Bookmark and Share
Please login to be able to add spectra, identifiers, links and publications.
  • Comments
  • Image
  • Spectrum
  • CIF
  • Identifier
  • Description
  • Add:
Inherent Properties, Identifiers and References
ChemSpider ID: 56094
Empirical Formula: C20H30O8
Molecular Weight: 398.4474
Nominal Mass: 398 Da
Average Mass: 398.4474 Da
Monoisotopic Mass: 398.194068 Da
Systematic Name: (2R,7S,7aR)-7-hydroxy-2,5,7-trimethyl-3a-[(3R,4S,5S,6R)-3,4,5-tri​hydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-spiro[3,7a-dihy​dro-2H-indene-6,1'-cyclopropane]-1-one
SMILES: O=C4[C@H]3C(OC1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO)(/C=C(/C)C2(CC​2)[C@]3(O)C)C[C@H]4C
InChI: InChI=1/C20H30O8/c1-9-6-20(28-17-15(25)14(24)13(23)11(8-21)27-17)​7-10(2)19(4-5-19)18(3,26)16(20)12(9)22/h7,9,11,13-17,21,23-26H,4-​6,8H2,1-3H3/t9-,11-,13-,14+,15-,16-,17?,18+,20?/m1/s1
InChIKey: GPHSJPVUEZFIDE-DUDRLGIABI
Std. InChI: InChI=1S/C20H30O8/c1-9-6-20(28-17-15(25)14(24)13(23)11(8-21)27-17​)7-10(2)19(4-5-19)18(3,26)16(20)12(9)22/h7,9,11,13-17,21,23-26H,4​-6,8H2,1-3H3/t9-,11-,13-,14+,15-,16-,17?,18+,20?/m1/s1
Std. InChIKey: GPHSJPVUEZFIDE-DUDRLGIASA-N
Associated Data Sources and Commercial Suppliers Filter
Patents
PubMed Articles
Names and Synonyms

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

87625-62-5 [RN]

Braxin C

piro(cycl​opropane-​1,5'-(5H)​indan)-3'​(2'H)-one​, 7'a-(be​ta-D-gluc​opyranosy​loxy)-1',​3'a,4',7'​a-tetrahy​dro-4'-hy​droxy-2',​4',6'-tri​methyl-, ​(2'R-(2'a​lpha,3'aa​lpha,4'be​ta.7'aalp​ha))-

ptaquilos​ide

Spiro(cyc​lopropane​-1,5'-(5H​)indan)-3​'(2'H)-on​e, 7'a-(b​eta-D-glu​copyranos​yloxy)-1'​,3'a,4',7​'a-tetrah​ydro-4'-h​ydroxy-2'​,4',6'-tr​imethyl-,​ (2'R,3'a​R,4'S,7'a​R)-

Spiro(cyc​lopropane​-1,5'-(5H​)inden)-3​'(2'H)-on​e, 1',3'-​alpha,4',​7'-alpha-​tetrahydr​o-7'-alph​a-(beta-D​-glucopyr​anosyloxy​)-4'-hydr​oxy-2',4'​,6'-trime​thyl-

Database ID(s)

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

ACD/LogP: -1.04 # of Rule of 5 Violations: 1
ACD/LogD (pH 5.5): -1.04 ACD/LogD (pH 7.4): -1.04
ACD/BCF (pH 5.5): 1 ACD/BCF (pH 7.4): 1
ACD/KOC (pH 5.5): 6.51 ACD/KOC (pH 7.4): 6.51
#H bond acceptors: 8 #H bond donors: 5
#Freely Rotating Bonds: 8 Polar Surface Area: 81.68 Å2
Index of Refraction: 1.62 Molar Refractivity: 97.3 cm3
Molar Volume: 276.8 cm3 Polarizability: 38.57 10-24cm3
Surface Tension: 70.6 dyne/cm Density: 1.43 g/cm3
Flash Point: 218.2 °C Enthalpy of Vaporization: 105.45 kJ/mol
Boiling Point: 620.7 °C at 760 mmHg Vapour Pressure: 5.26E-18 mmHg at 25°C
            
 Log Octanol-Water Partition Coef (SRC):
    Log Kow (KOWWIN v1.67 estimate) =  -0.95

 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42):
    Boiling Pt (deg C):  565.98  (Adapted Stein & Brown method)
    Melting Pt (deg C):  243.42  (Mean or Weighted MP)
    VP(mm Hg,25 deg C):  5.29E-016  (Modified Grain method)
    Subcooled liquid VP: 1.23E-013 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):  2.037e+004
       log Kow used: -0.95 (estimated)
       no-melting pt equation used

 Water Sol Estimate from Fragments:
    Wat Sol (v1.01 est) =  1e+006 mg/L

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

 Henrys Law Constant (25 deg C) [HENRYWIN v3.10]:
   Bond Method :   7.70E-019  atm-m3/mole
   Group Method:   Incomplete
 Henrys LC [VP/WSol estimate using EPI values]:  1.362E-020 atm-m3/mole

 Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]:
  Log Kow used:  -0.95  (KowWin est)
  Log Kaw used:  -16.502  (HenryWin est)
      Log Koa (KOAWIN v1.10 estimate):  15.552
      Log Koa (experimental database):  None

