Ellagic acid C14H6O8 structure – Flashcards

Flashcard maker : Noah Thomson

Molecular Formula C14H6O8
Average mass 302.193 Da
Density 2.1±0.1 g/cm3
Boiling Point 796.5±60.0 °C at 760 mmHg
Flash Point 310.1±26.4 °C
Molar Refractivity 67.7±0.3 cm3
Polarizability 26.9±0.5 10-24cm3
Surface Tension 140.4±3.0 dyne/cm
Molar Volume 146.2±3.0 cm3
  • Experimental data
  • Predicted – ACD/Labs
  • Predicted – EPISuite
  • Predicted – ChemAxon
  • Spectroscopy
    • Lambda Max:

      366 FooDB FDB012575
  • Experimental Physico-chemical Properties
    • Experimental Melting Point:

      450 °C (Decomposes) Alfa Aesar
      450 °C (Decomposes) Alfa Aesar A15722
      300 °C LKT Labs
      [E4444]
      450 °C Jean-Claude Bradley Open Melting Point Dataset 28062
      450 °C Biosynth W-202834
      300 °C (Decomposes) LabNetwork LN00196863
      350 °C Indofine
      [E-001]
      360 °C FooDB FDB012575
    • Experimental Boiling Point:

      796.5 °C Biosynth W-202834
    • Experimental Flash Point:

      310.11 °C Biosynth W-202834
    • Experimental Gravity:

      310.11 g/mL Biosynth W-202834
    • Experimental Solubility:

      1 M NaOH: 10 mg/mL, dark green Indofine
      [E-001]
      DMSO < 10 mg/ml MedChem Express HY-B0183
      DMSO:30mg/mL MedChem Express HY-B0183
      Soluble to 0.65 mM in ethanol Tocris Bioscience 3058
      Very slightly soluble in water. Soluble in 1 N NaOH (10mg/mL). LKT Labs
      [E4444]
  • Predicted Physico-chemical Properties
    • Predicted Melting Point:

      350 °C Indofine
      [E-001]
  • Miscellaneous
    • Appearance:

      cream to light yellow crystalline solid Oxford University Chemical Safety Data (No longer updated) More details
      tan to gray Indofine
      [E-001]
    • Stability:

      Stable. Combustible. Incompatible withstrong oxidizing agents. Oxford University Chemical Safety Data (No longer updated) More details
    • Safety:

      26-37 Alfa Aesar A15722
      36/37/38 Alfa Aesar A15722
      GHS07 Biosynth W-202834
      H315 H319 H335 LKT Labs
      [E4444]
      H315; H319; H335 Biosynth W-202834
      P261; P305+P351+P338 Biosynth W-202834
      R36/37/38 LKT Labs
      [E4444]
      Safety glasses. Oxford University Chemical Safety Data (No longer updated) More details
      Warning Biosynth W-202834
      WARNING: Irreversible damage risk, protect skin/eyes/lungs. Alfa Aesar A15722
      Xi LKT Labs
      [E4444]
    • Target Organs:

      Casein Kinase inhibitor;Carbonic anhydrase inhibitor;PKA inhibitor;PKC inhibitor;SMO inhibitor TargetMol T0465
    • Chemical Class:

      aromatic Microsource
      [01502245]
    • Drug Status:

      INN Microsource
      [01502245]
    • Compound Source:

      widely distributed in higher plants Microsource
      [01502245]
    • Bio Activity:

