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.

methyl (4S,18S)-4-[(1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-10-methoxycarbonyl-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraen-4-yl]-1-ethyl-2-oxa-6,16-diazapentacyclo[14.3.1.03,18.05,13.07,12]icosa-5(13),7,9,11-tetraene-4-carboxylate

PubChem CID: 327791

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

Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 143.0
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2C(C1)CC1C2CCC2CC3CC(C2)C(C3)C1C1CCC2CC3CCC4CCCC5CCC3(C2C1)C45
Np Classifier Class Aspidosperma type, Aspidosperma-Iboga hybrid type (Vinca alkaloids)
Deep Smiles CC[C@@]C=CCN[C@@H]6[C@@][C@H][C@@][C@@H]%10OC=O)C))))O)C=O)OC))))Ncc5cccc6)OC)))[C@@]C=O)OC)))COCC[C@H]5CNC6)CCcc%12[nH]cc5cccc6)))))))))))))))CC))))))))))C)))CC5
Heavy Atom Count 59.0
Classyfire Class Vinca alkaloids
Scaffold Graph Node Level C1CCC2C(C1)NC1C2CCN2CC3CC(C2)C(O3)C1C1CCC2NC3CCC4CCCN5CCC3(C2C1)C45
Isotope Atom Count 0.0
Molecular Complexity 1750.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name methyl (4S,18S)-4-[(1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-10-methoxycarbonyl-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraen-4-yl]-1-ethyl-2-oxa-6,16-diazapentacyclo[14.3.1.03,18.05,13.07,12]icosa-5(13),7,9,11-tetraene-4-carboxylate
Veber Rule False
Classyfire Superclass Alkaloids and derivatives
Xlogp 3.7
Gsk 4 400 Rule False
Molecular Formula C46H56N4O9
Scaffold Graph Node Bond Level C1=CC2CCC3Nc4ccc(C5c6[nH]c7ccccc7c6CCN6CC7CC(C6)C5O7)cc4C34CCN(C1)C24
Inchi Key KMWVJRBQGMUMID-CIASJWMASA-N
Silicos It Class Poorly soluble
Rotatable Bond Count 10.0
Synonyms catharanthamine
Esol Class Poorly soluble
Functional Groups CC(=O)OC, CC=CC, CN(C)C, CO, COC, COC(C)=O, cN(C)C, cOC, c[nH]c
Compound Name methyl (4S,18S)-4-[(1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-10-methoxycarbonyl-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraen-4-yl]-1-ethyl-2-oxa-6,16-diazapentacyclo[14.3.1.03,18.05,13.07,12]icosa-5(13),7,9,11-tetraene-4-carboxylate
Exact Mass 808.405
Formal Charge 0.0
Monoisotopic Mass 808.405
Hydrogen Bond Acceptor Count 12.0
Molecular Weight 809.0
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 10.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C46H56N4O9/c1-8-42-23-27-24-49(25-42)19-15-29-28-13-10-11-14-32(28)47-35(29)45(36(27)59-42,40(52)56-6)31-21-30-33(22-34(31)55-5)48(4)38-44(30)17-20-50-18-12-16-43(9-2,37(44)50)39(58-26(3)51)46(38,54)41(53)57-7/h10-14,16,21-22,27,36-39,47,54H,8-9,15,17-20,23-25H2,1-7H3/t27-,36?,37-,38+,39+,42?,43+,44+,45-,46-/m0/s1
Smiles CC[C@@]12C=CCN3[C@@H]1[C@]4(CC3)[C@H]([C@]([C@@H]2OC(=O)C)(C(=O)OC)O)N(C5=CC(=C(C=C45)[C@]6(C7[C@H]8CC(O7)(CN(C8)CCC9=C6NC1=CC=CC=C91)CC)C(=O)OC)OC)C
Np Classifier Biosynthetic Pathway Alkaloids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Tryptophan alkaloids

  • 1. Outgoing r'ship FOUND_IN to/from Catharanthus Roseus (Plant) Rel Props:Reference:ISBN:9788172361150