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(Q76285986)
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English
4-[(1Z,3S)-3-(4-hydroxyphenyl)penta-1,4-dienyl]phenol
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
chemical compound
0 references
mass
252.115029752
dalton
1 reference
based on heuristic
inferred from isomeric SMILES
stereoisomer of
CID 126090
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
Nyasol
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
(-)-hinokiresinol
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
(-)-nyasol
1 reference
based on heuristic
inferred from InChI
chemical formula
C₁₇H₁₆O₂
0 references
canonical SMILES
OC1=CC=C(C=C1)C=CC(C=C)C2=CC=C(O)C=C2
0 references
isomeric SMILES
C=C[C@@H](/C=C\C1=CC=C(C=C1)O)C2=CC=C(C=C2)O
0 references
found in taxon
Hypoxis obtusa
1 reference
stated in
Determination of the norlignan glucosides of Hypoxidaceae by high-performance liquid chromatography
Hypoxis angustifolia
2 references
stated in
Determination of the norlignan glucosides of Hypoxidaceae by high-performance liquid chromatography
stated in
Nyasol and 1,3(5)-diphenyl-1-pentene related glycosides from Hypoxis angustifolia
Anemarrhena asphodeloides
9 references
stated in
Identification of antiadipogenic constituents of the rhizomes of Anemarrhena asphodeloides.
stated in
Norlignans with Hyaluronidase Inhibitory Activity from Anemarrhena asphodeloides
stated in
Testosterone 5alpha-reductase inhibitory active constituents from Anemarrhenae Rhizoma
stated in
cis-hinokiresinol, a norlignan from Anemarrhena asphodeloides, inhibits angiogenic response in vitro and in vivo
stated in
Norlignans with Hyaluronidase Inhibitory Activity from Anemarrhena asphodeloides
stated in
cis-hinokiresinol, a norlignan from Anemarrhena asphodeloides, inhibits angiogenic response in vitro and in vivo
stated in
Testosterone 5alpha-reductase inhibitory active constituents from Anemarrhenae Rhizoma
stated in
7-hydroxy-3-(4-hydroxybenzyl)chroman and broussonin b: neurotrophic compounds, isolated from Anemarrhena asphodeloides BUNGE, function as proteasome inhibitors
stated in
Detection of antifungal activity in Anemarrhena asphodeloides by sensitive BCT method and isolation of its active compound
Asparagus africanus
1 reference
stated in
Antiprotozoal compounds from Asparagus africanus.
Asparagus cochinchinensis
2 references
stated in
(+)-Nyasol from Asparagus cochinchinensis
stated in
Bioactive constituents from Asparagus cochinchinensis.
Chamaecyparis formosensis
1 reference
stated in
Effects of Chamaecyparis formosensis Matasumura extractives on lipopolysaccharide-induced release of nitric oxide
Identifiers
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
0 references
InChIKey
VEAUNWQYYMXIRB-XSHSDMCLSA-N
0 references
PubChem CID
5281830
1 reference
matched by identifier from
InChIKey
InChIKey
VEAUNWQYYMXIRB-XSHSDMCLSA-N
ChEBI ID
131956
mapping relation type
exact match
2 references
stated in
ChEBI release 2021-03-01
matched by identifier from
International Chemical Identifier
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
UniChem compound ID
1068251
1 reference
stated in
UniChem
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