Detailed Information for S01231

Basic information about inhibitors

IPAD-DB ID S01231
Name Butyl caffeate
Category Synthetic compounds
2D Structure
3D Structure
Molecular Formula C 1 3 H 1 6 O 4
Molecular Weight 236.26 g/mol
IUPAC Name butyl(E)-3-(3, 4-dihydroxyphenyl)prop-2-enoate
InChI InChI=1S/C13H16O4/c1-2-3-8-17-13(16)7-5-10-4-6-11(14)12(15)9-10/h4-7, 9, 14-15H, 2-3, 8H2, 1H3/b7-5+
InChIKey DBBCBZIFZYILRL-FNORWQNLSA-N
Canonical SMILES CCCCOC(=O)C=CC1=CC(=C(C=C1)O)O
PubChem CID 9991705
DrugBank Accession Number -
CAS Registry Number 22020-28-6

Biological activity data

Ki -
EC50 12.0 μM(Aβ1-42) 
IC50
Inhibition <10%(10μM XOD inhibition), >90%(100μM XOD inhibition)
Toxicity
ROS(reactive oxygen species) 46%(100μM DPPH radical scavenging activity), 62%(500μM DPPH radical scavenging activity)
Metal Chelating
BBB(blood-brain barrier)
Target Protein Aβ1-42
Effects
Research Models Molecular docking
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME) 236.26
Hac(Computed by SwissADME) 17
Volume(Computed by ADMETlab 2.0) 246.826
Density(Computed by ADMETlab 2.0) 0.957
nRing(Computed by ADMETlab 2.0) 1
MaxRing(Computed by ADMETlab 2.0) 6
nHet(Computed by ADMETlab 2.0) 4
fChar(Computed by ADMETlab 2.0) 0
nRig(Computed by ADMETlab 2.0) 8
Flexibility(Computed by ADMETlab 2.0) 0.75
Stero Centers(Computed by ADMETlab 2.0) 0
LogS(Computed by ADMETlab 2.0) -2.631
LogD(Computed by ADMETlab 2.0) 3.027

ADMET properties

logP(Computed by ADMETlab 2.0) 3.128
TPSA(Computed by SwissADME) 66.76
Hbond Acceptor(Computed by SwissADME) 4
Hbond Donor(Computed by SwissADME) 2
Rotatable Bonds(Computed by SwissADME) 6

Pharmacokinetics

GI Absorption(Computed by SwissADME) High
BBB(blood-brain barrier) Permeant(Computed by SwissADME) Yes
P-gp Substrate(Computed by SwissADME) No
CYP1A2 Inhibitor(Computed by SwissADME) No
CYP2C19 Inhibitor(Computed by SwissADME) No
CYP2C9 Inhibitor(Computed by SwissADME) No
CYP2D6 Inhibitor(Computed by SwissADME) No
CYP3A4 Inhibitor(Computed by SwissADME) No
log Kp(Skin Permeation)(Computed by SwissADME) -5.23

Druglikeness

Lipinski(Computed by SwissADME) 0
Ghose(Computed by SwissADME) 0
Veber(Computed by SwissADME) 0
Egan(Computed by SwissADME) 0
Muegge(Computed by SwissADME) 0
Bioavailability Score(Computed by SwissADME) 0.55