Detailed Information for C00421

Basic information about inhibitors

IPAD-DB ID C00421
Name Mulberroside A
Category Natural compounds
2D Structure
3D Structure
Molecular Formula C 2 6 H 3 2 O 1 4
Molecular Weight 568.5g/mol
IUPAC Name (2S, 3R, 4S, 5S, 6R)-2-[3-hydroxy-4-[(E)-2-[3-hydroxy-5-[(2S, 3R, 4S, 5S, 6R)-3, 4, 5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3, 4, 5-triol
InChI InChI=1S/C26H32O14/c27-9-17-19(31)21(33)23(35)25(39-17)37-14-4-3-12(16(30)8-14)2-1-11-5-13(29)7-15(6-11)38-26-24(36)22(34)20(32)18(10-28)40-26/h1-8, 17-36H, 9-10H2/b2-1+/t17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-, 25-, 26-/m1/s1
InChIKey HPSWAEGGWLOOKT-VUNDNAJOSA-N
Canonical SMILES C1=CC(=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)C=CC3=CC(=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O
PubChem CID 6443484
DrugBank Accession Number -
CAS Registry Number 102841-42-9

Biological activity data

Ki -
EC50 -
IC50 -
Inhibition -
Toxicity -
ROS(reactive oxygen species) -
Metal Chelating -
BBB(blood-brain barrier) -
Target Protein Acetylcholinesterase (AChE)
Effects -
Research Models In vitro, Molecular docking, molecular dynamics (MD) simulations
Main Source From Morus macroura fruit
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME) 568.52
Hac(Computed by SwissADME) 40
Volume(Computed by ADMETlab 2.0) 528.634
Density(Computed by ADMETlab 2.0) 1.075
nRing(Computed by ADMETlab 2.0) 4
MaxRing(Computed by ADMETlab 2.0) 6
nHet(Computed by ADMETlab 2.0) 14
fChar(Computed by ADMETlab 2.0) 0
nRig(Computed by ADMETlab 2.0) 25
Flexibility(Computed by ADMETlab 2.0) 0.32
Stero Centers(Computed by ADMETlab 2.0) 10
LogS(Computed by ADMETlab 2.0) -1.66
LogD(Computed by ADMETlab 2.0) 0.647

ADMET properties

logP(Computed by ADMETlab 2.0) -2.37
TPSA(Computed by SwissADME) 239.22 Ų
Hbond Acceptor(Computed by SwissADME) 14
Hbond Donor(Computed by SwissADME) 10
Rotatable Bonds(Computed by SwissADME) 8

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) -10.36 cm/s

Druglikeness

Lipinski(Computed by SwissADME) No, 3 violations: MW>500, NorO>10, NHorOH>5
Ghose(Computed by SwissADME) No, 4 violations: MW>480, WLOGP<-0.4, MR>130, #atoms>70
Veber(Computed by SwissADME) No, 1 violation: TPSA>140
Egan(Computed by SwissADME) No, 1 violation: TPSA>131.6
Muegge(Computed by SwissADME) No, 3 violations: TPSA>150, H-acc>10, H-don>5
Bioavailability Score(Computed by SwissADME) 0.17