ChemSpider 2D Image | Radicicol | C18H17ClO6

Radicicol

  • Molecular FormulaC18H17ClO6
  • Average mass364.777 Da
  • Monoisotopic mass364.071381 Da
  • ChemSpider ID20137057

  • Double-bond stereo - Double-bond stereo

    defined stereocentres - 3 of 3 defined stereocentres

More details:

Featured data source
The Merck Index Online

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

(1aR,2Z,4E,14R,15aR)-8-Chlor-9,11-dihydroxy-14-methyl-1a,14,15,15a-tetrahydro-6H-oxireno[e][2]benzoxacyclotetradecin-6,12(7H)-dion [German] [ACD/IUPAC Name]
(1aR,2Z,4E,14R,15aR)-8-Chloro-9,11-dihydroxy-14-methyl-1a,14,15,15a-tetrahydro-6H-oxireno[e][2]benzoxacyclotetradecine-6,12(7H)-dione [ACD/IUPAC Name]
(1aR,2Z,4E,14R,15aR)-8-Chloro-9,11-dihydroxy-14-méthyl-1a,14,15,15a-tétrahydro-6H-oxiréno[e][2]benzoxacyclotétradécine-6,12(7H)-dione [French] [ACD/IUPAC Name]
[1aS-(1aR*,2Z,4E,14*,15aR*)]-8-Chloro-1a,14,15,15a-tetrahydro-9,11-dihydroxy-14-methyl-6H-oxireno[e][2]benzoxacyclotetradecin-6,12(7H)-dione
12772-57-5 [RN]
6H-Oxireno[e][2]benzoxacyclotetradecin-6,12(7H)-dione, 8-chloro-1a,14,15,15a-tetrahydro-9,11-dihydroxy-14-methyl-, (1aR,2Z,4E,14R,15aR)- [ACD/Index Name]
I60EH8GECX
LSM-6548
MFCD06795865
monorden
More...

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

R2146_SIGMA [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Chemical Class:

      An antifungal macrolactone antibiotic, obtained from <ital>Diheterospora chlamydosporia</ital> and <ital>Chaetomium chiversii</ital> that inhibits protein tyrosine kinase and heat shock protein 90 (Hs p90). ChEBI CHEBI:556075
      An antifungal macrolactone antibiotic, obtained from Diheterospora chlamydosporia and Chaetomium chiversii that inhibits protein tyrosine kinase and heat shock protein 90 (Hsp90). ChEBI CHEBI:556075

    • Bio Activity:

      Antibiotics Hello Bio HB4051
      Antifungal antibiotic. Inhibits heat shock protein 90 (Hsp90) activity by binding to the ATP-binding pocket, subsequently suppressing cell transformation induced by src, ras and mos. Represses estroge n receptor transcriptional activity and inhibits angiogenesis. Tocris Bioscience 1589
      Antifungal antibiotic. Inhibits heat shock protein 90 (Hsp90) activity by binding to the ATP-binding pocket, subsequently suppressing cell transformation induced by src, ras and mos. Represses estrogen receptor transcriptional activity and inhibits angiogenesis. Tocris Bioscience 1589
      Antifungal antibiotic. Potent HSP90 inhibitor. Also shows activity at many other kinases and suppresses iNOS expression. Induces differentiation of HL-60 cells into macrophages. Shows anticancer activity and protects against neuronal cell death. Hello Bio HB4051
      Cell signaling/Heatshock proteins/HSP90 Hello Bio HB4051
      Heat Shock Proteins Tocris Bioscience 1589
      Hsp90 Tocris Bioscience 1589
      Hsp90 inhibitor. Antifungal antibiotic Tocris Bioscience 1589
      Potent HSP90 inhibitor. Antifungal antibiotic. Hello Bio HB4051
      Signal Transduction Tocris Bioscience 1589

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

Density: 1.4±0.1 g/cm3
Boiling Point: 656.2±55.0 °C at 760 mmHg
Vapour Pressure: 0.0±2.0 mmHg at 25°C
Enthalpy of Vaporization: 100.1±3.0 kJ/mol
Flash Point: 350.7±31.5 °C
Index of Refraction: 1.583
Molar Refractivity: 89.4±0.3 cm3
#H bond acceptors: 6
#H bond donors: 2
#Freely Rotating Bonds: 0
#Rule of 5 Violations: 0
ACD/LogP: 1.53
ACD/LogD (pH 5.5): 2.71
ACD/BCF (pH 5.5): 64.60
ACD/KOC (pH 5.5): 653.99
ACD/LogD (pH 7.4): 1.49
ACD/BCF (pH 7.4): 3.87
ACD/KOC (pH 7.4): 39.15
Polar Surface Area: 96 Å2
Polarizability: 35.4±0.5 10-24cm3
Surface Tension: 50.1±3.0 dyne/cm
Molar Volume: 267.4±3.0 cm3

Click to predict properties on the Chemicalize site


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