Similar articles for PMID: 31838966

Year	Number of Results
2008	1
2009	1
2010	1
2012	2
2013	1
2014	7
2015	12
2016	7
2017	14
2018	13
2019	36
2020	21
2021	14
2022	16
2023	0

1

Synthesis, molecular docking and QSAR study of thiazole clubbed pyrazole hybrid as α-amylase inhibitor.

Duhan M, Singh R, Devi M, Sindhu J, Bhatia R, Kumar A, Kumar P. Duhan M, et al. J Biomol Struct Dyn. 2021 Jan;39(1):91-107. doi: 10.1080/07391102.2019.1704885. Epub 2019 Dec 27. J Biomol Struct Dyn. 2021. PMID: 31838966

2

Exploring biological efficacy of novel benzothiazole linked 2,5-disubstituted-1,3,4-oxadiazole hybrids as efficient α-amylase inhibitors: Synthesis, characterization, inhibition, molecular docking, molecular dynamics and Monte Carlo based QSAR studies.

Duhan M, Kumar P, Sindhu J, Singh R, Devi M, Kumar A, Kumar R, Lal S. Duhan M, et al. Comput Biol Med. 2021 Nov;138:104876. doi: 10.1016/j.compbiomed.2021.104876. Epub 2021 Sep 17. Comput Biol Med. 2021. PMID: 34598068

3

Quantitative structure activity relationship studies of novel hydrazone derivatives as α-amylase inhibitors with index of ideality of correlation.

Duhan M, Sindhu J, Kumar P, Devi M, Singh R, Kumar R, Lal S, Kumar A, Kumar S, Hussain K. Duhan M, et al. J Biomol Struct Dyn. 2022 Jul;40(11):4933-4953. doi: 10.1080/07391102.2020.1863861. Epub 2020 Dec 24. J Biomol Struct Dyn. 2022. PMID: 33357037

4

In-silico identification of fingerprint of pyrazolyl sulfonamide responsible for inhibition of N-myristoyltransferase using Monte Carlo method with index of ideality of correlation.

Kumar A, Sindhu J, Kumar P. Kumar A, et al. J Biomol Struct Dyn. 2021 Sep;39(14):5014-5025. doi: 10.1080/07391102.2020.1784286. Epub 2020 Jun 24. J Biomol Struct Dyn. 2021. PMID: 32579066

5

SMILES-based QSAR and molecular docking study of xanthone derivatives as α-glucosidase inhibitors.

Ahmadi S, Moradi Z, Kumar A, Almasirad A. Ahmadi S, et al. J Recept Signal Transduct Res. 2022 Aug;42(4):361-372. doi: 10.1080/10799893.2021.1957932. Epub 2021 Aug 12. J Recept Signal Transduct Res. 2022. PMID: 34384326

6

In vitro and in silico studies of fluorinated 2,3-disubstituted thiazolidinone-pyrazoles as potential α-amylase inhibitors and antioxidant agents.

Ganavi D, Ramu R, Kumar V, Patil SM, Martiz RM, Shirahatti PS, Sathyanarayana R, Poojary B, Holla BS, Poojary V, Kumari KPN, Shivachandra JC. Ganavi D, et al. Arch Pharm (Weinheim). 2022 Mar;355(3):e2100342. doi: 10.1002/ardp.202100342. Epub 2021 Dec 19. Arch Pharm (Weinheim). 2022. PMID: 34923670

7

New triazinoindole bearing thiazole/oxazole analogues: Synthesis, α-amylase inhibitory potential and molecular docking study.

Rahim F, Tariq S, Taha M, Ullah H, Zaman K, Uddin I, Wadood A, Khan AA, Rehman AU, Uddin N, Zafar S, Shah SAA. Rahim F, et al. Bioorg Chem. 2019 Nov;92:103284. doi: 10.1016/j.bioorg.2019.103284. Epub 2019 Sep 17. Bioorg Chem. 2019. PMID: 31546207

8

Design of novel benzimidazole derivatives as potential α-amylase inhibitors using QSAR, pharmacokinetics, molecular docking, and molecular dynamics simulation studies.

Abchir O, Daoui O, Belaidi S, Ouassaf M, Qais FA, ElKhattabi S, Belaaouad S, Chtita S. Abchir O, et al. J Mol Model. 2022 Mar 29;28(4):106. doi: 10.1007/s00894-022-05097-9. J Mol Model. 2022. PMID: 35352175

9

Identifications of good and bad structural fragments of hydrazone/2,5-disubstituted-1,3,4-oxadiazole hybrids with correlation intensity index and consensus modelling using Monte Carlo based QSAR studies, their molecular docking and ADME analysis.

Kumar P, Singh R, Kumar A, Toropova AP, Toropov AA, Devi M, Lal S, Sindhu J, Singh D. Kumar P, et al. SAR QSAR Environ Res. 2022 Sep;33(9):677-700. doi: 10.1080/1062936X.2022.2120068. Epub 2022 Sep 12. SAR QSAR Environ Res. 2022. PMID: 36093620

10

Design and development of novel focal adhesion kinase (FAK) inhibitors using Monte Carlo method with index of ideality of correlation to validate QSAR.

Kumar P, Kumar A, Sindhu J. Kumar P, et al. SAR QSAR Environ Res. 2019 Feb;30(2):63-80. doi: 10.1080/1062936X.2018.1564067. SAR QSAR Environ Res. 2019. PMID: 30793981

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