Attributes | Values |
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rdf:type
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description
| - химическое соединение (ru)
- chemical compound (en)
- composé chimique (fr)
- compositum chemicum (la)
- chemische Verbindung (de)
- քիմիական միացություն (hy)
- chemische verbinding (nl)
- compuestu químicu (ast)
- хімічна сполука (uk)
- রাসায়নিক যৌগ (bn)
- cheemsch Verbinnen (nds)
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rdfs:label
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skos:prefLabel
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name
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isomeric SMILES
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stereoisomer of
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isomeric SMILES
| - CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/[C@@]2(O)C(C)(C)C[C@H](O)C[C@@]2(C)O)C(C)(C)C[C@H](O)C1
|
stereoisomer of
| - 6-epi-Karpoxanthin
- 5,6-Di-epi-karpoxanthin
- (1R,2R,4R)-1-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol
|
instance of
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instance of
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subclass of
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subclass of
| - Carpoxanthin
- 6-Epikarpoxanthin
- 1-[(1E,3E,5E,7E,9E)-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl]-2,6,6-trimethylcyclohexane-1,2,4-triol
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found in taxon
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found in taxon
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UniChem compound ID
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CAS Registry Number
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canonical SMILES
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InChI
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InChIKey
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chemical formula
| |
PubChem CID
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ChEBI ID
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PubChem CID
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ChEBI ID
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UniChem compound ID
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CAS Registry Number
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canonical SMILES
| - OC1CC(=C(C=CC(=CC=CC(=CC=CC=C(C=CC=C(C=CC2(O)C(O)(C)CC(O)CC2(C)C)C)C)C)C)C(C)(C)C1)C
|
InChI
| - InChI=1S/C40H58O4/c1-29(17-13-19-31(3)21-22-36-33(5)25-34(41)26-37(36,6)7)15-11-12-16-30(2)18-14-20-32(4)23-24-40(44)38(8,9)27-35(42)28-39(40,10)43/h11-24,34-35,41-44H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,22-21+,24-23+,29-15+,30-16+,31-19+,32-20+/t34-,35+,39-,40-/m1/s1
|
InChIKey
| - DJOWTWWHMWQATC-SZYTUFQFSA-N
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chemical formula
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PubChem CID
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ChEBI ID
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LIPID MAPS ID
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LIPID MAPS ID
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mass
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mass
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is about
of | |
is stereoisomer of
of | - 6-epi-Karpoxanthin
- 5,6-Di-epi-karpoxanthin
- (1R,2R,4R)-1-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol
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is stereoisomer of
of | |
is main subject
of | |
is main subject
of | |