About: Vittatine, 11-hydroxy-

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About: Vittatine, 11-hydroxy- Goto Sponge NotDistinct Permalink

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group of stereoisomers with the chemical formula C₁₆H₁₇NO₄

Attributes	Values
rdf:type	Item
description	groep van stereo-isomeren (nl) group of stereoisomers with the chemical formula C₁₆H₁₇NO₄ (en) група стереоізомерів з хімічною формулою C₁₆H₁₇NO₄ (uk)
rdfs:label	Vittatine, 11-hydroxy- (en)
skos:prefLabel	Vittatine, 11-hydroxy- (en)
name	Vittatine, 11-hydroxy- (en)
instance of	wds:Q105146845-D6743482-1120-44A7-AC79-BB18A95931F0
instance of	group of stereoisomers
subclass of	wds:Q105146845-B61AF871-C1D3-4D8F-BA69-D4A3102CA5DF
subclass of	5,10b-ethanophenanthridine alkaloid
found in taxon	wds:Q105146845-0E0556F2-A658-4E85-B8EC-9D1497F65D52 wds:Q105146845-5621ABCA-3A16-4CA3-AF9D-6B269E64A62E wds:Q105146845-AE92F3C0-7969-49FC-8CDF-C1881E832717 wds:Q105146845-C702324A-6E5A-4348-8FA0-98410562B768 wds:Q105146845-C9BAB7D9-57A6-4D81-9321-AFFC9422B6CC
found in taxon	Brunsvigia josephinae Crinum asiaticum Galanthus elwesii Crinum asiaticum var. sinicum Brunsvigia radulosa
UniChem compound ID	wds:Q105146845-C46B96D0-E6C2-4A91-8258-B73115CE26FE
canonical SMILES	wds:Q105146845-C166806A-ABD6-439F-B006-5FC37CDB0025
InChI	wds:Q105146845-8A4AAAD6-F51C-441D-A49A-426D28EF9F3F
InChIKey	wds:Q105146845-82CD1994-5865-4290-A41E-EB930A25A2A4
chemical formula	wds:Q105146845-9028498B-10DF-4C53-87C7-603FA920A03E
PubChem CID	wds:Q105146845-3FA397BB-2BD6-44B7-B102-38EB5D32C3A4
PubChem CID	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID602595
UniChem compound ID	32698640
canonical SMILES	OC1C=CC23C4=CC=5OCOC5C=C4CN(CC2O)C3C1
InChI	InChI=1S/C16H17NO4/c18-10-1-2-16-11-5-13-12(20-8-21-13)3-9(11)6-17(7-15(16)19)14(16)4-10/h1-3,5,10,14-15,18-19H,4,6-8H2
InChIKey	KWAOMPWGIIXDPH-UHFFFAOYSA-N
chemical formula	C₁₆H₁₇NO₄
PubChem CID	602595
mass	wds:Q105146845-414AAD2B-7CF5-48A4-8228-BFD73F0FEC08
mass	287.115758024 (xsd:decimal)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q105146845
is subclass of of	bulbispermine (11S,13beta,19S)-1,2-Didehydrocrinan-3alpha,11-diol (1S,13S,15S,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.0¹,¹³.0²,¹⁰.0⁴,⁸]nonadeca-2,4(8),9,16-tetraene-15,18-diol hamayne (1R,13S,15R,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-15,18-diol
is subclass of of	wds:Q82096697-81806F23-7110-4A70-9BA9-315C0A293B97 wds:Q105146833-FA5D787B-7B7B-490D-AD95-0C893F6D9617 wds:Q105146838-8DDCCB65-20AC-4D68-9504-E551CE5D9A1E wds:Q105146840-2022ED01-B9DC-4B82-9253-FC6738FFED49 wds:Q104394675-FD1A99B1-1045-4A57-8448-7F2C407DF185
is main subject of	Alkaloids from Crinum lugardiae Alkaloids from Crinum kirkii Alkaloids from Galanthus nivalis Comprehensive study of alkaloids from Crinum asiaticum var. sinicum assisted by HPLC-DAD-SPE-NMR Further alkaloids from Brunsvigia josephinae Alkaloids from Crinum bulbispermum Investigation of the alkaloidal constituents of Crinum bulbispermum. Part II. Isolation and identification of crinamine, and other three alkaloids Choline esterase inhibitory properties of alkaloids from two Nigerian Crinum species Alkaloidal Constituents of Crinum bulbispermum III: Bulbispermine, a New Alkaloid of Crinum bulbispermum1. Bioactive alkaloids from Brunsvigia radulosa The alkaloidal constituents of Goda-manel (Crinum zeylanicum L.), a Sri Lankan folk medicine. Alkaloids from Crinum delagoense1Part 6 in the series “Alkaloids from South African Amaryllidaceae”. For part 5 see ref.[1].1
is main subject of	wds:Q47437828-7DE2FFD9-B750-4EB2-87EE-BD655FE16BE4 wds:Q46334649-6F9846E0-7FC9-4067-B21D-3F67EF00BD47 wds:Q104986101-92A837F8-1C66-460F-877C-1BEA4183472D wds:Q45121385-F923350B-D737-4B25-B06F-AA07B8A8604C wds:Q62141739-11134F49-3EC4-40D3-955E-9ED0EB3DCE3A wds:Q105146837-02EA8BA7-6C6D-4FE2-AC31-5B65ECEBF421 wds:Q95453208-64054BE1-4460-456D-A83D-11D7BD34868C wds:Q104990839-436F3005-1008-4A4F-BA94-10F92AD1DAD7 wds:Q46983505-822D997A-D7E1-467B-80A7-7DB5DA3A5D5D wds:Q38985267-ECE6587E-2220-41FA-9D35-CF62F1F08807 wds:Q73564044-000790DF-6BFD-4364-98FF-43C8D45CE3B5 wds:Q80255964-207C1D02-715A-44CC-B444-8D3700C1F918

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