Publication of Dr. Mohammad Sayed Alam
56. Alam M. S. and Ahmed J. U. “Synthesis, crystal structure, biological evaluation, in silico ADME properties, enzymatic target prediction and molecular docking studies of pyrazolone-azomethine analogs” J. Mol. Struct., 2023, 136504 https://doi.org/10.1016/j.molstruc.2023.136504 (IF 3.84)
55. Motiur Rahman A. F. M., Alam M. S., Kwon Y. “Editorial: Small organic molecules with anticancer activity” Front. Chem., 2023, 11, 1254312. (IF 5.5)
54. Alam M. S. and Lee D-U. “Hydrazide-hydrazones as small molecule tropomyosin receptor kinase A (TRKA) inhibitors: synthesis, anticancer activities, in silico ADME and molecular docking studies” Med. Chem., 2023, 19, 47-63. (IF 2.345)
53. Alam M. S. and Lee D-U. “Molecular structure, spectral (FT-IR, FT-Raman, Uv-Vis, and fluorescent) properties and quantum chemical analyses of azomethine derivative of 4-aminoantipyrine” J. Mol. Struct., 2021, 1227, 129512. (IF 3.196)
52. Lu Y., Jo H., , Lee H.-J., Yin W., Alam M. S., Karim M., Kadi A. A., Jahng Y., Kwon Y., Motiur Rahman A. F. M., Synthesis, biological evaluation and molecular docking study of cyclic diarylheptanoids as potential anticancer therapeutics, Anti-Cancer Agents in Medicinal Chemistry, 2020, 20, 464-475. (IF 2.556)
51. Alam M. S. and Hossain M. A. “Development of new generation broad spectrum antibiotics: preparation, biological evaluation and mode of action studies of novel pyrazolone heterocyclic compounds (PHC)” Journal of Science and Technology Research, 2019, 1(2), 92-98.
50. Alam M. A., Shimada K., Jahan A., Khan M. W., Bhuiyan M. M. H., Alam M. S., Matin M. M. Synthesis, reactions and medicinal importance of cyclic sulfone Derivatives: a review, Nat. Prod. Chem. Res., 2018, 6, 350.
49. Motiur Rahman A. F. M., Lu Y., Lee H.-J., Jo H., Yin W., Alam M. S., Cha H., Kadi A. A., Kwon Y., Jahng Y. Linear diarylheptanoids as potential anticancer therapeutics: synthesis, biological evaluation, and structure–activity relationship studies, Arch. Pharm. Res., 2018, 41, 1131-1148. (IF 2.49)
48. Alam M. S. Choi S-U. and Lee D-U. “Synthesis, anticancer, and docking studies of salicyl-hydrazone analogues: A novel series of small potent tropomyosin receptor kinase A inhibitors” Bioorg. Med. Chem., 2017, 25, 389-396. (IF-2.923)
47. Alam M. S. and Lee D-U. “Spectral (FT-IR, FT-Raman, UV, and fluorescence), DFT, and solid state interaction
analyses of (E)-4-(3,4-dimethoxybenzylideneamino)-1,5-dimethy1-2-pheny1-1H-pyrazol-3 (2H)-one”
J. Mol. Struct., 2017, 1128, 174-185. (IF 1.602)
46. Alam M. S. and Lee D-U. “Physicochemical analyses of a bioactive 4-aminoantipyrine analogue - synthesis,
crystal structure, solid state interactions, antibacterial, conformational and docking studies” EXCLI Journal 2016,
15, 614-629. (IF 1.292)
45. Alam M. S. Ahmed, J.U. and Lee D-U. “Biological features, drug-likeness, pharmacokinetic properties, and
docking of 2-arylidenehydrazinyl-4-arylthiazole analogues” Appl. Biol. Chem. 2016, 59, 181-192. (IF 0.655)
44. Alam M. S., Jebin S., Rahman M. M., Bari M. L., and Lee D-U. “Biological and quantitative-SAR evaluations,
and docking studies of (E)-N'-benzylidenebenzohydrazide analogues as potential antibacterial agents”
EXCLI Journal 2016, 15, 350-361. (IF 1.292)
43. Alam M. S. and Lee D-U. “Synthesis, biological evaluation, drug-likeness, and in silico screening of novel
benzylidene-hydrazone analogues as small molecule anticancer agents” Arch. Pharm. Res., 2016, 39, 191-201.
