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99028-49-6

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99028-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99028-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,0,2 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99028-49:
(7*9)+(6*9)+(5*0)+(4*2)+(3*8)+(2*4)+(1*9)=166
166 % 10 = 6
So 99028-49-6 is a valid CAS Registry Number.

99028-49-6Relevant academic research and scientific papers

Convenient synthesis of fused heterocyclic 1,3,5-triazines from some N-Acyl imidates and heterocyclic amines as anticancer and antioxidant agents

Bekircan, Olcay,Kuexuek, Murat,Kahveci, Bahittin,Kolayli, Sevgi

, p. 365 - 372 (2005)

N-Acyl imidates (2), reacting with 5-amino pyrazole (3), 2-aminobenzimidazole (4), 3-amino-1,2,4-triazole (5), 3,5-diamino-1,2,4-triazole (6), and 5-aminotetrazole (7) give pyrazolo[1,5-a][1,3,5]triazine (8), benzo[4,5]imidazo[1,2-a][1,3,5]triazine (9), [1,2,4]triazolo [2,3-a][1,3,5]triazine (10), [1,2,4]triazolo[2,3-a][1,3,5]triazin-5-ylamine (12), and tetrazolo-[1,5-a][1,3,5]triazine (14) derivatives, respectively. The synthesized compounds were characterized on the basis of IR, 1H-NMR, 13C-NMR, and mass spectral data and elemental analyses results. Five of the newly synthesized compounds, 8a, 9a, 10a, 12a, and 14a, were selected by National Cancer Institute and screened for their anticancer activity against three cancer cell lines MCF7, NCI-H460, and SF-268, where 12a exhibited moderate antiproliferation potential. 12a was, thus, further tested for anticancer activity against 60 human cancer cell lines and showed moderate growth inhibition potency. 12a showed a high growth inhibitory activity against A498 renal cancer cell line. All of the newly synthesized compounds 8-10, 12 and 14 were tested for their antioxidant capacity where they exhibited very high activity, even higher than the widely used reference antioxidants butylated hydroxytoluene and 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox) Compound 12a also showed the highest antioxidant activity.

Synthesis and evaluation of potent novel inhibitors of human sulfide:quinone oxidoreductase

Baugh, Simon D.P.,Jackson, Michael R.,Rashad, Adel Ahmed,Reitz, Allen B.,Lam, Patrick Y.S.,Jorns, Marilyn Schuman

supporting information, (2021/11/20)

Here we report the first small-molecule inhibitors of human sulfide:quinone oxidoreductase (SQOR) that decrease the rate of breakdown of hydrogen sulfide (H2S), a potent cardioprotective signaling molecule. SQOR is a mitochondrial membrane-boun

COMPOUNDS AND METHODS FOR TREATING OR PREVENTING HEART FAILURE

-

Page/Page column 104; 130-131, (2020/07/25)

The present invention relates to the discovery of novel compounds that can be used to treat and/or prevent heart failure in a subject. In certain embodiments, the compounds of the invention are sulfide: quinone oxidoreductase (SQOR) inhibitors. In other e

1,3-Oxazines and Related Compounds. XII. Facile Synthesis of 2,4-Disubstituted 6H-1,3-Oxazin-6-ones

Yamamoto, Yutaka,Morita, Yasuo,Minami, Keiko

, p. 1980 - 1986 (2007/10/02)

A convenient method for synthesis of 2,4-disubstituted 6H-1,3-oxazin-6-ones (8) was developed.Acylaminoalkylidene-1,3-dioxane-4,6-diones (5a-l), which were prepared from N-acylimidates (3a-l) and Meldrum's acid (4), readily underwent thermolysis upon heating, leading to a variety of 2,4-disubstituted 6H-1,3-oxazin-6-ones (8a-l).Keywords - 6H-1,3-oxazin-6-one; Meldrum's acid; acylaminoalkylidene-1,3-dioxane-4,6-dione; N-acylimidate; thermolysis

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