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ChemSpider ID: |
3509452
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Empirical Formula: |
C31H32N2O2
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Molecular Weight: |
464.598
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Nominal Mass: |
464
Da
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Average Mass: |
464.598
Da
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Monoisotopic Mass: |
464.246378
Da
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Systematic Name: |
5-hexanoyl-6,9-diphenyl-8,9,10,11-tetrahydro-6H-benzo[c][1,5]benzodiazepin-7-one
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SMILES: |
O=C5\C2=C(\Nc1ccccc1N(C(=O)CCCCC)C2c3ccccc3)CC(c4ccccc4)C5
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InChI: |
InChI=1/C31H32N2O2/c1-2-3-6-19-29(35)33-27-18-12-11-17-25(27)32-26-20-24(22-13-7-4-8-14-22)21-28(34)30(26)31(33)23-15-9-5-10-16-23/h4-5,7-18,24,31-32H,2-3,6,19-21H2,1H3
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InChIKey: |
MLLHNAXTYKLNBH-UHFFFAOYAF
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users,
Redirected by Users, Redirect Approved by Experts
10-hexanoyl-3,11-diphenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one
Validated by Experts, Validated by Users, Non-Validated, Removed by Users,
Redirected by Users, Redirect Approved by Experts
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LogP: |
ACD/LogP:
6.60
XLogP:
5.70
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# of Rule of 5 Violations: |
1
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ACD/LogD (pH 5.5): |
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ACD/LogD (pH 7.4): |
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ACD/BCF (pH 5.5): |
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ACD/BCF (pH 7.4): |
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ACD/KOC (pH 5.5): |
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ACD/KOC (pH 7.4): |
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#H bond acceptors: |
4
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#H bond donors: |
1
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#Freely Rotating Bonds: |
6
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Polar Surface Area: |
40.62
Å2
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Index of Refraction: |
1.645
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Molar Refractivity: |
139.45
cm3
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Molar Volume: |
384.5
cm3
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Polarizability: |
55.28
10-24cm3
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Surface Tension: |
56
dyne/cm
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Density: |
1.2
g/cm3
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Flash Point: |
365
°C
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Enthalpy of Vaporization: |
99.78
kJ/mol
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Boiling Point: |
680
°C at 760 mmHg
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Vapour Pressure: |
2.41E-18
mmHg at 25°C
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Log Octanol-Water Partition Coef (SRC):
Log Kow (KOWWIN v1.67 estimate) = 5.81
Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
Boiling Pt (deg C): 630.03 (Adapted Stein & Brown method)
Melting Pt (deg C): 273.34 (Mean or Weighted MP)
VP(mm Hg,25 deg C): 2.22E-014 (Modified Grain method)
Subcooled liquid VP: 1.2E-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): 0.01303
log Kow used: 5.81 (estimated)
no-melting pt equation used
Water Sol Estimate from Fragments:
Wat Sol (v1.01 est) = 0.00027939 mg/L
ECOSAR Class Program (ECOSAR v0.99h):
Class(es) found:
Vinyl/Allyl Ketones
Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
Bond Method : 7.03E-016 atm-m3/mole
Group Method: Incomplete
Henrys LC [VP/WSol estimate using EPI values]: 1.042E-012 atm-m3/mole
Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
Log Kow used: 5.81 (KowWin est)
Log Kaw used: -13.542 (HenryWin est)
Log Koa (KOAWIN v1.10 estimate): 19.352
Log Koa (experimental database): None
Probability of Rapid Biodegradation (BIOWIN v4.10):
Biowin1 (Linear Model) : 0.9289
Biowin2 (Non-Linear Model) : 0.9406
Expert Survey Biodegradation Results:
