About: 11-hydroxysugiol

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: 11-hydroxysugiol Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

chemical compound

Attributes	Values
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) cheemesch Verbindung (lb) 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)
rdfs:label	11-hydroxysugiol (en)
skos:prefLabel	11-hydroxysugiol (en)
name	11-hydroxysugiol (en)
isomeric SMILES	wds:Q74410660-68A105DE-007F-407E-998E-968421364457
stereoisomer of	wds:Q74410660-5A82A2BF-DDBC-4B7C-B9AC-DD4390FDE91F
isomeric SMILES	CC(C)C1=C(C(=C2C(=C1)C(=O)C[C@@H]3[C@@]2(CCCC3(C)C)C)O)O
stereoisomer of	(4aS,10aR)-5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one
instance of	wds:Q74410660-E534F560-2452-4295-AD23-BB5BC8ADEC03
instance of	type of chemical entity
subclass of	wds:Q74410660-679246AF-0D9A-4315-B2B1-22ED897AEBD7 wds:Q74410660-9366E2E9-EBB7-44D0-8212-F104031F8356
subclass of	catechol 11-Hydroxy-sugiol
found in taxon	wds:Q74410660-0C3323B9-FDFF-4ECB-A497-AFE87992DDC6 wds:Q74410660-2447D8BA-70E2-4665-9928-45273797BD80 wds:Q74410660-71E6CEA6-1255-4044-AAB5-3EE5EAB2078F wds:Q74410660-8883295F-037A-4389-B809-F3AF389A8010 wds:Q74410660-A1747E23-BC86-44E9-A1AC-54792F2AED91 wds:Q74410660-B522ADD4-046B-43AC-8EC4-F702BDA56944 wds:Q74410660-BD8D1F93-D44B-4F15-AB3D-2CF7ACC5DFDD wds:Q74410660-E1EB459F-4D4F-4A9C-837B-AACAF1D401C6 wds:Q74410660-F5E92C9D-4BAF-45B4-AC2E-B04EEEB504BC
found in taxon	Cryptomeria Salvinia adnata Plectranthus hadiensis Salvia canariensis Salvia broussonetii Crossopetalum gaumeri Salvia phlomoides Salvia montbretii Coleus hadiensis
UniChem compound ID	wds:Q74410660-BA122208-6D94-441E-B08D-E3089434B406
Reaxys registry number	wds:Q74410660-27332DE4-8FFD-44A5-B53D-1EF7A2FF4CCD
canonical SMILES	wds:Q74410660-DF39F65B-5322-4E21-B6DA-CF5868D1A59A
InChI	wds:Q74410660-DB6F2B3C-8199-4945-82E1-095849897E56
InChIKey	wds:Q74410660-6F39D827-4DA3-4471-BDB9-978A15A882D3
chemical formula	wds:Q74410660-781E4B82-70F5-44C1-BF42-ABD7BF4BD364
PubChem CID	wds:Q74410660-3F027068-6FAC-443A-B016-F3D3EBAF275E
ChEBI ID	wds:Q74410660-E3972A19-9731-42D5-B32D-CA3D6A2F2CB4
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10403490
ChEBI ID	http://purl.obolibrary.org/obo/CHEBI_138962
UniChem compound ID	33143204
Reaxys registry number	2060230
canonical SMILES	O=C1C=2C=C(C(O)=C(O)C2C3(C)CCCC(C)(C)C3C1)C(C)C
InChI	InChI=1S/C20H28O3/c1-11(2)12-9-13-14(21)10-15-19(3,4)7-6-8-20(15,5)16(13)18(23)17(12)22/h9,11,15,22-23H,6-8,10H2,1-5H3/t15-,20-/m0/s1
InChIKey	GDLRDIDXYBIPFY-YWZLYKJASA-N
chemical formula	C₂₀H₂₈O₃
PubChem CID	10403490
ChEBI ID	138962
mass	wds:Q74410660-49DAA0C2-901E-49F9-A496-417D161E2DC6
mass	316.203844756 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74410660
is stereoisomer of of	(4aS,10aR)-5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one
is stereoisomer of of	wds:Q105006783-388156C6-3E13-4189-A459-8B8BCE636CEE
is main subject of	Cytotoxic compounds from invasive giant salvinia (Salvinia molesta) against human tumor cells Abietanes and kauranes from leaves of Cryptomeria japonica Labdanes from Cryptomeria japonica Abietane diterpenoids from the bark of Cryptomeria fortunei Diterpenes from Salvia broussonetii transformed roots and their insecticidal activity

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 172 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software