(Q413192)

Falcarinol (English)

7 October 2016

2 references

inferred from InChIKey

(3S,9Z)-1,9-Heptadecadiene-4,6-diyn-3-ol

1 reference

(3R)-heptadeca-1,9-dien-4,6-diyn-3-ol

1 reference

(3S)-heptadeca-1,9-dien-4,6-diyn-3-ol

1 reference

chemical formula

C₁₇H₂₄O

1 reference

Falcarinol (English)

18 November 2016

CCCCCCCC=CCC#CC#CC(C=C)O

1 reference

Falcarinol (English)

18 November 2016

CCCCCCC/C=C\CC#CC#C[C@@H](C=C)O

1 reference

Antimycobacterial polyynes of Devil's Club (Oplopanax horridus), a North American native medicinal plant

Falcarinol (English)

18 November 2016

3 references

Antimycobacterial polyynes of Devil's Club (Oplopanax horridus), a North American native medicinal plant

Antimycobacterial polyynes of Devil's Club (Oplopanax horridus), a North American native medicinal plant

Angelica japonica

3 references

Antiproliferative constituents from umbelliferae plants. V. A new furanocoumarin and falcarindiol furanocoumarin ethers from the root of Angelica japonica

Novel antiproliferative falcarindiol furanocoumarin ethers from the root of Angelica japonica

Antiproliferative constituents from umbelliferae plants. V. A new furanocoumarin and falcarindiol furanocoumarin ethers from the root of Angelica japonica

Apium graveolens

2 references

Simultaneous HPLC Quantification of Two Dermatotoxins, 5-Methoxypsoralen and Falcarinol, in Healthy Celery

Bioactive polyacetylenes in food plants of the Apiaceae family: occurrence, bioactivity and analysis

Bunium paucifolium

1 reference

A sesquiterpene ketal from Bunium paucifolium

Chaerophyllum aureum

1 reference

Lignans, phenylpropanoids and polyacetylenes from Chaerophyllum aureum L. (Apiaceae).

Crithmum maritimum

1 reference

Bioactive metabolites from Sicilian marine fennel, Crithmum maritimum

Cussonia arborea

1 reference

Bioassay guided isolation of a new C18-polyacetylene, (+)-9(Z),17-octadecadiene-12,14-diyne-1,11,16-triol, from Cassonia barteri

Daucus carota

4 references

Analysis of myristicin and falcarinol in carrots by high-pressure liquid chromatography

Isolation and analysis of carrot constituents: myristicin, falcarinol, and falcarindiol

Isolation, identification, and bioassay of chemicals affecting nonpreference carrot-root resistance to carrot-fly larva.

Purple carrot (Daucus carota L.) polyacetylenes decrease lipopolysaccharide-induced expression of inflammatory proteins in macrophage and endothelial cells

Dendropanax arboreus

1 reference

Cytotoxic falcarinol oxylipins from Dendropanax arboreus

Eleutherococcus koreanus

1 reference

Studies on the chemical constituents ofAcanthopanax koreanum (II)

Eryngium dilatatum

1 reference

Acetylenes from roots of Eryngium bourgatii

Eryngium campestre

1 reference

Flavonolacyl glycosides of the aerial parts of Eryngium campestre

Fatsia japonica

1 reference

Glehnia littoralis

2 references

Furanocoumarin and polyacetylenic compound composition of wild Glehnia littoralis in North America

Chemical Constituents of the Halophyte Glehnia littoralis

Hedera canariensis

1 reference

Human maximization test of falcarinol, the principal contact allergen of English ivy and Algerian ivy (Hedera helix, H. canariensis).

Hedera helix

5 references

Allergic and irritant contact dermatitis from falcarinol and didehydrofalcarinol in common ivy (Hedera helix L.).

Human maximization test of falcarinol, the principal contact allergen of English ivy and Algerian ivy (Hedera helix, H. canariensis).

Polyacetylenes from the fruits of Hedera helix

The diacetylene 11,12-dehydrofalcarinol from Hedera helix

Heracleum moellendorffii

1 reference

Antiproliferative constituents in Umbelliferae plants II. Screening for polyacetylenes in some Umbelliferae plants, and isolation of panaxynol and falcarindiol from the root of Heracleum moellendorffii

Levisticum officinale

1 reference

Antimycobacterial polyacetylenes from Levisticum officinale

Niphogeton ternata

1 reference

Chemical constituents from the colombian medicinal plant Niphogeton ternata

Oenanthe javanica

2 references

A new phenylpropanoid glucoside and other constituents of Oenanthe javanica

A new phenylpropanoid glucoside and other constituents of Oenanthe javanica

Panax ginseng

9 references

Chemical Studies on Crude Drug Precession. I. On the Constituents of Ginseng Radix Rubra (1)

[Chemical studies on crude drug processing. V. On the constituents of ginseng radix rubra (2): Comparison of the constituents of white ginseng and red ginseng prepared from the same Panax ginseng root]

