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102783-24-4 分子结构
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(2S)-2-amino-5-[(E)-[amino(dimethylamino)methylidene]amino]pentanoic acid

ChemBase编号:1460
分子式:C8H18N4O2
平均质量:202.25412
单一同位素质量:202.14297584
SMILES和InChIs

SMILES:
CN(C)/C(=N/CCC[C@H](N)C(=O)O)/N
Canonical SMILES:
OC(=O)[C@H](CCC/N=C(/N(C)C)\N)N
InChI:
InChI=1S/C8H18N4O2/c1-12(2)8(10)11-5-3-4-6(9)7(13)14/h6H,3-5,9H2,1-2H3,(H2,10,11)(H,13,14)/t6-/m0/s1
InChIKey:
YDGMGEXADBMOMJ-LURJTMIESA-N

引用这个纪录

CBID:1460 http://www.chembase.cn/molecule-1460.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
(2S)-2-amino-5-[(E)-[amino(dimethylamino)methylidene]amino]pentanoic acid
IUPAC传统名
N,N-dimethylarginine
别名
ADMA
Asymmetric dimethylarginine
Dimethyl-l-arginine
Guanidino-n,n-dimethylarginine
Lopac-D-4268
N(5)-((Dimethylamino)iminomethyl)-L-ornithine
N(5)-[(dimethylamino)(imino)methyl]-L-ornithine
N(G1),N(G1)-Dimethylarginine
N(g),N(g)-dimethyl-l-arginine
N(g),N(g)-dimethylarginine
N(g)-dimethylarginine
N(omega),N(omega)-dimethyl-l-arginine
NG,NG-dimethyl-l-arginine
N,N-dimethylarginine
CAS号
102783-24-4
PubChem SID
46508091
160964919
PubChem CID
123831

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
DrugBank DB01686 external link
PubChem 123831 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 2.5392625  质子受体
质子供体 LogD (pH = 5.5) -5.5796237 
LogD (pH = 7.4) -4.3525457  Log P -2.672998 
摩尔折射率 53.6996 cm3 极化性 20.554567 Å3
极化表面积 104.94 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P -3.13  LOG S -1.48 
溶解度 6.77e+00 g/l 

分子性质

分子性质

生物活性(PubChem)

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB01686 external link
Item Information
Drug Groups experimental
Description Asymmetric dimethylarginine (ADMA) is a naturally occurring chemical found in blood plasma. It is a metabolic by-product of continual protein modification processes in the cytoplasm of all human cells. It is closely related to L-arginine, a conditionally-essential amino acid. ADMA interferes with L-arginine in the production of nitric oxide, a key chemical to endothelial and hence cardiovascular health. [Wikipedia]
Pharmacology Asymmetric dimethylarginine (ADMA), an endogenous inhibitor of nitric oxide synthase, is formed by methylation of arginine residues in proteins and released after proteolysis. In this reaction, S-adenosylmethionine is methyldonor and S-adenosylhomocysteine the demethylated product. ADMA and homocysteine are thus biochemically linked. Both plasma homocysteine and ADMA concentrations are increased in patients with renal dysfunction, probably as a result of an impairment in their metabolic, but not urinary, clearance. Hyperhomocysteinemia has been associated with an increased risk of cardiovascular disease in end-stage renal disease, especially in patients without malnutrition and inflammation. Also, plasma ADMA levels have been associated with cardiovascular disease in renal failure patients. Both homocysteine and ADMA are thought to mediate their adverse vascular effects by impairing endothelial, nitric oxide-dependent function resulting in decreased vasodilatation, increased smooth muscle cell proliferation, platelet dysfunction and increased monocyte adhesion.
Affected Organisms
Humans and other mammals
References
van Guldener C, Nanayakkara PW, Stehouwer CD: Review: Homocysteine and asymmetric dimethylarginine (ADMA): biochemically linked but differently related to vascular disease in chronic kidney disease. Clin Chem Lab Med. 2007 Oct 15;. [Pubmed]
External Links
Wikipedia

参考文献

参考文献

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  • van Guldener C, Nanayakkara PW, Stehouwer CD: Review: Homocysteine and asymmetric dimethylarginine (ADMA): biochemically linked but differently related to vascular disease in chronic kidney disease. Clin Chem Lab Med. 2007 Oct 15;. Pubmed
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专利

专利

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互联网资源

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