Kurnool Aravind

@swec.ac.in

Assistant Professor and Science and Humanities, Department of Chemistry
sridevi womens engineering college

Kurnool Aravind


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https://researchid.co/ammaammaamma

RESEARCH, TEACHING, or OTHER INTERESTS

Organic Chemistry, Analytical Chemistry, Materials Chemistry, Pharmaceutical Science
10

Scopus Publications

69

Scholar Citations

4

Scholar h-index

2

Scholar i10-index

Scopus Publications

  • Development of a series of thienopyrimidine-tagged 1,3,4-thiadiazole hybrids: synthesis, anti-diabetic activity and molecular docking studies
    Srawanthi Kotoori, Karuna Sree Merugu, Pooja Sahu, Aravind Kurnool, Baji Baba Shaik, Nagaraju Kerru
    Journal of the Indian Chemical Society, 2026
  • Quality by Design-Based Development of a Robust LC Method for Simultaneous Estimation of Process- and Degradation-Related Impurities in Rifapentine Drug Product for the Treatment of Active and Latent Tuberculosis
    Siva Prasad Korikana, Sreenivasa Rao Battula, Naresh Konduru, Aravind Kurnool, Divya Kumar Vemuri, Venkata Lakshamana Sagar Dantinapalli
    Biomedical Chromatography, 2026
    A precise, robust, and stability‐indicating liquid chromatographic (LC) method coupled with a photodiode array (PDA) detector was developed and validated for the quantitative estimation of rifapentine, an essential therapeutic agent for both active and latent tuberculosis (TB). The chromatographic separation was achieved on a YMC Pack C18 column (250 × 4.6 mm, 5 μm) using a gradient elution with Solvent A composed of phosphate buffer (pH 6.3) and acetonitrile (90:10, v/v), and Solvent B consisting of 100% acetonitrile. The optimized parameters included a flow rate of 1.0 mL min −1 , a column temperature of 30 °C, an injection volume of 25 μL, and UV detection at 330 nm. Method validation, conducted as per ICH Q2(R2) guidelines, confirmed excellent accuracy with recovery results between 97.0% and 103.0%. The method demonstrated linearity over a broad concentration range, from the limit of quantification (LOQ) to 200% of the target concentration, with correlation coefficients ( R 2 ) exceeding 0.998 for all impurities. Precision, expressed as relative standard deviation (RSD), was consistently below 5.0%. Forced degradation studies indicated that rifapentine undergoes degradation under acidic, basic, oxidative, thermal, and photolytic conditions, thus confirming the stability‐indicating nature of the developed LC method.
  • Microwave-Assisted, Multicomponent Synthesis of Pyrazolo [3, 4-b] Pyridines Under Green Conditions
    Shravya Pachipulusu, Karuna Sree Merugu, Ramakrishna Rao Bhonsle, Sirisha Surapaneni, Aravind Kurnool, Nagaraju Kerru
    Chemistryselect, 2024
    Developing novel and environmentally friendly green methodologies are critical in synthetic organic chemistry. Here, we investigated the one‐pot, efficient green synthesis of pyrazolo[3,4‐b]pyridine derivatives via a multicomponent approach. The reactions were operated in an aqueous medium by using microwave irradiation and conventional protocols. The green protocol offered high yields of desired product in swift reaction time, and good tolerance under reaction conditions.
  • A facile microwave-mediated method of 1,4-dihydropyridine carboxylates synthesis by multicomponent reaction
    Shravya Pachipulusu, Karuna Sree Merugu, Ramakrishna Rao Bhonsle, Aravind Kurnool
    Journal of Heterocyclic Chemistry, 2024
    An innovative green procedure has been devised to prepare derivatives of 1,4‐dihydropyridine (1,4‐DHP). This method works with a catalyst process using ethanol as solvent under microwave irradiation conditions, enabling swift reactions (<30 min) with impressive yields (90%–96%). It contributes to an environmentally friendly and easily executable process by using the energy efficiency method. Within 30 min, this method underscores ecologically conscious practices and offers simple purification, streamlining the process by omitting column chromatography. This method highlights the efficacy and eco‐friendly nature of synthesizing 1,4‐DHPs. This method combines four component reactions, utilizing EtOH as the solvent and triethylamine as the catalyst. Furthermore, the product was characterized by diverse spectroscopic analysis.
  • MARALIXIBAT IN RAT PLASMA AND ITS PHARMACOLOGICAL STUDIES (BIO-ANALYTICAL METHOD DEVELOPMENT AND VALIDATION BY LC-MS)