(IF 2.49)
42. Alam M. S. and Lee D-U. “Novel fluorescent Schiff base derivatives of 4-aminoantipyrine with large Stokes
shifts and dual emission properties: Crystal structure, molecular interactions, molecular surfaces, conformational
and DFT analyses” Bull. Kor. Chem. Soc., 2015, 36 (10), 2415-2428. (IF 0.871)
41. Alam M. S., Mostafizur Rahman S. M. and Lee D-U. “Synthesis, biological evaluation, quantitative-SAR and
docking studies of novel chalcone derivatives as antibacterial and antioxidant agents” Chemical Papers, 2015, 69,
1118-1129. (IF 1.468)
40. Alam M. S. and Lee D-U. “Syntheses, crystal structure, Hirshfeld surfaces, fluorescence properties, and DFT analysis of benzoic acid hydrazone Schiff bases” Spectrochimica Acta Part A: Mol. Biomol. Spectros., 2015, 145, 563–574. (IF 2.653)
39. Alam M. S. and Lee D-U. “Quantum-chemical studies to approach the antioxidant mechanism of non-phenolic
hydrazone Schiff base analogues: synthesis, molecular structure, Hirshfeld and DFT analyses” Bull. Kor. Chem.
Soc., 2015, 36(2), 682-691. (IF 0.871)
38. Alam M. S., Ahmed J. U. and Lee D-U. “Synthesis, antibacterial, antioxidant activity and QSAR studies of
novel 2-arylidenehydrazinyl-4-arylthiazole analogues” Chem. Pharm. Bull., 2014, 62(12), 1259-1268. (IF 1.375)
37. Alam M. S., Saha S. and Lee D-U. “Antibacterial and in vivo cytotoxic activities of the leaves of Leucas aspera” J. Korean Soc. Appl. Biol. Chem., 2014, 57, 551-554. (IF 0.69)
36. Alam M. S., Lee D-U. and Bari M. L. “Antibacterial and cytotoxic activities of Schiff base analogues of 4-aminoantipyrine” J. Korean Soc. Appl. Biol. Chem., 2014, 57, 613-619. (IF 0.69)
35. Islam M. A. A. A., Sheikh M. C., Alam M. S., Zangrando E., Alam M. A., Tarafder M. T. H., Miyatake R. “Synthesis, characterization and bio-activity of a bidentate NS Schiff base of S-allyldithiocarbazate and its divalent metal complexes: X-ray crystal structures of the free ligand and its nickel(II) complex” Transition Met. Chem. 2014 39, 141–149. (IF 1.306)
34. Naher S., Alam M. S., Rahman, M. M. and Aziz, S. “Comparative Studies on Physico-chemical properties and GC-MS Analysis of essential oil of Myristica fragrans” Jagannth Univ. J. Sci., 2013, 2(II), 19-25.
33. Alam M. S., Nam Y-J. and Lee D-U. “Synthesis and evaluation of (Z)-2,3-diphenyl acrylonitrile analogues as anticancer and antimicrobial agent” Eur. J. Med. Chem. 2013, 69, 790-797. (IF 3.432)
32. Alam M. S., Naher S.; Mahmud A., Bhuyan N. H.; Khan M. and Islam S. “Physico-chemical properties and GC-MS analysis of essential oil of Sapindus trifoliatus” Jagannth Univ. J. Sci., 2013, 2(I), 69-78.
