IPAD-DB ID | C01294 |
Name | 4-Aminobutanoic acid |
Category | Natural compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 4 H 9 N O 2 |
Molecular Weight | 103.12g/mol |
IUPAC Name | 4-aminobutanoic acid |
InChI | InChI=1S/C4H9NO2/c5-3-1-2-4(6)7/h1-3, 5H2, (H, 6, 7) |
InChIKey | BTCSSZJGUNDROE-UHFFFAOYSA-N |
Canonical SMILES | C(CC(=O)O)CN |
PubChem CID | 119 |
DrugBank Accession Number | - |
CAS Registry Number | 1956-12-2 |
Molecular Weight(Computed by SwissADME) | 103.12 |
Hac(Computed by SwissADME) | 7 |
Volume(Computed by ADMETlab 2.0) | 103.681 |
Density(Computed by ADMETlab 2.0) | 0.994 |
nRing(Computed by ADMETlab 2.0) | 0 |
MaxRing(Computed by ADMETlab 2.0) | 0 |
nHet(Computed by ADMETlab 2.0) | 3 |
fChar(Computed by ADMETlab 2.0) | 0 |
nRig(Computed by ADMETlab 2.0) | 1 |
Flexibility(Computed by ADMETlab 2.0) | 3 |
Stero Centers(Computed by ADMETlab 2.0) | 0 |
LogS(Computed by ADMETlab 2.0) | 0.681 |
LogD(Computed by ADMETlab 2.0) | -1.383 |
logP(Computed by ADMETlab 2.0) | -0.19 |
TPSA(Computed by SwissADME) | 63.32 Ų |
Hbond Acceptor(Computed by SwissADME) | 3 |
Hbond Donor(Computed by SwissADME) | 2 |
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) | -9.18 cm/s |
Lipinski(Computed by SwissADME) | Yes, 0 violation |
Ghose(Computed by SwissADME) | No, 3 violations: MW<160, MR<40, #atoms<20 |
Veber(Computed by SwissADME) | Yes |
Egan(Computed by SwissADME) | Yes |
Muegge(Computed by SwissADME) | No, 3 violations: MW<200, XLOGP3<-2, #C<5 |
Bioavailability Score(Computed by SwissADME) | 0.55 |