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Search term: VHXGVJKLCIYCNY-UHFFFAOYAQ
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Inherent Properties, Identifiers and References
ChemSpider ID: 2790205
Empirical Formula: C24H23BrN6O
Molecular Weight: 491.383
Nominal Mass: 490 Da
Average Mass: 491.383 Da
Monoisotopic Mass: 490.111664 Da
Systematic Name: 1-[4-[1-(benzotriazol-1-ylmethyl)imidazol-2-yl]-1-piperidyl]-3-(2​-bromophenyl)prop-2-en-1-one
SMILES: Brc1ccccc1C=CC(=O)N5CCC(c2nccn2Cn4nnc3ccccc34)CC5
InChI: InChI=1/C24H23BrN6O/c25-20-6-2-1-5-18(20)9-10-23(32)29-14-11-19(1​2-15-29)24-26-13-16-30(24)17-31-22-8-4-3-7-21(22)27-28-31/h1-10,1​3,16,19H,11-12,14-15,17H2
InChIKey: VHXGVJKLCIYCNY-UHFFFAOYAQ
Std. InChI: InChI=1S/C24H23BrN6O/c25-20-6-2-1-5-18(20)9-10-23(32)29-14-11-19(​12-15-29)24-26-13-16-30(24)17-31-22-8-4-3-7-21(22)27-28-31/h1-10,​13,16,19H,11-12,14-15,17H2
Std. InChIKey: VHXGVJKLCIYCNY-UHFFFAOYSA-N
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ACD/LogP: 3.91 # of Rule of 5 Violations: 0
ACD/LogD (pH 5.5): 3.04 ACD/LogD (pH 7.4): 3.87
ACD/BCF (pH 5.5): 73.76 ACD/BCF (pH 7.4): 506.76
ACD/KOC (pH 5.5): 427.47 ACD/KOC (pH 7.4): 2936.89
#H bond acceptors: 7 #H bond donors: 0
#Freely Rotating Bonds: 5 Polar Surface Area: 68.84 Å2
Index of Refraction: 1.709 Molar Refractivity: 129.85 cm3
Molar Volume: 332.3 cm3 Polarizability: 51.47 10-24cm3
Surface Tension: 58.1 dyne/cm Density: 1.47 g/cm3
Flash Point: 412.5 °C Enthalpy of Vaporization: 110.5 kJ/mol
Boiling Point: 758.5 °C at 760 mmHg Vapour Pressure: 6.66E-23 mmHg at 25°C
            
 Log Octanol-Water Partition Coef (SRC):
    Log Kow (KOWWIN v1.67 estimate) =  4.30

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  662.67  (Adapted Stein & Brown method)
    Melting Pt (deg C):  288.58  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  1.96E-015  (Modified Grain method)
    Subcooled liquid VP: 1.65E-012 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):  0.1724
       log Kow used: 4.30 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  3.5662 mg/L

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

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   2.67E-017  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  7.351E-015 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  4.30  (KowWin est)
  Log Kaw used:  -14.962  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  19.262
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :   0.6681
   Biowin2 (Non-Linear Model)     :   0.0848
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   1.8482  (months      )
   Biowin4 (Primary Survey Model) :   3.1222  (weeks       )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :  -0.2432
   Biowin6 (MITI Non-Linear Model):   0.0017
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model): -1.3686
 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):  2.2E-010 Pa (1.65E-012 mm Hg)
  Log Koa (Koawin est  ): 19.262
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  1.36E+004 
       Octanol/air (Koa) model:  4.49E+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 = 138.4182 E-12 cm3/molecule-sec [Cis-isomer]
      OVERALL OH Rate Constant = 141.0782 E-12 cm3/molecule-sec [Trans-isomer]
      Half-Life =    0.927 Hrs (12-hr day; 1.5E6 OH/cm3) [Cis-isomer]
      Half-Life =    0.910 Hrs (12-hr day; 1.5E6 OH/cm3) [Trans-isomer]
   Ozone Reaction:
      OVERALL Ozone Rate Constant =     1.050000 E-17 cm3/molecule-sec [Cis-]
      OVERALL Ozone Rate Constant =     2.100000 E-17 cm3/molecule-sec [Trans-]
      Half-Life =     1.091 Days (at 7E11 mol/cm3) [Cis-isomer]
      Half-Life =    13.097 Hrs (at 7E11 mol/cm3) [Trans-isomer]
   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    :  8.702E+006
      Log Koc:  6.940 

