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Search term: MSHPPRCEXZALPL-UHFFFAOYAC
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Inherent Properties, Identifiers and References
ChemSpider ID: 630188
Empirical Formula: C17H16O4
Molecular Weight: 284.3065
Nominal Mass: 284 Da
Average Mass: 284.3065 Da
Monoisotopic Mass: 284.104859 Da
Systematic Name: (4-phenylphenyl) methyl butanedioate
SMILES: O=C(Oc1ccc(cc1)c2ccccc2)CCC(=O)OC
InChI: InChI=1/C17H16O4/c1-20-16(18)11-12-17(19)21-15-9-7-14(8-10-15)13-​5-3-2-4-6-13/h2-10H,11-12H2,1H3
InChIKey: MSHPPRCEXZALPL-UHFFFAOYAC
Std. InChI: InChI=1S/C17H16O4/c1-20-16(18)11-12-17(19)21-15-9-7-14(8-10-15)13​-5-3-2-4-6-13/h2-10H,11-12H2,1H3
Std. InChIKey: MSHPPRCEXZALPL-UHFFFAOYSA-N
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Otava ChemicalsAcetylcholinesterase (AChE)
Names and Synonyms

Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts

biphenyl-​4-yl meth​yl butane​dioate

butanedio​ic acid, ​[1,1'-bip​henyl]-4-​yl methyl​ ester

1-[1,1'-b​iphenyl]-​4-yl 4-me​thyl succ​inate

4-bipheny​lyl methy​l succina​te

Database ID(s)

Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts

ACD/LogP: 3.83 # of Rule of 5 Violations: 0
ACD/LogD (pH 5.5): ACD/LogD (pH 7.4):
ACD/BCF (pH 5.5): ACD/BCF (pH 7.4):
ACD/KOC (pH 5.5): ACD/KOC (pH 7.4):
#H bond acceptors: 4 #H bond donors: 0
#Freely Rotating Bonds: 7 Polar Surface Area: 52.6 Å2
Index of Refraction: 1.547 Molar Refractivity: 77.85 cm3
Molar Volume: 245.3 cm3 Polarizability: 30.86 10-24cm3
Surface Tension: 42.4 dyne/cm Density: 1.158 g/cm3
Flash Point: 217.7 °C Enthalpy of Vaporization: 68.76 kJ/mol
Boiling Point: 431.9 °C at 760 mmHg Vapour Pressure: 1.16E-07 mmHg at 25°C
            
 Log Octanol-Water Partition Coef (SRC):
    Log Kow (KOWWIN v1.67 estimate) =  3.39

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  378.33  (Adapted Stein & Brown method)
    Melting Pt (deg C):  41.38  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  1.97E-005  (Modified Grain method)
    Subcooled liquid VP: 2.78E-005 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):  19.44
       log Kow used: 3.39 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  6.5549 mg/L

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

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   1.57E-008  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  3.791E-007 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  3.39  (KowWin est)
  Log Kaw used:  -6.193  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  9.583
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :   1.0886
   Biowin2 (Non-Linear Model)     :   0.9999
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   2.8733  (weeks       )
   Biowin4 (Primary Survey Model) :   3.9004  (days        )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :   0.7270
   Biowin6 (MITI Non-Linear Model):   0.7631
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model):  0.5115
 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):  0.00371 Pa (2.78E-005 mm Hg)
  Log Koa (Koawin est  ): 9.583
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  0.000809 
       Octanol/air (Koa) model:  0.00094 
   Fraction sorbed to airborne particulates (phi):
       Junge-Pankow model     :  0.0284 
       Mackay model           :  0.0608 
       Octanol/air (Koa) model:  0.0699 

 Atmospheric Oxidation (25 deg C) [AopWin v1.92]:
   Hydroxyl Radicals Reaction:
      OVERALL OH Rate Constant =   6.8053 E-12 cm3/molecule-sec
      Half-Life =     1.572 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =    18.861 Hrs
   Ozone Reaction:
      No Ozone Reaction Estimation
   Fraction sorbed to airborne particulates (phi): 0.0446 (Junge,Mackay)
    Note: the sorbed fraction may be resistant to atmospheric oxidation

 Soil Adsorption Coefficient (PCKOCWIN v1.66):
      Koc    :  2640
      Log Koc:  3.422 

