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check_image( "../cid_thumbs/cid_2825893.png" ); ?>
check_image( "../cid_thumbs/cid_1774581.png" ); ?>
check_image( "../cid_thumbs/cid_1149778.png" ); ?>
check_image( "../cid_thumbs/cid_5715178.png" ); ?>
check_image( "../cid_thumbs/cid_2142908.png" ); ?>
check_image( "../cid_thumbs/cid_65564.png" ); ?>
check_image( "../cid_thumbs/cid_1035.png" ); ?>
check_image( "../cid_thumbs/cid_493034.png" ); ?>
check_image( "../cid_thumbs/cid_94515.png" ); ?>
check_image( "../cid_thumbs/cid_4091709.png" ); ?>
check_image( "../cid_thumbs/cid_4465532.png" ); ?>
check_image( "../cid_thumbs/cid_754880.png" ); ?>
check_image( "../cid_thumbs/cid_90364.png" ); ?>
check_image( "../cid_thumbs/cid_20200.png" ); ?>
check_image( "../cid_thumbs/cid_1603781.png" ); ?>
check_image( "../cid_thumbs/cid_70111.png" ); ?>
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Oxidized vitamin C
PubChem Notes:
Dehydroascorbic Acid The reversibly oxidized form of ascorbic acid. It is the lactone of 2,3-DIKETOGULONIC ACID and has antiscorbutic activity in man on oral ingestion.
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Molecular Formula:
C6H6O6
InChI: InChI=1/C6H6O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-8H,1H2/t2?,5-/m1/s1
InChIKey: InChIKey=SBJKKFFYIZUCET-DOAHDZERBV
SMILES: C(C(C1C(=O)C(=O)C(=O)O1)O)O
Names:
dehydroascorbate
DEHYDROASCORBIC ACID
Dehydro-L-ascorbic acid
DHAA
EINECS 207-720-6
L-Ascorbic acid, dehydro-
L-Dehydroascorbic acid
L-Threo-hexo-2,3-diulosono-1,4-lactone
Oxidized ascorbic acid
Oxidized vitamin C
(5R)-5-(1,2-dihydroxyethyl)oxolane-2,3,4-trione
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Registries:
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PubChem CID 10280
PubChem ID 153544
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