Preparation of deoxypeganine hydrochloride

1991 ◽  
Vol 26 (4) ◽  
pp. 427-429
Author(s):  
K. D. Sargazakov ◽  
Kh. N. Arupov ◽  
L. V. Molchanov ◽  
V. N. Plugar'
Keyword(s):  
Deoxypeganine Hydrochloride

scholarly journals Identification of natural products and their derivatives as promising inhibitors of protein glycation with non-toxic nature against mouse fibroblast 3T3 cells

2017 ◽  
Vol 8 (4) ◽  
pp. 533 ◽  
Author(s):  
Ghulam Abbas ◽  
Ahmed Suliman Al-Harrasi ◽  
Hidayat Hussain ◽  
Samina Abdul Sattar ◽  
M. Iqbal Choudhary
Keyword(s):  
Acetic Acid ◽  
Significant Inhibition ◽  
Mouse Fibroblast ◽  
Protein Glycation ◽  
Fibroblast Cells ◽  
Inhibition Activity ◽  
3T3 Cells ◽  
Gossypol Acetic Acid ◽  
Deoxypeganine Hydrochloride

<p>This study was performed to identify new inhibitors of protein glycation <em>in vitro</em>. Protein glycation is one of the major causes of late diabetic complications. In this study, terpenoids and alkaloids, isolated from different medicinal plants, along with their derivatives, were evaluated for their antiglycation activity <em>in vitro,</em> while MTT assay on mouse fibroblast 3T3 cells was used to assess their potential cytotoxicity. Among the tested compounds, gossypol (2,2′-<em>bis</em>-(formyl-1,6,7-trihydroxy-5-isopropyl-3-methylnaphthalene) (<strong>1</strong>), isolated from<em> Gossypium herbaceum, </em>and its derivatives,<em> </em>gossypol acetic acid (<strong>2</strong>), gossypolidene- 4-aminoantipyrine (<strong>4</strong>), and gazolidone (<strong>6</strong>), showed a potent antiglycation activity (IC<sub>50</sub> &lt; 16 <em>µ</em>M), while gossypolidene-4-aminoantipyrine (<strong>5</strong>) showed a significant antiglycation activity with IC<sub>50 </sub>value 82.934±2.924<em> µ</em>M, in BSA-fluorescence assay. Alkaloid, noscapine (3S)-6,7-Dimethoxy-3-[(5R)-4-methoxy-6-methyl-5,6,7,8-tetrahy-dro-1,3-dioxolo[4,5-g]isoquinolin-5-yl] isobenzofuran-1(3<em>H</em>)-one (<strong>7</strong>), isolated from <em>Papaver somniferum, N</em>-nitrosoaphyllinic acid (<strong>9</strong>), a derivative of alkaloid aphylline<em>, </em>and 2<em>H</em>-quinolizine, octahydro salt (<strong>11</strong>), a salt of alkaloid lupinine, exhibited significant inhibition activity with<em> </em>IC<sub>50 </sub>values 152.662±5.432, 393.758 ±4.001 µM and 110.203±4.816µM, respectively. Similarly, compounds<strong> </strong>gossypolidene thiocarbamide (<strong>3</strong>), deoxypeganine hydrochloride (<strong>8</strong>)<strong>, </strong>lupinine (<strong>10</strong>) and cytisine (<strong>12</strong>) showed moderate inhibition with IC<sub>50</sub> values of 401.865 ±18.450, 863.322 ±6.415, 712.176±7.745, and 728.462±2.331<em> </em>µM, respectively. The results were compared with the standard antiglycation agent, rutin (<strong>13</strong>) (IC<sub>50 </sub>=98.012±2.030 µM).</p>Cellular cytotoxicity assay showed only gossypol acetic acid (<strong>2</strong>) and gossypolidene thiocarbamide (<strong>3</strong>) as somewhat toxic to 3T3 (mouse fibroblast) cells with IC<sub>50 </sub>values<em> </em>2.07 ±0.61 and 5.00 ±1.89 µM, respectively. Cycloheximide was used as a standard in this assay with IC<sub>50</sub> value 0.3 ± 0.089 μM

Quantitative determination of deoxypeganine hydrochloride

1985 ◽  
Vol 21 (1) ◽  
pp. 80-82
Author(s):  
A. Kh. Sattarova ◽  
E. K. Dobronravova ◽  
T. T. Shakirov
Keyword(s):  
Quantitative Determination ◽  
Deoxypeganine Hydrochloride

Crystal and molecular structure of deoxypeganine hydrochloride dihydrate

1996 ◽  
Vol 31 (3) ◽  
pp. 349-352 ◽  
Author(s):  
B. Tashkhodzhaev ◽  
L. V. Molchanov ◽  
K. K. Turgunov ◽  
M. K. Makhmudov ◽  
Kh. N. Aripov
Keyword(s):  
Molecular Structure ◽  
Crystal And Molecular Structure ◽  
Deoxypeganine Hydrochloride
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