Oxypalmatine

AlkaPlorer ID: AK020658

Synonym: ''

IUPAC Name: 2,3,9,10-tetramethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-8-one

Structure

SMILES: COC1=C(OC)C=C2C(=C1)CCN1C2=CC2=CC=C(OC)C(OC)=C2C1=O

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InChI: InChI=1S/C21H21NO5/c1-24-16-6-5-13-9-15-14-11-18(26-3)17(25-2)10-12(14)7-8-22(15)21(23)19(13)20(16)27-4/h5-6,9-11H,7-8H2,1-4H3

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InChIKey: MZIUUCTTWZPXOV-UHFFFAOYSA-N

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Reference

The isoindolobenzazepine alkaloids

PubChem CID: 10926678

CAS: 19716-59-7

LOTUS: LTS0238575

SuperNatural Ⅲ: SN0239397

COCONUT: CNP0204644

data_source: manually

Source

Properties Information

Molecule Weight: 367.4010000000001

TPSA: 58.92000000000001

MolLogP: 3.259000000000002

Number of H-Donors: 0

Number of H-Acceptors: 6

RingCount: 4

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Candida albicans Candida albicans MIC 250.0 ug.mL-1 10.1016/j.bmc.2018.04.025
Escherichia coli Escherichia coli MIC 250.0 ug.mL-1 10.1016/j.bmc.2018.04.025
Homo sapiens HEK293 Activity nan None 10.1021/acs.jnatprod.6b00409
Rattus norvegicus IEC-6 Survival 70.0 % 10.1016/j.bmc.2018.04.025
Staphylococcus aureus Staphylococcus aureus MIC 250.0 ug.mL-1 10.1016/j.bmc.2018.04.025
None Molecular identity unknown IC50 600.0 nM 10.1021/acs.jnatprod.6b00409
None NON-PROTEIN TARGET Activity nan None 10.1021/acs.jnatprod.6b00409

Metabolism Information