アッセイ
~98%
形状
triethylamine:hexane solution
官能基
ester
輸送温度
dry ice
保管温度
−20°C
SMILES記法
CCCCC\C=C/C/C=C\C=C\C=C\[C@@H]1O[C@H]1CCCC(=O)OC
InChI
1S/C21H32O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-16-19-20(24-19)17-15-18-21(22)23-2/h7-8,10-14,16,19-20H,3-6,9,15,17-18H2,1-2H3/b8-7-,11-10-,13-12+,16-14+/t19-,20-/m0/s1
InChI Key
WTKAVFHPLJFCMZ-NIBLXIPLSA-N
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生物化学的/生理学的作用
ロイコトリエンC4の前駆物質。
包装
アルゴン封入包装。
注意
遊離酸は不安定; 加水分解は推奨されません。
物理的形状
トリエチルアミン:ヘキサン (2:98)溶液
保管分類コード
10 - Combustible liquids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
試験成績書(COA)
製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Prostaglandins, 37(2), 251-258 (1989-02-01)
C-20 Trideuterated leukotriene A4 methyl ester was prepared by Wittig condensation of a deuterated C9-phosphonium salt with a C11-epoxydienal. It was then treated separately with glutathione, cysteinylglycine and cysteine. The resulting esters were saponified to give C-20 trideuterated leukotrienes C4
Biochemistry international, 15(6), 1127-1135 (1987-12-01)
It has been shown that various glutathione transferases can synthesize leukotriene C4, or its methyl ester, from glutathione and leukotriene A4. We questioned whether the same enzymes could be used to resolve racemic leukotriene A4 methyl ester (more easily prepared
Proceedings of the National Academy of Sciences of the USA, 81, 689-689 (1987)
FEBS letters, 175(2), 289-293 (1984-10-01)
Six major basic cytosolic glutathione transferases from rat liver catalyzed the conversion of leukotriene A4 methyl ester to the corresponding leukotriene C4 monomethyl ester. Glutathione transferase 4-4, the most active among these enzymes, had a Vmax of 615 nmol X
The Biochemical journal, 250(3), 713-718 (1988-03-15)
Leukotriene C4 synthesis was studied in preparations from mouse mastocytoma cells. Enzymic conjugation of leukotriene A4 with glutathione was catalysed by both the cytosol and the microsomal fraction. The specific activity of the microsomal fraction (7.8 nmol/min per mg of
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