InChI=1S/C16H17NO3/c1-20-14-8-12-10(6-13(14)19)9-17-5-4-16(12)3-2-11(18)7-15(16)17/h2-3,6,8,15,19H,4-5,7,9H2,1H3/t15-,16-/m0/s1 |
VEXDOCFQMVMPHJ-HOTGVXAUSA-N |
C1(=C(C=C2C(=C1)[C@@]34[C@@](N(C2)CC3)(CC(C=C4)=O)[H])O)OC |
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Galanthus elwesii
(NCBI:txid82232)
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See:
PubMed
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Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
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View more via ChEBI Ontology
Outgoing
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(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
has role
plant metabolite
(CHEBI:76924)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is a
aromatic ether
(CHEBI:35618)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is a
bridged compound
(CHEBI:35990)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is a
cyclic ketone
(CHEBI:3992)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is a
enone
(CHEBI:51689)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is a
isoquinoline alkaloid
(CHEBI:24921)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is a
organic heterotetracyclic compound
(CHEBI:38163)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is a
phenols
(CHEBI:33853)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is a
tertiary amino compound
(CHEBI:50996)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is conjugate base of
(4aS,10bR)-noroxomaritidine(1+)
(CHEBI:133995)
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
is enantiomer of
(4aR,10bS)-noroxomaritidine
(CHEBI:136560)
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Incoming
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(4aS,10bR)-noroxomaritidine(1+)
(CHEBI:133995)
is conjugate acid of
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
(4aR,10bS)-noroxomaritidine
(CHEBI:136560)
is enantiomer of
(4aS,10bR)-noroxomaritidine
(CHEBI:136557)
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(4aS,10bR)-8-hydroxy-9-methoxy-4,4a-dihydro-3H,6H-5,10b-ethanophenanthridin-3-one
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1545884
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Reaxys Registry Number
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Reaxys
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21385538
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Reaxys Registry Number
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Reaxys
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26941773
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PubMed citation
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Europe PMC
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