Carlos Rangel Rodrigues

Author

Universidade Federal do Rio de Janeiro ORCID

Also Known As

C R Rodrigues, C. R. Rodrigues, C.R Rodrigues, C.R. Rodrigues, C.R.F. Rodrigues, CARLOS R. RODRIGUES, Carlos R Rodrigues, Carlos R. Rodrigues, Carlos Rangel RODRIGUES, Carlos Rangel Rodrigues

262

Publications

5.4K

Citations

H-Index

134

Concepts

All Affiliations

Universidade Federal do Rio de Janeiro Universidade Federal Fluminense Fundação Oswaldo Cruz Hospital Universitário Antônio Pedro Universidade do Estado do Rio de Janeiro

About

Carlos Rangel Rodrigues is an author at Universidade Federal do Rio de Janeiro specializing in pharmacology, medicine, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	65	2.2K
2	Biochemistry	18	26	713
3	Engineering	17	23	684
4	Natural Sciences	17	21	631
5	Health Sciences	2	2	22

Carlos Rangel Rodrigues

113

Publications

3.7K

Citations

H-Index

Page 1

	Year	Citations
Synthesis, tuberculosis inhibitory activity, and SAR study of N-substituted-phenyl-1,2,3-triazole derivatives Marilia S. Costa, Núbia Boechat, Érica A. Rangel, Bioorganic & Medicinal Chemistry Derivative (Chemistry)DerivativesMedicineOrganic ChemistryChemistry	2006	216
Design, Synthesis, and Pharmacological Profile of Novel Fused Pyrazolo[4,3-<i>d</i>]pyridine and Pyrazolo[3,4-<i>b</i>][1,8]naphthyridine Isosteres: A New Class of Potent and Selective Acetylcholinesterase Inhibitors Eliezer J. Barreiro, Celso A. Câmara, Hugo Verli, Journal of Medicinal Chemistry	2003	109
Design, synthesis, SAR, and biological evaluation of new 4-(phenylamino)thieno[2,3-b]pyridine derivatives Alice M. R. Bernardino, Luiz C. S. Pinheiro, Carlos Rangel Rodrigues, Bioorganic & Medicinal Chemistry DerivativesMedicineOrganic ChemistryBiological EvaluationChemistry	2006	102
Structure−Activity Relationships of the Antimalarial Agent Artemisinin. 6. The Development of Predictive In Vitro Potency Models Using CoMFA and HQSAR Methodologies Mitchell A. Avery, Maria Alvim‐Gaston, Carlos Rangel Rodrigues, Journal of Medicinal Chemistry	2001	85
Trypanocidal agents with low cytotoxicity to mammalian cell line: A comparison of the theoretical and biological features of lapachone derivatives Vı́tor F. Ferreira, Alessandra Jorqueira, Alessandra Mendonça Teles de Souza, Bioorganic & Medicinal Chemistry Mammalian Cell LineBiochemistryAntiparasitic AgentMedicineAfrican Trypanosomiasis	2006	83
Synthesis, antiplatelet and in silico evaluations of novel N-substituted-phenylamino-5-methyl-1H-1,2,3-triazole-4-carbohydrazides Alessandro K. Jordão, Vı́tor F. Ferreira, Émerson Silva Lima, Bioorganic & Medicinal Chemistry Medicinal ChemistryDerivative (Chemistry)Organic ChemistrySilico EvaluationsPharmacology	2009	79
Synthesis, in vitro evaluation, and SAR studies of a potential antichagasic 1H-pyrazolo[3,4-b]pyridine series Luiza R.S. Dias, Marcelo Bannwart Santos, Sérgio de Albuquerque, Bioorganic & Medicinal Chemistry Sar StudiesMedicinal ChemistryBioorganic ChemistryNatural SciencesMedicine	2006	78
Synthesis, antichagasic in vitro evaluation, cytotoxicity assays, molecular modeling and SAR/QSAR studies of a 2-phenyl-3-(1-phenyl-1H-pyrazol-4-yl)-acrylic acid benzylidene-carbohydrazide series Maria A.F. Vera-DiVaio, Antonio C. C. Freitas, Helena Carla Castro, Bioorganic & Medicinal Chemistry EngineeringCytotoxicity AssaysMedicineOrganic ChemistryAnti-cancer Agent	2008	74
Photoprotection assessment of olive (Olea europaea L.) leaves extract standardized to oleuropein: In vitro and in silico approach for improved sunscreens Anne C.P. da Silva, Juliana Patrão de Paiva, Raiane R. Diniz, Journal of Photochemistry and Photobiology B Biology Olea Europaea L.PhotochemistryBotanyMedicineImproved Sunscreens	2019	70
Antibacterial profile against drug-resistant Staphylococcus epidermidis clinical strain and structure–activity relationship studies of 1H-pyrazolo[3,4-b]pyridine and thieno[2,3-b]pyridine derivatives Bruno Leal, Ilídio F. Afonso, Carlos Rangel Rodrigues, Bioorganic & Medicinal Chemistry Clinical StrainDrug-resistant StaphylococcusMedicineAntibacterial ProfileAntibacterial Agent	2008	68

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