Crinan-6,11-diol, 1,2-didehydro-3-methoxy-, (3beta,5alpha,6beta,11R,13beta,19alpha)- (Q105382717)

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group of stereoisomers with the chemical formula C₁₇H₁₉NO₅

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Language	Label	Description	Also known as
English	Crinan-6,11-diol, 1,2-didehydro-3-methoxy-, (3beta,5alpha,6beta,11R,13beta,19alpha)-	group of stereoisomers with the chemical formula C₁₇H₁₉NO₅

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

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canonical SMILES

OC1C2=CC=3OCOC3C=C2C45C=CC(OC)CC5N1CC4O

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found in taxon

Ungernia trisphaera

1 reference

stated in

Alkaloids of Ungernia 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

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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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