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4345-03-3 分子结构
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4-oxo-4-{[(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-yl]oxy}butanoic acid

ChemBase编号:155437
分子式:C33H54O5
平均质量:530.77886
单一同位素质量:530.39712483
SMILES和InChIs

SMILES:
Cc1c(c(c(c2c1O[C@](CC2)(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C)OC(=O)CCC(=O)O)C
Canonical SMILES:
C[C@@H](CCC[C@]1(C)CCc2c(O1)c(C)c(c(c2C)OC(=O)CCC(=O)O)C)CCC[C@@H](CCCC(C)C)C
InChI:
InChI=1S/C33H54O5/c1-22(2)12-9-13-23(3)14-10-15-24(4)16-11-20-33(8)21-19-28-27(7)31(25(5)26(6)32(28)38-33)37-30(36)18-17-29(34)35/h22-24H,9-21H2,1-8H3,(H,34,35)/t23-,24-,33-/m1/s1
InChIKey:
IELOKBJPULMYRW-NJQVLOCASA-N

引用这个纪录

CBID:155437 http://www.chembase.cn/molecule-155437.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
4-oxo-4-{[(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-yl]oxy}butanoic acid
IUPAC传统名
4-oxo-4-{[(2R)-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-3,4-dihydro-1-benzopyran-6-yl]oxy}butanoic acid
别名
维生素 E 琥珀酸酯
D-α-生育酚琥珀酸酯
CV 104
Covitol 1210
NSC 173849
d-α-Tocopherol Acid Succinate
Butanedioic Acid 1-[(2R)-3,4-Dihydro-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-2H-1-benzopyran-6-yl] Ester
(+)-2,5,7,8-Tetramethyl-2-(4,8,12-trimethyltridecyl)-6-chromanol Hydrogen Succinate
d-α-Tocopheryl Acid Succinate
(+)-α-Tocopheryl Succinate
Succinic Acid (+)-mono[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-6-chromanyl] ester
α-Vitamin E Succinate
Vitamin E d-α-Tocosuccinate
α-Tocopheryl Succinate
Vitamin E succinate
D-α-Tocopherol succinate
CAS号
4345-03-3
EC号
224-403-8
MDL号
MFCD00072055
Beilstein号
4038233
PubChem SID
24871418
24900107
24890110
162249575
PubChem CID
20353

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
PubChem 20353 external link

理论计算性质

理论计算性质

JChem
Acid pKa 3.9952197  质子受体
质子供体 LogD (pH = 5.5) 8.729335 
LogD (pH = 7.4) 7.0816007  Log P 10.243406 
摩尔折射率 155.4189 cm3 极化性 60.94539 Å3
极化表面积 72.83 Å2 可自由旋转的化学键 17 
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)
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
1 expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
保存温度
-20°C expand 查看数据来源
2-8°C expand 查看数据来源
纯度
≥98.0% (HPLC) expand 查看数据来源
级别
analytical standard expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
包装
ampule of 100 mg expand 查看数据来源
生物来源
semisynthetic expand 查看数据来源
特征
standard type fat soluble vitamin expand 查看数据来源
产品线
BioXtra expand 查看数据来源
Pharmacopeia Traceability
traceable to PhEur T1610000 expand 查看数据来源
traceable to USP 1667803 expand 查看数据来源
Empirical Formula (Hill Notation)
C33H54O5 expand 查看数据来源

详细说明

详细说明

Sigma Aldrich Sigma Aldrich TRC TRC
Sigma Aldrich -  T3126 external link
Biochem/physiol Actions
Tocopherols (TCP) (vitamin E) are a series (α, β, γ and δ) of chiral organic molecules that vary in their degree of methylation of the phenol moiety of the chromanol ring. Tocopherols are lipid soluble anti-oxidants that protect cell membranes from oxidative damage. α-Tocopherol is the form of tocopherol preferentially absorbed by homo sapiens. α-Tocopherol succinate is used along the α-Tocopherol acetate, α-Tocopherol nicotinate and other esterified forms as a vitamin E supplement with similar but differential activities.
Sigma Aldrich -  95255 external link
Biochem/physiol Actions
Tocopherols (TCP) (vitamin E) are a series (α, β, γ and δ) of chiral organic molecules that vary in their degree of methylation of the phenol moiety of the chromanol ring. Tocopherols are lipid soluble anti-oxidants that protect cell membranes from oxidative damage. α-Tocopherol is the form of tocopherol preferentially absorbed by homo sapiens. α-Tocopherol succinate is used along the α-Tocopherol acetate, α-Tocopherol nicotinate and other esterified forms as a vitamin E supplement with similar but differential activities.
Toronto Research Chemicals -  T539950 external link
A potent novel antineoplastic agent with high selectivity and cooperativity with tumor necrosis factor-related apoptosis-inducing ligand (Apo2 ligand). It inhibits proliferation of mesothelioma cells by selective down-regulation of fibroblast growth facto

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Weber, T. et al.: Clin. Can Res., 8, 863 (2002)
  • Staphelberg, M. et al.: Biochem. Biophys. Res. Comm., 318, 636 (2002)
  • Ramathapuram, L.V. et al.: Cancer Immunol. Immununother., 55, 166 (2002)
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专利

专利

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互联网资源

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