IPAD-DB ID | C01295 |
Name | 5-Aminopentanoic acid |
Category | Natural compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 5 H 1 1 N O 2 |
Molecular Weight | 117.15g/mol |
IUPAC Name | 5-aminopentanoic acid |
InChI | InChI=1S/C5H11NO2/c6-4-2-1-3-5(7)8/h1-4, 6H2, (H, 7, 8) |
InChIKey | JJMDCOVWQOJGCB-UHFFFAOYSA-N |
Canonical SMILES | C(CCN)CC(=O)O |
PubChem CID | 138 |
DrugBank Accession Number | - |
CAS Registry Number | 660-88-8 |
Molecular Weight(Computed by SwissADME) | 117.15 |
Hac(Computed by SwissADME) | 8 |
Volume(Computed by ADMETlab 2.0) | 120.977 |
Density(Computed by ADMETlab 2.0) | 0.968 |
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) | 4 |
Stero Centers(Computed by ADMETlab 2.0) | 0 |
LogS(Computed by ADMETlab 2.0) | 0.648 |
LogD(Computed by ADMETlab 2.0) | -1.255 |
logP(Computed by ADMETlab 2.0) | 0.2 |
TPSA(Computed by SwissADME) | 63.32 Ų |
Hbond Acceptor(Computed by SwissADME) | 3 |
Hbond Donor(Computed by SwissADME) | 2 |
Rotatable Bonds(Computed by SwissADME) | 4 |
GI Absorption(Computed by SwissADME) | High |
BBB(blood-brain barrier) Permeant(Computed by SwissADME) | Yes |
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) | -6.02 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, 2 violations: MW<200, XLOGP3<-2 |
Bioavailability Score(Computed by SwissADME) | 0.55 |