    Shravya Pachipulusu, Karunasree Merugu, Aravind Kurnool
    Rasayan Journal of Chemistry, 2024
    The bio-analytical method development of Maralixibat using Elobixibat as an internal standard is a convenient, fast, accurate, and consistent new LC-MS technique and was validated. The present work explains the development of the LC-MS/MS bio-analytical method by RP-18(150x4.6 mm, 3.5µ) column and a binary mixture(0.1% formic acid & methanol) of organic mobile phase in the ratio 60:40. By using liquid-liquid extraction process, these drugs are removed from rat plasma. The linearity in the standard curve was observed under the experimental concentration range. 10%-200% (6-12ng/ml) of Maralixibat. The calibration plots were linear with a regression coefficient of R2> 0.999. Precision, Accuracy, Stability results, and Matrix effect were observed within the acceptable limit. The method is more accessible and effective for analyzing the sample in the body fluids. The work represents that Specificity, Suitability, Accuracy, and linearity parameters ideally agree with the USFDA guidelines and are efficiently practiced in rat plasma for pharmacokinetic studies
  • An Antiviral Drug—Peramivir: Degradation and Identification of Impurities and the Endorsement of an HPLC–MS Method
    Thulaseedhar Alumuri, Karuna Sree Merugu, L A Amarababu Namburi, Aravınd Kurnool, Arunachalam SaravanaVadivu, Selvakumar Balasubramanian
    Journal of AOAC International, 2023
    Background Peramivir is a neuraminidase inhibitor that serves as a transition state analogue for influenza neuraminidase, inhibiting the formation of new viruses in infected cells, and has been approved for intravenous administration. Objective To validate an HPLC method used to identify the degraded products of the antiviral drug peramivir. Methods Herein, we report the identification of compounds formed after the degradation of peramivir through acid, alkali, peroxide, thermal, and photolytic degradation. At the level of toxicology, a technique was devised for the isolation and measurement of peramivir. Results A sensitive and reliable LC–tandem mass spectrometry technique for the quantitative measurement of Peramivir and its impurities was developed and verified in order to comply with the recommendations made by the International Council for Harmonisation (ICH). The proposed protocol was in the 50–750 µg/mL range. Relative Standard Deviation values of less than 2.0% indicated good recovery in the range of 98.36–102.57%. Within the studied range, the calibration curves demonstrated good linearity and, in addition, the fitting of correlation coefficient was more than 0.999 for every impurity. Quantitative analysis of contaminants revealed the high efficiency at a low level. Conclusion Given its ability to separate degradation products, quantitative analysis is used to detect and quantify known and unknown impurities and degradants in the peramivir drug substance during routine analysis and stability studies. No significant degradation was found in peroxide and photolytic degradation studies. Highlights An HPLC method was developed and put to the test in order to analyze the behavior of the impurities of peramivir as they degraded when subjected to the stress conditions suggested by the ICH. Peramivir was found to be stable under peroxide and photolysis conditions but not stable or degradable when exposed to the acid, base, and thermal stress conditions. The method developed was extremely precise, linear, accurate, robust, and rugged. As a result, this technology has the potential to be used in the medication production process for regular impurity analysis as well as for the stability analysis of peramivir.
  • PERAMIVIR AND RELATED IMPURITIES IN RAT PLASMA AND ITS APPLICATIONS IN PHARMACOKINETIC STUDIES (BIOANALYTICAL METHOD DEVELOPMENT AND VALIDATION BY LC-MS/MS)
    THULASEEDHAR ALUMURI, KARUNASREE MERUGU, NAMBURI L. A. AMARABABU, ARAVIND KURNOOL
    International Journal of Applied Pharmaceutics, 2022
