Basic information about inhibitors

IPAD-DB ID	C01274
Name	Chlorogenic acide
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 1 6 H 1 8 O 9
Molecular Weight	354.31 g/mol
IUPAC Name	(1S, 3R, 4R, 5R)-3-(((E)-3-(3, 4-dihydroxyphenyl)acryloyl)oxy)-1, 4, 5-trihydroxycyclohexane-1-carboxylic acid
InChI	InChI=1S/C16H18O9/c17-9-3-1-8(5-10(9)18)2-4-13(20)25-12-7-16(24, 15(22)23)6-11(19)14(12)21/h1-5, 11-12, 14, 17-19, 21, 24H, 6-7H2, (H, 22, 23)/b4-2+/t11-, 12-, 14-, 16+/m1/s1
InChIKey	CWVRJTMFETXNAD-JUHZACGLSA-N
Canonical SMILES	C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O
PubChem CID	1794427
DrugBank Accession Number	DB12029
CAS Registry Number	202650-88-2

Biological activity data

Ki	-
EC50	-
IC50	-
Inhibition	-
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	β-site amyloid precursor protein cleaving enzyme 1 (BACE1)
Effects	-
Research Models	In vitro, Molecular docking, molecular dynamics (MD) simulations
Main Source	From Morus macroura fruit and M. macroura leaf
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	354.31
Hac(Computed by SwissADME)	25
Volume(Computed by ADMETlab 2.0)	331.473
Density(Computed by ADMETlab 2.0)	1.068
nRing(Computed by ADMETlab 2.0)	2
MaxRing(Computed by ADMETlab 2.0)	6
nHet(Computed by ADMETlab 2.0)	9
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	15
Flexibility(Computed by ADMETlab 2.0)	0.333
Stero Centers(Computed by ADMETlab 2.0)	4
LogS(Computed by ADMETlab 2.0)	-1.198
LogD(Computed by ADMETlab 2.0)	0.005

ADMET properties

logP(Computed by ADMETlab 2.0)	-0.162
TPSA(Computed by SwissADME)	164.75
Hbond Acceptor(Computed by SwissADME)	9
Hbond Donor(Computed by SwissADME)	6
Rotatable Bonds(Computed by SwissADME)

Pharmacokinetics

GI Absorption(Computed by SwissADME)	Low
BBB(blood-brain barrier) Permeant(Computed by SwissADME)	No
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)	-8.76

Druglikeness

Lipinski(Computed by SwissADME)	1
Ghose(Computed by SwissADME)	1
Veber(Computed by SwissADME)	1
Egan(Computed by SwissADME)	1
Muegge(Computed by SwissADME)	2
Bioavailability Score(Computed by SwissADME)	0.11