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> Main
CHEBI:435764 - (−)-hinokiresinol
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ChEBI Name
(−)-hinokiresinol
ChEBI ID
CHEBI:435764
ChEBI ASCII Name
(-)-hinokiresinol
Definition
A 1,3-bis(
p
-hydroxyphenyl)pentane-1,4-diene that has 1
E
,3
S
configuration. A natural product found in
Chamaecyparis obtusa
.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:10484, CHEBI:69979
Supplier Information
Download
Molfile
XML
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Molfile
Molfile
Formula
C17H16O2
Net Charge
0
Average Mass
252.308
Monoisotopic Mass
252.11503
InChI
InChI=1S/C17H16O2/c1-
2-
14(15-
7-
11-
17(19)
12-
8-
15)
6-
3-
13-
4-
9-
16(18)
10-
5-
13/h2-
12,14,18-
19H,1H2/b6-
3+/t14-
/m0/s1
InChIKey
VEAUNWQYYMXIRB-ZRFDWSJLSA-N
SMILES
C=1C(=CC=C(C1)O)[C@@H](C=C)/C=C/C2=CC=C(C=C2)O
Metabolite of Species
Details
Metasequoia glyptostroboides
(NCBI:txid3371)
Found in stem
(BTO:0001300)
. 95% ethanolic extract of air-dried, powdered stems and leaves See:
PubMed
Metasequoia glyptostroboides
(NCBI:txid3371)
Found in leaf
(BTO:0000713)
. 95% ethanolic extract of air-dried, powdered stems and leaves See:
PubMed
Roles Classification
Biological Role
(s):
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via
1,3-bis(p-hydroxyphenyl)pentane-1,4-diene
)
(via
norlignan
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(−)-hinokiresinol (
CHEBI:435764
)
has role
metabolite (
CHEBI:25212
)
(−)-hinokiresinol (
CHEBI:435764
)
is a
1,3-bis(
p
-hydroxyphenyl)pentane-1,4-diene (
CHEBI:131953
)
(−)-hinokiresinol (
CHEBI:435764
)
is a
norlignan (
CHEBI:53629
)
IUPAC Name
4-[(1
E
,3
S
)-1-(4-hydroxyphenyl)penta-1,4-dien-3-yl]phenol
Synonym
Source
4-[(1E,3S)-3-(4-hydroxyphenyl)penta-1,4-dienyl]phenol
ChEBI
Manual Xrefs
Databases
C00000722
KNApSAcK
C10628
KEGG COMPOUND
EP2323641
Patent
US2009312274
Patent
View more database links
Registry Numbers
Types
Sources
17676-24-3
CAS Registry Number
ChemIDplus
1971903
Beilstein Registry Number
Beilstein
Citations
Types
Sources
10909263
PubMed citation
Europe PMC
11684179
PubMed citation
Europe PMC
14561517
PubMed citation
Europe PMC
16309307
PubMed citation
Europe PMC
16884819
PubMed citation
Europe PMC
17051467
PubMed citation
Europe PMC
17886842
PubMed citation
Europe PMC
18093914
PubMed citation
Europe PMC
20091263
PubMed citation
Europe PMC
20165801
PubMed citation
Europe PMC
Last Modified
19 May 2016