      Casein Kinase 2 Tocris Bioscience 3058
      Cell Cycle/DNA Damage MedChem Express HY-B0183
      Cell Cycle/DNA Damage; MedChem Express HY-B0183
      CK2 MedChem Express HY-B0183
      Ellagic Acid is a cell permeable and strong casein kinase 2 (CK2) inhibitor (Ki = 20 nM) which acts as a potent antioxidant and anti-mutagenic. MedChem Express
      Ellagic Acid is a cell permeable and strong casein kinase 2 (CK2) inhibitor (Ki = 20 nM) which acts as a potent antioxidant and anti-mutagenic.; Target: CK2; Ellagic acid is a natural phenol antioxidant found in numerous fruits and vegetables. MedChem Express HY-B0183
      Ellagic Acid is a cell permeable and strong casein kinase 2 (CK2) inhibitor (Ki = 20 nM) which acts as a potent antioxidant and anti-mutagenic.;Target: CK2Ellagic acid is a natural phenol antioxidant found in numerous fruits and vegetables. The antiproliferative and antioxidant properties of ellagic acid have spurred preliminary research into the potential health benefits of ellagic acid consumption. Ellagic acid is the dilactone of hexahydroxydiphenic acid. Plants produce ellagic acid from hydrolysis of tannins such as ellagitannin and geraniin.Ellagic acid has antiproliferative and antioxidant properties in a number of in vitro and small-animal models. The antiproliferative properties of ellagic acid may be due to its ability to directly inhibit the DNA binding of certain carcinogens, including nitrosamines and polycyclic aromatic hydrocarbons. As with other polyphenol antioxidants, ellagic acid has a chemoprotective effect in cellular models by reducing oxidative stress. MedChem Express HY-B0183
      Enzyme; Metabolism; Cell Cycle/Checkpoint TargetMol T0465
      Enzymes Tocris Bioscience 3058
      Kinases Tocris Bioscience 3058
      Selective inhibitor of CK2. Also inhibits glutathione S-transferase Tocris Bioscience 3058
      Selective, ATP-competitive inhibitor of casein kinase 2 (CK2) (IC50 values are 40, 2900, 3500, 4300 and 9400 nM for CK2, Lyn, PKA, Syk and FGR respectively). Exhibits antioxidant, antitumor and antic
      arcinogenic activity and also inhibits glutathione S-transferase. Tocris Bioscience 3058
      Selective, ATP-competitive inhibitor of casein kinase 2 (CK2) (IC50 values are 40, 2900, 3500, 4300 and 9400 nM for CK2, Lyn, PKA, Syk and FGR respectively). Exhibits antioxidant, antitumor and anticarcinogenic activity and also inhibits glutathione S-transferase. Tocris Bioscience 3058
      SYK, Casein kinase II;CA;PKA;PKC;SMO TargetMol T0465
  • Gas Chromatography
    • Retention Index (Kovats):

      3070 (estimated with error: 174) NIST Spectra mainlib_235205

Predicted data is generated using the ACD/Labs Percepta Platform – PhysChem Module

Density: 2.1±0.1 g/cm3
Boiling Point: 796.5±60.0 °C at 760 mmHg
Vapour Pressure: 0.0±2.9 mmHg at 25°C
Enthalpy of Vaporization: 119.9±3.0 kJ/mol
Flash Point: 310.1±26.4 °C
Index of Refraction: 1.895
Molar Refractivity: 67.7±0.3 cm3
#H bond acceptors: 8
#H bond donors: 4
#Freely Rotating Bonds: 0
#Rule of 5 Violations: 0
ACD/LogP: 0.52
ACD/LogD (pH 5.5): 0.83
ACD/BCF (pH 5.5): 1.71
ACD/KOC (pH 5.5): 32.22
ACD/LogD (pH 7.4): -2.08
ACD/BCF (pH 7.4): 1.00
ACD/KOC (pH 7.4): 1.00
Polar Surface Area: 134 Å2
Polarizability: 26.9±0.5 10-24cm3
Surface Tension: 140.4±3.0 dyne/cm
Molar Volume: 146.2±3.0 cm3

Predicted data is generated using the US Environmental Protection Agency’s EPISuite™

 
 Log Octanol-Water Partition Coef (SRC):
 Log Kow (KOWWIN v1.67 estimate) = -2.05

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
 Boiling Pt (deg C): 593.63 (Adapted Stein & Brown method)
 Melting Pt (deg C): 256.33 (Mean or Weighted MP)
 VP(mm Hg,25 deg C): 2.81E-015 (Modified Grain method)
 Subcooled liquid VP: 9.41E-013 mm Hg (25 deg C, Mod-Grain method)

 Water Solubility Estimate from Log Kow (WSKOW v1.41):
 Water Solubility at 25 deg C (mg/L): 1.964e+005
 log Kow used: -2.05 (estimated)
 no-melting pt equation used

