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isoliquiritigenin

chemical compound
Class type of: chalcone, 2-phenylchromane flavonoid Q3155537

Facts

10 properties
Instance of
type of chemical entity
Subclass of
chalcone, 2-phenylchromane flavonoid[4][5]
Canonical SMILES
C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O[2]
Chemical formula
C₁₅H₁₂O₄[3]
Found in taxon
Calanticaria bicolor, Calanticaria brevifolia, Calanticaria greggii, liquorice, Butea monosperma, Tephrosia sinapou, Agapanthus africanus, Brosimum acutifolium, Clausena excavata, Crinum bulbispermum, Dahlia tenuicaulis, Dipteryx odorata, Dorstenia prorepens, Dracaena draco, Glycyrrhiza inflata, Glycyrrhiza pallidiflora, Lespedeza bicolor, Millettia usaramensis, Onobrychis viciifolia, Pancratium maritimum, Psorothamnus arborescens, Pterocarpus santalinus, Allium chinense, Artemisia ludoviciana, Ateleia herbert-smithii, Broussonetia papyrifera, cicer arietinum, Cissus sicyoides, Dalbergia louvelii, Dalbergia sissoides, Dalbergia sissoo, Dorstenia zenkeri, soybean, Glycyrrhiza aspera, Glycyrrhiza echinata, Glycyrrhiza uralensis, Hedysarum polybotrys, Helianthus angustifolius, common sunflower, Helianthus carnosus, Helianthus floridanus, Helianthus heterophyllus, Helianthus longifolius, Helianthus radula, Helianthus simulans, Isatis tinctoria, Luxemburgia octandra, Medicago sativa, Morus cathayana, Morus mongolica, Muntingia calabura, Platymiscium floribundum, Platymiscium yucatanum, Pterocarpus macrocarpus, Pterocarpus marsupium, Pueraria montana var. lobata, Senna lindheimeriana, Sinofranchetia chinensis, Sophora chrysophylla, Sophora mollis, Dendroviguiera splendens, Xanthorrhoea glauca, Zollernia paraensis, Anemarrhena asphodeloides, Dalbergia parviflora, Morinda citrifolia, Albizia julibrissin, Amburana cearensis, Artemisia palustris, Clematis hexapetala, Dalbergia retusa, Dracaena cambodiana, Erythrina fusca, Hydnophytum formicarum, Lespedeza cyrtobotrya, Millettia leucantha, Mimosa tenuiflora, Oxytropis falcata, Pterocarpus indicus, Robinia pseudoacacia, Medicago truncatula, Astragalus laxmannii, Biancaea decapetala, Wisteriopsis reticulata, Spatholobus sinensis, Bahiopsis laciniata, Bahiopsis parishii, Bahiopsis triangularis, Garcinia nervosa, Schnella guianensis, Dalbergia odorifera, Millettia vatkei, Toxicodendron vernicifluum, Euphorbia helioscopia, Crinum augustum, Artemisia campestris, Pisum sativum, Dermatophyllum gypsophilum, Cyclolobium brasiliense, Cyclolobium claussenii, Cissus discolor, Propolis, Saccharomonospora[6][7][8][9][10][11][12][13][14][15][16][17][18][19]
Has characteristic
bitterness
Isomeric SMILES
C1=CC(=CC=C1/C=C/C(=O)C2=C(C=C(C=C2)O)O)O
Mass
+256.074
Melting point
+186
Subject has role
enzyme inhibitor
🏷️ Also known as
en 2',4,4'-Trihydroxychalcone en (E)-1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)-2-propene-1-one en (E)-1-(2,4-Dihydroxy-phenyl)-3-(4-hydroxy-phenyl)-propenone en ILTG en isoliquiritigenin en trans-2',4,4'-trihydroxychalcone es Isoliquiritigenina fa ازوئگوئتیدین fr C15H12O4 fr isoliquiritigénine ja イソリクイリチゲニン
🔖 Identifiers · 32
OpenAlex ID
C2776974645
CAS Registry Number
961-29-5
Cannabis Database ID
005186
ChEBI ID
310312
ChEMBL ID
CHEMBL129795
ChemSpider ID
553829
DSSTOX compound identifier
DTXCID202466
DSSTox substance ID
DTXSID2022466
DrugBank ID
DB03285
EC number
677-489-8
ECHA Substance Infocard ID
100.202.617
Freebase ID
/m/0b5r4h
Show all 32 identifiers +20
Human Metabolome Database ID
HMDB0037316
InChI
InChI=1S/C15H12O4/c16-11-4-1-10(2-5-11)3-8-14(18)13-7-6-12(17)9-15(13)19/h1-9,16-17,19H/b8-3+
InChIKey
DXDRHHKMWQZJHT-FPYGCLRLSA-N
KEGG ID
C08650
KNApSAcK ID
C00006925, C00035173
LIPID MAPS ID
LMPK12120096
MassBank accession ID
MSBNK-BS-BS003260, MSBNK-BS-BS003261
MeSH descriptor ID
C040920
Microsoft Academic ID (discontinued)
2776974645
NMRShiftDB structure ID
10017704
PDB ligand ID
HCC
PDB structure ID
1FP1, 4RLU
Probes And Drugs ID
PD001236
PubChem CID
638278
Reaxys registry number
1914296
SPLASH
splash10-014r-0900000000-e7c4095e90f57884e80c, splash10-0a4i-0090000000-788e4464b6a542aa7c22, splash10-000i-1930000000-6d143294fc9a6a343052, splash10-0a4i-0751900000-7ab528549936a64f02c3, splash10-0nmu-3960000000-432bdec43fcc4c3cc08f, splash10-0a4i-0090000000-e0ef2b922828538142d6, splash10-0a4i-0000009000-afd1640b539ec58a4616
SureChEMBL ID
161168, 161169
UMLS CUI
C0045137
UNII
B9CTI9GB8F
UniChem compound ID
8121

