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About:
(4S)-4-hydroxy-3,4-dihydro-2H-naphthalen-1-one
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New Facet based on Instances of this Class
chemical compound
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rdf:type
Item
description
composto chimico
(it)
химическое соединение
(ru)
chemical compound
(en)
composé chimique
(fr)
תרכובת
(he)
kemisk forbindelse
(da)
compositum chemicum
(la)
chemische Verbindung
(de)
քիմիական միացություն
(hy)
chemická sloučenina
(cs)
chemická zlúčenina
(sk)
chemische verbinding
(nl)
kemia kombinaĵo
(eo)
związek chemiczny
(pl)
chemical compound
(en-ca)
chemical compound
(en-gb)
chemiese verbinding
(af)
chemische Verbindung
(de-ch)
component quimic
(oc)
compost químic
(ca)
composto químico
(gl)
composto químico
(pt)
composto químico
(pt-br)
compuesto quimico
(an)
compuestu químicu
(ast)
compus chimic
(ro)
kemiallinen yhdiste
(fi)
kjemisk forbindelse
(nb)
kjemisk sambinding
(nn)
komponim kimik
(sq)
konposatu kimiko
(eu)
senyawa kimia
(id)
ķīmisks savienojums
(lv)
хімічна сполука
(uk)
مركب كيميائي
(ar)
রাসায়নিক যৌগ
(bn)
compuesto químico
(es)
payvastagii khimiyaviy
(tg-latn)
пайвастагии химиявӣ
(tg-cyrl)
chemesch Verbindung
(lb)
rdfs:label
(4S)-4-hydroxy-3,4-dihydro-2H-naphthalen-1-one
(en)
skos:prefLabel
(4S)-4-hydroxy-3,4-dihydro-2H-naphthalen-1-one
(en)
name
(4S)-4-hydroxy-3,4-dihydro-2H-naphthalen-1-one
(en)
isomeric SMILES
wds:Q104935668-F2372419-AE48-4D51-AFD0-A74A06E8DC37
stereoisomer of
wds:Q104935668-E8C495EC-7230-4540-A4E5-BE6F25C81F1E
isomeric SMILES
O=C1CC[C@H](O)c2ccccc21
stereoisomer of
(4R)-4-hydroxy-3,4-dihydro-2H-naphthalen-1-one
instance of
wds:Q104935668-261079BC-466F-4749-81A9-FCE9C3A38DC5
instance of
type of chemical entity
subclass of
wds:Q104935668-ED4CF931-57D5-4AE1-9CDF-7530C8B2EF4B
subclass of
chemical substance
found in taxon
wds:Q104935668-74606EFB-097A-4F1B-ABD6-50415271364F
wds:Q104935668-86FBD8E2-B61A-4401-9607-15D9AA295239
wds:Q104935668-C8CBFB68-744E-4860-A0F3-7DA34444456C
found in taxon
Juglans sigillata
Juglans mandshurica
Ampelocera edentula
UniChem compound ID
wds:Q104935668-4EF6D6BC-91B0-440D-8570-F91100095D16
canonical SMILES
wds:Q104935668-12B4E290-6A8F-4F4D-B955-2BCEBA6F7BEC
InChI
wds:Q104935668-7F8AA446-EBFA-433E-9BE9-FB7675487B0B
InChIKey
wds:Q104935668-B573232D-7754-422F-81AF-898461F910E0
chemical formula
wds:Q104935668-4C017E9C-0983-4DF9-BD65-3D0D682203CA
PubChem CID
wds:Q104935668-432C65E2-01FD-4953-A4B8-C2F9B54557D1
PubChem CID
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11240662
UniChem compound ID
5349785
canonical SMILES
O=C1C=2C=CC=CC2C(O)CC1
InChI
InChI=1S/C10H10O2/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-4,9,11H,5-6H2/t9-/m0/s1
InChIKey
BGPJTIXJFAGUIF-VIFPVBQESA-N
chemical formula
C₁₀H₁₀O₂
PubChem CID
11240662
mass
wds:Q104935668-56B84953-1BFE-4E46-BC38-E422D47B1A8C
mass
162.06807956
(
xsd:decimal
)
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q104935668
is
stereoisomer of
of
(4R)-4-hydroxy-3,4-dihydro-2H-naphthalen-1-one
is
stereoisomer of
of
wds:Q104935667-66937CF3-4325-4A46-9239-2D5A022F6338
is
main subject
of
Studies on the constituents of Juglans species. I. Structural determination of (4S)- and (4R)-4-hydroxy-alpha-tetralone derivatives from the fruit of Juglans mandshurica MAXIM. var. sieboldiana MAKINO.
New α-Tetralone Galloylglucosides from the Fresh Pericarps of Juglans sigillata
Antileishmanial activity of a tetralone isolated from Ampelocera edentula, a Bolivian plant used as a treatment for cutaneous leishmaniasis.
is
main subject
of
wds:Q37284553-AF2A938D-3B4D-40A8-9A64-8927F30D3EC5
wds:Q47339661-541042FD-E998-46AD-BC99-97C7FD943A86
wds:Q46633968-B9F45822-7F3F-4E0B-B39B-E6BFB2916826
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