IPAD-DB ID | C01350 |
Name | Terpinen-4-ol |
Category | Natural compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 1 0 H 1 8 O |
Molecular Weight | 154.25 g/mol |
IUPAC Name | 4-methyl-1-propan-2-ylcyclohex-3-en-1-ol |
InChI | InChI=1S/C10H18O/c1-8(2)10(11)6-4-9(3)5-7-10/h4, 8, 11H, 5-7H2, 1-3H3 |
InChIKey | WRYLYDPHFGVWKC-UHFFFAOYSA-N |
Canonical SMILES | CC1=CCC(CC1)(C(C)C)O |
PubChem CID | 11230 |
DrugBank Accession Number | - |
CAS Registry Number | 562-74-3 |
Molecular Weight(Computed by SwissADME) | 154.25 |
Hac(Computed by SwissADME) | 11 |
Volume(Computed by ADMETlab 2.0) | 179.114 |
Density(Computed by ADMETlab 2.0) | 0.861 |
nRing(Computed by ADMETlab 2.0) | 1 |
MaxRing(Computed by ADMETlab 2.0) | 6 |
nHet(Computed by ADMETlab 2.0) | 1 |
fChar(Computed by ADMETlab 2.0) | 0 |
nRig(Computed by ADMETlab 2.0) | 6 |
Flexibility(Computed by ADMETlab 2.0) | 0.167 |
Stero Centers(Computed by ADMETlab 2.0) | 1 |
LogS(Computed by ADMETlab 2.0) | -2.371 |
LogD(Computed by ADMETlab 2.0) | 2.017 |
logP(Computed by ADMETlab 2.0) | 3.06 |
TPSA(Computed by SwissADME) | 20.23 |
Hbond Acceptor(Computed by SwissADME) | 1 |
Hbond Donor(Computed by SwissADME) | 1 |
Rotatable Bonds(Computed by SwissADME) |
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) | -4.93 |
Lipinski(Computed by SwissADME) | 0 |
Ghose(Computed by SwissADME) | 1 |
Veber(Computed by SwissADME) | 0 |
Egan(Computed by SwissADME) | 0 |
Muegge(Computed by SwissADME) | 2 |
Bioavailability Score(Computed by SwissADME) | 0.55 |