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(9S)-9-hydroxy-14-oxa-7-azatetracyclo[6.6.1.01,11.02,7]pentadec-11-en-13-one

PubChem CID: 5321219

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Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 49.8
Hydrogen Bond Donor Count 1.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CC2CCC3CC2(C1)C1CCCCC31
Np Classifier Class Quinolizidine alkaloids
Deep Smiles O=CC=CCO5)CC[C@H]C6)O))NC5CCCC6
Heavy Atom Count 17.0
Classyfire Class Indolizidines
Scaffold Graph Node Level OC1CC2CCC3CC2(O1)C1CCCCN31
Isotope Atom Count 0.0
Molecular Complexity 419.0
Database Name cmaup_ingredients;imppat_phytochem;pubchem
Defined Atom Stereocenter Count 1.0
Iupac Name (9S)-9-hydroxy-14-oxa-7-azatetracyclo[6.6.1.01,11.02,7]pentadec-11-en-13-one
Prediction Hob 1.0
Veber Rule True
Classyfire Superclass Organoheterocyclic compounds
Xlogp 0.2
Gsk 4 400 Rule True
Molecular Formula C13H17NO3
Scaffold Graph Node Bond Level O=C1C=C2CCC3CC2(O1)C1CCCCN31
Prediction Swissadme 0.0
Inchi Key OHLFUILALUNTGR-CIYITXRRSA-N
Silicos It Class Soluble
Fcsp3 0.7692307692307693
Rotatable Bond Count 0.0
Synonyms securinol b
Esol Class Very soluble
Functional Groups CC1=CC(=O)OC1, CN(C)C, CO
Compound Name (9S)-9-hydroxy-14-oxa-7-azatetracyclo[6.6.1.01,11.02,7]pentadec-11-en-13-one
Prediction Hob Swissadme 0.0
Exact Mass 235.121
Formal Charge 0.0
Monoisotopic Mass 235.121
Hydrogen Bond Acceptor Count 4.0
Molecular Weight 235.28
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 4.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -1.4184545999999998
Inchi InChI=1S/C13H17NO3/c15-10-5-8-6-12(16)17-13(8)7-9(10)14-4-2-1-3-11(13)14/h6,9-11,15H,1-5,7H2/t9?,10-,11?,13?/m0/s1
Smiles C1CCN2C(C1)C34CC2[C@H](CC3=CC(=O)O4)O
Np Classifier Biosynthetic Pathway Alkaloids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Lysine alkaloids