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79-83-4 分子结构
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3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoic acid

ChemBase编号:1555
分子式:C9H17NO5
平均质量:219.23498
单一同位素质量:219.11067265
SMILES和InChIs

SMILES:
CC(C)(CO)[C@@H](O)C(=O)NCCC(=O)O
Canonical SMILES:
OCC([C@H](C(=O)NCCC(=O)O)O)(C)C
InChI:
InChI=1S/C9H17NO5/c1-9(2,5-11)7(14)8(15)10-4-3-6(12)13/h7,11,14H,3-5H2,1-2H3,(H,10,15)(H,12,13)/t7-/m0/s1
InChIKey:
GHOKWGTUZJEAQD-ZETCQYMHSA-N

引用这个纪录

CBID:1555 http://www.chembase.cn/molecule-1555.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
3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoic acid
IUPAC传统名
(+)-pantothenic acid
DL-pantothenic acid
别名
pantothenate
vitamin B5
Pantothenic acid
N-[(2r)-2,4-Dihydroxy-3,3-Dimethylbutanoyl]-Beta-Alanine
CAS号
79-83-4
MDL号
MFCD00020513
PubChem SID
160965012
46505022
PubChem CID
6613

数据来源

数据来源

所有数据来源 商品来源 非商品来源

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 4.3547416  质子受体
质子供体 LogD (pH = 5.5) -2.5288656 
LogD (pH = 7.4) -4.2778497  Log P -1.355375 
摩尔折射率 51.5111 cm3 极化性 20.437252 Å3
极化表面积 106.86 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P -1.12  LOG S -0.56 
溶解度 6.05e+01 g/l 

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
纯度
95+% 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

DrugBank DrugBank Selleck Chemicals Selleck Chemicals
DrugBank -  DB01783 external link
Item Information
Drug Groups experimental
Description A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE. [PubChem]
Selleck Chemicals -  S2498 external link
Research Area: Metabolic Disease
Biological Activity:
Pantothenic acid(pantothenate) is a water-soluble vitamin and an essential nutrient for for many animals. Pantothenic acid is used in the synthesis of coenzyme A (CoA). Coenzyme A may act as an acyl group carrier to form acetyl-CoA and other related compounds; this is a way to transport carbon atoms within the cell. CoA is important in energy metabolism for pyruvate to enter the tricarboxylic acid cycle(TCA cycle) as acetyl-CoA, and for α-ketoglutarate to be transformed to succinyl-CoA in the cycle. CoA is also important in the biosynthesis of many important compounds such as fatty acids, cholesterol, and acetylcholine. [1]

参考文献

参考文献

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专利

专利

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