 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 = 2.612 (BCF = 409.4)
       log Kow used: 4.30 (estimated)

 Volatilization from Water:
    Henry LC:  2.67E-017 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 4.861E+013  hours   (2.025E+012 days)
    Half-Life from Model Lake : 5.303E+014  hours   (2.209E+013 days)

 Removal In Wastewater Treatment:
    Total removal:              45.27  percent
    Total biodegradation:        0.44  percent
    Total sludge adsorption:    44.83  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       0.000137        1.73         1000       
   Water     8.07            1.44e+003    1000       
   Soil      86.9            2.88e+003    1000       
   Sediment  4.99            1.3e+004     0          
     Persistence Time: 3e+003 hr




        
Descriptors: 0, 0, 0, 0, 1, 0, 0, 5, 0, 0, 0, 0, 11, 9, 0, 2, 20, 2, 1, 0, 2, 3, 0, 0
CategoryTargetPDB CodeLASSO Score
KinasesPDGFrb, platelet derived growth factor receptor kinaseN/A0.70
KinasesP38 MAP, P38 mitogen activated protein1kv20.07
Other EnzymesInhA, enoyl ACP reductase1p440.07
Nuclear Hormone ReceptorsPPARg, peroxisome proliferator activated receptor1fm90.05
Other EnzymesHIVRT, HIV reverse transcriptase1rt10.02
KinasesVEGFr2, vascular endothelial growth factor receptor1vr20.02
Other EnzymesCOX-1, cyclooxygenase-11p4g0.02
Serine ProteasesFXa, factor Xa1f0r0.02
Nuclear Hormone ReceptorsGR, glucocorticoid receptor1m2z0.01
KinasesSRC, tyrosine kinase SRC2src0.01
Serine ProteasesThrombin1ba80.01
Other EnzymesHMGR, hydroxymethylglutaryl-CoA reductase1hw80.01
Other EnzymesHIVPR, HIV protease1hpx0.01
KinasesHSP90, human heat shock protein 901uy60.01
Nuclear Hormone ReceptorsMR, mineralocorticoid receptor2aa20.01
Other EnzymesAChE, acetylcholinesterase1eve0.01
Nuclear Hormone ReceptorsPR, progesterone receptor1sr70.01
Other EnzymesPARP, poly(ADP-ribose) polymerase1efy0.01
Nuclear Hormone ReceptorsER, estrogen receptor; antagonist3ert0.01
Other EnzymesAmpC, AmpC beta-lactamase1xgj0.00
Other EnzymesPNP, purine nucleoside phosphorylase1b8o0.00
Nuclear Hormone ReceptorsRXRa, retinoic X receptor R1mvc0.00
Nuclear Hormone ReceptorsER, estrogen receptor; agonist1l2i0.00
Folate EnzymesDHFR, dihydrofolate reductase3dfr0.00
MetalloenzymesACE, angiotensin-converting enzyme1o860.00
Serine ProteasesTrypsin1bju0.00
Other EnzymesGPB, glycogen phosphorylase1a8i0.00
MetalloenzymesPDE5, phosphodiesterase 51xp00.00
Other EnzymesSAHH, S-adenosyl-homocysteine hydrolase1a7a0.00
KinasesFGFr1, fibroblast growth factor receptor kinase1agw0.00
Other EnzymesCOX-2, cyclooxygenase-21cx20.00
KinasesCDK2, cyclindependent kinase 21ckp0.00
MetalloenzymesCOMT, catechol O-methyltransferase1h1d0.00
Other EnzymesALR2, aldose reductase1ah30.00
Other EnzymesNA, neuraminidase1a4g0.00
KinasesTK, thymidine kinase1kim0.00
MetalloenzymesADA, adenosine deaminase1stw0.00
Nuclear Hormone ReceptorsAR, androgen receptor1xq20.00
Folate EnzymesGART, glycinamide ribonucleotide transformylase1c2t0.00
KinasesEGFr, epidermal growth factor receptor1m170.00