分子量
321.3
儲存溫度
−20°C
SMILES 字串
N[C@@H](CCC(O)=O)C(O)=O.O=C(O)[C@@H](N)CCCNC(N)=N
InChI
1S/C6H14N4O2.C5H9NO4/c7-4(5(11)12)2-1-3-10-6(8)9;6-3(5(9)10)1-2-4(7)8/h4H,1-3,7H2,(H,11,12)(H4,8,9,10);3H,1-2,6H2,(H,7,8)(H,9,10)/t4-;3-/m00/s1
InChI 密鑰
RVEWUBJVAHOGKA-WOYAITHZSA-N
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生化/生理作用
Substrate of nitric oxide synthase, which is converted to citrulline and nitric oxide (NO). Induces insulin release by a nitric oxide-dependent mechanism.
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
Likars'ka sprava, (7)(7), 25-28 (2005-02-24)
The study of protein and carbohydrate components of extracellular matrix in patients with alcoholic and non alcoholic steatohepatitis developed on the background of type 2 diabetes mellitus has shown a significant increase in collagen and glycosaminoglycan synthesis along with the
Likars'ka sprava, (3-4)(3-4), 68-79 (2011-01-28)
The complex open randomized clinical, instrumental and biochemical research with including 89 patients with type 2 diabetes mellitus (DM), complicated with distal symmetric polyneuropathy (DDSP) has been conducted. It is proved that the antioxidant "cocktail" application (Dialipon, Byocerulin, hepatoprotector with
La Clinica terapeutica, 155(2-3), 57-59 (2004-07-13)
This study was carried out to confirm the results obtained in a previous trial, where Stressen had reduced homocysteinemia in patients with elevated concentrations of this amino acid and affected by vascular disease. 50 patients were enrolled and they received
La Clinica terapeutica, 155(1), 17-20 (2004-05-19)
Elevated plasma concentrations of homocysteine may occur because of impaired metabolism of this amino acid as a result of genetic factors or can be attributed to inadeguate blood levels of folate and vitamin B12. Recent studies demonstrated that STRESSEN decreases
Conformational analysis in a multidimensional energy landscape: study of an arginylglutamate repeat.
The journal of physical chemistry. B, 113(49), 15989-16001 (2009-09-26)
The identification of the distinct conformation classes of a molecule is a common and often crucial step in establishing structure-function relationships. Many different methods have been suggested for that purpose which differ in their choice of a (dis)similarity measure and
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