IPAD-DB ID | C00783 |
Name | (-)-Epigallocatechin (EGC) |
Category | Natural compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 1 5 H 1 4 O 7 |
Molecular Weight | 306.27 g/mol |
IUPAC Name | (2R, 3R)-2-(3, 4, 5-trihydroxyphenyl)-3, 4-dihydro-2H-chromene-3, 5, 7-triol |
InChI | InChI=1S/C15H14O7/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6/h1-4, 12, 15-21H, 5H2/t12-, 15-/m1/s1 |
InChIKey | XMOCLSLCDHWDHP-IUODEOHRSA-N |
Canonical SMILES | C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O |
PubChem CID | 72277 |
DrugBank Accession Number | - |
CAS Registry Number | 970-74-1 |
Molecular Weight(Computed by SwissADME) | 306.27 |
Hac(Computed by SwissADME) | 22 |
Volume(Computed by ADMETlab 2.0) | 288.04 |
Density(Computed by ADMETlab 2.0) | 1.063 |
nRing(Computed by ADMETlab 2.0) | 3 |
MaxRing(Computed by ADMETlab 2.0) | 10 |
nHet(Computed by ADMETlab 2.0) | 7 |
fChar(Computed by ADMETlab 2.0) | 0 |
nRig(Computed by ADMETlab 2.0) | 17 |
Flexibility(Computed by ADMETlab 2.0) | 0.059 |
Stero Centers(Computed by ADMETlab 2.0) | 2 |
LogS(Computed by ADMETlab 2.0) | -2.88 |
LogD(Computed by ADMETlab 2.0) | 0.905 |
logP(Computed by ADMETlab 2.0) | 0.736 |
TPSA(Computed by SwissADME) | 130.61 |
Hbond Acceptor(Computed by SwissADME) | 7 |
Hbond Donor(Computed by SwissADME) | 6 |
Rotatable Bonds(Computed by SwissADME) |
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) | -8.17 |
Lipinski(Computed by SwissADME) | 1 |
Ghose(Computed by SwissADME) | 0 |
Veber(Computed by SwissADME) | 0 |
Egan(Computed by SwissADME) | 0 |
Muegge(Computed by SwissADME) | 1 |
Bioavailability Score(Computed by SwissADME) | 0.55 |