 Probability of Rapid Biodegradation (BIOWIN v4.10):
   Biowin1 (Linear Model)         :  -0.0469
   Biowin2 (Non-Linear Model)     :   0.0000
 Expert Survey Biodegradation Results:
   Biowin3 (Ultimate Survey Model):   2.2823  (weeks-months)
   Biowin4 (Primary Survey Model) :   3.2886  (days-weeks  )
 MITI Biodegradation Probability:
   Biowin5 (MITI Linear Model)    :   0.6979
   Biowin6 (MITI Non-Linear Model):   0.0560
 Anaerobic Biodegradation Probability:
   Biowin7 (Anaerobic Linear Model): -0.9121
 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):  1.64E-011 Pa (1.23E-013 mm Hg)
  Log Koa (Koawin est  ): 15.552
   Kp (particle/gas partition coef. (m3/ug)):
       Mackay model           :  1.83E+005 
       Octanol/air (Koa) model:  875 
   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 = 172.0053 E-12 cm3/molecule-sec
      Half-Life =     0.062 Days (12-hr day; 1.5E6 OH/cm3)
      Half-Life =     0.746 Hrs
   Ozone Reaction:
      OVERALL Ozone Rate Constant =     1.137500 E-17 cm3/molecule-sec
      Half-Life =     1.007 Days (at 7E11 mol/cm3)
      Half-Life =     24.179 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    :  10
      Log Koc:  1.000 

 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 = 0.500 (BCF = 3.162)
       log Kow used: -0.95 (estimated)

 Volatilization from Water:
    Henry LC:  7.7E-019 atm-m3/mole  (estimated by Bond SAR Method)
    Half-Life from Model River: 1.518E+015  hours   (6.324E+013 days)
    Half-Life from Model Lake : 1.656E+016  hours   (6.899E+014 days)

 Removal In Wastewater Treatment:
    Total removal:               1.85  percent
    Total biodegradation:        0.09  percent
    Total sludge adsorption:     1.75  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       0.000127        1.41         1000       
   Water     46.4            900          1000       
   Soil      53.5            1.8e+003     1000       
   Sediment  0.0891          8.1e+003     0          
     Persistence Time: 973 hr




        
Descriptors: 0, 0, 0, 0, 0, 0, 0, 6, 0, 0, 5, 10, 17, 0, 7, 1, 0, 0, 1, 1, 2, 0, 0, 0
CategoryTargetPDB CodeLASSO Score
Other EnzymesSAHH, S-adenosyl-homocysteine hydrolase1a7a0.10
Nuclear Hormone ReceptorsRXRa, retinoic X receptor R1mvc0.03
Nuclear Hormone ReceptorsPPARg, peroxisome proliferator activated receptor1fm90.03
Other EnzymesGPB, glycogen phosphorylase1a8i0.02
KinasesSRC, tyrosine kinase SRC2src0.01
Other EnzymesHMGR, hydroxymethylglutaryl-CoA reductase1hw80.01
Other EnzymesHIVPR, HIV protease1hpx0.01
KinasesHSP90, human heat shock protein 901uy60.01
MetalloenzymesPDE5, phosphodiesterase 51xp00.01
Nuclear Hormone ReceptorsMR, mineralocorticoid receptor2aa20.01
MetalloenzymesADA, adenosine deaminase1stw0.01
Other EnzymesPARP, poly(ADP-ribose) polymerase1efy0.01
Other EnzymesPNP, purine nucleoside phosphorylase1b8o0.00
Other EnzymesAmpC, AmpC beta-lactamase1xgj0.00
Other EnzymesNA, neuraminidase1a4g0.00
Nuclear Hormone ReceptorsER, estrogen receptor; agonist1l2i0.00
MetalloenzymesACE, angiotensin-converting enzyme1o860.00
Nuclear Hormone ReceptorsPR, progesterone receptor1sr70.00
Folate EnzymesDHFR, dihydrofolate reductase3dfr0.00
KinasesVEGFr2, vascular endothelial growth factor receptor1vr20.00
KinasesFGFr1, fibroblast growth factor receptor kinase1agw0.00
Serine ProteasesThrombin1ba80.00
KinasesTK, thymidine kinase1kim0.00
Other EnzymesCOX-1, cyclooxygenase-11p4g0.00
Nuclear Hormone ReceptorsAR, androgen receptor1xq20.00
Other EnzymesAChE, acetylcholinesterase1eve0.00
Nuclear Hormone ReceptorsGR, glucocorticoid receptor1m2z0.00
Other EnzymesInhA, enoyl ACP reductase1p440.00
Folate EnzymesGART, glycinamide ribonucleotide transformylase1c2t0.00
KinasesPDGFrb, platelet derived growth factor receptor kinaseN/A0.00
Nuclear Hormone ReceptorsER, estrogen receptor; antagonist3ert0.00
Serine ProteasesFXa, factor Xa1f0r0.00
Other EnzymesCOX-2, cyclooxygenase-21cx20.00
KinasesEGFr, epidermal growth factor receptor1m170.00
Other EnzymesALR2, aldose reductase1ah30.00
KinasesCDK2, cyclindependent kinase 21ckp0.00
MetalloenzymesCOMT, catechol O-methyltransferase1h1d0.00
KinasesP38 MAP, P38 mitogen activated protein1kv20.00
Other EnzymesHIVRT, HIV reverse transcriptase1rt10.00
Serine ProteasesTrypsin1bju0.00