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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376488생성일: 2026년 10월 26일

2-Mercaptoethanol → AD 5075

https://huagongshe.com/reaction/376488

반응식

참여 물질

역할이름HCID투입량
반응물2-MercaptoethanolHCID 1567—
반응물BenzamideHCID 2331—
반응물Phenylmethylsulfonyl FluorideHCID 4784—
반응물ThiazolidinedioneHCID 5437—
반응물Ethylenediaminetetraacetic AcidHCID 6049—
반응물Tris(hydroxymethyl)aminomethaneHCID 6503—
반응물Leupeptin acidHCID 189069—
반응물D-1,4-DithiothreitolHCID 446094—
용매GlycerolHCID 753—
생성물AD 5075HCID 128440—

반응 단계

For each assay, an aliquot of receptor (1:1000-1:3000 dilution) was incubated in TEGM (10 mM Tris, pH 7.2, 1 mM EDTA, 10% glycerol, 7 μl/100 ml β-mercaptoethanol, 10 mM Na molybdate, 1 mM dithiothreitol, 5 μg/ml aprotinin, 2 μg/ml leupeptin, 2 μg/ml benzamide and 0.5 mM PMSF) containing 5-10% COS-1 cell cytoplasmic lysate and 10 nM labeled thiazolidinedione ([3H2 ]AD-5075, 21 Ci/mmole), ± test compound compound, [3H2 ]Example 11, 17 Ci/mmole), ± test compound, respectively. Assays were incubated for ~16 h at 4 ° C. in a final volume of 300 μl. Unbound ligand was removed by addition of 200 μl dextran/gelatin-coated charcoal, on ice, for ~10 minutes. After centrifugation at 3000 rpm for 10 min at 4° C., 200 μl of the supernatant fraction was counted in a liquid scintillation counter. In this assay the KD for AD-5075 and Example 11 is 1 nM, respectively.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06020382
출처 데이터셋uspto-grants-2000_02
ORD IDord-02cc420f906c4c0687d2f648116f01e1
출처 메모uspto-grants-2000_02