C)C)O
Canonical SMILES:
OC(=O)[C@@H]1CC(C)(C)C[C@@H]2C1CC[C@@]1(C2=CC[C@H]2[C@@]1(C)CC[C@@H]1[C@]2(C)CC[C@@H](C1(C)C)O)C
InChI:
InChI=1S/C30H48O3/c1-26(2)16-19-18(20(17-26)25(32)33)10-14-29(6)21(19)8-9-23-28(5)13-12-24(31)27(3,4)22(28)11-15-30(23,29)7/h8,18-20,22-24,31H,9-17H2,1-7H3,(H,32,33)/t18?,19-,20-,22+,23-,24+,28+,29-,30-/m1/s1
InChIKey:
AOWMBRPPHGNFDX-HPPBOAITSA-N

引用这个纪录

CBID:72965 http://www.chembase.cn/molecule-72965.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
(4R,6aS,6bR,8aR,10S,12aR,12bR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4-carboxylic acid
IUPAC传统名
(4R,6aS,6bR,8aR,10S,12aR,12bR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1H-picene-4-carboxylic acid
别名
Caryophyllin
Astrantiagenin C
Giganteumgenin C
Virgaureagenin B
Oleanolic Acid
CAS号
508-02-1
PubChem SID
162037885
PubChem CID
49867939

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
S2334 external link 加入购物车 请登录
数据来源 数据ID
PubChem 49867939 external link

理论计算性质

理论计算性质

JChem
Acid pKa 4.6560044  质子受体
质子供体 LogD (pH = 5.5) 5.4246063 
LogD (pH = 7.4) 3.6469674  Log P 6.325838 
摩尔折射率 133.6721 cm3 极化性 53.23124 Å3
极化表面积 57.53 Å2 可自由旋转的化学键
里宾斯基五规则 false 

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 -  S2334 external link
Research Area: Inflammation
Biological Activity:
Oleanolic acid(Caryophyllin) is a naturally occurring triterpenoid, widely distributed in food and medicinal plants, related to betulinic acid. It is relatively non-toxic, antitumor, and hepatoprotective, as well as exhibiting antiviral properties. An extremely potent synthetic triterpenoid analogue of oleanolic acid was found in 2005, which are powerful inhibitors of cellular inflammatory processes. [1]

参考文献

参考文献

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  • http://en.wikipedia.org/wiki/Oleanolic_acid
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专利

专利

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互联网资源

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