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Detail of "13224-99-2"

  • CAS Number:
  • 13224-99-2
  • Name:
  • a-D-Glucopyranose,4,6-O-ethylidene-

  • Superlist Name:
  • 4,6-O-Ethylidene-alpha-D-glucose
  • Molecular Structure:
  • Formula:
  • C8H14 O6
  • Molecular Weight:
  • 206.19
  • Synonyms:
  • Glucopyranose,4,6-O-ethylidene-, a-D- (8CI); Pyrano[3,2-d]-1,3-dioxin, a-D-glucopyranose deriv.; 4,6-O-Ethylidene a-D-glucopyranose;4,6-O-Ethylidene-a-D-glucose;Ethylidene glucose; NSC 89726
  • EINECS:
  • 236-198-2
  • Melting Point:
  • 168-170 ºC
  • Safety:
  • WGK Germany 3
    Details

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CAS No.13224-99-2 4,6-O-Ethylidene-alpha-D-glucose

4,6-O-Ethylidene-D-glucose

Supplier:Carborine (Beijing) technologies Ltd [ China (Mainland)]

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CAS No.13224-99-2 4,6-O-Ethylidene-alpha-D-glucose

NO:GLU-018

Supplier:Shamrock (SMK) Bio-chemical Technology Co., Ltd. [ China (Mainland)]

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Tel:86-571-88384880

Address:26-2-301 Daoxiangyuan Hangzhou, Zhejiang Province, China 310014

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Reference

Sugars and sugar derivatives which inhibit the short-circuit current of the everted small intestine of the rat
Sugars and sugar derivatives which inhibit the short-circuit current of the everted small intestine of the rat. Muflih, I. W.; Widdas, W. F. (Dep. Physiol., Bedford Coll., London, Engl.). J. Physiol. (London), 263(2), 101-14 (English) 1976.Several reagents with their cas registry numbers 63-42-3 and 146-72-5 are used here. CODEN: JPHYA7. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) Ethylidene glucose (I) [13224-99-2] (.ltoreq.20mM) and benzylidene glucose (II) [25152-90-3] (.ltoreq.5mM) reduced the short-circuit current generated in everted rat intestine by transportable sugars such as galactose [59-23-4] (5.5mM) and 3-O-methyl glucose [146-72-5] (12mM). I and II also reduced the basal short-circuit current established by the everted intestine in a sugar-free Krebs soln. Both types of inhibition approached satn. at the higher concns. used. Similar inhibitory properties were shown by mannose [3458-28-4], lactose [63-42-3], and cellobiose [528-50-7]. These compds. possibly react with the sites for active hexose transfer without translocation by the system, and the significance of the results is discussed in this context. .
The effects of transportable ('blockers') and nontransportable inhibitors ('lockers') on rat transjejunal potential difference in vivo
The effects of transportable ('blockers') and nontransportable inhibitors ('lockers') on rat transjejunal potential difference in vivo. Levin, R. J.; McGourty, J. (Dep. Physiol., Univ. Sheffield, Sheffield, Engl.). J. Physiol. (London), 263(1), 226P-227P (English) 1976. CODEN: JPHYA7. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) Rat basal transjejunal p.d. was not depressed by 'lockers'; e.g. 25mM ethylidene glucose [13224-99-2], of the electrogenic hexose transfer system. In contrast, the 'blocker' arbutin [497-76-7] increased the p.d. and displayed electrogenic transport, the increases in p.d. showing satn. kinetics, apparent Km 10-12mM and max. p.d. 3-5 mV. The 'locker' phloridzin [60-81-1] behaved anomalously as a 'blocker', stimulating basal p.d. 60-81-1 and 25152-90-3 which are cas registry numbers of substances are two of reagents here. in 52% of rats and showing satn. kinetics with an apparent Km of 2-3mM and a max. p.d. of 2-3 mV. .
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