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Inherent Properties, Identifiers and References
ChemSpider ID: 34272
Empirical Formula: C20H25N3O
Molecular Weight: 323.432
Nominal Mass: 323 Da
Average Mass: 323.432 Da
Monoisotopic Mass: 323.199762 Da
Quick Links: Permalink Similar Isomers
Systematic Name:
SMILES: O(c1ccc3c(c1)C(c2c(nccc2)CC3)N4CCN(CC4)C)C
InChI: InChI=1/C20H25N3O/c1-22-10-12-23(13-11-22)20-17-4-3-9-21-19(17)8-​6-15-5-7-16(24-2)14-18(15)20/h3-5,7,9,14,20H,6,8,10-13H2,1-2H3
InChIKey: KZKGAKPGDZFAIK-UHFFFAOYAM
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Names and Synonyms

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

10,11-Dih​ydro-7-me​thoxy-5-(​N-methylp​iperaziny​l)-5H-ben​zo(4,5)cy​clohepta(​1,2-b)pyr​idine

36040-30-9 [RN]

5H-BENZO(​4,5)CYCLO​HEPTA(1,2​-b)PYRIDI​NE, 10,11​-DIHYDRO-​7-METHOXY​-5-(N-MET​HYLPIPER

5H-Benzo(​4,5)cyclo​hepta(1,2​-b)pyridi​ne, 10,11​-dihydro-​7-methoxy​-5-(N-met​hylpipera​zinyl)-

Database ID(s)

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

(Details...) Predicted Properties
LogP: ACD/LogP: 1.73
XLogP: 1.60
ALOGPS: 2.66
# of Rule of 5 Violations: 0
ACD/LogD (pH 5.5): -0.95 ACD/LogD (pH 7.4): 0.85
ACD/BCF (pH 5.5): 1 ACD/BCF (pH 7.4): 1.62
ACD/KOC (pH 5.5): 1 ACD/KOC (pH 7.4): 27.77
#H bond acceptors: 4 #H bond donors: 0
#Freely Rotating Bonds: 2 Polar Surface Area: 28.6 Å2
Index of Refraction: 1.594 Molar Refractivity: 96.12 cm3
Molar Volume: 283.2 cm3 Polarizability: 38.1 10-24cm3
Surface Tension: 46.6 dyne/cm Density: 1.141 g/cm3
Flash Point: 217.3 °C Enthalpy of Vaporization: 69.21 kJ/mol
Boiling Point: 435.7 °C at 760 mmHg Vapour Pressure: 8.55E-08 mmHg at 25°C
            
 Log Octanol-Water Partition Coef (SRC):
    Log Kow (KOWWIN v1.67 estimate) =  1.55

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  425.78  (Adapted Stein & Brown method)
    Melting Pt (deg C):  177.93  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  5.02E-008  (Modified Grain method)
    Subcooled liquid VP: 1.95E-006 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):  8.666e+004
       log Kow used: 1.55 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  2.8615e+005 mg/L

 ECOSAR Class Program (ECOSAR v0.99h):
    Class(es) found:
       Aliphatic Amines
       Vinyl/Allyl Ethers

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   8.31E-014  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  2.465E-013 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  1.55  (KowWin est)
  Log Kaw used:  -11.469  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  13.019
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :  -0.2642
   Biowin2 (Non-Linear Model)     :   0.0000
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   1.6771  (recalcitrant)
   Biowin4 (Primary Survey Model) :   2.7081  (weeks-months)
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :  -0.3746
   Biowin6 (MITI Non-Linear Model):   0.0007
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model): -2.2846
 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):  0.00026 Pa (1.95E-006 mm Hg)
  Log Koa (Koawin est  ): 13.019
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  0.0115 
       Octanol/air (Koa) model:  2.56 
   Fraction sorbed to airborne particulates (phi):
       Junge-Pankow model     :  0.294 
       Mackay model           :  0.48 
       Octanol/air (Koa) model:  0.995 

 Atmospheric Oxidation (25 deg C) [AopWin v1.92]:
   Hydroxyl Radicals Reaction:
      OVERALL OH Rate Constant = 456.2090 E-12 cm3/molecule-sec
      Half-Life =     0.023 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =    16.881 Min
   Ozone Reaction:
      OVERALL Ozone Rate Constant =    11.443750 E-17 cm3/molecule-sec
      Half-Life =     0.100 Days (at 7E11 mol/cm3)
      Half-Life =      2.403 Hrs
   Fraction sorbed to airborne particulates (phi): 0.387 (Junge,Mackay)
    Note: the sorbed fraction may be resistant to atmospheric oxidation

