Difference between revisions of "Adrenochrome"
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[[File:Adrenochrome 3D ball.png|alt=|thumb|226x226px|Chemical structure of Adrenochrome]] | [[File:Adrenochrome 3D ball.png|alt=|thumb|226x226px|Chemical structure of Adrenochrome]] | ||
| + | <ref name=":0"><nowiki>https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome</nowiki></ref><ref name=":0" /> | ||
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| + | <ref>https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome</ref> | ||
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| + | [[File:Adrenochrome 3D spacefill.png|alt=|thumb|Adrenochrome ]] | ||
| + | <ref>https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome</ref><ref>https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome</ref> | ||
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| + | <ref>https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome</ref> | ||
==References== | ==References== | ||
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Revision as of 19:09, 25 August 2020
Adrenochrome, chemical formula C9H9NO3, is a pigment obtained by the oxidation of adrenaline (epinephrine). Adrenochrome monosemicarbazone, also known as carbazochrome, is a hemostatic, meaning it reduces capillary bleeding.[1]
References
- ^ https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome
- ^ a b https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome
- ^ https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome
- ^ https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome
- ^ https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome
- ^ https://pubchem.ncbi.nlm.nih.gov/compound/Adrenochrome
