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ChemSpider 2D Image | Troglitazone | C24H27NO5S

Troglitazone

  • Molecular FormulaC24H27NO5S
  • Average mass441.540 Da
  • Monoisotopic mass441.160980 Da
  • ChemSpider ID5389

More details:

Featured data source
The Merck Index Online

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

(±)-5-[4-[(6-Hydroxy-2,5,7,8-tetramethylchroman-2-yl)methoxy]benzyl]-2,4-thiazolidinedione
2,4-Thiazolidinedione, 5-[[4-[(3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)methoxy]phenyl]methyl]- [ACD/Index Name]
5-({4-[(6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methoxy]phenyl}methyl)-1,3-thiazolidine-2,4-dione
5-[(4-{[(6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromen-2-yl)methyl]oxy}phenyl)methyl]-1,3-thiazolidine-2,4-dione
5-{4-[(6-Hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromen-2-yl)methoxy]benzyl}-1,3-thiazolidin-2,4-dion [German] [ACD/IUPAC Name]
5-{4-[(6-Hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromen-2-yl)methoxy]benzyl}-1,3-thiazolidine-2,4-dione [ACD/IUPAC Name]
5-{4-[(6-Hydroxy-2,5,7,8-tétraméthyl-3,4-dihydro-2H-chromén-2-yl)méthoxy]benzyl}-1,3-thiazolidine-2,4-dione [French] [ACD/IUPAC Name]
97322-87-7 [RN]
MFCD00878416
troglitazona [Spanish] [INN]
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

CS-045 [DBID]
1A70L3TM4P [DBID]
BFQ06OHW4R [DBID]
BRN 4338399 [DBID]
CCRIS 8969 [DBID]
CHEBI:9753 [DBID]
CI 991 [DBID]
CI-991 [DBID]
CS 045 [DBID]
D00395 [DBID]
More...
  • References
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Toxicity:

      Organic Compound; Amine; Ether; Amide; Drug; Synthetic Compound Toxin, Toxin-Target Database T3D4789

    • Safety:

      A10BG01 Wikidata Q7844989

    • Bio Activity:

      Biochemicals & small molecules/Agonists & activators Hello Bio HB2559
      Cell Cycle/DNA Damage MedChem Express HY-50935
      Cell Cycle/DNA Damage; NF-KB; MedChem Express HY-50935
      Cell process/Stem cells/Proliferation Hello Bio HB2559
      Nuclear Receptors Tocris Bioscience 3114
      Potent, selective PPARγ agonist with no activity at PPARα or PPARδ. Decreases insulin resistance and shows potent glucose-lowering effects. Also stimulates adipogenesis and induces cellcycle arrest and apoptosis in several cancer cell lines. Shows anti-diabetic and anti-inflammatory activity. Hello Bio HB2559
      Potent, selective PPARγ agonist. Inhibits hematopoietic cell line growth. Hello Bio HB2559
      PPAR MedChem Express HY-50935
      PPAR Receptors Tocris Bioscience 3114
      PPARgamma Receptors Tocris Bioscience 3114
      PPARs Tocris Bioscience 3114
      Receptors & Transporters/Nuclear hormone/PPAR/PPARγ Hello Bio HB2559
      Selective PPAR? agonist; antidiabetic agent Tocris Bioscience 3114
      Selective PPAR? receptor agonist (EC50 values are 780 and 555 nM at murine and human PPAR? receptors respectively). Displays no activity at PPAR? or PPAR? receptors. Antidiabetic agent; exerts potent glucose-lowering effects in insulin-resistant diabetic mice. Displays anti-invasive effect on human breast cancer cells; reduces migration, adhesion and spreading on fibronectin-coated plates. Also in hibits cell growth of hematopoietic cell lines. Inhibits lamellipodia formation and actin polymerization. Tocris Bioscience 3114
      Selective PPAR? receptor agonist (EC50 values are 780 and 555 nM at murine and human PPAR? receptors respectively). Displays no activity at PPAR? or PPAR? receptors. Antidiabetic agent; exerts potent glucose-lowering effects in insulin-resistant diabetic mice. Displays anti-invasive effect on human breast cancer cells; reduces migration, adhesion and spreading on fibronectin-coated plates. Also inhibits cell growth of hematopoietic cell lines. Inhibits lamellipodia formation and actin polymerization. Tocris Bioscience 3114
      Selective PPARgamma agonist; antidiabetic agent Tocris Bioscience 3114
      Selective PPARgamma receptor agonist (EC50 values are 780 and 555 nM at murine and human PPARgamma receptors respectively). Displays no activity at PPARalpha or PPARdelta receptors. Antidiabetic agent; exerts potent glucose-lowering effects in insulin-resistant diabetic mice. Displays anti-invasive effect on human breast cancer cells; reduces migration, adhesion and spreading on fibronectin-coated plates. Also inhibits cell growth of hematopoietic cell lines. Inhibits lamellipodia formation and actin polymerization. Tocris Bioscience 3114
      Troglitazone(CS-045), PPAR? agonist, is an anti-diabetic thiazolidinedione (TZD) with anti-inflammatory and anti-tumor activity.; IC50 Value: 5.71 uM and 8.38 uM (in 786-O and A498 cells) [1]; Target: PPAR?; in vitro: PPARgamma ligands inhibited RCC cell growth in a dose-dependent manner with IC50 values of 7.08 micromol/L and 11.32 micromol/L for pioglitazone, and 5.71 micromol/L and 8.38 micromol/L for troglitazone in 786-O and A498 cells, respectively [1]. MedChem Express HY-50935