    Objective: New LC-MS/MS method for the estimation of Peramivir and its associated substances was developed and validated Methods: Optimized (Developed) method includes gradient elution of peramivir and its related substances with a flow of 1 ml/min and waters X-bridge C18 column of dimensions 150 mmx4.6 mm, 3.5µ. 0.1% formic acid and acetonitrile were used as the mobile phase. Sarilumab was used as an internal standard. 40 min run time was used to separate peramivir and its related substances. Results: The calibration curve was linear in the concentration percentage range from 10%-200% of Peramivir and its related substances. The calibration charts plotted were linear with a regression coefficient of R2>0.999. Accuracy, precision, recovery, matrix effect and stability results were found to be within the suitable limits. A Simple and efficient method was developed and utilized in pharmacokinetic studies to see the investigated analyte in body fluids. Conclusion: This application denotes all parameters such as accuracy, precision, recovery, stability etc, which are in good agreement with the USFDA guidelines and are effectively applied to the investigation of the pharmacokinetic studies in rat plasma.
  • DEVELOPMENT AND VALIDATION OF A STABILITY INDICATING RELATED SUBSTANCES OF ATENOLOL AND NITRENDIPINE BY RP-HPLC
    THULASEEDHAR ALUMURI, NAMBURI L. A. AMARABABU, ARAVİND KURNOOL, PHANI RAJA KANUPARTHY, KARUNASREE MERUGU
    International Journal of Applied Pharmaceutics, 2022
    Objective: A validated stability-indicating RP-HPLC method for Atenolol and Nitrendipine was developed by separating its related impurities. Methods: By using Waters HPLC e-2695 quaternary pump with a PDA detector of 2998 instrument, the chromatographic separation of Atenolol, Nitrendipine and its related impurities was achieved on the column of Agilent eclipse C18 (150x4.6 mm, 3.5 µ) using gradient elution with a buffer containing 0.1percent formic acid and acetonitrile as a mobile phase with a flow rate of 1 ml/min at ambient temperature. A detector wavelength of 218 nm utilizing the PDA detector was given in the instrumental settings. The linearity was studied between the concentration range of 6.25-37.5 µg/ml of Atenolol, 0.75-4.5 µg/ml each of Atenolol imp-A, imp-B and 5-30 µg/ml of Nitrendipine, 0.5-3 µg/ml each of Nitrendipine imp-1, imp-2 were injected with a run time of 40 min. Validation of the proposed method was carried out according to an International Conference on Harmonization (ICH) guidelines. Results: LOD and LOQ for the Atenolol and its impurities were established with respect to test concentration. The plotted calibration curves were linear with a regression coefficient of R2>0.999, indicating that the linearity was with in the limit. As a part of method validation the parameters like specificity, linearity, accuracy, ruggedness, robustness were determined and the results were found to be within the allowable limit. Conclusion: The method developed was found to be applicable to routine analysis and to be used for the measurement of active pharmaceutical ingredients (i. e, Atenolol, Nitrendipine and their related impurities). Since there is no HPLC method reported in the literature for the estimation of Atenolol, Nitrendipine and their related impurities, there is a need to develop quantitative methods under different conditions to achieve improvement in specificity selectivity etc.
  • Synthesis, biological evaluation and docking studies of 1,2,4,5-tetrasubstituted imidazoles as antibacterial agents: Use of niobia supported heteropoly tungstate as an efficient reusable catalyst
    Aravind Kurnool, Karunasree Merugu, Pachipulusu Shravya, P. Malleswarareddy
    Asian Journal of Chemistry, 2021
    The synthesis of novel 1,2,4,5-tetrasubstituted imidazoles was carried out in a single molecular motif using niobia supported heteropoly tungstate as a mild and efficient reusable catalyst. The condensation of 3-aryl-1-phenyl-1H-pyrazole-4-carbaldehyde, aromatic amine, benzil, ammonium acetate and heteropoly tungstate supported on niobia was achieved under both conventional and non-conventional conditions. The employed protocol provides significant advantages, as it exhibits a remarkable catalytic activity on recovery, excellent yields and excellent reaction efficacy within short reaction times between 1-2 h (conventional) and 1-3 min (microwave radiation). All the obtained compounds were characterized by means of spectral data and elemental analysis. They were also screened for their antibacterial activity. To predict the binding mode of compounds with glutamine-fructose-6-phosphate transaminase (GlcN6P synthase), docking studies were performed.
  • Synthesis, characterization and biological activities of 2,5-disubstituted 1,3,4-oxadiazoles
    Der Pharma Chemica, 2011

