Phyto4Health

Olvanil

Representations & DB's id

ChEBI: None
ChEMBL: CHEMBL76903
PubChem: 5311093
IUPAC: (Z)-N-[(4-hydroxy-3-methoxyphenyl)methyl]octadec-9-enamide
Standard InChI: InChI=1S/C26H43NO3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-26(29)27-22-23-19-20-24(28)25(21-23)30-2/h10-11,19-21,28H,3-9,12-18,22H2,1-2H3,(H,27,29)/b11-10-
Standard InChI Key: OPZKBPQVWDSATI-KHPPLWFESA-N
SMILES: CCCCCCCC/C=CCCCCCCCC(=NCc1ccc(c(c1)OC)O)O

Molecular propeties

AlogP: 7.05
Hydrogen bonds acceptors: 3
Hydrogen bonds donors: 2
Rotatable bonds: 18
Number of rings: 1
Molecular Weight: 417.32
Topological polar surface area: 58.6
Number of aromatic rings: 1
Fsp3: 0.654
Number of carbons: 26

Plant sources

Part of plant Plant name Ref.
FructusCapsicum annuum

In vitro data

Activity Type Activity Value Target Name UniProt ID Ref.
Potency1648.2 nMSerine/threonine-protein kinase mTORP42345
Potency3548.1 nMMicrotubule-associated protein tauP10636
Potency13091.8 nMSerine/threonine-protein kinase mTORP42345
Potency25118.9 nM15-hydroxyprostaglandin dehydrogenase [NAD+]P15428
Potency31622.8 nMCellular tumor antigen p53P04637
Potency31622.8 nMCellular tumor antigen p53P04637
Potency3162.3 nMCytochrome P450 2D6P10635
Potency10000 nMCytochrome P450 3A4P08684
Potency10000 nMCytochrome P450 3A4P08684
Potency1458 nMDopamine D1 receptorP21728
Potency125.9 nMHistone-lysine N-methyltransferase, H3 lysine-9 specific 3Q96KQ7
Potency23715 nMGemininO75496