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

Density: 1.3±0.1 g/cm3
Boiling Point: 657.0±55.0 °C at 760 mmHg
Vapour Pressure: 0.0±2.1 mmHg at 25°C
Enthalpy of Vaporization: 100.2±3.0 kJ/mol
Flash Point: 351.2±31.5 °C
Index of Refraction: 1.608
Molar Refractivity: 120.5±0.3 cm3
#H bond acceptors: 6
#H bond donors: 2
#Freely Rotating Bonds: 5
#Rule of 5 Violations: 0
ACD/LogP: 4.99
ACD/LogD (pH 5.5): 4.24
ACD/BCF (pH 5.5): 960.50
ACD/KOC (pH 5.5): 4572.52
ACD/LogD (pH 7.4): 3.26
ACD/BCF (pH 7.4): 98.79
ACD/KOC (pH 7.4): 470.31
Polar Surface Area: 110 Å2
Polarizability: 47.8±0.5 10-24cm3
Surface Tension: 51.0±3.0 dyne/cm
Molar Volume: 348.5±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) =  6.11

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  713.95  (Adapted Stein & Brown method)
    Melting Pt (deg C):  312.54  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  1.81E-018  (Modified Grain method)
    Subcooled liquid VP: 3.07E-015 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):  0.03863
       log Kow used: 6.11 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  0.054832 mg/L

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

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   5.77E-015  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  2.722E-017 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  6.11  (KowWin est)
  Log Kaw used:  -12.627  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  18.737
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :   1.0064
   Biowin2 (Non-Linear Model)     :   0.9646
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   1.5772  (recalcitrant)
   Biowin4 (Primary Survey Model) :   2.9085  (weeks       )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :   0.0487
   Biowin6 (MITI Non-Linear Model):   0.0068
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model): -0.9361
 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):  4.09E-013 Pa (3.07E-015 mm Hg)
  Log Koa (Koawin est  ): 18.737
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  7.33E+006 
       Octanol/air (Koa) model:  1.34E+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 = 246.3732 E-12 cm3/molecule-sec
      Half-Life =     0.043 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =     0.521 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    :  1.99E+005
      Log Koc:  5.299 

 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 = 4.006 (BCF = 1.014e+004)
       log Kow used: 6.11 (estimated)

 Volatilization from Water:
    Henry LC:  5.77E-015 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 2.132E+011  hours   (8.884E+009 days)
    Half-Life from Model Lake : 2.326E+012  hours   (9.692E+010 days)

 Removal In Wastewater Treatment:
    Total removal:              92.57  percent
    Total biodegradation:        0.77  percent
    Total sludge adsorption:    91.80  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       0.00509         1.04         1000       
   Water     1.42            4.32e+003    1000       
   Soil      46.5            8.64e+003    1000       
   Sediment  52.1            3.89e+004    0          
     Persistence Time: 9.28e+003 hr

Click to predict properties on the Chemicalize site


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