IPAD-DB ID | D00060 |
Name | Levodopa |
Category | Drugs |
2D Structure |
|
3D Structure | |
Molecular Formula | C 9 H 1 1 N O 4 |
Molecular Weight | 197.19 g/mol |
IUPAC Name | (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid |
InChI | InChI=1S/C9H11NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6,11-12H,3,10H2,(H,13,14)/t6-/m0/s1 |
InChIKey | WTDRDQBEARUVNC-LURJTMIESA-N |
Canonical SMILES | C1=CC(=C(C=C1CC(C(=O)O)N)O)O |
PubChem CID | 6047 |
DrugBank Accession Number | DB01235 |
CAS Registry Number | 59-92-7 |
Molecular Weight(Computed by SwissADME) | 197.19 |
Hac(Computed by SwissADME) | 14 |
Volume(Computed by ADMETlab 2.0) | 191.276 |
Density(Computed by ADMETlab 2.0) | 1.03 |
nRing(Computed by ADMETlab 2.0) | 1 |
MaxRing(Computed by ADMETlab 2.0) | 6 |
nHet(Computed by ADMETlab 2.0) | 5 |
fChar(Computed by ADMETlab 2.0) | 0 |
nRig(Computed by ADMETlab 2.0) | 7 |
Flexibility(Computed by ADMETlab 2.0) | 0.429 |
Stero Centers(Computed by ADMETlab 2.0) | 1 |
LogS(Computed by ADMETlab 2.0) | -2.194 |
LogD(Computed by ADMETlab 2.0) | -0.173 |
logP(Computed by ADMETlab 2.0) | -2.551 |
TPSA(Computed by SwissADME) | 103.78 |
Hbond Acceptor(Computed by SwissADME) | 5 |
Hbond Donor(Computed by SwissADME) | 4 |
Rotatable Bonds(Computed by SwissADME) | 3 |
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) | -9.45 |
Lipinski(Computed by SwissADME) | 0 |
Ghose(Computed by SwissADME) | 0 |
Veber(Computed by SwissADME) | 0 |
Egan(Computed by SwissADME) | 0 |
Muegge(Computed by SwissADME) | 2 |
Bioavailability Score(Computed by SwissADME) | 0.55 |