グレード
technical grade
アッセイ
≥85%
フォーム
powder
不純物
<5 wt. % ethanol
mp
200 °C (dec.) (lit.)
保管温度
2-8°C
SMILES記法
[Na+].[O-]C(=O)C(=O)CS
InChI
1S/C3H4O3S.Na/c4-2(1-7)3(5)6;/h7H,1H2,(H,5,6);/q;+1/p-1
InChI Key
CODUSAVZTZYYDD-UHFFFAOYSA-M
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アプリケーション
Sodium mercaptopyruvate is suitable for use in the thiosulfate sulfurtransferase activity assay.[1]
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
dust mask type N95 (US), Eyeshields, Gloves
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
359394-VAR:
359394-1G:
359394-BULK:
359394-100MG:
Herbert T Nagasawa et al.
Journal of medicinal chemistry, 50(26), 6462-6464 (2007-11-28)
A series of prodrugs of 3-mercaptopyruvate (3-MP), the substrate for the enzyme 3-mercaptopyruvate/cyanide sulfurtransferase (3-MPST) that converts cyanide to the nontoxic thiocyanate, which are highly effective cyanide antidotes, have been developed. These prodrugs of 3-MP are unique in being not
T Nakamura et al.
European journal of biochemistry, 267(17), 5621-5630 (2000-08-22)
Mercaptopyruvate sulfurtransferase (MST, EC 2.8.1.2) and thiosulfate sulfurtransferase (TST, rhodanese, EC 2.8.1.1) are evolutionarily related enzymes that catalyze the transfer of sulfur ions from mercaptopyruvate and thiosulfate, respectively, to cyanide ions. We have isolated and characterized two cDNAs, AtMST1 and
Steven E Patterson et al.
Journal of medicinal chemistry, 56(3), 1346-1349 (2013-01-11)
Current cyanide antidotes are administered by IV infusion, which is suboptimal for mass casualties. Therefore, in a cyanide disaster, intramuscular (IM) injectable antidotes would be more appropriate. We report the discovery of the highly water-soluble sulfanegen triethanolamine as a promising
N E Labrou et al.
Journal of chromatography. A, 718(1), 35-44 (1995-12-01)
Three biomimetic dye ligands bearing as a triazine-linked terminal moiety a carboxylated structure, which mimics substrates and inhibitors of L-lactate dehydrogenase (LDH), were immobilized on cross-linked agarose Ultrogel A6R. These biomimetic dyes are purpose-designed analogues of commercial monochlorotriazine Cibacron Blue
J Papenbrock et al.
European journal of biochemistry, 267(1), 145-154 (1999-12-22)
A database search for similarities between sequenced parts of the Arabidopsis thaliana genome with known sulfurtransferase sequences from Escherichia coli and mammals was undertaken to obtain information about plant sulfurtransferase-like proteins. One gene and several homologous EST clones were identified.
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