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词条 L-Dopaquinone
释义

  1. References

  2. External links

{{DISPLAYTITLE:L-Dopaquinone}}{{chembox
| Name = L-Dopaquinone
| ImageFile = L-Dopachinon.svg
| ImageSize =
| IUPACName = (2S)-2-Amino-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)propanoic acid
| OtherNames = o-Dopaquinone
|Section1={{Chembox Identifiers
| CASNo = 4430-97-1
| PubChem = 439316
| ChEBI = 16852
| SMILES = N[C@@H](CC1=CC(=O)C(=O)C=C1)C(O)=O
| ChemSpiderID = 388447
| InChI = 1/C9H9NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6H,3,10H2,(H,13,14)/t6-/m0/s1
| InChIKey = AHMIDUVKSGCHAU-LURJTMIEBS
| StdInChI = 1S/C9H9NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6H,3,10H2,(H,13,14)/t6-/m0/s1
| StdInChIKey = AHMIDUVKSGCHAU-LURJTMIESA-N
|Section2={{Chembox Properties
| C=9 | H=9 | N=1 | O=4
| Appearance=
| Density=
| MeltingPt=
| BoilingPt=
| Solubility=
|Section3={{Chembox Hazards
| MainHazards=
| FlashPt=
| AutoignitionPt =
}}L-Dopaquinone also known as o-dopaquinone is a metabolite of L-DOPA and a precursor of melanin.[1][2]

References

1. ^{{cite journal | author = Ito S, Wakamatsu K | title = Chemistry of mixed melanogenesis – pivotal roles of dopaquinone | journal = Photochem. Photobiol. | volume = 84 | issue = 3 | pages = 582–92 | year = 2008 | pmid = 18435614 | doi = 10.1111/j.1751-1097.2007.00238.x }}
2. ^{{cite journal | author = Hearing VJ | title = Determination of melanin synthetic pathways | journal = J. Invest. Dermatol. | volume = 131 | issue = E1 | pages = E8–E11 | year = 2011 | pmid = 22094404 | doi = 10.1038/skinbio.2011.4 | url = }}

External links

  • {{MeSH name|dopaquinone}}
{{DEFAULTSORT:Dopaquinone, L-}}

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