(Q27107626)

inferred from SMILES

chemical structure

Parthenin.svg
360 × 430; 25 KB

0 references

mass

262.120509±0 dalton

1 reference

UNII-982DJP4W6A (English)

5 October 2016

2 references

inferred from InChIKey

(3aR,6S,6aS,9aS,9bR)-6a-hydroxy-6,9a-dimethyl-3-methylidene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione

inferred from InChI

1 reference

(3aS,6R,6aS,9aS,9bS)-6a-hydroxy-6,9a-dimethyl-3-methylidene-4,5,6,9b-tetrahydro-3aH-azuleno[8,7-b]furan-2,9-dione

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₁₅H₁₈O₄

1 reference

UNII-982DJP4W6A (English)

20 November 2016

canonical SMILES

CC1CCC2C(C3(C1(C=CC3=O)O)C)OC(=O)C2=C

1 reference

UNII-982DJP4W6A (English)

20 November 2016

isomeric SMILES

C[C@H]1CC[C@@H]2[C@H]([C@]3([C@]1(C=CC3=O)O)C)OC(=O)C2=C

1 reference

UNII-982DJP4W6A (English)

20 November 2016

found in taxon

Parthenium hysterophorus

27 references

Sesquiterpene lactones in various populations of Parthenium hysterophorus

Ecogeographic distribution of secondary constituents in Parthenium (compositae)

The sesquiterpene lactone chemistry of the genus Parthenium (compositae)

Flavonoids of four species of Parthenium (compositae)

Charminarone, a seco-Pseudoguaianolide from Parthenium hysterophorus.

Characterization of a toxin fromParthenium hysterophorus and its mode of excretion in animals

Structural analysis of sesquiterpene lactones from Hymenoclea salsola

Dihydroparthenin, a pseudoguaianolide from tissue culture of Parthenium hysterophorus

Sesquiterpene lactone variability in Parthenium hysterophorus L

Minor sesquiterpenes of flowers of Parthenium hysterophorus

Pseudoguaianolides from the flowers of Parthenium hysterophorus

Chemotaxonomy of Parthenium: P. Hysterophorus—P. Glomeratum

Three ambrosanolides from Parthenium hysterophorus

Parthenin, a sesquiterpene lactone of Parthenium hysterophorus L. is a high toxicity clastogen

Effects of Sesquiterpene Lactones on Development of Aedes atropalpus and Relation to Partition Coefficient

Plant based antiamoebic drugs; Part II. Amoebicidal activity of parthenin isolated from Parthenium hysterophorus

Occurrence of hysterin and dihydroisoparthenin in Parthenium hysterophorus

Occurrence of hysterin and dihydroisoparthenin in Parthenium hysterophorus

Two New Pseudoguaianolides from the Flowers ofParthenium hysterophorus

Acetylated pseudoguaianolides from Parthenium hysterophorus and their cytotoxic activity

A new highly oxygenated pseudoguaianolide from a collection of the flowers of Parthenium hysterophorus

Chemotaxonomy of Parthenium: P. Hysterophorus—P. Glomeratum

Determination of parthenin in Parthenium hysterophorus L. by means of HPLC-UV: Method development and validation

Coronopilin—another major sesquiterpene lactone in Parthenium hysterophorus

Pseudoguaianolides from the flowers of Parthenium hysterophorus

Minor sesquiterpenes of flowers of Parthenium hysterophorus

Dihydroparthenin, a pseudoguaianolide from tissue culture of Parthenium hysterophorus

Stylissa carteri

1 reference

New alkaloids from the indopacific sponge Stylissa carteri

Ambrosia maritima

4 references

Sesquiterpene lactones from Ambrosia maritima (Damssissa)

Sesquiterpene lactones from Ambrosia maritima (Damssissa)

New Pseudoguaianolides from Ambrosia maritima

Sesquiterpene lactones from Ambrosia maritima (Damssissa)

Dichrocephala integrifolia

2 references

Pseudoguaiane-type sesquiterpenes and inhibitors on nitric oxide production from Dichrocephala integrifolia

Pseudoguaiane-type sesquiterpenes and inhibitors on nitric oxide production from Dichrocephala integrifolia

Ambrosia monogyra

1 reference

Pseudoguaianolides and other constituents from Hymenoxys linearifolium

Ambrosia psilostachya

1 reference

Arrivacins, novel pseudoguaianolide esters with potent angiotensin II binding activity from Ambrosia psilostachya

Ambrosia artemisiifolia

2 references

New Pseudoguaianolides from Ambrosia maritima

Sesquiterpene lactones from Ambrosia maritima (Damssissa)

1 reference

Identifiers

InChI

InChI=1S/C15H18O4/c1-8-4-5-10-9(2)13(17)19-12(10)14(3)11(16)6-7-15(8,14)18/h6-8,10,12,18H,2,4-5H2,1,3H3/t8-,10-,12+,14-,15+/m0/s1

1 reference

UNII-982DJP4W6A (English)

20 November 2016

2 references

UNII-982DJP4W6A (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

508-59-8

2 references

Global Substance Registration System

UNII

982DJP4W6A

parthenin (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=508-59-8

10 April 2021

1 reference

parthenicin (English)

20 November 2016

1 reference

UNII-982DJP4W6A (English)

20 November 2016

ChEBI ID

7938

mapping relation type

2 references

PARTHENIN (English)

20 November 2016

International Chemical Identifier

InChI

InChI=1S/C15H18O4/c1-8-4-5-10-9(2)13(17)19-12(10)14(3)11(16)6-7-15(8,14)18/h6-8,10,12,18H,2,4-5H2,1,3H3/t8-,10-,12+,14-,15+/m0/s1

1 reference

PARTHENIN (English)

20 November 2016

2 references

inferred from InChIKey

1 reference

NMRShiftDB structure ID

20028270

1 reference

DSSTox substance ID

DTXSID40877834

1 reference

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

Parthenin (English)

5 October 2016

2 references

UNII

982DJP4W6A

parthenin (English)

20 November 2016

1 reference

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

Parthenin (English)

5 October 2016

1 reference