6-Keto cholestanol

Suppliers

Names

[ CAS No. ]:
1175-06-0

[ Name ]:
6-Keto cholestanol

[Synonym ]:
MFCD00003572
EINECS 214-640-5
6-ketocholestanol

Chemical & Physical Properties

[ Density]:
1 g/cm3

[ Boiling Point ]:
501.3ºC at 760 mmHg

[ Melting Point ]:
140-142 °C

[ Molecular Formula ]:
C27H46O2

[ Molecular Weight ]:
402.65300

[ Flash Point ]:
212.4ºC

[ Exact Mass ]:
402.35000

[ PSA ]:
37.30000

[ LogP ]:
6.64760

[ Index of Refraction ]:
1.51

[ Storage condition ]:
-20°C Freezer

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Risk Phrases ]:
R24/25

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Precursor & DownStream

Precursor

  • 6-(Hydroxy(oxido)amino)cholest-5-en-3-ol

DownStream

Articles

SR4 Uncouples Mitochondrial Oxidative Phosphorylation, Modulates AMP-dependent Kinase (AMPK)-Mammalian Target of Rapamycin (mTOR) Signaling, and Inhibits Proliferation of HepG2 Hepatocarcinoma Cells.

J. Biol. Chem. 290 , 30321-41, (2015)

Mitochondrial oxidative phosphorylation produces most of the energy in aerobic cells by coupling respiration to the production of ATP. Mitochondrial uncouplers, which reduce the proton gradient across...

Probing amphotericin B single channel activity by membrane dipole modifiers.

PLoS ONE 7(1) , e30261, (2012)

The effects of dipole modifiers and their structural analogs on the single channel activity of amphotericin B in sterol-containing planar phosphocholine membranes are studied. It is shown that the add...

Effect of agents modifying the membrane dipole potential on properties of syringomycin E channels.

Langmuir 23(13) , 6889-92, (2007)

We evaluated the effect of agents modifying the membrane dipole potential: phloretin, 6-ketocholestanol and RH 421 on the properties of single channels formed by lipodepsipeptide syringomycin E (SRE) ...


More Articles


Related Compounds

  • 6-ketocholestanol
  • 6-ketocholestanol
  • 6-chloro-3-[[ethoxy(ethylsulfanyl)phosphoryl]sulfanylmethyl]-1,3-benzoxazol-2-one
  • 6-Chloro-N-(3-pyridinylmethyl)-4-pyrimidinamine
  • 6-chloro-3,3,4,4,5,5,6,6-octafluorohexan-1-ol
  • 6-bromo-3-chloroquinoxalin-2-amine
  • Tert-butyl 4-(1-benzyltetrazol-5-yl)piperidine-1-carboxylate
  • 3-[(1-Ethyl-5-piperidin-4-ylpyrazol-3-yl)methyl]pyridine
  • Tert-butyl 4-(2-nitroacetyl)piperidine-1-carboxylate
  • 3-[(3-piperidin-4-yl-1H-pyrazol-5-yl)methyl]pyridine
  • 2-((4-Acetamidophenyl)amino)-3-allyl-4-(2,4-dichlorophenyl)thiazol-3-ium chloride
  • GlcNAc3Ac4Ac6Ac(b1-4)GlcNAc3Ac6Ac(b)-O-allyl
  • EThyl (2S)-2-(trifluoroacetamido)propanoate
  • 4-Bromo-2-chloro-5-(chlorosulfonyl)benzoic acid
  • N-[(1S)-1-[[[(4R)-1-[(2,4-Dichlorophenyl)sulfonyl]hexahydro-1H-azepin-4-yl]amino]carbonyl]-3-methylbutyl]benzo[b]thiophene-2-carboxamide
  • N-butyl-3-{2-chloroimidazo[1,2-a]pyridin-3-yl}-2-cyanoprop-2-enamide
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