ChemSpider 2D Image | Isobutyl (3Z)-2-oxo-3-{[(4-sulfamoylphenyl)amino]methylene}-5-indolinecarboxylate | C20H21N3O5S

Isobutyl (3Z)-2-oxo-3-{[(4-sulfamoylphenyl)amino]methylene}-5-indolinecarboxylate

  • Molecular FormulaC20H21N3O5S
  • Average mass415.463 Da
  • Monoisotopic mass415.120178 Da
  • ChemSpider ID5021549
  • Double-bond stereo - Double-bond stereo


More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

(3Z)-2-Oxo-3-{[(4-sulfamoylphényl)amino]méthylène}-5-indolinecarboxylate d'isobutyle [French] [ACD/IUPAC Name]
1H-Indole-5-carboxylic acid, 3-[[[4-(aminosulfonyl)phenyl]amino]methylene]-2,3-dihydro-2-oxo-, 2-methylpropyl ester, (3Z)- [ACD/Index Name]
2-methylpropyl (3Z)-2-oxo-3-{[(4-sulfamoylphenyl)amino]methylidene}-2,3-dihydro-1H-indole-5-carboxylate
Isobutyl (3Z)-2-oxo-3-{[(4-sulfamoylphenyl)amino]methylene}-5-indolinecarboxylate [ACD/IUPAC Name]
Isobutyl-(3Z)-2-oxo-3-{[(4-sulfamoylphenyl)amino]methylen}-5-indolincarboxylat [German] [ACD/IUPAC Name]
2-oxo-3-[1-(4-sulfamoyl-phenylamino)-meth-(Z)-ylidene]-2,3-dihydro-1H-indole-5-carboxylic acid isobutyl ester
GW416981X
https://www.ebi.ac.uk/chembl/compoundreportcard/CHEMBL269883/
Oxindole-Based Inhibitor 54

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

Density: 1.4±0.1 g/cm3
Boiling Point:
Vapour Pressure:
Enthalpy of Vaporization:
Flash Point:
Index of Refraction: 1.659
Molar Refractivity: 107.8±0.4 cm3
#H bond acceptors: 8
#H bond donors: 4
#Freely Rotating Bonds: 7
#Rule of 5 Violations: 0
ACD/LogP: 3.93
ACD/LogD (pH 5.5): 2.32
ACD/BCF (pH 5.5): 34.08
ACD/KOC (pH 5.5): 435.11
ACD/LogD (pH 7.4): 2.32
ACD/BCF (pH 7.4): 34.01
ACD/KOC (pH 7.4): 434.25
Polar Surface Area: 136 Å2
Polarizability: 42.7±0.5 10-24cm3
Surface Tension: 68.7±3.0 dyne/cm
Molar Volume: 292.3±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) =  1.78

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  628.39  (Adapted Stein & Brown method)
    Melting Pt (deg C):  272.57  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  2.5E-014  (Modified Grain method)
    Subcooled liquid VP: 1.33E-011 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):  74.26
       log Kow used: 1.78 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  22.74 mg/L

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

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   9.27E-020  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  1.840E-016 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  1.78  (KowWin est)
  Log Kaw used:  -17.421  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  19.201
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :   0.7003
   Biowin2 (Non-Linear Model)     :   0.8779
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   2.2321  (months      )
   Biowin4 (Primary Survey Model) :   3.5743  (days-weeks  )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :  -0.1479
   Biowin6 (MITI Non-Linear Model):   0.0022
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model): -0.8783
 Ready Biodegradability Prediction:   NO

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

 Sorption to aerosols (25 Dec C)[AEROWIN v1.00]:
  Vapor pressure (liquid/subcooled):  1.77E-009 Pa (1.33E-011 mm Hg)
  Log Koa (Koawin est  ): 19.201
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  1.69E+003 
       Octanol/air (Koa) model:  3.9E+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 =  44.8926 E-12 cm3/molecule-sec
      Half-Life =     0.238 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =     2.859 Hrs
   Ozone Reaction:
      OVERALL Ozone Rate Constant =     2.100000 E-17 cm3/molecule-sec
      Half-Life =     0.546 Days (at 7E11 mol/cm3)
      Half-Life =     13.097 Hrs
   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    :  9086
      Log Koc:  3.958 

 Aqueous Base/Acid-Catalyzed Hydrolysis (25 deg C) [HYDROWIN v1.67]:
  Total Kb for pH > 8 at 25 deg C :  3.338E-002  L/mol-sec
  Kb Half-Life at pH 8:     240.316  days   
  Kb Half-Life at pH 7:       6.579  years  

 Bioaccumulation Estimates from Log Kow (BCFWIN v2.17):
   Log BCF from regression-based method = 0.670 (BCF = 4.675)
       log Kow used: 1.78 (estimated)

 Volatilization from Water:
    Henry LC:  9.27E-020 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 1.287E+016  hours   (5.364E+014 days)
    Half-Life from Model Lake : 1.404E+017  hours   (5.852E+015 days)

 Removal In Wastewater Treatment:
    Total removal:               2.09  percent
    Total biodegradation:        0.09  percent
    Total sludge adsorption:     1.99  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       9.56e-008       3.98         1000       
   Water     28.2            1.44e+003    1000       
   Soil      71.7            2.88e+003    1000       
   Sediment  0.0885          1.3e+004     0          
     Persistence Time: 1.7e+003 hr




                    

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