This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration. This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration.

Paratocarpin B

PubChem CID: 42607541

Connections displayed (default: 10).
Loading graph...

Compound Synonyms Paratocarpin B, UNII-0536M66IHB, 0536M66IHB, 161099-57-6, 2-Propen-1-one, 1-(5-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl)-, (2E)-, CHEMBL4059903, 3-Prenyl-6'',6''-dimethylpyrano[2'',3'':4',3']-4,2'-dihydroxychalcone, CHEBI:187700, BDBM50267180, LMPK12120091, Q27236063, (E)-1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 66.8
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC(CCC1CCCCC1)C1CCC2CCCCC2C1
Np Classifier Class Chalcones
Deep Smiles CC=CCccc/C=C/C=O)cccccc6O))C=CCO6)C)C))))))))))))ccc6O)))))))))C
Heavy Atom Count 29.0
Classyfire Class Linear 1,3-diarylpropanoids
Scaffold Graph Node Level OC(CCC1CCCCC1)C1CCC2OCCCC2C1
Classyfire Subclass Chalcones and dihydrochalcones
Isotope Atom Count 0.0
Molecular Complexity 670.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 0.0
Uniprot Id P14679, P18031, Q16236
Iupac Name (E)-1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one
Prediction Hob 1.0
Veber Rule True
Classyfire Superclass Phenylpropanoids and polyketides
Target Id NPT178
Xlogp 6.4
Gsk 4 400 Rule False
Molecular Formula C25H26O4
Scaffold Graph Node Bond Level O=C(C=Cc1ccccc1)c1ccc2c(c1)C=CCO2
Prediction Swissadme 0.0
Inchi Key WRNYEZGVIHDIGH-YRNVUSSQSA-N
Silicos It Class Moderately soluble
Fcsp3 0.24
Logs -3.889
Rotatable Bond Count 5.0
Logd 4.655
Synonyms paratocarpin b
Esol Class Poorly soluble
Functional Groups CC=C(C)C, c/C=C/C(c)=O, cC=CC, cO, cOC
Compound Name Paratocarpin B
Prediction Hob Swissadme 0.0
Exact Mass 390.183
Formal Charge 0.0
Monoisotopic Mass 390.183
Hydrogen Bond Acceptor Count 4.0
Molecular Weight 390.5
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 0.0
Total Bond Stereocenter Count 1.0
Lipinski Rule Of 5 True
Esol -6.256576696551725
Inchi InChI=1S/C25H26O4/c1-16(2)5-8-18-15-17(6-10-21(18)26)7-11-22(27)19-9-12-23-20(24(19)28)13-14-25(3,4)29-23/h5-7,9-15,26,28H,8H2,1-4H3/b11-7+
Smiles CC(=CCC1=C(C=CC(=C1)/C=C/C(=O)C2=C(C3=C(C=C2)OC(C=C3)(C)C)O)O)C
Nring 3.0
Np Classifier Biosynthetic Pathway Shikimates and Phenylpropanoids
Defined Bond Stereocenter Count 1.0
Egan Rule True
Np Classifier Superclass Flavonoids

  • 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