DENV2SEQ10

Peptide Sequence

Gly Trp Val Pro Arg Val Val Asp Glu Val Phe His Ile Thr Lys Arg Ser Ala

Single Letter Code: GWVPRVVDEVFHITKRSA

3D Structure Visualization

ADMET Properties

Comprehensive Drug Property Analysis

Absorption

  • Water solubility -2.892 (log mol/L)
  • Caco2 permeability -0.756 (log Papp in 10-6 cm/s)
  • Intestinal absorption (human) 0 (% Absorbed)
  • Skin Permeability -2.735 (log Kp)
  • P-glycoprotein substrate Yes
  • P-glycoprotein I inhibitor Yes
  • P-glycoprotein II inhibitor Yes

Distribution

  • VDss (human) -0.024 (log L/kg)
  • Fraction unbound (human) 0.38 (Fu)
  • BBB permeability -5.562 (log BB)
  • CNS permeability -10.158 (log PS)

Metabolism

  • CYP2D6 substrate No
  • CYP3A4 substrate Yes
  • CYP1A2 inhibitior No
  • CYP2C19 inhibitior No
  • CYP2C9 inhibitior No
  • CYP2D6 inhibitior No
  • CYP3A4 inhibitior No

Excretion

  • Total Clearance -0.609 (log ml/min/kg)
  • Renal OCT2 substrate No

Toxicity

  • AMES toxicity No
  • Max. tolerated dose (human) 0.438 (log mg/kg/day)
  • hERG I inhibitor No
  • hERG II inhibitor Yes
  • Oral Rat Acute Toxicity (LD50) 2.482 (mol/kg)
  • Oral Rat Chronic Toxicity (LOAEL) 4.65 (log mg/kg_bw/day)
  • Hepatotoxicity Yes
  • Skin Sensitisation No
  • T.Pyriformis toxicity 0.285 (log ug/L)
  • Minnow toxicity 3.594 (log mM)