Determination of absolute stereochemistry of panaxynol

Extraction of panaxynol and panaxydol compounds from Korean ginseng

Isolation of cholesteryl ester transfer protein inhibitors from Panax ginseng roots

Polyacetylene analogs, isolated from hairy roots of Panax ginseng, inhibit Acyl-CoA : cholesterol acyltransferase

Polyacetylenes from Panax ginseng roots

The first specific antibody against cytotoxic polyacetylenic alcohol, panaxynol

Cytotoxic activity of polyacetylene compounds in Panax ginseng C. A. Meyer

Panax pseudoginseng

2 references

Bioactive saponins and glycosides. XIX. Notoginseng (3): immunological adjuvant activity of notoginsenosides and related saponins: structures of notoginsenosides-L, -M, and -N from the roots of Panax notoginseng (Burk.) F. H. Chen

Saponins of plants of Panax species collected in Central Nepal, and their chemotaxonomical significance. III.

American ginseng

2 references

Bioactive saponins and glycosides. XI. Structures of new dammarane-type triterpene oligoglycosides, quinquenosides I, II, III, IV, and V, from American ginseng, the roots of Panax quinquefolium L

Inducible nitric oxide synthase inhibitors from Saposhnikovia divaricata and Panax quinquefolium

parsley

2 references

C17 polyacetylenic alcohols as the major constituents in roots of Petroselinum crispum Mill. ssp. tuberosum

Bioactive polyacetylenes in food plants of the Apiaceae family: occurrence, bioactivity and analysis

Saposhnikovia divaricata

2 references

Analgesic components of saposhnikovia root (Saposhnikovia divaricata)

Inducible nitric oxide synthase inhibitors from Saposhnikovia divaricata and Panax quinquefolium

Schefflera arboricola

1 reference

The polyacetylenic falcarinol as the major allergen in schefflera arboricola

Schefflera tomentosa

1 reference

Schefflera venulosa

1 reference

Todaroa aurea

1 reference

Two phenylpropanoids from Todaroa aurea subsp. Suaveolens

Trevesia palmata

1 reference

Trevesia sundaica

1 reference

Panax bipinnatifidus var. bipinnatifidus

1 reference

Bioactive constituents from the roots of Panax japonicus var. major and development of a LC-MS/MS method for distinguishing between natural and artifactual compounds

Panax notoginseng

1 reference

Induction of apoptosis in human promyelocytic leukemia HL60 cells by panaxynol and panaxydol.

tomato

1 reference

Occurrence of Falcarinol and Falcarindiol In Tomato Plants after Infection with Verticillium albo-atrum and Characterization of Four Phytoalexins by Capillary Gas Chromatography-Mass Spectrometry

Didymopanax macrocarpus

1 reference

Polyacetylenes of Brazilian species of Didymopanax (Araliaceae)

Anethum graveolens

1 reference

Bioactive polyacetylenes in food plants of the Apiaceae family: occurrence, bioactivity and analysis

Pastinaca sativa

1 reference

Bioactive polyacetylenes in food plants of the Apiaceae family: occurrence, bioactivity and analysis

Eleutherococcus senticosus

2 references

Studies on the chemical constituents ofAcanthopanax koreanum (II)

Antifatigue activity of the liposoluble fraction from Acanthopanax senticosus

Eryngium bourgatii

1 reference

Acetylenes from roots of Eryngium bourgatii

Heptapleurum calyptratum

1 reference

InChI=1S/C17H24O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h4,10-11,17-18H,2-3,5-9,12H2,1H3/b11-10-/t17-/m1/s1

1 reference

0 references

0 references

0 references

Falcarinol

0 references

Identifiers

InChI

1 reference

Falcarinol (English)

18 November 2016

2 references

Falcarinol (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

21852-80-2

2 references

Global Substance Registration System

UNII

8P1DJD416I

panaxynol (English)

18 November 2016

https://commonchemistry.cas.org/detail?cas_rn=21852-80-2

10 April 2021

1 reference

(R)-(-)-Falcarinol (English)

18 November 2016

2 references

Falcarinol (English)

retrieved

18 November 2016

ChEBI ID

66722

mapping relation type

2 references

CHEMBL71260 (English)

retrieved

18 November 2016

International Chemical Identifier

InChI

InChI=1S/C17H24O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h4,10-11,17-18H,2-3,5-9,12H2,1H3/b11-10-/t17-/m1/s1

1 reference

CHEMBL71260 (English)

18 November 2016

2 references

inferred from InChIKey

Hazardous Substances Data Bank

1 reference

1 reference

28 October 2019

FALCARINOL (English)

10 May 2021

1 reference

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

Panaxynol (English)

7 October 2016

2 references

UNII

8P1DJD416I

panaxynol (English)

retrieved

18 November 2016

0 references

1 reference