RECENT SCHOLAR PUBLICATIONS

  • Development of a series of thienopyrimidine-tagged 1,3,4-thiadiazole hybrids: synthesis, anti-diabetic activity and molecular docking studies.
    NK Srawanthi Kotoori, Karuna Sree Merugu, Pooja Sahu, Aravind Kurnool,Baji ...
    Journal of the Indian Chemical Society , 2026
    2026.0
  • Quality by Design-Based Development of a Robust LC Method for Simultaneous Estimation of Processand Degradation-Related Impurities in Rifapentine Drug Product for the …
    VLSD Siva Prasad Korikana, Sreenivasa Rao Battula, Naresh Konduru, Aravind ...
    Biomedical Chromatography, 1-21 , 2026
    2026.0
  • Microwave‐Assisted, Multicomponent Synthesis of Pyrazolo [3, 4‐b] Pyridines Under Green Conditions
    S Pachipulusu, KS Merugu, RR Bhonsle, S Surapaneni, A Kurnool, ...
    ChemistrySelect 9 (38), e202403569 , 2024
    2024.0
    Citations: 3
  • A facile microwave‐mediated method of 1, 4‐dihydropyridine carboxylates synthesis by multicomponent reaction
    S Pachipulusu, KS Merugu, RR Bhonsle, A Kurnool
    Journal of Heterocyclic Chemistry 61 (6), 1009-1014 , 2024
    2024.0
    Citations: 2
  • MARALIXIBAT IN RAT PLASMA AND ITS PHARMACOLOGICAL STUDIES (BIO-ANALYTICAL METHOD DEVELOPMENT AND VALIDATION BY LC-MS).
    S Pachipulusu, K Merugu, A Kurnool
    Rasayan Journal of Chemistry 17 (1) , 2024
    2024.0
  • An Antiviral Drug—Peramivir: Degradation and Identification of Impurities and the Endorsement of HPLC-MS Method
    BS Thulaseedhar Alumuri1, Karuna Sree Merugu1*, Namburi L A Amarababu2 ...
    J.AOAC INTERNATIONAL , 2023
    2023.0
    Citations: 2
  • Devising a Robust Rp-Hplc Method for the Determination of Relugolix's Related Substances and Characterization of its Degradant Using LC-MS/MS
    SKBASV Thulseedhar Alumuri, Merugu Karunasree, Namburi L. A. Amarababu ...
    SSRN (Social Science Research Network), 17 , 2023
    2023.0
  • Development and validation of a stability indicating related substances of Atenolol and nitrendipine by RP-HPLC
    K Merugu, T Alumuri, A Kurnool
    Current Overview on Pharmaceutical Science Vol. 3, 52-74 , 2023
    2023.0
    Citations: 1
  • DEVELOPMENT AND VALIDATION OF A STABILITY INDICATING RELATED SUBSTANCES OF ATENOLOL AND NITRENDIPINE BY RP-HPLC
    KM THULASEEDHAR ALUMURI, NAMBURI L. A. AMARABABU, ARAVİND KURNOOL, PHANI ...
    International Journal of Applied Pharmaceutics 14 (4), 265-273 , 2022
    2022.0
    Citations: 4
  • PERAMIVIR AND RELATED IMPURITIES IN RAT PLASMA AND ITS APPLICATIONS IN PHARMACOKINETIC STUDIES (BIOANALYTICAL METHOD DEVELOPMENT AND VALIDATION BY LC-MS/MS)
    AK THULASEEDHAR ALUMURI, KARUNASREE MERUGU, NAMBURI L. A. AMARABABU
    International Journal of Applied Pharmaceutics 14 (4), 53-61 , 2022
    2022.0
    Citations: 8
  • Synthesis, Biological Evaluation and Docking Studies of 1,2,4,5-Tetrasubstituted Imidazoles as Antibacterial Agents: Use of Niobia Supported Heteropoly Tungstate as an …
    PM Aravind Kurnool, Karunasree Merugu, Pachipulusu Shravya
    Asian Journal of Chemistry 33 (10), 2423-2429 , 2021
    2021.0
  • Ruthenium (II) ethylenediamine complexes with dipyridophenazine ligands: synthesis, characterization, DNA interactions, and antiproliferative activities
    M Shilpa, C Shobha Devi, P Nagababu, J Naveena Lavanya Latha, ...
    Journal of Coordination Chemistry 66 (10), 1661-1675 , 2013
    2013.0
    Citations: 13
  • Microwave-assisted synthesis and characterization of 1-[4-(3-substituted-acryloyl)-phenyl]-pyrrole-2, 5-diones
    K Aravind, A Ganesh
    Pharma Chem 5, 261-264 , 2013
    2013.0
    Citations: 4
  • Efficient solvent-free microwave assisted organic synthesis of 1-{2, 4-dihydroxy-5-[3-imidazol-1-yl-3-aryl-propionyl]}-3-aryl-propenone and their antibacterial activity
    K Aravind, A Ganesh, D Ashok
    Journal of Chemical and Pharmaceutical Research 5 (6), 34-39 , 2013
    2013.0
    Citations: 3
  • Microwave assisted synthesis, characterization and antibacterial activity of quinoxaline derivatives
    K Aravind, A Ganesh, D Ashok
    J. Chem. Pharm. Res 5 (2), 48-52 , 2013
    2013.0
    Citations: 22
  • Discovery of Novel and Potent Molecules against Plasmodium falciparum Farnesyltransferase (PfFT) by Improved Virtual Screening Strategy
    AK Pradeep Kumar M, Kranthi Raj. K , Radha Vaddavalli , Pavan Kumar MNS
    International Journal of Drug Design and Discovery 2 (4), 666-673 , 2011
    2011.0
    Citations: 1
  • Synthesis, characterization and biological activities of 2, 5-disubstituted-1, 3, 4-oxadiazoles
    KS Merugu, A Kurnool, V Kumar, LJN Pujari
    Der Pharma Chem 3, 130-137 , 2011
    2011.0
    Citations: 3
  • Microwave Assisted Synthesis of New 1‐{2, 4‐Dihydroxy‐5‐[5‐(aryl)‐1‐pyridine/pyrimidine‐4‐carbonyl)‐4, 5‐dihydro‐1 H ‐pyrazol‐3‐yl]‐phenyl}‐3‐(aryl …
    D Ashok, K Aravind
    Journal of Chemistry 6 (2), 323-331 , 2009
    2009.0
    Citations: 3
  • MICROWAVE ASSISTED SYNTHESIS OF SOME NEW (E)-1-[2′,4′-DIHYDROXY-5′-(3"-ARYL-3"-(1 H -1,2,4-TRIAZOL-1-YL) PROPANOYL) PHENYL]-3-ARYL …
    D Ashok, K Aravind
    INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY 18 (2), 117-120 , 2008
    2008.0
  • Maralixibat In Rat Plasma And Its Application In Pharmacokinetic Studies (Bioanalytical Method Development And Validation By LC-MS/MS)
    S Pachipulusu, K Merugu, A Kurnool

