HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 29719, compound → HCID 54574623, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 29719 | HCID 29719 | — |
| Reactant | HCID 54032006 | HCID 54032006 | — |
| Product | HCID 54574623 | HCID 54574623 | — |
Reaction Steps
The other pathway from dopaquinone to melanin involves the addition of cysteine to dopaquinone to produce 5-S-cysteinyldopa, followed by the oxidation of 5-S-cysteinyldopa to 5-S-cysteinyldopaquinone. A ring closure of the 5-S-cysteinyldopaquinone then yields 7-alanyl-5-hydroxy-3-carboxy-2H-1,4-benzothiazine which is subsequently decarboxylated to yield 7-alanyl-5-hydroxy-2H-1,4-benzothiazine. At this point, the 7-alanyl-5-hydroxy-2H-1,4-benzothiazine is converted to melanin and pheomelanin. Tyrosinase does not play any additional role in this melanin production pathway.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05817631 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-99a96f93134d4e79950b7a838582d115 |
| Source note | uspto-grants-1998_10 |