| 1 |
Nagy ET, Ahmed AAS, Elmongy EI, El-Gendy SM, Elmadbouh I, El Sayed IET, Abd Eldaim MA, El-Gokha AA. Design and cytotoxic evaluation via apoptotic and antiproliferative activity for novel 11(4-aminophenylamino)neocryptolepine on hepatocellular and colorectal cancer cells. Apoptosis 2023. [PMID: 36719468 DOI: 10.1007/s10495-023-01810-y] [Reference Citation Analysis]
|
| 2 |
Ma Y, Xu H, Zhou Z, Tian Y, Du K, Zhang H, Jiang X, Lu J, Niu Y, Tu L, Liu H, Zhu H, Chen P, Liu Y. CFNC, a neocryptolepine derivative, inhibited the growth of gastric cancer AGS cells by inhibiting PI3K/AKT signaling pathway. Eur J Pharmacol 2022;938:175408. [PMID: 36442620 DOI: 10.1016/j.ejphar.2022.175408] [Reference Citation Analysis]
|
| 3 |
Li D, Yang R, Wu J, Zhong B, Li Y. Comprehensive review of α-carboline alkaloids: Natural products, updated synthesis, and biological activities. Front Chem 2022;10:988327. [DOI: 10.3389/fchem.2022.988327] [Reference Citation Analysis]
|
| 4 |
Nuthakki VK, Mudududdla R, Bharate SB. Role of basic aminoalkyl chains in the lead optimization of Indoloquinoline alkaloids. Eur J Med Chem 2021;227:113938. [PMID: 34710743 DOI: 10.1016/j.ejmech.2021.113938] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
|
| 5 |
Håheim KS, Lindbäck E, Tan KN, Albrigtsen M, Urdal Helgeland IT, Lauga C, Matringe T, Kennedy EK, Andersen JH, Avery VM, Sydnes MO. Synthesis and Evaluation of the Tetracyclic Ring-System of Isocryptolepine and Regioiso-Mers for Antimalarial, Antiproliferative and Antimicrobial Activities. Molecules 2021;26:3268. [PMID: 34070798 DOI: 10.3390/molecules26113268] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
|
| 6 |
Nischitha R, Shivanna MB. Antimicrobial activity and metabolite profiling of endophytic fungi in Digitaria bicornis (Lam) Roem. and Schult. and Paspalidium flavidum (Retz.) A. Camus. 3 Biotech 2021;11:53. [PMID: 33489672 DOI: 10.1007/s13205-020-02590-x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
|
| 7 |
Zarnowski R, Jaromin A, Zagórska A, Dominguez EG, Sidoryk K, Gubernator J, Andes DR. A Label-Free Cellular Proteomics Approach to Decipher the Antifungal Action of DiMIQ, a Potent Indolo[2,3-b]Quinoline Agent, against Candida albicans Biofilms. Int J Mol Sci 2020;22:E108. [PMID: 33374351 DOI: 10.3390/ijms22010108] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
|
| 8 |
Sidoryk K, Michalak O, Kubiszewski M, Leś A, Cybulski M, Stolarczyk EU, Doubsky J. Synthesis of Thiol Derivatives of Biological Active Compounds for Nanotechnology Application. Molecules 2020;25:E3470. [PMID: 32751592 DOI: 10.3390/molecules25153470] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
|
| 9 |
Nagalakshmamma V, Venkataswamy M, Pasala C, Umamaheswari A, Thyagaraju K, Nagaraju C, Chalapathi PV. Design, synthesis, anti-tobacco mosaic viral and molecule docking simulations of urea/thiourea derivatives of 2-(piperazine-1-yl)-pyrimidine and 1-(4-Fluoro/4-Chloro phenyl)-piperazine and 1-(4-Chloro phenyl)-piperazine - A study. Bioorg Chem 2020;102:104084. [PMID: 32693309 DOI: 10.1016/j.bioorg.2020.104084] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
|
| 10 |
Anil SM, Rajeev N, Kiran KR, Swaroop TR, Mallesha N, Shobith R, Sadashiva MP. Multi-pharmacophore Approach to Bio-therapeutics: Piperazine Bridged Pseudo-peptidic Urea/Thiourea Derivatives as Anti-oxidant Agents. Int J Pept Res Ther 2020;26:151-158. [DOI: 10.1007/s10989-019-09824-4] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
|
| 11 |
Zhu J, Gao J, Yang C, Shang X, Zhao Z, Lawoe RK, Zhou R, Sun Y, Yin X, Liu Y. Design, Synthesis, and Antifungal Evaluation of Neocryptolepine Derivatives against Phytopathogenic Fungi. J Agric Food Chem 2020;68:2306-15. [DOI: 10.1021/acs.jafc.9b06793] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 6.7] [Reference Citation Analysis]
|
| 12 |
Stompor M, Świtalska M, Bajek A, Wietrzyk J. Influence of amide versus ester linkages on the anticancer properties of the new flavone-biotin conjugates. Z Naturforsch C J Biosci 2019;74:193-200. [PMID: 31100057 DOI: 10.1515/znc-2018-0195] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
|
| 13 |
Marepu N, Gosi M, Vedula SS, Yeturu S, Pal M. Ultrasound-assisted Synthesis of 6-substituted indolo[2,3-b]quinolines: their Evaluation as Potential Cytotoxic Agents. Mini Rev Med Chem 2019;19:599-608. [PMID: 30058486 DOI: 10.2174/1389557518666180727170055] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
|
| 14 |
Wang M, Rakesh KP, Leng J, Fang WY, Ravindar L, Channe Gowda D, Qin HL. Amino acids/peptides conjugated heterocycles: A tool for the recent development of novel therapeutic agents. Bioorg Chem 2018;76:113-29. [PMID: 29169078 DOI: 10.1016/j.bioorg.2017.11.007] [Cited by in Crossref: 48] [Cited by in F6Publishing: 43] [Article Influence: 8.0] [Reference Citation Analysis]
|
| 15 |
Stompor M, Świtalska M, Wietrzyk J. Synthesis and biological evaluation of acyl derivatives of hydroxyflavones as potent antiproliferative agents against drug resistance cell lines. Zeitschrift für Naturforschung C 2018;73:87-93. [DOI: 10.1515/znc-2017-0093] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.2] [Reference Citation Analysis]
|
| 16 |
Challa C, Ravindran J, Konai MM, Varughese S, Jacob J, Kumar BSD, Haldar J, Lankalapalli RS. Expedient Synthesis of Indolo[2,3-b]quinolines, Chromeno[2,3-b]indoles, and 3-Alkenyl-oxindoles from 3,3'-Diindolylmethanes and Evaluation of Their Antibiotic Activity against Methicillin-Resistant Staphylococcus aureus. ACS Omega 2017;2:5187-95. [PMID: 30023741 DOI: 10.1021/acsomega.7b00840] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 3.2] [Reference Citation Analysis]
|
| 17 |
Kukowska M. Amino acid or peptide conjugates of acridine/acridone and quinoline/quinolone-containing drugs. A critical examination of their clinical effectiveness within a twenty-year timeframe in antitumor chemotherapy and treatment of infectious diseases. Eur J Pharm Sci 2017;109:587-615. [PMID: 28842352 DOI: 10.1016/j.ejps.2017.08.027] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 4.2] [Reference Citation Analysis]
|
| 18 |
An YS, Hao ZF, Zhang XJ, Wang LZ. Efficient Synthesis and Biological Evaluation of a Novel Series of 1,5-Benzodiazepine Derivatives as Potential Antimicrobial Agents. Chem Biol Drug Des 2016;88:110-21. [PMID: 26850700 DOI: 10.1111/cbdd.12739] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 2.7] [Reference Citation Analysis]
|
| 19 |
Mieczkowski A, Makowska M, Sekula J, Tomczyk E, Zalewska E, Nasulewicz-goldeman A, Wietrzyk J. Bicyclic cytarabine analogues: synthesis and investigation of antitumor properties of novel, 6-aryl- and 6-alkyl-3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one arabinosides. Tetrahedron 2015;71:8454-61. [DOI: 10.1016/j.tet.2015.09.015] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
|
| 20 |
Sidoryk K, Świtalska M, Jaromin A, Cmoch P, Bujak I, Kaczmarska M, Wietrzyk J, Dominguez EG, Żarnowski R, Andes DR, Bańkowski K, Cybulski M, Kaczmarek Ł. The synthesis of indolo[2,3-b]quinoline derivatives with a guanidine group: highly selective cytotoxic agents. Eur J Med Chem 2015;105:208-19. [PMID: 26496013 DOI: 10.1016/j.ejmech.2015.10.022] [Cited by in Crossref: 34] [Cited by in F6Publishing: 36] [Article Influence: 4.3] [Reference Citation Analysis]
|
| 21 |
Wang L, Świtalska M, Wang N, Du ZJ, Fukumoto Y, Diep NK, Kiguchi R, Nokami J, Wietrzyk J, Inokuchi T. Design, synthesis, and biological evaluation of artemisinin-indoloquinoline hybrids as potent antiproliferative agents. Molecules 2014;19:19021-35. [PMID: 25412047 DOI: 10.3390/molecules191119021] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 1.6] [Reference Citation Analysis]
|
| 22 |
Bracca ABJ, Heredia DA, Larghi EL, Kaufman TS. Neocryptolepine (Cryprotackieine), A Unique Bioactive Natural Product: Isolation, Synthesis, and Profile of Its Biological Activity: Neocryptolepine: Isolation, Synthesis, and Biological Activity. Eur J Org Chem 2014;2014:7979-8003. [DOI: 10.1002/ejoc.201402910] [Cited by in Crossref: 42] [Cited by in F6Publishing: 43] [Article Influence: 4.7] [Reference Citation Analysis]
|
