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Toroko base II
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group of stereoisomers with the chemical formula C₂₅H₄₁NO₆
Attributes
Values
rdf:type
Item
description
groep van stereo-isomeren
(nl)
група стереоізомерів з хімічною формулою C₂₅H₄₁NO₆
(uk)
group of stereoisomers with the chemical formula C₂₅H₄₁NO₆
(en)
rdfs:label
Toroko base II
(en)
skos:prefLabel
Toroko base II
(en)
name
Toroko base II
(en)
isomeric SMILES
wds:Q104974642-98AC70DC-1F8F-4CBB-98DC-3FA1789A578A
isomeric SMILES
CCN1C[C@]2(COC)CC[C@H](OC)[C@]34C1[C@H]([C@H](OC)[C@H]23)[C@@]1(O)C[C@H](OC)[C@H]2C[C@@H]4[C@@H]1[C@H]2O
instance of
wds:Q104974642-B2EBE3D7-A65B-4299-ADE9-5D9BBC0B2D11
instance of
group of stereoisomers
subclass of
wds:Q104974642-DF43397E-5A31-49A2-9D7D-293B23C3875A
subclass of
(2R,3R,4S,5S,6S,8R,13S,16S,17R,18R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol
found in taxon
wds:Q104974642-03448A56-091D-4B29-8823-FD7818B3F37F
wds:Q104974642-4EEFF88E-7EEE-4CC8-B383-4F9A879478EC
wds:Q104974642-5AC114C4-6141-4C3F-ADA3-1A2C8C658A76
wds:Q104974642-61D9DC65-9F62-423F-8625-0C58EC284F30
wds:Q104974642-67F4718D-757F-4A14-8177-DE174E0E18CF
wds:Q104974642-76EAA5D5-F3DC-44AE-B7D3-30A7C42CA80B
wds:Q104974642-890BC3EF-AF2D-45E7-AB53-CDAD31E1685A
wds:Q104974642-8F2B3310-3573-4496-B46A-0A5D7E83DBFF
wds:Q104974642-952EB5A0-897B-4740-AC4C-58758A557339
wds:Q104974642-AF39550C-9A74-4F3C-AAA5-06E2E80C6310
wds:Q104974642-BAC4BDD4-250A-41DA-9DAB-1FDA20C5946E
wds:Q104974642-BD4993D9-C5AC-4C19-9F74-6425E1E6C911
wds:Q104974642-F6503AC1-16CA-4119-9D9B-0BFDD0A138CE
found in taxon
Aconitum carmichaelii
Aconitum henryi
Aconitum
Delphinium staphisagria
Delphinium staphisagria
Aconitum napellus
Aconitum burnatii
Aconitum episcopale
Aconitum hemsleyanum
Aconitum forrestii
Aconitum carmichaeli
Aconitum sungpanense
Aconitum nevadense
UniChem compound ID
wds:Q104974642-A2B4A694-D814-44F3-8FD2-15225B9C7ACF
canonical SMILES
wds:Q104974642-63B7F27D-47A4-4EC5-A794-A6BAC26CC19C
InChI
wds:Q104974642-F53CF538-B384-4961-A17A-E5743CB955E4
InChIKey
wds:Q104974642-F14A7C32-4F60-4BCB-A3F3-7B3B9F214939
chemical formula
wds:Q104974642-67352D81-941B-4930-A855-DFCE798491F2
PubChem CID
wds:Q104974642-B3C53C3E-57CD-47F9-959B-0D95A745B123
ChEBI ID
wds:Q104974642-4DCCF583-21A8-45D8-B95F-E8690BCA597A
PubChem CID
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20055812
ChEBI ID
http://purl.obolibrary.org/obo/CHEBI_132641
UniChem compound ID
60680583
canonical SMILES
OC1C2CC3C1C(O)(CC2OC)C4C(OC)C5C6(COC)CN(CC)C4C35C(OC)CC6
InChI
InChI=1S/C25H41NO6/c1-6-26-11-23(12-29-2)8-7-16(31-4)25-14-9-13-15(30-3)10-24(28,17(14)19(13)27)18(22(25)26)20(32-5)21(23)25/h13-22,27-28H,6-12H2,1-5H3/t13-,14-,15+,16+,17-,18+,19+,20+,21-,22?,23+,24-,25+/m1/s1
InChIKey
DBODJJZRZFZBBD-RIVIBFSZSA-N
chemical formula
C₂₅H₄₁NO₆
PubChem CID
20055812
ChEBI ID
132641
mass
wds:Q104974642-7E49D6D0-91C8-4702-B9FF-E8D1ADBE1FA8
mass
451.293388032
(
xsd:decimal
)
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q104974642
is
subclass of
of
(1S,2R,3R,4R,5S,6R,8R,9R,10R,13S,16R,17R,18S)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol
Chasmanine
(1S,2R,3R,4S,5S,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol
is
subclass of
of
wds:Q72516752-8A110F95-87DE-4732-B22D-B66B847B8E72
wds:Q104974643-010082BB-0DB5-4573-ADB4-27C5F5E27B12
wds:Q104974647-5AA77314-96D9-4363-9662-A60596123119
is
main subject
of
Hemsleyatine, a Novel C19-Diterpenoid Alkaloid with 8-Amino Group from Aconitum hemsleyanum
Alkaloids from Delphinium staphisagria
Feeding deterrents from Aconitum episcopale roots against the red flour beetle, Tribolium castaneum.
The Diterpenoid Alkaloids from Aconitum napellus
Hypaconitine, the dominant constituent responsible for the neuromuscular blocking action of the Japanese-sino medicine "bushi" (aconite root)
The Structures of Forestine and Foresticine, Two New C19-Diterpenoid Alkaloids from Aconitum forrestii Stapf
Diterpenoid Alkaloids from Aconitum crassicaule
Hemsleyatine, a Novel C19-Diterpenoid Alkaloid with 8-Amino Group from Aconitum hemsleyanum.
Nevadenine and Nevadensine, Two New Diterpenoid Alkaloids from Aconitum nevadense Vechtr.
New Alkaloids from Delphinium staphisagria
Diterpenoid Alkaloids of Aconitum sungpanase
Diterpenoid alkaloids from Delphinium gracile
is
main subject
of
wds:Q33917068-9882A792-77D9-4FD2-9EA1-C5194049068C
wds:Q73367547-47AA856E-BA9B-47C2-B995-E00A2EA9F5DA
wds:Q104911441-2FC45ACD-D9D5-4770-B6C1-F9D6AA2A2721
wds:Q81244116-9A05CDCA-B59B-4A12-A400-8D04D13FCAD8
wds:Q79704174-C87BF936-F2DA-47A8-A9CD-F3F76C77BF7D
wds:Q104974644-354C6517-465E-4FAC-B28F-3C5B70F56039
wds:Q104974646-A375CD4B-4566-4EBC-AE6C-CB07875349D3
wds:Q50542172-30383204-00A0-4BED-B9D5-3547D9B17B03
wds:Q104393766-0CBD4A13-D0DB-4F23-BE96-094B9648EE9E
wds:Q104390796-EA27B32F-64FD-4F2B-A19E-A2DEA2778968
wds:Q68003441-C308AABB-3FA5-4E1F-A4F8-0A023AA91EEE
wds:Q104923883-AAED3B19-5B65-411D-B3BE-73016BA4AB31
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