Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Epinephrine → (2S)-3-(4-hydroxyphenyl)-2-nitramidopropanoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Epinephrine | HCID 5816 | — |
| 반응물 | Arachidonic Acid | HCID 444899 | — |
| 반응물 | Prostaglandin H2 | HCID 445049 | — |
| 반응물 | HCID 178511350 | HCID 178511350 | — |
| 촉매 | Ferriheme hydroxide | HCID 27337 | — |
| 용매 | Phosphate | HCID 1061 | — |
| 생성물 | (2S)-3-(4-hydroxyphenyl)-2-nitramidopropanoic acid | HCID 9834478 | — |
반응 단계
Reaction mixture in 100 mM phosphate buffer, pH 7.4, (total volume, 200 μl) was incubated at 37° C. for 30 minutes. The reaction mixture contained a combination of cytochrome c (40 μg), ovine prostaglandin H2 synthase form 2 (104 units), arachidonic acid (590 μM), epinephrine (31 μg), hematin (1 μM), and DETA NONOate, an NO donor, (300 μM) as indicated in FIG. 2. After incubation, the proteins were separated by SDS-PAGE followed by Western blot analysis with an alkaline phosphatase system using monoclonal antibodies produced against nitrotyrosine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06812212B2 |
| 출처 데이터셋 | uspto-grants-2004_11 |
| ORD ID | ord-76199e79b92a4202aea748587ed7142b |
| 출처 메모 | uspto-grants-2004_11 |