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.

14-O-Acetylbrowniine

PubChem CID: 441704

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

Compound Synonyms 14-O-Acetylbrowniine, Acetylbrowniine, Browniine 14-acetate, Browniine 14-O-acetate, 14-Acetylbrowniine, 65601-04-9, CHEBI:2414, [(1S,2R,3R,4S,5R,6S,8R,9S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate, 20-ethyl-7,8-dihydroxy-1alpha,6beta,16beta-trimethoxy-4-(methoxymethyl)aconitan-14alpha-yl acetate, ((1S,2R,3R,4S,5R,6S,8R,9S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo(7.7.2.12,5.01,10.03,8.013,17)nonadecan-4-yl) acetate, Browniine 14-acetic acid, Browniine 14-O-acetic acid, DTXSID60984175, C08654, Q27105657, 20-Ethyl-7,8-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl acetate
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 107.0
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule True
Scaffold Graph Level C1CC2CCC3C4CC2C3(C1)C1CC2CCC4C1C2
Np Classifier Class Terpenoid alkaloids
Deep Smiles COC[C@@]CC[C@@H][C@@][C@@H]6[C@H]OC))[C@]C5NC%11)CC))))O)[C@@][C@@H][C@H]7C[C@@H][C@@H]5OC=O)C))))[C@H]C7)OC)))))))O))))))OC
Heavy Atom Count 36.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CC2CNC3C4CC2C3(C1)C1CC2CCC4C1C2
Classyfire Subclass Diterpenoids
Isotope Atom Count 0.0
Molecular Complexity 918.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 12.0
Iupac Name [(1S,2R,3R,4S,5R,6S,8R,9S,13S,16S,17R,18S)-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 0.0
Gsk 4 400 Rule False
Molecular Formula C27H43NO8
Scaffold Graph Node Bond Level C1CC2CNC3C4CC2C3(C1)C1CC2CCC4C1C2
Inchi Key BQMFTYVYHRJVMQ-VEUWJJFUSA-N
Silicos It Class Soluble
Rotatable Bond Count 8.0
Synonyms 14-acetylbrowniine
Esol Class Soluble
Functional Groups CC(=O)OC, CN(C)C, CO, COC
Compound Name 14-O-Acetylbrowniine
Exact Mass 509.299
Formal Charge 0.0
Monoisotopic Mass 509.299
Hydrogen Bond Acceptor Count 9.0
Molecular Weight 509.6
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 13.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C27H43NO8/c1-7-28-12-24(13-32-3)9-8-18(34-5)26-16-10-15-17(33-4)11-25(30,19(16)20(15)36-14(2)29)27(31,23(26)28)22(35-6)21(24)26/h15-23,30-31H,7-13H2,1-6H3/t15-,16-,17+,18+,19-,20+,21-,22+,23?,24+,25-,26+,27-/m1/s1
Smiles CCN1C[C@@]2(CC[C@@H]([C@@]34[C@@H]2[C@@H]([C@@](C31)([C@]5(C[C@@H]([C@H]6C[C@@H]4[C@@H]5[C@H]6OC(=O)C)OC)O)O)OC)OC)COC
Np Classifier Biosynthetic Pathway Alkaloids, Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Pseudoalkaloids

  • 1. Outgoing r'ship FOUND_IN to/from Consolida Ajacis (Plant) Rel Props:Reference:ISBN:9788172362133; ISBN:9788185042114