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1-[(4-hydroxyphenyl)methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol

PubChem CID: 21817819

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Compound Synonyms CHEMBL3828751, SCHEMBL12807694
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 52.9
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC(CC2CCCC3CCCCC32)CC1
Np Classifier Class Isoquinoline alkaloids, Tetrahydroisoquinoline alkaloids
Deep Smiles COcccccc6O)))CCNC6Ccccccc6))O)))))))C
Heavy Atom Count 22.0
Classyfire Class Isoquinolines and derivatives
Scaffold Graph Node Level C1CCC(CC2NCCC3CCCCC32)CC1
Classyfire Subclass Benzylisoquinolines
Isotope Atom Count 0.0
Molecular Complexity 356.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 0.0
Uniprot Id O42275, P81908
Iupac Name 1-[(4-hydroxyphenyl)methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol
Prediction Hob 1.0
Veber Rule True
Classyfire Superclass Organoheterocyclic compounds
Xlogp 3.0
Gsk 4 400 Rule True
Molecular Formula C18H21NO3
Scaffold Graph Node Bond Level c1ccc(CC2NCCc3ccccc32)cc1
Prediction Swissadme 1.0
Inchi Key HTSOYRHMEMWMRT-UHFFFAOYSA-N
Silicos It Class Moderately soluble
Fcsp3 0.3333333333333333
Logs -1.781
Rotatable Bond Count 3.0
Logd 2.78
Synonyms n-methylisococlaurine
Esol Class Soluble
Functional Groups CN(C)C, cO, cOC
Compound Name 1-[(4-hydroxyphenyl)methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol
Prediction Hob Swissadme 1.0
Exact Mass 299.152
Formal Charge 0.0
Monoisotopic Mass 299.152
Hydrogen Bond Acceptor Count 4.0
Molecular Weight 299.4
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 -3.816930363636364
Inchi InChI=1S/C18H21NO3/c1-19-8-7-13-10-17(21)18(22-2)11-15(13)16(19)9-12-3-5-14(20)6-4-12/h3-6,10-11,16,20-21H,7-9H2,1-2H3
Smiles CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)O
Nring 3.0
Np Classifier Biosynthetic Pathway Alkaloids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Tyrosine alkaloids