MOST CITED SCHOLAR PUBLICATIONS

  • Microwave assisted synthesis, characterization and antibacterial activity of quinoxaline derivatives
    K Aravind, A Ganesh, D Ashok
    J. Chem. Pharm. Res 5 (2), 48-52 , 2013
    2013.0
    Citations: 22
  • Ruthenium (II) ethylenediamine complexes with dipyridophenazine ligands: synthesis, characterization, DNA interactions, and antiproliferative activities
    M Shilpa, C Shobha Devi, P Nagababu, J Naveena Lavanya Latha, ...
    Journal of Coordination Chemistry 66 (10), 1661-1675 , 2013
    2013.0
    Citations: 13
  • PERAMIVIR AND RELATED IMPURITIES IN RAT PLASMA AND ITS APPLICATIONS IN PHARMACOKINETIC STUDIES (BIOANALYTICAL METHOD DEVELOPMENT AND VALIDATION BY LC-MS/MS)
    AK THULASEEDHAR ALUMURI, KARUNASREE MERUGU, NAMBURI L. A. AMARABABU
    International Journal of Applied Pharmaceutics 14 (4), 53-61 , 2022
    2022.0
    Citations: 8
  • DEVELOPMENT AND VALIDATION OF A STABILITY INDICATING RELATED SUBSTANCES OF ATENOLOL AND NITRENDIPINE BY RP-HPLC
    KM THULASEEDHAR ALUMURI, NAMBURI L. A. AMARABABU, ARAVİND KURNOOL, PHANI ...
    International Journal of Applied Pharmaceutics 14 (4), 265-273 , 2022
    2022.0
    Citations: 4
  • Microwave-assisted synthesis and characterization of 1-[4-(3-substituted-acryloyl)-phenyl]-pyrrole-2, 5-diones
    K Aravind, A Ganesh
    Pharma Chem 5, 261-264 , 2013
    2013.0
    Citations: 4
  • Microwave‐Assisted, Multicomponent Synthesis of Pyrazolo [3, 4‐b] Pyridines Under Green Conditions
    S Pachipulusu, KS Merugu, RR Bhonsle, S Surapaneni, A Kurnool, ...
    ChemistrySelect 9 (38), e202403569 , 2024
    2024.0
    Citations: 3
  • Efficient solvent-free microwave assisted organic synthesis of 1-{2, 4-dihydroxy-5-[3-imidazol-1-yl-3-aryl-propionyl]}-3-aryl-propenone and their antibacterial activity
    K Aravind, A Ganesh, D Ashok
    Journal of Chemical and Pharmaceutical Research 5 (6), 34-39 , 2013
    2013.0
    Citations: 3
  • Synthesis, characterization and biological activities of 2, 5-disubstituted-1, 3, 4-oxadiazoles
    KS Merugu, A Kurnool, V Kumar, LJN Pujari
    Der Pharma Chem 3, 130-137 , 2011
    2011.0
    Citations: 3
  • Microwave Assisted Synthesis of New 1‐{2, 4‐Dihydroxy‐5‐[5‐(aryl)‐1‐pyridine/pyrimidine‐4‐carbonyl)‐4, 5‐dihydro‐1 H ‐pyrazol‐3‐yl]‐phenyl}‐3‐(aryl …
    D Ashok, K Aravind
    Journal of Chemistry 6 (2), 323-331 , 2009
    2009.0
    Citations: 3
  • A facile microwave‐mediated method of 1, 4‐dihydropyridine carboxylates synthesis by multicomponent reaction
    S Pachipulusu, KS Merugu, RR Bhonsle, A Kurnool
    Journal of Heterocyclic Chemistry 61 (6), 1009-1014 , 2024
    2024.0
    Citations: 2
