(Q27137421)

Licoricidin (English)

4-[(3S)-7-hydroxy-5-methoxy-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-3-yl]-2-(3-methylbut-2-enyl)benzene-1,3-diol

7 October 2016

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

chemical formula

C₂₆H₃₂O₅

1 reference

Licoricidin (English)

7 October 2016

canonical SMILES

CC(=CCC1=C(C=CC(=C1O)C2CC3=C(C(=C(C=C3OC2)O)CC=C(C)C)OC)O)C

1 reference

Licoricidin (English)

7 October 2016

isomeric SMILES

CC(=CCC1=C(C=CC(=C1O)[C@H]2CC3=C(C(=C(C=C3OC2)O)CC=C(C)C)OC)O)C

1 reference

Licoricidin (English)

7 October 2016

found in taxon

Glycyrrhiza uralensis

9 references

Five New Isoprenoid-substitued Flavonoids, Kanzonols F - J, from Glycyrrhiza uralensis

Studies on the Index Compounds for HPLC Analysis of Glycyrrhiza uralensis

Hexane-ethanol extract of Glycyrrhiza uralensis containing licoricidin inhibits the metastatic capacity of DU145 human prostate cancer cells

Isoflavonoids and coumarins from Glycyrrhiza uralensis: antibacterial activity against oral pathogens and conversion of isoflavans into isoflavan-quinones during purification

Anti-Helicobacter pylori flavonoids from licorice extract

Phenolic constituents of licorice. VIII. Structures of glicophenone and glicoisoflavanone, and effects of licorice phenolics on methicillin-resistant Staphylococcus aureus

Isoflavonoids and coumarins from Glycyrrhiza uralensis: antibacterial activity against oral pathogens and conversion of isoflavans into isoflavan-quinones during purification

Preliminary evaluation of antinephritis and radical scavenging activities of glabridin from Glycyrrhiza glabra.

Isoflavonoids and coumarins from Glycyrrhiza uralensis: antibacterial activity against oral pathogens and conversion of isoflavans into isoflavan-quinones during purification

Glycyrrhiza

2 references

Four New Phenolic Constituents from Licorice (Root of Glycyrrhiza Sp.)

Structures of Six Isoprenoid-substituted Flavonoids, Gancaonins F, G, H, I, Glycyrol, and Isoglycyrol from Xibei Licorice (Glycyrrhiza Sp.)

Glycyrrhiza aspera

1 reference

Four New Prenylated Flavonoids, Glyasperins A, B, C, and D from the Roots of Glycyrrhiza aspera

liquorice

1 reference

Inhibition of lysoPAF acetyltransferase activity by components of licorice root

Lycoris traubii

1 reference

New lycorine-type alkaloid from Lycoris traubii and evaluation of antitrypanosomal and antimalarial activities of lycorine derivatives

Identifiers

InChI

InChI=1S/C26H32O5/c1-15(2)6-8-19-22(27)11-10-18(25(19)29)17-12-21-24(31-14-17)13-23(28)20(26(21)30-5)9-7-16(3)4/h6-7,10-11,13,17,27-29H,8-9,12,14H2,1-5H3/t17-/m0/s1

1 reference

Licoricidin (English)

7 October 2016

2 references

Licoricidin (English)

7 October 2016

ChEBI release 2020-09-01

2 references

licoricidin (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=30508-27-1

10 April 2021

1 reference

4-[(3R)-7-Hydroxy-5-methoxy-6-(3-methyl-2-buten-1-yl)-3,4-dihydro-2H-chromen-3-yl]-2-(3-methyl-2-buten-1-yl)-1,3-benzenediol (English)

7 October 2016

2 references

Licoricidin (English)

7 October 2016

Reaxys registry number

5362788

1 reference

licoricidin (English)

7 October 2016

ChEBI ID

69082

mapping relation type

2 references

licoricidin (English)

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C26H32O5/c1-15(2)6-8-19-22(27)11-10-18(25(19)29)17-12-21-24(31-14-17)13-23(28)20(26(21)30-5)9-7-16(3)4/h6-7,10-11,13,17,27-29H,8-9,12,14H2,1-5H3/t17-/m0/s1

1 reference

LICORICIDIN (English)

7 October 2016

2 references

inferred from InChIKey

splash10-0hg9-0913000000-ec2bfa032d0d078ebbb3

1 reference

0 references

DSSTox substance ID

DTXSID30952821

1 reference

DSSTOX compound identifier

0 references

2 references

Global Substance Registration System

UNII

929XTD20VK

LICORICIDIN (English)

7 October 2016

1 reference

licoricidin (English)