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Licoricidin

PubChem CID: 480865

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Compound Synonyms Licoricidin, 30508-27-1, CHEBI:69082, UNII-929XTD20VK, 929XTD20VK, LICORISOFLAVAN B, 7-O-DEMETHYLLICORISOFLAVAN A, 4-[(3R)-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, 4-((R)-7-Hydroxy-5-methoxy-6-(3-methyl-but-2-enyl)-1-benzopyran-3-yl)-2-((E)-3-methyl-but-2-enyl)-benzene-1,3-diol, 4-[(3r)-7-hydroxy-5-methoxy-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-2h-chromen-3-yl]-2-(3-methylbut-2-en-1-yl)benzene-1,3-diol, 4-[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, 2',4',7'-trihydroxy-5-methoxy-3',6-diisopentenyl-isoflavan, 1,3-BENZENEDIOL, 4-((3R)-3,4-DIHYDRO-7-HYDROXY-5-METHOXY-6-(3-METHYL-2-BUTENYL)-2H-1-BENZOPYRAN-3-YL)-2-(3-METHYL-2-BUTENYL)-, 4-((3R)-7-hydroxy-5-methoxy-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-2H-chromen-3-yl)-2-(3-methylbut-2-en-1-yl)benzene-1,3-diol, 4-[(R)-7-Hydroxy-5-methoxy-6-(3-methyl-but-2-enyl)-1-benzopyran-3-yl]-2-((E)-3-methyl-but-2-enyl)-benzene-1,3-diol, (+)-LICORICIDIN, LicoricidinLICORISOFLAVAN B, CHEMBL1929043, SCHEMBL22704769, DTXSID30952821, HY-N3387, BDBM50172098, MSK168286, AKOS032949058, 1,3-Benzenediol,4-[(3R)-3,4-dihydro-7-hydroxy-5-methoxy-6-(3-methyl-2-buten-1-yl)-2H-1-benzopyran-3-yl]-2-(3-methyl-2-buten-1-yl)-, DA-64965, MS-27469, CS-0024069, C16986, G16869, Q27137421, 4-[(3R)-7-hydroxy-5-methoxy-6-(3-methylbut-2-enyl)chroman-3-yl]-2-(3-methylbut-2-enyl)benzene-1,3-diol, 4-[7-Hydroxy-5-methoxy-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-2H-1-benzopyran-3-yl]-2-(3-methylbut-2-en-1-yl)benzene-1,3-diol
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 79.2
Hydrogen Bond Donor Count 3.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC(C2CCC3CCCCC3C2)CC1
Np Classifier Class Isoflavanones
Deep Smiles COccC[C@@H]COc6ccc%10CC=CC)C)))))O))))))cccccc6O))CC=CC)C)))))O
Heavy Atom Count 31.0
Classyfire Class Isoflavonoids
Scaffold Graph Node Level C1CCC(C2COC3CCCCC3C2)CC1
Classyfire Subclass O-methylated isoflavonoids
Isotope Atom Count 0.0
Molecular Complexity 636.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 1.0
Uniprot Id n.a., P18031, P22303
Iupac Name 4-[(3R)-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
Prediction Hob 0.0
Veber Rule True
Classyfire Superclass Phenylpropanoids and polyketides
Target Id NPT204, NPT178
Xlogp 6.4
Gsk 4 400 Rule False
Molecular Formula C26H32O5
Scaffold Graph Node Bond Level c1ccc(C2COc3ccccc3C2)cc1
Prediction Swissadme 0.0
Inchi Key GBRZTUJCDFSIHM-KRWDZBQOSA-N
Silicos It Class Poorly soluble
Fcsp3 0.3846153846153846
Logs -3.065
Rotatable Bond Count 6.0
Logd 4.1
Synonyms licoricidin
Esol Class Poorly soluble
Functional Groups CC=C(C)C, cO, cOC
Compound Name Licoricidin
Prediction Hob Swissadme 0.0
Exact Mass 424.225
Formal Charge 0.0
Monoisotopic Mass 424.225
Hydrogen Bond Acceptor Count 5.0
Molecular Weight 424.5
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 1.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -6.413481012903226
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
Smiles CC(=CCC1=C(C=CC(=C1O)[C@H]2CC3=C(C=C(C(=C3OC)CC=C(C)C)O)OC2)O)C
Nring 3.0
Np Classifier Biosynthetic Pathway Shikimates and Phenylpropanoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Isoflavonoids

  • 1. Outgoing r'ship FOUND_IN to/from Glycyrrhiza Glabra (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 2. Outgoing r'ship FOUND_IN to/from Glycyrrhiza Inflata (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 3. Outgoing r'ship FOUND_IN to/from Glycyrrhiza Uralensis (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 4. Outgoing r'ship FOUND_IN to/from Mitracarpus Scaber (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all