Basic information about inhibitors

IPAD-DB ID	C01102
Name	Diosgenin
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 2 7 H 4 2 O 3
Molecular Weight	414.6g/mol
IUPAC Name	(1S, 2S, 4S, 5'R, 6R, 7S, 8R, 9S, 12S, 13R, 16S)-5', 7, 9, 13-tetramethylspiro[5-oxapentacyclo[10.8.0.02, 9.04, 8.013, 18]icos-18-ene-6, 2'-oxane]-16-ol
InChI	InChI=1S/C27H42O3/c1-16-7-12-27(29-15-16)17(2)24-23(30-27)14-22-20-6-5-18-13-19(28)8-10-25(18, 3)21(20)9-11-26(22, 24)4/h5, 16-17, 19-24, 28H, 6-15H2, 1-4H3/t16-, 17+, 19+, 20-, 21+, 22+, 23+, 24+, 25+, 26+, 27-/m1/s1
InChIKey	WQLVFSAGQJTQCK-VKROHFNGSA-N
Canonical SMILES	CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1
PubChem CID	99474
DrugBank Accession Number	-
CAS Registry Number	512-04-9

Biological activity data

Ki	-
EC50	-
IC50	-
Inhibition	-
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	S-Shaped Aβ42
Effects	-
Research Models	Ensemble docking and molecular dynamics (MD) simulations
Main Source	-
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	414.62
Hac(Computed by SwissADME)	30
Volume(Computed by ADMETlab 2.0)	447.944
Density(Computed by ADMETlab 2.0)	0.925
nRing(Computed by ADMETlab 2.0)	6
MaxRing(Computed by ADMETlab 2.0)	20
nHet(Computed by ADMETlab 2.0)	3
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	30
Flexibility(Computed by ADMETlab 2.0)	0
Stero Centers(Computed by ADMETlab 2.0)	11
LogS(Computed by ADMETlab 2.0)	-5.869
LogD(Computed by ADMETlab 2.0)	4.972

ADMET properties

logP(Computed by ADMETlab 2.0)	5.71
TPSA(Computed by SwissADME)	38.69 Ų
Hbond Acceptor(Computed by SwissADME)	3
Hbond Donor(Computed by SwissADME)	1
Rotatable Bonds(Computed by SwissADME)	0

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)	-4.80 cm/s

Druglikeness

Lipinski(Computed by SwissADME)	Yes, 1 violation: MLOGP>4.15
Ghose(Computed by SwissADME)	No, 2 violations: WLOGP>5.6, #atoms>70
Veber(Computed by SwissADME)	Yes
Egan(Computed by SwissADME)	Yes
Muegge(Computed by SwissADME)	No, 1 violation: XLOGP3>5
Bioavailability Score(Computed by SwissADME)	0.55