Detailed Information for C01363

Basic information about inhibitors

IPAD-DB ID C01363
Name Brazilin
Category Natural compounds
2D Structure
3D Structure
Molecular Formula C 1 6 H 1 4 O 5
Molecular Weight 286.28 g/mol
IUPAC Name (6aS, 11bR)-7, 11b-dihydro-6H-indeno[2, 1-c]chromene-3, 6a, 9, 10-tetrol
InChI InChI=1S/C16H14O5/c17-9-1-2-10-14(4-9)21-7-16(20)6-8-3-12(18)13(19)5-11(8)15(10)16/h1-5, 15, 17-20H, 6-7H2/t15-, 16+/m0/s1
InChIKey UWHUTZOCTZJUKC-JKSUJKDBSA-N
Canonical SMILES C1C2=CC(=C(C=C2C3C1(COC4=C3C=CC(=C4)O)O)O)O
PubChem CID 73384
DrugBank Accession Number -
CAS Registry Number 474-07-7

Biological activity data

Ki -
EC50 -
IC50 1.5μM(Aβ43 fibrils)
Inhibition -
Toxicity -
ROS(reactive oxygen species) -
Metal Chelating -
BBB(blood-brain barrier) -
Target Protein Aβ42 fibrils
Effects -
Research Models -
Main Source -
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME) 286.28
Hac(Computed by SwissADME) 21
Volume(Computed by ADMETlab 2.0) 279.199
Density(Computed by ADMETlab 2.0) 1.025
nRing(Computed by ADMETlab 2.0) 4
MaxRing(Computed by ADMETlab 2.0) 17
nHet(Computed by ADMETlab 2.0) 5
fChar(Computed by ADMETlab 2.0) 0
nRig(Computed by ADMETlab 2.0) 20
Flexibility(Computed by ADMETlab 2.0) 0
Stero Centers(Computed by ADMETlab 2.0) 2
LogS(Computed by ADMETlab 2.0) -3.174
LogD(Computed by ADMETlab 2.0) 2.178

ADMET properties

logP(Computed by ADMETlab 2.0) 2.183
TPSA(Computed by SwissADME) 90.15
Hbond Acceptor(Computed by SwissADME) 5
Hbond Donor(Computed by SwissADME) 4
Rotatable Bonds(Computed by SwissADME) 0

Pharmacokinetics

GI Absorption(Computed by SwissADME) High
BBB(blood-brain barrier) Permeant(Computed by SwissADME) No
P-gp Substrate(Computed by SwissADME) Yes
CYP1A2 Inhibitor(Computed by SwissADME) Yes
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) -6.95

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