Detailed Information for C00637

Basic information about inhibitors

IPAD-DB ID C00637
Name Salvianolic Acid B
Category Natural compounds
2D Structure
3D Structure
Molecular Formula C 3 6 H 3 0 O 1 6
Molecular Weight 718.6 g/mol
IUPAC Name 2-[(E)-3-[3-[1-carboxy-2-(3, 4-dihydroxyphenyl)ethoxy]carbonyl-2-(3, 4-dihydroxyphenyl)-7-hydroxy-2, 3-dihydro-1-benzofuran-4-yl]prop-2-enoyl]oxy-3-(3, 4-dihydroxyphenyl)propanoic acid
InChI InChI=1S/C36H30O16/c37-20-6-1-16(11-24(20)41)13-27(34(45)46)50-29(44)10-5-18-3-9-23(40)33-30(18)31(32(52-33)19-4-8-22(39)26(43)15-19)36(49)51-28(35(47)48)14-17-2-7-21(38)25(42)12-17/h1-12, 15, 27-28, 31-32, 37-43H, 13-14H2, (H, 45, 46)(H, 47, 48)/b10-5+
InChIKey SNKFFCBZYFGCQN-BJMVGYQFSA-N
Canonical SMILES C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O
PubChem CID 5316299
DrugBank Accession Number -
CAS Registry Number 121521-90-2

Biological activity data

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

Physicochemical properties

Molecular Weight(Computed by SwissADME) 718.61
Hac(Computed by SwissADME) 52
Volume(Computed by ADMETlab 2.0) 684.253
Density(Computed by ADMETlab 2.0) 1.05
nRing(Computed by ADMETlab 2.0) 5
MaxRing(Computed by ADMETlab 2.0) 9
nHet(Computed by ADMETlab 2.0) 16
fChar(Computed by ADMETlab 2.0) 0
nRig(Computed by ADMETlab 2.0) 33
Flexibility(Computed by ADMETlab 2.0) 0.424
Stero Centers(Computed by ADMETlab 2.0) 4
LogS(Computed by ADMETlab 2.0) -3.88
LogD(Computed by ADMETlab 2.0) 2.836

ADMET properties

logP(Computed by ADMETlab 2.0) 3.33
TPSA(Computed by SwissADME) 278.04 Ų
Hbond Acceptor(Computed by SwissADME) 16
Hbond Donor(Computed by SwissADME) 9
Rotatable Bonds(Computed by SwissADME) 14

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) -7.86 cm/s

Druglikeness

Lipinski(Computed by SwissADME) No, 3 violations: MW>500, NorO>10, NHorOH>5
Ghose(Computed by SwissADME) No, 3 violations: MW>480, MR>130, #atoms>70
Veber(Computed by SwissADME) No, 2 violations: Rotors>10, TPSA>140
Egan(Computed by SwissADME) No, 1 violation: TPSA>131.6
Muegge(Computed by SwissADME) No, 4 violations: MW>600, TPSA>150, H-acc>10, H-don>5
Bioavailability Score(Computed by SwissADME) 0.11