Found: 22
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Development of spiro-3-indolin-2-one containing compounds of antiproliferative and anti-SARS-CoV-2 properties.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-17883-9
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- Article
Indole Compounds in Oncology: Therapeutic Potential and Mechanistic Insights.
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- Pharmaceuticals (14248247), 2024, v. 17, n. 7, p. 922, doi. 10.3390/ph17070922
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- Article
Synthesis, Antibacterial Evaluation, and Computational Studies of a Diverse Set of Linezolid Conjugates.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 2, p. 191, doi. 10.3390/ph15020191
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- Article
Design, synthesis, antimicrobial, and DNA gyrase inhibitory properties of fluoroquinolone–dichloroacetic acid hybrids.
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- Chemical Biology & Drug Design, 2020, v. 95, n. 2, p. 248, doi. 10.1111/cbdd.13638
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- Article
Efficient Synthesis and Computational Studies of Useful Guanylating Agents: 1H‐Benzotriazole‐1‐carboximidamides.
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- ChemistrySelect, 2020, v. 5, n. 44, p. 13963, doi. 10.1002/slct.202003796
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- Article
Development of Isatin‐Based Schiff Bases Targeting VEGFR‐2 Inhibition: Synthesis, Characterization, Antiproliferative Properties, and QSAR Studies.
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- ChemMedChem, 2022, v. 17, n. 13, p. 1, doi. 10.1002/cmdc.202200164
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- Article
New Pyrazine Conjugates: Synthesis, Computational Studies, and Antiviral Properties against SARS‐CoV‐2.
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- ChemMedChem, 2021, v. 16, n. 22, p. 3418, doi. 10.1002/cmdc.202100476
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- Article
Stereoselective Synthesis, Structural and Spectroscopic Study of 4,5,11-Triazatricyclo[6.2.1.0*2,6*]Undec-5-ene.
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- Journal of Heterocyclic Chemistry, 2016, v. 53, n. 4, p. 1074, doi. 10.1002/jhet.2440
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- Article
Regio- and stereoselective synthesis of spiro[1-benzothiepine-4(5 h), 3′(3 h)-pyrazol]-5-ones.
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- Journal of Heterocyclic Chemistry, 2006, v. 43, n. 6, p. 1549, doi. 10.1002/jhet.5570430618
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- Article
Novel regioselective synthesis of 3′ H,4 H-spiro[chromene-3,2′-[1,3,4]thiadiazol]-4-one containing compounds.
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- Journal of Heterocyclic Chemistry, 2006, v. 43, n. 5, p. 1237, doi. 10.1002/jhet.5570430515
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- Article
New 2,4‐disubstituted‐2‐thiopyrimidines as VEGFR‐2 inhibitors: Design, synthesis, and biological evaluation.
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- Archiv der Pharmazie, 2019, v. 352, n. 11, p. N.PAG, doi. 10.1002/ardp.201900089
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- Article
Indole-Based Compounds as Potential Drug Candidates for SARS-CoV-2.
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- Molecules, 2023, v. 28, n. 18, p. 6603, doi. 10.3390/molecules28186603
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- Article
New NSAID Conjugates as Potent and Selective COX-2 Inhibitors: Synthesis, Molecular Modeling and Biological Investigation.
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- Molecules, 2023, v. 28, n. 4, p. 1945, doi. 10.3390/molecules28041945
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- Article
Azomethine Ylides—Versatile Synthons for Pyrrolidinyl-Heterocyclic Compounds.
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- Molecules, 2023, v. 28, n. 2, p. 668, doi. 10.3390/molecules28020668
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- Article
Spirooxindole: A Versatile Biologically Active Heterocyclic Scaffold.
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- Molecules, 2023, v. 28, n. 2, p. 618, doi. 10.3390/molecules28020618
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- Article
Synthesis of Potential Antiviral Agents for SARS-CoV-2 Using Molecular Hybridization Approach.
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- Molecules, 2022, v. 27, n. 18, p. 5923, doi. 10.3390/molecules27185923
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- Article
Molecular structure studies of novel bronchodilatory-active 4-azafluorenes.
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- Zeitschrift für Kristallographie. Crystalline Materials, 2016, v. 231, n. 3, p. 179, doi. 10.1515/zkri-2015-1892
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- Article
Synthesis, X-ray powder diffraction and DFT-D studies of indole-based compounds.
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- Zeitschrift für Kristallographie. Crystalline Materials, 2018, v. 233, n. 6, p. 421, doi. 10.1515/zkri-2017-2106
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- Article
A convenient synthesis of thiamacrocyclic dilactams.
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- Heteroatom Chemistry, 2007, v. 18, n. 3, p. 249, doi. 10.1002/hc.20292
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- Article
Synthesis and X-ray studies of novel azaphenanthrenes.
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- Journal of Chemical Research, 2018, v. 42, p. 90, doi. 10.3184/174751918X15183538282993
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- Article
Synthesis and X-ray studies of novel azaphenanthrenes.
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- Journal of Chemical Research, 2018, v. 42, n. 2, p. 90, doi. 10.3184/174751918X15183538282993
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- Article
Novel Curcumin Mimics: Design, Synthesis, Biological Properties and Computational Studies of Piperidone‐Piperazine Conjugates.
- Published in:
- ChemistrySelect, 2022, v. 7, n. 31, p. 1, doi. 10.1002/slct.202201406
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- Article