31. Alam M. S. and Ozoe Y. “Antimicrobial activity and drug-likeness of 4,5-disubstituted 1-(phenyl)-1H-1,2,3-triazole analogues” Jagannth Univ. J. Sci., 2012, 1 (II), 15-26.
30. Liu L., Alam M. S. and Lee D-U. “Synthesis, antioxidant activity, fluorescence properties of new europium complexes with 2-hydroxynaphth-1-aldehyde benzoyl hydrazone Schiff base” Bull. Kor. Chem. Soc.,2012, 33, 3361-3367. (IF 0.982)
29. Motiur Rahman A. F. M., Alam M. S. and Kadi A. A. “Synthesis and antimicrobial activity of novel tetrabromo-a,a'-bis(substituted-benzyl)cycloalkanones” J. Serb. Chem. Soc. 2012, 77, 717–723. (IF 0.912)
28. Alam M. S., Choi J.-H. and Lee D-U. “Synthesis of novel Schiff base analogues of 4-amino-1,5-dimethyl-2-phenyl pyrazol-3-one and their evaluation for antioxidant and anti-inflammatory activity” Bioorg. Med. Chem. 2012, 20, 4103–4108.(IF 2.903)
27. Alam M. S. and Lee D-U. “Synthesis, molecular structure and antioxidant activity of (E)-4-[benzylideneamino]-
1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one, a schiff base derivative of antipyrine” J. Chem. Crystal., 2012, 42,
93-102. (IF 0.513)
26. Alam M. S., Liu L. and Lee D-U. “Cytotoxicity of new 5-phenyl-4,5-dihydro-1,3,4-thiadiazole analogues ” Chem. Pharm. Bull., 2011, 59 (11), 1413-1416. (IF 1.592)
25. Alam M. S. and Lee D-U. “Cytotoxic and antimicrobial properties of furoflavones and furochalcones” J. Korean Soc. Appl. Biol. Chem., 2011, 54 (5), 725-730. (IF 0.365)
24. Alam M. S., Liu L., Lee Y-E. and Lee D-U. “Synthesis, antibacterial activity and quantum-chemical studies of novel 2-arylidenehydrazinyl-4-arylthiazole analogues” Chem. Pharm. Bull., 2011, 59 (5), 568-573. (IF 1.592)
23. Alam M. S., Ozoe Y. and Lee D-U. “Structure-antimicrobial activity of 4- or 5-substituted 1-(2,6-dichloro-4-trifluoromethylphenyl)-1H-1,2,3-triazole analogues” J. Korean Soc. Appl. Biol. Chem., 2011, 54 (1), 149-153. (IF 0.365)
22. Alam M. S. and Lee D-U. “Facile synthesis and antibacterial activity of naturally occurring 5-methoxyfuroflavone” Chem. Pharm. Bull., 2010, 58 (12), 1643-45. (IF 1.507)
21. Watanabe T., Arisawa M., Narusuye K., Alam M. S., Ozoe, Y. and Nishida, A. “Alantrypinone and its derivatives: synthesis and antagonist activity toward insect GABA receptors” Bioorg. Med. Chem. 2009, 17, 94-110. (IF 2.822)
20. Liu L., Alam M. S, Hirata H., Matsuda K. and Ozoe Y. “Actions of quinolizidine alkaloids on Periplaneta americana nicotinic acetylcholine receptors” Pest Manag. Sci., 2008, 64, 1222-1228. (IF 2.040)
19. Alam M. S., Huang J., Ozoe F., Matsumura F. and Ozoe Y. “Synthesis, 3D-QSAR, and docking studies of 1-phenyl-1H-1,2,3-triazoles as selective antagonists for b3 over a1b2g2 GABA receptors” Bioorg. Med. Chem., 2007, 15 (15), 5090-5104. (IF- 2.83)
18. Alam S., Miah M. A. J. and Islam A. “Synthesis and studies of biological activity of benzyl and methyl derivatives of 7-hydroxyflavone” Pak. J. Scient. Ind. Res., 2007, 50 (2), 80-84. (IF- 0.26)
17. Mostahar S., Alam S. and Islam A. “Cytotoxic and antimicrobial activities of two new synthetic 2'-oxygenated flavones reported from Andrographis viscosula” J. Serb. Chem. Soc., 2007, 72(4), 321-329. (IF 0.611)
16. Alam M. S, Kajiki R; Hanatani H., Kong X., Ozoe F., Matsui Y., Matsumura F. and Ozoe Y. “Synthesis and structure-activity relationships of 1-phenyl-1H-1,2,3-triazoles as selective insect GABA receptor antagonists” J. Agric. Food Chem., 2006, 54(4), 1361-1372. (IF 3.13)
15. Mostahar S., Alam S. and Islam A. “Cytotoxic and antimicrobial activities of some synthetic flavones” Indian J. Chem., 2006, 45B, 1478-1486. (IF 0.466)
14. Alam S., Miah M. A. J. and Islam A. “Synthesis and studies of antimicrobial activity of two benzylated flavones” J. Ban. Chem. Soc., 2005, 18(1), 30-40.
