(Q27108515)

(1S,3R,5S,7R,10R,12R,14R,15R,18R,19R,22S,23R)-10,22-dihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2H-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.03,12.05,10.015,23.018,22]pentacosane-14-carbaldehyde

Uscharidin (English)

5 October 2016

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₂₉H₃₈O₉

1 reference

Uscharidin (English)

20 November 2016

CC1CC(=O)C2(C(O1)OC3CC4CCC5C(C4(CC3O2)C=O)CCC6(C5(CCC6C7=CC(=O)OC7)O)C)O

1 reference

Uscharidin (English)

20 November 2016

C[C@@H]1CC(=O)[C@]2([C@@H](O1)O[C@@H]3C[C@@H]4CC[C@@H]5[C@@H]([C@]4(C[C@H]3O2)C=O)CC[C@]6([C@@]5(CC[C@@H]6C7=CC(=O)OC7)O)C)O

1 reference

Nutrient and cardenolide composition of unextracted and solvent-extracted Calotropis procera

Uscharidin (English)

20 November 2016

1 reference

Asclepias curassavica

8 references

New cardenolide and acylated lignan glycosides from the aerial parts of Asclepias curassavica

Biosynthetic preparation of cardenolides from [1-14C]acetic acid by stem discs of the milkweed Asclepias curassavica

Cardenolide biosynthesis from malonate in Asclepias curassavica

Cardenolide biosynthesis from acetate in Asclepias curassavica

Some quantitative aspects of cardenolide synthesis from malonate inAsclepias curassa vica

Cytotoxic principles from the formosan milkweed, Asclepias curassavica

Cytotoxicity of cardenolides and cardenolide glycosides from Asclepias curassavica

New cardenolide and acylated lignan glycosides from the aerial parts of Asclepias curassavica

Gomphocarpus fruticosus

1 reference

Cardenolide glycosides of the asclepiadaceae. New glycosides from asclepias fruticosa and the stereochemistry of uscharin, voruscharin and calotoxin

Thymus vulgaris

1 reference

Influence of fibre coating in headspace solid-phase microextraction-gas chromatographic analysis of aromatic and medicinal plants

Asclepias subulata

1 reference

Cardenolides and a lignan from asclepias subulata

Identifiers

InChI

InChI=1S/C29H38O9/c1-15-9-23(31)29(34)25(36-15)37-21-11-17-3-4-20-19(27(17,14-30)12-22(21)38-29)5-7-26(2)18(6-8-28(20,26)33)16-10-24(32)35-13-16/h10,14-15,17-22,25,33-34H,3-9,11-13H2,1-2H3/t15-,17 ,18-,19 ,20-,21-,22-,25 ,26-,27-,28 ,29 /m1/s1

1 reference

Uscharidin (English)

20 November 2016

2 references

Uscharidin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

24321-47-9

1 reference

Global Substance Registration System

UNII

2GU13C5298

uscharidin (English)

20 November 2016

1 reference

2,14-Dihydroxy-19-oxo-3-[(tetrahydro-6-methyl-2,3-dioxo-2H-pyran-2-yl)oxy]card-20(22)-enolide (English)

20 November 2016

2 references

Uscharidin (English)

20 November 2016

ChEBI ID

9913

mapping relation type

2 references

USCHARIDIN (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C29H38O9/c1-15-9-23(31)29(34)25(36-15)37-21-11-17-3-4-20-19(27(17,14-30)12-22(21)38-29)5-7-26(2)18(6-8-28(20,26)33)16-10-24(32)35-13-16/h10,14-15,17-22,25,33-34H,3-9,11-13H2,1-2H3/t15-,17 ,18-,19 ,20-,21-,22-,25 ,26-,27-,28 ,29 /m1/s1

1 reference

USCHARIDIN (English)

20 November 2016

2 references

inferred from InChIKey

1 reference

1 reference

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

Uscharidin (English)

5 October 2016

2 references

UNII

2GU13C5298

uscharidin (English)

20 November 2016

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

Uscharidin (English)

5 October 2016

1 reference

31 December 2022