 Water Sol Estimate from Fragments:
 Wat Sol (v1.01 est) = 7.0721 mg/L

 ECOSAR Class Program (ECOSAR v0.99h):
 Class(es) found:
 Esters
 Phenols

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
 Bond Method : 5.67E-024 atm-m3/mole
 Group Method: Incomplete
 Henrys LC [VP/WSol estimate using EPI values]: 5.689E-021 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
 Log Kow used: -2.05 (KowWin est)
 Log Kaw used: -21.635 (HenryWin est)
 Log Koa (KOAWIN v1.10 estimate): 19.585
 Log Koa (experimental database): None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
 Biowin1 (Linear Model) : 1.4153
 Biowin2 (Non-Linear Model) : 1.0000
 Expert Survey Biodegradation Results:
 Biowin3 (Ultimate Survey Model): 3.0373 (weeks )
 Biowin4 (Primary Survey Model) : 4.0284 (days )
 MITI Biodegradation Probability:
 Biowin5 (MITI Linear Model) : 0.7739
 Biowin6 (MITI Non-Linear Model): 0.7084
 Anaerobic Biodegradation Probability:
 Biowin7 (Anaerobic Linear Model): 1.3118
 Ready Biodegradability Prediction: YES

Hydrocarbon Biodegradation (BioHCwin v1.01):
 Structure incompatible with current estimation method!

 Sorption to aerosols (25 Dec C)[AEROWIN v1.00]:
 Vapor pressure (liquid/subcooled): 1.25E-010 Pa (9.41E-013 mm Hg)
 Log Koa (Koawin est ): 19.585
 Kp (particle/gas partition coef. (m3/ug)):
 Mackay model : 2.39E+004 
 Octanol/air (Koa) model: 9.44E+006 
 Fraction sorbed to airborne particulates (phi):
 Junge-Pankow model : 1 
 Mackay model : 1 
 Octanol/air (Koa) model: 1 

 Atmospheric Oxidation (25 deg C) [AopWin v1.92]:
 Hydroxyl Radicals Reaction:
 OVERALL OH Rate Constant = 14.8105 E-12 cm3/molecule-sec
 Half-Life = 0.722 Days (12-hr day; 1.5E6 OH/cm3)
 Half-Life = 8.666 Hrs
 Ozone Reaction:
 No Ozone Reaction Estimation
 Reaction With Nitrate Radicals May Be Important!
 Fraction sorbed to airborne particulates (phi): 1 (Junge,Mackay)
 Note: the sorbed fraction may be resistant to atmospheric oxidation

 Soil Adsorption Coefficient (PCKOCWIN v1.66):
 Koc : 3418
 Log Koc: 3.534 

 Aqueous Base/Acid-Catalyzed Hydrolysis (25 deg C) [HYDROWIN v1.67]:
 Rate constants can NOT be estimated for this structure!

 Bioaccumulation Estimates from Log Kow (BCFWIN v2.17):
 Log BCF from regression-based method = 0.500 (BCF = 3.162)
 log Kow used: -2.05 (estimated)

 Volatilization from Water:
 Henry LC: 5.67E-024 atm-m3/mole (estimated by Bond SAR Method)
 Half-Life from Model River: 1.795E+020 hours (7.479E+018 days)
 Half-Life from Model Lake : 1.958E+021 hours (8.159E+019 days)

 Removal In Wastewater Treatment:
 Total removal: 1.85 percent
 Total biodegradation: 0.09 percent
 Total sludge adsorption: 1.75 percent
 Total to Air: 0.00 percent
 (using 10000 hr Bio P,A,S)

 Level III Fugacity Model:
 Mass Amount Half-Life Emissions
 (percent) (hr) (kg/hr)
 Air 2.21e-010 17.3 1000 
 Water 39 360 1000 
 Soil 60.9 720 1000 
 Sediment 0.0713 3.24e+003 0 
 Persistence Time: 579 hr




 

Click to predict properties on the Chemicalize site

Get an explanation on any task
Get unstuck with the help of our AI assistant in seconds
New