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Found in taxon 87
soybean, Pisum sativum, common sunflower, cicer arietinum, liquorice, Medicago sativa, Robinia pseudoacacia, Morinda citrifolia +79 more
Has characteristic 1
bitterness
Subject has role 1
enzyme inhibitor
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Summary

isoliquiritigenin is a type of chemical entity[1].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . PubChem. Retrieved . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Flavonoids of Viguiera series Brevifoliae. wikidata.org.
  6. [7] ↑ . Flavonoids of Viguiera series Brevifoliae. wikidata.org.
  7. [8] ↑ . Flavonoids of Viguiera series Brevifoliae. wikidata.org.
  8. [9] ↑ . Application of supercritical fluid extraction to components of crude drugs and plants. III. Extraction of pigments from lithospermum root and licorice root. wikidata.org.
  9. [10] ↑ . Bioactive flavonoids of the flowers of Butea monosperma. wikidata.org.
  10. [11] ↑ . Potential cancer chemopreventive flavonoids from the stems of Tephrosia toxicaria. wikidata.org.
  11. [12] ↑ . Isolation and synthesis of a dimeric dihydrochalcone from Agapanthus africanus. wikidata.org.
  12. [13] ↑ . Flavonoids from Brosimum acutifolium. wikidata.org.
  13. [14] ↑ . Alkaloidal and other constituents from the root bark of Clausena excavata. wikidata.org.
  14. [15] ↑ . Minor phenolics from Crinum bulbispermum bulbs. wikidata.org.
  15. [16] ↑ . Flavonoids and polyacetylenes in Dahlia tenuicaulis. wikidata.org.
  16. [17] ↑ . Potential cancer chemopreventive constituents of the seeds of Dipteryx odorata (tonka bean).. wikidata.org.
  17. [18] ↑ . Chalcones and other constituents of Dorstenia prorepens and Dorstenia zenkeri. wikidata.org.
  18. [19] ↑ . Phenolic compounds of Dragon's blood from Dracaena draco. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). isoliquiritigenin. Retrieved November 11, 2026, from https://4ort.xyz/entity/isoliquiritigenin
MLA “isoliquiritigenin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 11 Nov. 2026, https://4ort.xyz/entity/isoliquiritigenin.
BibTeX @misc{4ortxyz_isoliquiritigenin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{isoliquiritigenin}}, year = {2026}, url = {https://4ort.xyz/entity/isoliquiritigenin}, note = {Accessed: 2026-11-11}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 20w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Instance of → type of chemical entity
    Has characteristic → bitterness
    Found in taxon → Calanticaria bicolor, Calanticaria brevifolia, Calanticaria greggii +1
    Subclass of → chalcone, 2-phenylchromane flavonoid
    + 3 other properties edited (see Wikidata diff for full list)
    "Changed [tr] labels, descriptions or aliases: QuickStatements 3.0 batch #37300"
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