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ArticleMedicinal chemistry (Shariqah (United Arab Emirates))2024

Synthesis and Structural Activity Relationship Study of Ursolic Acid Derivatives as Antitubercular Agent.

Sadhna Vishwakarma, Santosh K Srivastava, Naveen K Khare, Shiwa Chaubey, Vinita Chaturvedi, Priyanka Trivedi, Sana Khan, Feroz Khan

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Article in Medicinal chemistry (Shariqah (United Arab Emirates)), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Sadhna VishwakarmaDepartment of Medicinal Chemistry, CSIR-Central Institute of Medicinal and Aromatic Plants (CIMAP), Lucknow, 226015, India.
Santosh K SrivastavaDepartment of Medicinal Chemistry, CSIR-Central Institute of Medicinal and Aromatic Plants (CIMAP), Lucknow, 226015, India.
Naveen K KhareDepartment of Chemistry, University of Lucknow, Lucknow, 226007, India.
Shiwa ChaubeyDepartment of Chemistry, University of Lucknow, Lucknow, 226007, India.
Vinita ChaturvediDivision of Biochemistry and Structural Biology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Priyanka TrivediDivision of Biochemistry and Structural Biology, CSIR-Central Drug Research Institute, Lucknow, 226031, India.
Sana KhanDepartment of Metabolic and Structural Biology, CSIR-Central Institute of Medicinal and Aromatic Plants (CIMAP), Lucknow, 226015, India.
Feroz KhanDepartment of Metabolic and Structural Biology, CSIR-Central Institute of Medicinal and Aromatic Plants (CIMAP), Lucknow, 226015, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe chemical transformation of ursolic acid (UA) into novel C-3 aryl ester derivatives and

backgroundUA is a natural pentacyclic triterpenoid with many pharmacological properties. Semisynthetic UA analogs have demonstrated enhanced anticancer, antimalarial, and antifilarial properties in our previous studies.

methodsThe C-30 carboxylic group of previously isolated UA was protected, and various C-3 aryl ester derivatives were semi-synthesized. The agar dilution method was used to evaluate the

resultsThe derivative 3-O-(2-amino,3-methyl benzoic acid)-ethyl ursolate (UA-1H) was the most active among the eight derivatives (MIC1 2.5 μg/mL) against Mtb H

conclusionThe ursolic acid derivative UA-1H possesses significant

Indexed as

Antitubercular AgentsMolecular Docking SimulationMycobacterium tuberculosisTriterpenesUrsolic AcidMicrobial Sensitivity TestsMolecular StructureStructure-Activity RelationshipAntitubercular AgentsTriterpenesUrsolic Acidantituberculareucalyptus tereticornisin silico docking.in vitrotriterpenoidUrsolic acid

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.