Molecule

vilmorisine

AlkaPlorer ID: AK009518

Synonym: None

IUPAC Name: None

Structure

SMILES: CCN1C(O2)[C@]34C([C@@H]2C=C5C6C4C[C@H](C(OC)C5)[C@@H]6OC(C)=O)[C@@](C1)(COC)CC[C@@H]3OC

InChI: InChI=1S/C26H39NO6/c1-6-27-12-25(13-29-3)8-7-20(31-5)26-17-11-16-18(30-4)9-15(21(17)22(16)32-14(2)28)10-19(23(25)26)33-24(26)27/h10,16-24H,6-9,11-13H2,1-5H3/t16-,17?,18?,19+,20+,21?,22+,23?,24?,25+,26+/m1/s1

InChIKey: NSBYDRRVBINIHE-OQRVKYAASA-N

Reference

Biologically active franchetine-type diterpenoid alkaloids: Isolation, synthesis, anti-inflammatory, agalgesic activities, and molecular docking

data_source: manually

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Penicillium crustosum	Penicillium	Aspergillaceae	Eurotiales	Eurotiomycetes	Ascomycota	Fungi	Eukaryota

Properties Information

Molecule Weight: 461.59900000000033

TPSA？: 66.46000000000001

MolLogP？: 2.633700000000001

Number of H-Donors: 0

Number of H-Acceptors: 7

RingCount: 6

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi