Year |
Citation |
Score |
2020 |
Yaseen M, Rashid MA, Iqbal MA, Farooq Z, Idrees M, Qayyum MA, Intisar A, Mahmood MHR, Khan I, Latif M. Synthesis, photoinduced, amination and topological indices of novel porphyrin dyads Journal of Porphyrins and Phthalocyanines. 24: 1054-1065. DOI: 10.1142/S1088424620500200 |
0.362 |
|
2019 |
Nazir Y, Saeed A, Rafiq M, Afzal S, Ali A, Latif M, Zuegg J, Hussein WM, Fercher C, Barnard RT, Cooper MA, Blaskovich MAT, Ashraf Z, Ziora ZM. Hydroxyl substituted benzoic acid/cinnamic acid derivatives: Tyrosinase inhibitory kinetics, anti-melanogenic activity and molecular docking studies. Bioorganic & Medicinal Chemistry Letters. 126722. PMID 31732410 DOI: 10.1016/J.Bmcl.2019.126722 |
0.352 |
|
2019 |
Iqbal Z, Iqbal A, Ashraf Z, Latif M, Hassan M, Nadeem H. Synthesis and docking studies of N-(5-(alkylthio)-1,3,4-oxadiazol-2-yl)methyl)benzamide analogues as potential alkaline phosphatase inhibitors. Drug Development Research. PMID 31032540 DOI: 10.1002/Ddr.21542 |
0.369 |
|
2018 |
Mah S, Jang J, Song D, Shin Y, Latif M, Jung Y, Hong S. Discovery of fluorescent 3-heteroarylcoumarin derivatives as novel inhibitors of anaplastic lymphoma kinase. Organic & Biomolecular Chemistry. PMID 30534706 DOI: 10.1039/C8Ob02874E |
0.4 |
|
2018 |
Latif M, Ashraf Z, Basit S, Ghaffar A, Zafar MS, Saeed A, Meo SA. Latest perspectives of orally bioavailable 2,4-diarylaminopyrimidine analogues (DAAPalogues) as anaplastic lymphoma kinase inhibitors: discovery and clinical developments Rsc Advances. 8: 16470-16493. DOI: 10.1039/C8Ra01934G |
0.362 |
|
2017 |
Abbas Q, Ashraf Z, Hassan M, Nadeem H, Latif M, Afzal S, Seo SY. Development of highly potent melanogenesis inhibitor by in vitro, in vivo and computational studies. Drug Design, Development and Therapy. 11: 2029-2046. PMID 28740364 DOI: 10.2147/Dddt.S137550 |
0.344 |
|
2017 |
Basit S, Ashraf Z, Lee K, Latif M. First macrocyclic 3(rd)-generation ALK inhibitor for treatment of ALK/ROS1 cancer: Clinical and designing strategy update of lorlatinib. European Journal of Medicinal Chemistry. 134: 348-356. PMID 28431340 DOI: 10.1016/J.Ejmech.2017.04.032 |
0.391 |
|
2016 |
Choe H, Pham TT, Lee JY, Latif M, Park H, Kang YK, Lee J. Remote Stereoinductive Intramolecular Nitrile Oxide Cycloaddition: Asymmetric Total Synthesis and Structure Revision of (-)-11beta-Hydroxycurvularin. The Journal of Organic Chemistry. PMID 26894643 DOI: 10.1021/Acs.Joc.5B02760 |
0.698 |
|
2015 |
Latif M, Yun JI, Seshadri K, Kim HR, Park CH, Park H, Kim H, Lee J. Stereoselective construction of 2,6-cis-disubstituted tetrahydropyrans via intramolecular amide enolate alkylation: total synthesis of (-)-centrolobine. The Journal of Organic Chemistry. 80: 3315-20. PMID 25723100 DOI: 10.1021/Acs.Joc.5B00046 |
0.681 |
|
2015 |
Saeed A, Ejaz SA, Khurshid A, Hassan S, Al-Rashida M, Latif M, Lecka J, Sévigny J, Iqbal J. Synthesis, characterization and biological evaluation of N-(2,3-dimethyl-5-oxo-1-phenyl-2,5-dihydro-1H-pyrazol-4-yl)benzamides Rsc Advances. 5: 86428-86439. DOI: 10.1039/C5Ra17568B |
0.325 |
|
2015 |
Latif M, Park S, Ali I, Choe H, Chae CH, Park CH, Kim HR, Yun CS, Lee K. Design, synthesis, and evaluation of 2-anilino-4-(3,5-dicarboxamidespiperidine)-pyrimidines as anaplastic lymphoma kinase inhibitors Bulletin of the Korean Chemical Society. 36: 2397-2400. DOI: 10.1002/Bkcs.10454 |
0.675 |
|
2015 |
Moon SH, Latif M, Qasim M, Choi SW, Lee JY, Byun BJ, Saeed A, Kim SH. Synthesis, characterization, and biological evaluation of oxadiazole derivatives bearing 5-phenyl-tetrazole as osteoclast differentiation inhibitors Bulletin of the Korean Chemical Society. 36: 2247-2253. DOI: 10.1002/Bkcs.10436 |
0.392 |
|
2015 |
Latif M, Byun BJ, Lee K. Synthesis of 4-(3,4-dicarboxamido-1H-pyrrole)pyrimidines as anaplastic lymphoma kinase inhibitors Bulletin of the Korean Chemical Society. 36: 520-525. DOI: 10.1002/Bkcs.10097 |
0.368 |
|
2014 |
Lee HJ, Latif M, Choe H, Ali I, Lee HK, Yang EH, Yun JI, Chae CH, Jung JK, Kim HR, Lee CO, Park CH, Lee K. ALK inhibitors of bis-ortho-alkoxy-para-piperazinesubstituted-pyrimidines and -triazines for cancer treatment. Archives of Pharmacal Research. 37: 1130-8. PMID 24446111 DOI: 10.1007/S12272-013-0323-Z |
0.733 |
|
2014 |
Yun JI, Yang EH, Latif M, Lee HJ, Lee K, Yun CS, Park CH, Lee CO, Chae CH, Cho SY, Jung HJ, Kim P, Choi SU, Kim HR. Novel 2,4-dianilino-5-fluoropyrimidine derivatives possessing ALK inhibitory activities. Archives of Pharmacal Research. 37: 873-81. PMID 24129617 DOI: 10.1007/S12272-013-0247-7 |
0.689 |
|
2014 |
Latif M, Jung ME, Lee K, Choi G. Synthesis and biological evaluation of tetrapeptide ketones as reversible 20S proteasome inhibitors Bulletin of the Korean Chemical Society. 35: 3571-3575. DOI: 10.5012/Bkcs.2014.35.12.3571 |
0.381 |
|
2013 |
Park CH, Choe H, Jang IY, Kwon SY, Latif M, Lee HK, Lee HJ, Yang EH, Yun JI, Chae CH, Cho SY, Choi SU, Ha JD, Jung H, Kim HR, et al. Novel bis-ortho-alkoxy-para-piperazinesubstituted-2,4-dianilinopyrimidines (KRCA-0008) as potent and selective ALK inhibitors for anticancer treatment. Bioorganic & Medicinal Chemistry Letters. 23: 6192-6. PMID 24095090 DOI: 10.1016/J.Bmcl.2013.08.090 |
0.731 |
|
2013 |
Saeed A, Al-Masoudi NA, Latif M. Synthesis and antiviral activity of new substituted methyl [2-(arylmethylene-hydrazino)-4-oxo-thiazolidin-5-ylidene]acetates. Archiv Der Pharmazie. 346: 618-25. PMID 23828482 DOI: 10.1002/Ardp.201300057 |
0.343 |
|
2013 |
Latif M, Saeed A, Kim SH. Journey of the ALK-inhibitor CH5424802 to phase II clinical trial. Archives of Pharmacal Research. 36: 1051-4. PMID 23700294 DOI: 10.1007/S12272-013-0157-8 |
0.335 |
|
2013 |
Yang EH, Yun JI, Latif M, Lee HJ, Yun C, Lee K, Park CH, Cho SY, Jung HJ, Kim P, Ha JD, Kim HR. New Pyrimidine Derivatives possessing ALK Inhibitory Activities Bulletin of the Korean Chemical Society. 34: 3129-3132. DOI: 10.5012/Bkcs.2013.34.10.3129 |
0.696 |
|
2010 |
Saeed A, Khera RA, Abbas N, Latif M, Sajid I, Flörke U. Synthesis, characterization, crystal structures, and antibacterial activity of some new 1-(3,4,5-trimethoxybenzoyl)-3-aryl thioureas Turkish Journal of Chemistry. 34: 335-345. DOI: 10.3906/Kim-0810-44 |
0.356 |
|
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