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(Q105382717)
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English
Crinan-6,11-diol, 1,2-didehydro-3-methoxy-, (3beta,5alpha,6beta,11R,13beta,19alpha)-
group of stereoisomers with the chemical formula C₁₇H₁₉NO₅
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Statements
instance of
group of stereoisomers
0 references
subclass of
5,10b-ethanophenanthridine alkaloid
1 reference
inferred from
5,10b-ethanophenanthridine alkaloid
mass
317.126322708
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₁₇H₁₉NO₅
0 references
canonical SMILES
OC1C2=CC=3OCOC3C=C2C45C=CC(OC)CC5N1CC4O
0 references
found in taxon
Ungernia trisphaera
1 reference
stated in
Alkaloids ofUngernia vvedenskyi
Hymenocallis arenicola
2 references
stated in
Alkaloids fromHymenocallis littoralis
stated in
Antiproliferative amaryllidaceae alkaloids isolated from the bulbs of Sprekelia formosissima and Hymenocallis x festalis
Pancratium foetidum
1 reference
stated in
Two New Alkaloids of the Crinane Series from Pancratium sickenbergeri
Narcissus cuneiflorus
1 reference
stated in
Isolation of O-methylmaritidine from bulbs of Narcissus tazetta L.
Narcissus asturiensis
1 reference
stated in
Isolation of O-methylmaritidine from bulbs of Narcissus tazetta L.
Crinum bulbispermum
3 references
stated in
Alkaloids from Crinum delagoense1Part 6 in the series “Alkaloids from South African Amaryllidaceae”. For part 5 see ref.[1].1
stated in
The alkaloidal constituents of Goda-manel (Crinum zeylanicum L.), a Sri Lankan folk medicine
stated in
Alkaloids of the Amaryllidaceae. 27. Structures of 9-O-demethylhomolycorine and 5.alpha.-hydroxyhomolycorine. Alkaloids of Crinum defixum, C. scabrum, and C. latifolium. Assignment of aromatic substitution patterns from 1H-coupled carbon-13 spectra
Pancratium trianthum
1 reference
stated in
Two New Alkaloids of the Crinane Series from Pancratium sickenbergeri
Pancratium canariense
1 reference
stated in
Two New Alkaloids of the Crinane Series from Pancratium sickenbergeri
Narcissus tazetta
1 reference
stated in
Alkaloids from Narcissus asturiensis
Crinum zeylanicum
3 references
stated in
Alkaloids of the Amaryllidaceae. 27. Structures of 9-O-demethylhomolycorine and 5.alpha.-hydroxyhomolycorine. Alkaloids of Crinum defixum, C. scabrum, and C. latifolium. Assignment of aromatic substitution patterns from 1H-coupled carbon-13 spectra
stated in
Alkaloids from Crinum bulbispermum
stated in
Alkaloids from Crinum delagoense1Part 6 in the series “Alkaloids from South African Amaryllidaceae”. For part 5 see ref.[1].1
Identifiers
InChI
InChI=1S/C17H19NO5/c1-21-9-2-3-17-11-6-13-12(22-8-23-13)5-10(11)16(20)18(7-15(17)19)14(17)4-9/h2-3,5-6,9,14-16,19-20H,4,7-8H2,1H3
0 references
InChIKey
ZSTPNQLNQBRLQF-UHFFFAOYSA-N
0 references
PubChem CID
544807
1 reference
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
UniChem compound ID
48552767
1 reference
stated in
UniChem
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