Metabolite Card

Formula: C18H10N2O4 (318.0641)
SMILES: CC1=C2NC=C3C2=C(C2=CNC4=C(C)C(=O)C(=O)C3=C24)C(=O)C1=O

Synonyms [en]

Melanin; Phaeomelanins; Melanin from Sepia officinalis; 6,14-dimethyl-4,12-diazapentacyclo[8.6.1.1^{2,5}.0^{13,17}.0^{9,18}]octadeca-1(17),2,5,9(18),10,13-hexaene-7,8,15,16-tetrone; Allomelanins; Melanins

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Melanin. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000020317). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Dermal melanin is produced by melanocytes, which are found in the stratum basale of the epidermis. Although human beings generally possess a similar concentration of melanocytes in their skin, the melanocytes in some individuals and races more frequently or less frequently express the melanin-producing genes, thereby conferring a greater or lesser concentration of skin melanin. Some individual animals and humans have no or very little melanin in their bodies, which is a condition known as albinism. Higher eumelanin levels also can be a disadvantage, however, beyond a higher disposition toward vitamin D deficiency. Dark skin is a complicating factor in the laser removal of port-wine stains. Effective in treating fair skin, lasers generally are less successful in removing port-wine stains in Asians and people of African descent. Higher concentrations of melanin in darker-skinned individuals simply diffuse and absorb the laser radiation, inhibiting light absorption by the targeted tissue. Melanin similarly can complicate laser treatment of other dermatological conditions in people with darker skin. Under the microscope melanin is brown, non-refractile and finely granular with individual granules having a diameter of less than 800 nanometers. This differentiates melanin from common blood breakdown pigments which are larger, chunky and refractile and range in color from green to yellow or red-brown. In heavily pigmented lesions, dense aggregates of melanin can obscure histologic detail. A dilute solution of potassium permanganate is an effective melanin bleach. Pigments causing darkness in skin, hair, feathers, etc. They are irregular polymeric structures and are divided into three groups: allomelanins in the plant kingdom and eumelanins and phaeomelanins in the animal kingdom. Because melanin is an aggregate of smaller component molecules, there are a number of different types of melanin with differing proportions and bonding patterns of these component molecules. Both pheomelanin and eumelanin are found in human skin and hair, but eumelanin is the most abundant melanin in humans, as well as the form most likely to be deficient in albinism. Freckles and moles are formed where there is a localized concentration of melanin in the skin. They are highly associated with pale skin. Melanin is a biopolymer and a neuropeptide. In the early 1970s, John McGinness, Peter Corry, and Peter Proctor reported that melanin is a high-conductivity organic semiconductor (Science, vol 183, 853-855 (1974)). Studies revealed that melanin acted as a voltage-controlled solid-state threshold switch. Further, it emitting a flash of light electroluminescence when it switched.

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 8049-97-6
  • PubChem: 6325610
  • ChEBI: ChEBI:89634
  • HMDB: HMDB0004068
  • HMDB: HMDB04068
  • KEGG: C05606
  • BioCyc: MELANIN
  • NCBI MeSH: Melanins
  • Wikipedia: Melanin
  • RefMet: RM0136253
  • MoNA: BAF_UVA_POS000932
  • MoNA: BAF_UVA_POS001489
  • Metlin: METLIN_7011
  • Coconut NaturalProduct: CNP0301754.0

Class / Ontology

Metabolic Network
ID EC Number Name
View More
Organism Source

Taxonomy Source

  1. Capra hircus [ncbi taxid: 9925]
  2. Dalbergia odorifera [ncbi taxid: 499988]
  3. Ercolania funerea [ncbi taxid: ]
  4. Gomophia watsoni [ncbi taxid: ]
  5. Helichrysum stirlingii [ncbi taxid: ]
  6. Heptacyclum zenkeri [ncbi taxid: ]
  7. Homo sapiens [ncbi taxid: 9606]
  8. Jaborosa parviflora [ncbi taxid: 1608015]
  9. Lachnum YM156 [ncbi taxid: ]
  10. Luffa aegyptiaca [ncbi taxid: 3670]
  11. Luffa cylindrica [ncbi taxid: ]
  12. Mallotus nudiflorus [ncbi taxid: 300977]
  13. Ormocarpum kirkii [ncbi taxid: 77284]
  14. Ovis aries [ncbi taxid: 9940]
  15. Pamburus missionis [ncbi taxid: 159062]
  16. Pithecellobium dulce [ncbi taxid: 404691]
  17. Pithomyces chartarum [ncbi taxid: ]
  18. Ruppia maritima [ncbi taxid: 29652]
  19. Stellaria heterophylla [ncbi taxid: ]
  20. Streptomyces avermitilis MA4680 [ncbi taxid: ]
  21. Streptomyces griseus [ncbi taxid: 1911]
  22. Streptomyces kathirae [ncbi taxid: 151424]
  23. Streptomyces nodosus [ncbi taxid: 40318]
  24. Streptomyces parvulus strain 03 [ncbi taxid: ]
  25. Streptomyces spectabilis NRRL-2792 [ncbi taxid: ]
  26. Tephrosia obovata [ncbi taxid: 185973]
  27. Vaccaria hispanica [ncbi taxid: ]
  28. Vaccaria segetalis [ncbi taxid: ]
  29. Zingiber montanum [ncbi taxid: 336856]

Pathway Synthetic

pathway id name
WikiPathways:WP3604 Biochemical pathways: part I
WikiPathways:WP662 Amino acid metabolism
WikiPathways:WP3925 Amino acid metabolism
PathBank:SMP0120674 Alkaptonuria
PathBank:SMP0120782 Dopamine beta-Hydroxylase Deficiency
PathBank:SMP0000190 Hawkinsinuria
PathBank:SMP0087450 Tyrosine Metabolism
PathBank:SMP0120729 Tyrosinemia Type I
PathBank:SMP0120817 Monoamine Oxidase-A Deficiency (MAO-A)
PathBank:SMP0120491 Hawkinsinuria
PathBank:SMP0000169 Alkaptonuria
PathBank:SMP0000429 Disulfiram Action Pathway
PathBank:SMP0063684 Tyrosine Metabolism
PathBank:SMP0120453 Alkaptonuria
PathBank:SMP0120509 Tyrosinemia Type I
PathBank:SMP0120598 Monoamine Oxidase-A Deficiency (MAO-A)
PathBank:SMP0000218 Tyrosinemia Type I
PathBank:SMP0000533 Monoamine Oxidase-A Deficiency (MAO-A)
PathBank:SMP0087328 Tyrosine Metabolism
PathBank:SMP0120711 Hawkinsinuria
View All Pathways