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One-Pot Synthesis of Novel Thiazoles as Potential Anti-Cancer Agents

Sayed, Abdelwahed R. (författare)
KFU, Fac Sci, Dept Chem, Al Hufuf, Saudi Arabia.;Beni Suef Univ, Fac Sci, Dept Chem, Bani Suwayf, Egypt.
Gomha, Sobhi M. (författare)
Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt.;Islamic Univ Almadinah Almonawara, Fac Sci, Dept Chem, Almadinah Almonawara 42351, Saudi Arabia.
Taher, Eman A. (författare)
NODCAR, Dept Pharmaceut Chem, Giza 12311, Egypt.;Menoufia Univ, Fac Sci, Chem Dept, Shibin Al Kawm 32512, Egypt.
visa fler...
Muhammad, Zeinab A. (författare)
NODCAR, Dept Pharmaceut Chem, Giza 12311, Egypt.
El-Seedi, Hesham (författare)
Uppsala universitet,Farmakognosi,Menoufia Univ, Fac Sci, Chem Dept, Shibin Al Kawm 32512, Egypt
Gaber, Hatem M. (författare)
NODCAR, Dept Pharmaceut Chem, Giza 12311, Egypt.
Ahmed, Mahgoub M. (författare)
NODCAR, Mol Drug Evaluat Dept, Giza 12311, Egypt.
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KFU, Fac Sci, Dept Chem, Al Hufuf, Saudi Arabia;Beni Suef Univ, Fac Sci, Dept Chem, Bani Suwayf, Egypt. Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt.;Islamic Univ Almadinah Almonawara, Fac Sci, Dept Chem, Almadinah Almonawara 42351, Saudi Arabia. (creator_code:org_t)
2020
2020
Engelska.
Ingår i: Drug Design, Development and Therapy. - 1177-8881. ; 14, s. 1363-1375
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: Thiazole and thiosemicarbazone derivatives are known to have potential anticancer activity with a mechanism of action related to inhibition of matrix metallo-proteinases, kinases and anti-apoptotic BCL2 family proteins.Materials and Methods: A novel three series of 5-(1-(2-(thiazol-2-yl)hydrazono)ethyl) thiazole derivatives were prepared in a one-pot three-component reaction using 2-(2-benzylidene hydrazinyl)-4-methylthiazole as a starting precursor. MS, IR, H-1-NMR and C-13-NMR were used to elucidate the structures of the synthesized compounds. Most of the synthesized products were evaluated for their in vitro anticancer screening against HCT-116, HT-29 and HepG2 using the MTT colorimetric assay.Results: The results indicated that compounds 4c, 4d and 8c showed growth inhibition activity against HCT-116 with IC50 values of 3.80 +/- 0.80, 3.65 +/- 0.90 and 3.16 +/- 0.90 mu M, respectively, compared to harmine (IC50 = 2.40 +/- 0.12 mu M) and cisplatin (IC50 = 5.18 +/- 0.94 mu M) reference drugs. Also, compounds 8c, 4d and 4c showed promising IC(50 )values of 3.47 +/- 0.79, 4.13 +/- 0.51 and 7.24 +/- 0.62 mu M, respectively, against the more resistant human colorectal cancer (HT-29) cell line compared with harmine (IC50 = 4.59 +/- 0.67 mu M) and cisplatin (IC50 = 11.68 +/- 1.54 mu M). On the other hand, compounds 4d, 4c, 8c and llc were the most active (IC50 values of 2.31 +/- 0.43, 2.94 +/- 0.62, 4.57 +/- 0.85 and 9.86 +/- 0.78 mu M, respectively) against the hepatocellular carcinoma (HepG2) cell line compared with harmine (IC50 = 2.54 +/- 0.82 mu M) and cisplatin (IC50 = 41 +/- 0.63 pM). The study also suggested that the mechanism of the anticancer action exerted by the most active compounds (4c, 4d and 8c) inside HCT-116 cells was apoptosis through the Bcl-2 family.Conclusion: Thiazole scaffolds 4c, 4d and 8c showed anticancer activities in the micromolar range and are appropriate as a candidate for cancer treatment.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)

Nyckelord

hydrazones
hydrazonoyl halides
cyclization
harmine
HCT-116
HepG2
HT-29

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