IPAD-DB ID | S00191 |
Name | Dihydrolipoic acid |
Category | Synthetic compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 8 H 1 6 O 2 S 2 |
Molecular Weight | 208.3 g/mol |
IUPAC Name | 6, 8-bis(sulfanyl)octanoic acid |
InChI | InChI=1S/C8H16O2S2/c9-8(10)4-2-1-3-7(12)5-6-11/h7, 11-12H, 1-6H2, (H, 9, 10) |
InChIKey | IZFHEQBZOYJLPK-UHFFFAOYSA-N |
Canonical SMILES | C(CCC(=O)O)CC(CCS)S |
PubChem CID | 421 |
DrugBank Accession Number | - |
CAS Registry Number | 462-20-4 |
Molecular Weight(Computed by SwissADME) | 208.34 |
Hac(Computed by SwissADME) | 12 |
Volume(Computed by ADMETlab 2.0) | 198.886 |
Density(Computed by ADMETlab 2.0) | 1.046 |
nRing(Computed by ADMETlab 2.0) | 0 |
MaxRing(Computed by ADMETlab 2.0) | 0 |
nHet(Computed by ADMETlab 2.0) | 4 |
fChar(Computed by ADMETlab 2.0) | 0 |
nRig(Computed by ADMETlab 2.0) | 1 |
Flexibility(Computed by ADMETlab 2.0) | 7 |
Stero Centers(Computed by ADMETlab 2.0) | 1 |
LogS(Computed by ADMETlab 2.0) | -2.24 |
LogD(Computed by ADMETlab 2.0) | 0.868 |
logP(Computed by ADMETlab 2.0) | 2.08 |
TPSA(Computed by SwissADME) | 114.9 |
Hbond Acceptor(Computed by SwissADME) | 2 |
Hbond Donor(Computed by SwissADME) | 1 |
Rotatable Bonds(Computed by SwissADME) | 7 |
GI Absorption(Computed by SwissADME) | High |
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) | -5.86 |
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) | 0.56 |