Detailed Information for S00813

Basic information about inhibitors

IPAD-DB ID S00813
Name Methyl caffeate
Category Synthetic compounds
2D Structure
3D Structure
Molecular Formula C 1 0 H 1 0 O 4
Molecular Weight 194.18 g/mol
IUPAC Name methyl(E)-3-(3, 4-dihydroxyphenyl)prop-2-enoate
InChI InChI=1S/C10H10O4/c1-14-10(13)5-3-7-2-4-8(11)9(12)6-7/h2-6, 11-12H, 1H3/b5-3+
InChIKey OCNYGKNIVPVPPX-HWKANZROSA-N
Canonical SMILES COC(=O)C=CC1=CC(=C(C=C1)O)O
PubChem CID 689075
DrugBank Accession Number -
CAS Registry Number 3843-74-1

Biological activity data

Ki -
EC50 67.7 μM(Aβ1-42) 
IC50
Inhibition <10%(10μM XOD inhibition), 22%(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) 194.18
Hac(Computed by SwissADME) 14
Volume(Computed by ADMETlab 2.0) 194.938
Density(Computed by ADMETlab 2.0) 0.995
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) 0.375
Stero Centers(Computed by ADMETlab 2.0) 0
LogS(Computed by ADMETlab 2.0) -1.27
LogD(Computed by ADMETlab 2.0) 1.979

ADMET properties

logP(Computed by ADMETlab 2.0) 1.957
TPSA(Computed by SwissADME) 66.76
Hbond Acceptor(Computed by SwissADME) 4
Hbond Donor(Computed by SwissADME) 2
Rotatable Bonds(Computed by SwissADME) 3

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) -6.43

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) 1
Bioavailability Score(Computed by SwissADME) 0.55