  • An Antiviral Drug—Peramivir: Degradation and Identification of Impurities and the Endorsement of HPLC-MS Method
    BS Thulaseedhar Alumuri1, Karuna Sree Merugu1*, Namburi L A Amarababu2 ...
    J.AOAC INTERNATIONAL , 2023
    2023.0
    Citations: 2
  • Development and validation of a stability indicating related substances of Atenolol and nitrendipine by RP-HPLC
    K Merugu, T Alumuri, A Kurnool
    Current Overview on Pharmaceutical Science Vol. 3, 52-74 , 2023
    2023.0
    Citations: 1
  • Discovery of Novel and Potent Molecules against Plasmodium falciparum Farnesyltransferase (PfFT) by Improved Virtual Screening Strategy
    AK Pradeep Kumar M, Kranthi Raj. K , Radha Vaddavalli , Pavan Kumar MNS
    International Journal of Drug Design and Discovery 2 (4), 666-673 , 2011
    2011.0
    Citations: 1
  • Development of a series of thienopyrimidine-tagged 1,3,4-thiadiazole hybrids: synthesis, anti-diabetic activity and molecular docking studies.
    NK Srawanthi Kotoori, Karuna Sree Merugu, Pooja Sahu, Aravind Kurnool,Baji ...
    Journal of the Indian Chemical Society , 2026
    2026.0
  • Quality by Design-Based Development of a Robust LC Method for Simultaneous Estimation of Processand Degradation-Related Impurities in Rifapentine Drug Product for the …
    VLSD Siva Prasad Korikana, Sreenivasa Rao Battula, Naresh Konduru, Aravind ...
    Biomedical Chromatography, 1-21 , 2026
    2026.0
  • MARALIXIBAT IN RAT PLASMA AND ITS PHARMACOLOGICAL STUDIES (BIO-ANALYTICAL METHOD DEVELOPMENT AND VALIDATION BY LC-MS).
    S Pachipulusu, K Merugu, A Kurnool
    Rasayan Journal of Chemistry 17 (1) , 2024
    2024.0
  • Devising a Robust Rp-Hplc Method for the Determination of Relugolix's Related Substances and Characterization of its Degradant Using LC-MS/MS
    SKBASV Thulseedhar Alumuri, Merugu Karunasree, Namburi L. A. Amarababu ...
    SSRN (Social Science Research Network), 17 , 2023
    2023.0
  • Synthesis, Biological Evaluation and Docking Studies of 1,2,4,5-Tetrasubstituted Imidazoles as Antibacterial Agents: Use of Niobia Supported Heteropoly Tungstate as an …
    PM Aravind Kurnool, Karunasree Merugu, Pachipulusu Shravya
    Asian Journal of Chemistry 33 (10), 2423-2429 , 2021
    2021.0
  • MICROWAVE ASSISTED SYNTHESIS OF SOME NEW (E)-1-[2′,4′-DIHYDROXY-5′-(3"-ARYL-3"-(1 H -1,2,4-TRIAZOL-1-YL) PROPANOYL) PHENYL]-3-ARYL …
    D Ashok, K Aravind
    INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY 18 (2), 117-120 , 2008
    2008.0
  • Maralixibat In Rat Plasma And Its Application In Pharmacokinetic Studies (Bioanalytical Method Development And Validation By LC-MS/MS)
    S Pachipulusu, K Merugu, A Kurnool