 Soil Adsorption Coefficient (PCKOCWIN v1.66):
      Koc    :  4.456E+004
      Log Koc:  4.649 

 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 = 0.491 (BCF = 3.1)
       log Kow used: 1.55 (estimated)

 Volatilization from Water:
    Henry LC:  8.31E-014 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 1.267E+010  hours   (5.28E+008 days)
    Half-Life from Model Lake : 1.382E+011  hours   (5.76E+009 days)

 Removal In Wastewater Treatment:
    Total removal:               1.99  percent
    Total biodegradation:        0.09  percent
    Total sludge adsorption:     1.90  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       8.25e-007       0.456        1000       
   Water     36              4.32e+003    1000       
   Soil      63.9            8.64e+003    1000       
   Sediment  0.0971          3.89e+004    0          
     Persistence Time: 2.13e+003 hr




        
Descriptors: 0, 0, 0, 0, 1, 0, 0, 5, 0, 0, 0, 0, 4, 5, 15, 0, 12, 0, 0, 0, 0, 0, 0, 0
CategoryTargetPDB CodeLASSO Score
MetalloenzymesACE, angiotensin-converting enzyme;1o860.00
Other EnzymesAChE, acetylcholinesterase;1eve0.00
MetalloenzymesADA, adenosine deaminase;1stw0.00
Other EnzymesALR2, aldose reductase;1ah30.00
Other EnzymesAmpC, AmpC beta-lactamase;1xgj0.00
Nuclear Hormone ReceptorsAR, androgen receptor;1xq20.00
KinasesCDK2, cyclindependent kinase 2;1ckp0.10
MetalloenzymesCOMT, catechol O-methyltransferase;1h1d0.00
Other EnzymesCOX-1, cyclooxygenase-1;1p4g0.00
Other Enzymescyclooxygenase-21cx20.00
Folate EnzymesDHFR, dihydrofolate reductase;3dfr0.00
KinasesEGFr, epidermal growth factor receptor;1m170.09
Nuclear Hormone ReceptorsER, estrogen receptor; agonist1l2i0.00
Nuclear Hormone ReceptorsER, estrogen receptor; antagonist3ert0.01
KinasesFGFr1, fibroblast growth factor receptor kinase;1agw0.00
Serine ProteasesFXa, factor Xa;1f0r0.00
Folate EnzymesGART, glycinamide ribonucleotide transformylase;1c2t0.00
Other EnzymesGPB, glycogen phosphorylase â;1a8i0.00
Nuclear Hormone ReceptorsGR, glucocorticoid receptor;1m2z0.00
Other EnzymesHIVPR, HIV protease;1hpx0.01
Other EnzymesHIVRT, HIV reverse transcriptase;1rt10.02
Other EnzymesHMGR, hydroxymethylglutaryl-CoA reductase;1hw80.01
KinasesHSP90, human heat shock protein 90;1uy60.00
Other EnzymesInhA, enoyl ACP reductase;1p440.02
Nuclear Hormone ReceptorsMR, mineralocorticoid receptor;2aa20.01
Other EnzymesNA, neuraminidase;1a4g0.00
KinasesP38 MAP, P38 mitogen activated protein;1kv20.00
Other EnzymesPARP, poly(ADP-ribose) polymerase;1efy0.01
MetalloenzymesPDE5, phosphodiesterase 5;1xp00.01
KinasesPDGFrb, platelet derived growth factor receptor kinase;0.02
Other EnzymesPNP, purine nucleoside phosphorylase;1b8o0.00
Nuclear Hormone ReceptorsPPARg, peroxisome proliferator activated receptor ç;1fm90.03
Nuclear Hormone ReceptorsPR, progesterone receptor;1sr70.00
Nuclear Hormone ReceptorsRXRa, retinoic X receptor R;1mvc0.00
Other EnzymesSAHH, S-adenosyl-homocysteine hydrolase;1a7a0.00
KinasesSRC, tyrosine kinase SRC;2src0.01
Serine ProteasesThrombin1ba80.01
KinasesTK, thymidine kinase;1kim0.00
Serine ProteasesTrypsin1bju0.00
KinasesVEGFr2, vascular endothelial growth factor receptor;1vr20.00