化工社化工社 化学情報印刷レポート · 研究参考用
3,4-Dihydro-3,6,8-trihydoroxy-1(2H)-napthalenone → 1,3,6,8-Naphthalenetetrol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,4-Dihydro-3,6,8-trihydoroxy-1(2H)-napthalenone | HCID 439309 | — |
| 反応物 | 1,3,8-Trihydroxynaphthalene | HCID 439428 | — |
| 反応物 | Malonyl CoA | HCID 644066 | — |
| 生成物 | 1,3,6,8-Naphthalenetetrol | HCID 440202 | — |
反応手順
Biosynthesis of DHN melanin is synthesized by a polyketide pathway, through the genes encoding Polyketide synthase (PKS), Scytalone dehydratase (SCD), and 1,3,8-trihydroxynaphthalene reductase (THN). It started with a PKS using malonyl-CoA as a substrate to produce 1,3,6,8-tetrahydroxynaphthalene, 1,3,6,8-THN (Fujii et al., 2000), followed by reducatse catalysis to produce scytalone, dehydration by SCD to yield 1,3,8-trihydroxynaphthalene (1,3,8-THN), reduction by THN to yield vermelone, dehydration to produce melanin precursor 1,8-dihydroxynaphthalene (1,8-DHN), and then oxidation and polymerization to yield melanin.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08518393B2 |
| 出典データセット | uspto-grants-2013_08 |
| ORD ID | ord-ce00f41e87b947328bc4cb0434182911 |
| 出典メモ | uspto-grants-2013_08 |