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Otosenine

PubChem CID: 6438142

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Compound Synonyms otosenine, Othosenine, Tomentosine, Othosenin, d-Otocenime, d-Otosenine, 16958-29-5, (-)-Octosenine, Otosenin, Z999A1E7I4, (1R,3'S,4S,6R,7R,11Z)-7-hydroxy-3',6,7,14-tetramethylspiro[2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-4,2'-oxirane]-3,8,17-trione, OTOSENINE (NEUTRAL), OTOSENINE, (+)-, CHEBI:136467, Spiro(2,9-dioxa-14-azabicyclo(9,5,1)heptadec-11-ene-4,2'-oxirane)-3,8,17-trione, 7-hydroxy-3',6,7,14-tetramethyl-, (1R,2'S,3'S,6R,7R)-, (1R,3'S,4S,6R,7R,11Z)-7-hydroxy-3',6,7,14-tetramethyl-3H,8H,17H-spiro[2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-4,2'-oxirane]-3,8,17-trione, 4,8-SECOSENECIONAN-8,11,16-TRIONE, 15,20-EPOXY-15,20-DIHYDRO-12-HYDROXY-4-METHYL-, (15.ALPHA.,20S)-, SPIRO(2,9-DIOXA-14-AZABICYCLO(9.5.1)HEPTADEC-11-ENE-4,2'-OXIRANE)-3,8,17-TRIONE, 7-HYDROXY-3',6,7,14-TETRAMETHYL-, (1R,2'S,3'S,6R,7R)-, SPIRO(2,9-DIOXA-14-AZABICYCLO(9.5.1)HEPTADEC-11-ENE-4,2'-OXIRANE)-3,8,17-TRIONE, 7-HYDROXY-3',6,7,14-TETRAMETHYL-, (1R-(1R*,4S*(S*),6R*,7R*))-, UNII-Z999A1E7I4, (1R,3'S,4S,6R,7R,11Z)-7-hydroxy-3',6,7,14-tetramethyl-3H,8H,17H-spiro(2,9-dioxa-14-azabicyclo(9.5.1)heptadec-11-ene-4,2'-oxirane)-3,8,17-trione, (1R,3'S,4S,6R,7R,11Z)-7-hydroxy-3',6,7,14-tetramethylspiro(2,9-dioxa-14-azabicyclo(9.5.1)heptadec-11-ene-4,2'-oxirane)-3,8,17-trione, CHEMBL511627, DTXSID701102927, AKOS032428314, AKOS040762156, FS-6741, HY-124413, CS-0086429, NS00094199, Q27295184, (1R,2a(2)S,3a(2)S,6R,7R)-7-Hydroxy-3a(2),6,7,14-tetramethylspiro[2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-4,2a(2)-oxirane]-3,8,17-trione, 4,8-SECOSENECIONAN-8,11,16-TRIONE, 15,20-EPOXY-15,20-DIHYDRO-12-HYDROXY-4-METHYL-, (15ALPHA,20S)-
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 106.0
Hydrogen Bond Donor Count 1.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CCCC2(CC2)C(C)CC2CCCCCC(CC1)C2C
Np Classifier Class Pyrrolizidine alkaloids
Deep Smiles CNCC[C@H]OC=O)[C@]O[C@H]3C)))C[C@H][C@@]C=O)OCC=CC%16))C%12=O))))))C)O))C
Heavy Atom Count 27.0
Classyfire Class Azaspirodecane derivatives
Scaffold Graph Node Level OC1CCCC2(CO2)C(O)OC2CCNCCC(CO1)C2O
Isotope Atom Count 0.0
Molecular Complexity 690.0
Database Name imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name (1R,3'S,4S,6R,7R,11Z)-7-hydroxy-3',6,7,14-tetramethylspiro[2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-4,2'-oxirane]-3,8,17-trione
Nih Violation False
Veber Rule True
Classyfire Superclass Organoheterocyclic compounds
Xlogp 0.6
Is Pains False
Gsk 4 400 Rule True
Molecular Formula C19H27NO7
Scaffold Graph Node Bond Level O=C1CCCC2(CO2)C(=O)OC2CCNCC=C(CO1)C2=O
Inchi Key CZQLULNMKQAIQL-GZSSMBGUSA-N
Silicos It Class Soluble
Rotatable Bond Count 0.0
Synonyms othosenine, otosenine, tomentosine
Esol Class Soluble
Functional Groups C/C=C(/C)C(C)=O, CN(C)C, CO, COC(C)=O, C[C@@H]1O[C@]1(C)C(=O)OC
Compound Name Otosenine
Exact Mass 381.179
Formal Charge 0.0
Brenk Violation True
Monoisotopic Mass 381.179
Hydrogen Bond Acceptor Count 8.0
Molecular Weight 381.4
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 5.0
Total Bond Stereocenter Count 1.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C19H27NO7/c1-11-9-19(12(2)27-19)17(23)26-14-6-8-20(4)7-5-13(15(14)21)10-25-16(22)18(11,3)24/h5,11-12,14,24H,6-10H2,1-4H3/b13-5-/t11-,12+,14-,18-,19+/m1/s1
Smiles C[C@@H]1C[C@]2([C@@H](O2)C)C(=O)O[C@@H]3CCN(C/C=C(\C3=O)/COC(=O)[C@]1(C)O)C
Np Classifier Biosynthetic Pathway Alkaloids
Defined Bond Stereocenter Count 1.0
Egan Rule True
Np Classifier Superclass Ornithine alkaloids