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N-Acetylbongaridine

PubChem CID: 78411088

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Compound Synonyms N-Acetylbongaridine, (-)-N-Acetylanonaine, SCHEMBL15800848, (7R)-6,7,7a,8-Tetrahydro-7-acetyl-5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 38.8
Hydrogen Bond Donor Count 0.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2C(C1)CC1CCCC3CC4CCCC4C2C13
Np Classifier Class Aporphine alkaloids, Isoquinoline alkaloids
Deep Smiles CC=O)NCCccC6Ccccccc6-c%10ccc%14)OCO5
Heavy Atom Count 23.0
Classyfire Class Aporphines
Scaffold Graph Node Level C1CCC2C(C1)CC1NCCC3CC4OCOC4C2C31
Isotope Atom Count 0.0
Molecular Complexity 495.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name 1-(3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-11-yl)ethanone
Veber Rule True
Classyfire Superclass Alkaloids and derivatives
Xlogp 2.8
Gsk 4 400 Rule True
Molecular Formula C19H17NO3
Scaffold Graph Node Bond Level c1ccc2c(c1)CC1NCCc3cc4c(c-2c31)OCO4
Inchi Key XVIHBNVDAPQBRH-UHFFFAOYSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 0.0
Synonyms (-)n-acetylanonaine
Esol Class Soluble
Functional Groups CC(=O)N(C)C, c1cOCO1
Compound Name N-Acetylbongaridine
Exact Mass 307.121
Formal Charge 0.0
Monoisotopic Mass 307.121
Hydrogen Bond Acceptor Count 3.0
Molecular Weight 307.3
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
Inchi InChI=1S/C19H17NO3/c1-11(21)20-7-6-13-9-16-19(23-10-22-16)18-14-5-3-2-4-12(14)8-15(20)17(13)18/h2-5,9,15H,6-8,10H2,1H3
Smiles CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3
Np Classifier Biosynthetic Pathway Alkaloids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Tyrosine alkaloids