 Aqueous Base/Acid-Catalyzed Hydrolysis (25 deg C) [HYDROWIN v1.67]:
  Total Kb for pH > 8 at 25 deg C :  5.161E-001  L/mol-sec
  Kb Half-Life at pH 8:      15.544  days   
  Kb Half-Life at pH 7:     155.439  days   

 Bioaccumulation Estimates from Log Kow (BCFWIN v2.17):
   Log BCF from regression-based method = 1.907 (BCF = 80.69)
       log Kow used: 3.39 (estimated)

 Volatilization from Water:
    Henry LC:  1.57E-008 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 6.288E+004  hours   (2620 days)
    Half-Life from Model Lake : 6.861E+005  hours   (2.859E+004 days)

 Removal In Wastewater Treatment:
    Total removal:              10.76  percent
    Total biodegradation:        0.17  percent
    Total sludge adsorption:    10.60  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       0.247           37.7         1000       
   Water     17.1            360          1000       
   Soil      82.1            720          1000       
   Sediment  0.607           3.24e+003    0          
     Persistence Time: 735 hr




        
Descriptors: 0, 0, 0, 0, 0, 0, 0, 4, 2, 0, 0, 0, 4, 9, 3, 0, 12, 4, 2, 0, 0, 0, 0, 0
CategoryTargetPDB CodeLASSO Score
Nuclear Hormone ReceptorsPPARg, peroxisome proliferator activated receptor1fm90.08
Other EnzymesInhA, enoyl ACP reductase1p440.04
Other EnzymesAChE, acetylcholinesterase1eve0.03
Other EnzymesHIVRT, HIV reverse transcriptase1rt10.02
Serine ProteasesFXa, factor Xa1f0r0.02
KinasesSRC, tyrosine kinase SRC2src0.01
Other EnzymesHMGR, hydroxymethylglutaryl-CoA reductase1hw80.01
MetalloenzymesPDE5, phosphodiesterase 51xp00.01
Nuclear Hormone ReceptorsMR, mineralocorticoid receptor2aa20.01
Other EnzymesHIVPR, HIV protease1hpx0.01
KinasesVEGFr2, vascular endothelial growth factor receptor1vr20.01
Nuclear Hormone ReceptorsPR, progesterone receptor1sr70.01
Nuclear Hormone ReceptorsER, estrogen receptor; antagonist3ert0.01
Other EnzymesPARP, poly(ADP-ribose) polymerase1efy0.01
KinasesPDGFrb, platelet derived growth factor receptor kinaseN/A0.00
Other EnzymesAmpC, AmpC beta-lactamase1xgj0.00
Other EnzymesPNP, purine nucleoside phosphorylase1b8o0.00
Serine ProteasesThrombin1ba80.00
Nuclear Hormone ReceptorsER, estrogen receptor; agonist1l2i0.00
MetalloenzymesACE, angiotensin-converting enzyme1o860.00
Folate EnzymesDHFR, dihydrofolate reductase3dfr0.00
Other EnzymesGPB, glycogen phosphorylase1a8i0.00
Serine ProteasesTrypsin1bju0.00
KinasesFGFr1, fibroblast growth factor receptor kinase1agw0.00
Nuclear Hormone ReceptorsRXRa, retinoic X receptor R1mvc0.00
Other EnzymesSAHH, S-adenosyl-homocysteine hydrolase1a7a0.00
MetalloenzymesCOMT, catechol O-methyltransferase1h1d0.00
Folate EnzymesGART, glycinamide ribonucleotide transformylase1c2t0.00
Other EnzymesCOX-1, cyclooxygenase-11p4g0.00
Other EnzymesALR2, aldose reductase1ah30.00
Other EnzymesNA, neuraminidase1a4g0.00
MetalloenzymesADA, adenosine deaminase1stw0.00
KinasesP38 MAP, P38 mitogen activated protein1kv20.00
Nuclear Hormone ReceptorsAR, androgen receptor1xq20.00
Nuclear Hormone ReceptorsGR, glucocorticoid receptor1m2z0.00
KinasesTK, thymidine kinase1kim0.00
KinasesHSP90, human heat shock protein 901uy60.00
KinasesCDK2, cyclindependent kinase 21ckp0.00
Other EnzymesCOX-2, cyclooxygenase-21cx20.00
KinasesEGFr, epidermal growth factor receptor1m170.00