13. Alam S., Miah M. A. J. and Islam A. “Antibactaerial and Antifungal Activities of Synthetic Apigenin Trimethyl Ether” ACGC Chem. Res. Comm., 2005, 18:1-6.
12. Alam S. and Mostahar S. “Studies of Antimicrobial Activity of two Synthetic 2', 4', 6'-Trioxygenated Flavones” J. Applied Sci., 2005, 5(3), 327-333.
11. Alam S., Sharkar Z. and Islam A. “Synthesis and studies of antibacterial activity of pongaglabol” J. Chem. Sci., 2004, 116 (1), 29-32. (IF 1.075)
10. Alam S., “Synthesis and studies of antimicrobial activity of lanceolatin B” Acta Chim. Slov. 2004, 51 (3), 447-452. (IF 0.895)
9. Alam S., Miah M. A. J. and Islam A. “In vitro studies of antimicrobial activity of synthetic ovaliflavone” J. Bio. Sci., 2004, 4 (4), 527-531.
8. Alam S., Das N. C. and Islam A. “Synthesis of maximaflavanone-A and its derivative” J. Ban. Acad. Sci., 2004, 28(2), 117-120.
7. Alam S. “Synthesis, antibacterial and antifungal activity of some derivatives of 2-phenyl-chromen-4-one” J. Chem. Sci., 2004, 116(6), 325-331. (IF 1.075)
6. Alam S. and Islam A. “Synthesis of 2',4',4-trihydroxy-6¢-methoxydihydro chalcone and 2', 4'-dihydroxy-4, 6'-dimethoxydihydrochalcone” Act. Cien. Ind., 2003, Vol. XXIX (2), 83-86.
5. Alam S. and Islam A. “Synthesis of 2', 4'-dihydroxy-6'-methoxy-3, 4-methylenedioxydihydrochalcone and 2', 4', 6'-trihydroxy-4-methoxydihydrochalcone” Pak. J. Sci. Ind. Res., 2003, 46 (1), 27-29. (IF- 0.26)
4. Alam S., Easmin S., Islam A. “Synthesis of sanaganone, a naturally occurring flavone” J. Ban. Acad. Sci., 2003, 27(1), 21-25.
3. Alam S., Hasan T. and Islam A. “Synthesis of 4-hydroxy-2-methoxydihydrochalcone and 4,4'-dihydroxy-2-methoxydihydrochalcone” Orient. J. Chem., 2000, 16(2), 233-237.
2. Ali R., Hasan T., Alam S. and Islam A. “Synthesis of lespedezaflavanone-A & B, the naturally occurring prenylatedflavanone” J. Ban. Chem. Soc., 2000, 13 (1 & 2), 33-40.
1. Ali R., Hasan T., Alam S. and Islam A. “Synthesis of Euchrenone a3-a naturally occurring prenylatedflavanone” J. Ban. Chem. Soc., 1999, 12(2), 125-131.
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