Biowin3 (Ultimate Survey Model): 2.2283 (months )
Biowin4 (Primary Survey Model) : 3.4626 (days-weeks )
MITI Biodegradation Probability:
Biowin5 (MITI Linear Model) : -0.2503
Biowin6 (MITI Non-Linear Model): 0.0025
Anaerobic Biodegradation Probability:
Biowin7 (Anaerobic Linear Model): -1.8828
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): 1.6E-009 Pa (1.2E-011 mm Hg)
Log Koa (Koawin est ): 19.352
Kp (particle/gas partition coef. (m3/ug)):
Mackay model : 1.87E+003
Octanol/air (Koa) model: 5.52E+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 = 114.2348 E-12 cm3/molecule-sec
Half-Life = 0.094 Days (12-hr day; 1.5E6 OH/cm3)
Half-Life = 1.124 Hrs
Ozone Reaction:
OVERALL Ozone Rate Constant = 13.650000 E-17 cm3/molecule-sec
Half-Life = 0.084 Days (at 7E11 mol/cm3)
Half-Life = 2.015 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 : 2.825E+006
Log Koc: 6.451
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 = 3.777 (BCF = 5991)
log Kow used: 5.81 (estimated)
Volatilization from Water:
Henry LC: 7.03E-016 atm-m3/mole (estimated by Bond SAR Method)
Half-Life from Model River: 1.795E+012 hours (7.48E+010 days)
Half-Life from Model Lake : 1.958E+013 hours (8.16E+011 days)
Removal In Wastewater Treatment:
Total removal: 91.15 percent
Total biodegradation: 0.76 percent
Total sludge adsorption: 90.38 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 0.000273 1.06 1000
Water 2.93 1.44e+003 1000
Soil 53.5 2.88e+003 1000
Sediment 43.5 1.3e+004 0
Persistence Time: 4.85e+003 hr
Descriptors:
0, 0, 0, 1, 0, 0, 0, 4, 0, 0, 0, 0, 17, 14, 0, 0, 18, 2, 2, 2, 2, 0, 0, 0
| Category | Target | PDB Code | LASSO Score |
| Metalloenzymes | ACE, angiotensin-converting enzyme; | 1o86 | 0.00 |
| Other Enzymes | AChE, acetylcholinesterase; | 1eve | 0.04 |
| Metalloenzymes | ADA, adenosine deaminase; | 1stw | 0.00 |
| Other Enzymes | ALR2, aldose reductase; | 1ah3 | 0.00 |
| Other Enzymes | AmpC, AmpC beta-lactamase; | 1xgj | 0.00 |
| Nuclear Hormone Receptors | AR, androgen receptor; | 1xq2 | 0.00 |
| Kinases | CDK2, cyclindependent kinase 2; | 1ckp | 0.00 |
| Metalloenzymes | COMT, catechol O-methyltransferase; | 1h1d | 0.00 |
| Other Enzymes | COX-1, cyclooxygenase-1; | 1p4g | 0.02 |
| Other Enzymes | cyclooxygenase-2 | 1cx2 | 0.00 |
| Folate Enzymes | DHFR, dihydrofolate reductase; | 3dfr | 0.00 |
| Kinases | EGFr, epidermal growth factor receptor; | 1m17 | 0.00 |
| Nuclear Hormone Receptors | ER, estrogen receptor; agonist | 1l2i | 0.00 |
| Nuclear Hormone Receptors | ER, estrogen receptor; antagonist | 3ert | 0.01 |
| Kinases | FGFr1, fibroblast growth factor receptor kinase; | 1agw | 0.00 |
| Serine Proteases | FXa, factor Xa; | 1f0r | 0.02 |
| Folate Enzymes | GART, glycinamide ribonucleotide transformylase; | 1c2t | 0.00 |
| Other Enzymes | GPB, glycogen phosphorylase â; | 1a8i | 0.00 |
| Nuclear Hormone Receptors | GR, glucocorticoid receptor; | 1m2z | 0.10 |
| Other Enzymes | HIVPR, HIV protease; | 1hpx | 0.01 |
| Other Enzymes | HIVRT, HIV reverse transcriptase; | 1rt1 | 0.03 |
| Other Enzymes | HMGR, hydroxymethylglutaryl-CoA reductase; | 1hw8 | 0.01 |
| Kinases | HSP90, human heat shock protein 90; | 1uy6 | 0.00 |
| Other Enzymes | InhA, enoyl ACP reductase; | 1p44 | 0.08 |
| Nuclear Hormone Receptors | MR, mineralocorticoid receptor; | 2aa2 | 0.01 |
| Other Enzymes | NA, neuraminidase; | 1a4g | 0.00 |
| Kinases | P38 MAP, P38 mitogen activated protein; | 1kv2 | 0.00 |
| Other Enzymes | PARP, poly(ADP-ribose) polymerase; | 1efy | 0.01 |
| Metalloenzymes | PDE5, phosphodiesterase 5; | 1xp0 | 0.01 |
| Kinases | PDGFrb, platelet derived growth factor receptor kinase; | | 0.00 |
| Other Enzymes | PNP, purine nucleoside phosphorylase; | 1b8o | 0.00 |
| Nuclear Hormone Receptors | PPARg, peroxisome proliferator activated receptor ç; | 1fm9 | 0.03 |
| Nuclear Hormone Receptors | PR, progesterone receptor; | 1sr7 | 0.12 |
| Nuclear Hormone Receptors | RXRa, retinoic X receptor R; | 1mvc | 0.00 |
| Other Enzymes | SAHH, S-adenosyl-homocysteine hydrolase; | 1a7a | 0.00 |
| Kinases | SRC, tyrosine kinase SRC; | 2src | 0.01 |
| Serine Proteases | Thrombin | 1ba8 | 0.01 |
| Kinases | TK, thymidine kinase; | 1kim | 0.00 |
| Serine Proteases | Trypsin | 1bju | 0.00 |
| Kinases | VEGFr2, vascular endothelial growth factor receptor; | 1vr2 | 0.02 |
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