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Butyrospermol acetate
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group of stereoisomers with the chemical formula C₃₂H₅₂O₂
Attributes
Values
rdf:type
Item
description
groep van stereo-isomeren
(nl)
group of stereoisomers with the chemical formula C₃₂H₅₂O₂
(en)
група стереоізомерів з хімічною формулою C₃₂H₅₂O₂
(uk)
rdfs:label
Butyrospermol acetate
(en)
skos:prefLabel
Butyrospermol acetate
(en)
name
Butyrospermol acetate
(en)
isomeric SMILES
wds:Q104403120-FF7A1132-2DCB-4B22-9456-100F282F939A
isomeric SMILES
CC(=O)OC1CCC2(C)C3CC[C@@]4(C)[C@H](C(C)CCC=C(C)C)CC[C@]4(C)C3=CC[C@H]2C1(C)C
instance of
wds:Q104403120-042B77CD-51A0-43F4-9547-A397CAC1266A
instance of
group of stereoisomers
subclass of
wds:Q104403120-08028E96-6659-41CF-8393-D37B80BD13D4
subclass of
lanostane triterpenoid
found in taxon
wds:Q104403120-1274AB18-8038-4CF3-9968-48234F5461AD
wds:Q104403120-41324A05-C55F-4483-B06E-81B4BFF3DCAD
wds:Q104403120-5D5CA582-926F-4629-AD18-734548A6E27C
wds:Q104403120-BA24C166-0D19-4441-8F8B-7D8AB4A51D5A
wds:Q104403120-D09E87A5-6FEF-4386-9034-15AB8C12C4B0
found in taxon
Buddleja officinalis
Broussonetia papyrifera
Maclura pomifera
Maclura cochinchinensis
Euphorbia broteri
UniChem compound ID
wds:Q104403120-11AC6DC0-C268-45DD-A093-EAE2F4269CBA
canonical SMILES
wds:Q104403120-029B8844-DDEE-4592-A13D-980AB4104972
InChI
wds:Q104403120-75B5F9C4-FD1D-4B84-A2F1-0C1F1E81C9BE
InChIKey
wds:Q104403120-C517871C-20D9-43D2-AD6B-F61AC4396220
chemical formula
wds:Q104403120-DC9EF9E6-D2D8-4612-954A-AB2373E98B0F
PubChem CID
wds:Q104403120-5A0D3493-26A7-4296-83E1-7A49586D0D07
PubChem CID
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6427349
UniChem compound ID
57657128
canonical SMILES
O=C(OC1CCC2(C)C3C(=CCC2C1(C)C)C4(C)CCC(C(C)CCC=C(C)C)C4(C)CC3)C
InChI
InChI=1S/C32H52O2/c1-21(2)11-10-12-22(3)24-15-19-32(9)26-13-14-27-29(5,6)28(34-23(4)33)17-18-30(27,7)25(26)16-20-31(24,32)8/h11,13,22,24-25,27-28H,10,12,14-20H2,1-9H3/t22?,24-,25?,27-,28?,30?,31-,32+/m0/s1
InChIKey
LJPRHQWBGLMFJJ-XBUARUJWSA-N
chemical formula
C₃₂H₅₂O₂
PubChem CID
6427349
mass
wds:Q104403120-E9BC2A54-505F-490C-B88F-4426AC3E4510
mass
468.396730904
(
xsd:decimal
)
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q104403120
is
subclass of
of
5alpha-Tirucalla-7,24-dien-3beta-ol acetate
[(3S,5R,9S,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
[(3S,5R,9R,10R,13S,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
[(3S,5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
is
subclass of
of
wds:Q105152710-164464E4-EA3F-4F0D-A9EF-A2602C68605E
wds:Q105152712-FB19CB61-31B5-405B-AAC9-B897859A18EE
wds:Q105152708-AD2CA182-5606-4A9F-B2D0-F5E71570BC29
wds:Q105152706-8179FAEE-B1DE-42F7-9981-A7050470A254
is
main subject
of
Flavonoids and a prenylated xanthone from Cudrania cochinchinensis var. gerontogea
Osage orange (Maclura pomifera): History and economic uses
Triterpenes from Euphorbia broteri
Two isoflavones and a flavone from the fruits of Maclura pomifera
Phenolic constituents of formosan Broussonetia papyrifera
Sulfated Triterpenes from Melissa officinalis L.
is
main subject
of
wds:Q55969995-B5BDD8EB-837E-4685-8F4E-468DA275801E
wds:Q104884679-8A7E1118-69BC-4D0C-876C-5CEA10EA78AC
wds:Q60360623-00B22BA1-CF2E-43A6-A307-9865F8EFEF95
wds:Q104403111-BC45E19E-9727-4A75-8B15-BC28B276B013
wds:Q104846157-91B64CC5-F7F9-4277-932B-4423DD4FD4C7
wds:Q104847847-E19D6CA4-6D37-4D92-AB7E-2008A1E66547
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