DEOXYVACISINONE HCl

For research use only. Not for therapeutic Use.

  • CAT Number: T000016
  • CAS Number: 2446-62-0 (parent)
  • Molecular Formula: C12H12N2O.HCl
  • Purity: ≥95%
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<p>
DEOXYVACISINONE HCl inhibits cholinesterase activity <em>in vitro</em>.</p>
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<em>In vivo</em>, high doses induce sleep and enhance the effect of soporifics.</p>
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Quinazolone alkaloid<!–C<sub>12</sub>H<sub>12</sub>N<sub>2</sub>O.HCl–>, synthetic.<br />
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High dose inhibits orientation reaction and motor functions. So, it induces somnolence, even sleep.</p>
<p>
Half and quarter LD&lt;sub&gt;50&lt;/sub&gt; doses (= moderate doses) enhance the effect of soporifics. <em>In vitro</em>, it causes weak inhibition of cholinesterase acitivity with IC&lt;sub&gt;50&lt;/sub&gt; = 6.2×10&lt;sup&gt;-4&lt;/sup&gt; g/ml, and of monoaminoxidase at 10&lt;sup&gt;-4&lt;/sup&gt; M reduces by 18.8 % its activity.</p>
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Catalog Number T000016
CAS Number 2446-62-0 (parent)
Synonyms

6,7,8,9-Tetrahydro-11H-pyrido[2,1-b]quinazolin-11-one hydrochloride

Molecular Formula C12H12N2O.HCl
Purity ≥95%
Solubility In ethanol and water<br>Not well in chloroform and acetone
Storage Stable in freeze-dried stateStore at +4°C, in dark place.
Reference

– Fitzgerald et al., /6, 7, 8, 9-tetrahydropyrido-quinazoline, a new class of alkaloids from Mackinlava species (Araliaceae)/ Aust. J. Chem. (1966). 19(1):151-159<br />
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– Spath et al., /Uber Derivate des Peganins und ihre Ring-Homologen/ J. Mitt. Uber Peganin, Chem. Ber. 6 (1935). 68:2221-2226<br />
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– Jen et al., /A new class of antihypertensive agents, 1, 2, 3, 5-Tetrahydroimidazo [2,1-b] quinazoline./ J. Med. Chem.1 (1972). 15(7):727-731<br />
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– Touliaganov, Ph. D. Thesis, Moscow (1981) (Russian).<br />
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