Parvin Kumar
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Explore the profile of Parvin Kumar including associated specialties, affiliations and a list of published articles.
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70
Citations
278
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Recent Articles
1.
Singh R, Sindhu J, Singh D, Kumar P
Future Med Chem
. 2025 Jan;
17(3):347-362.
PMID: 39835704
The escalating cases of type II diabetes combined with adverse side effects of current antidiabetic drugs spurred the advancement of innovative approaches for the management of postprandial glucose levels. α-Amylase...
2.
Aggarwal V, Singh D, Bhagwan S, Saini R, Jakhar K, Kumar S, et al.
RSC Adv
. 2024 Dec;
14(53):39569-39587.
PMID: 39691219
The combination of 4,4,4-trifluoro-1-phenyl-1,3-butanedione (TFPB) and pyrazine (pyz) with Tb ions forms two distinct types of complexes, represented by the formulas [Tb(TFPB)(L)], where L is either HO or pyz, and...
3.
Shweta , Chahal S, Dhaka R, Rana A, Joshi G, Singh R, et al.
J Agric Food Chem
. 2024 Dec;
72(50):27762-27774.
PMID: 39630023
Herein, a novel, biocatalyzed, and on-water microwave-assisted multicomponent methodology have been developed for the synthesis of trisubstituted thiazoles (-). The reaction was catalyzed using a sulfonated peanut shell residue-derived carbonaceous...
4.
Nivins S, Kumar P, Chen X, Gissler M, Lavebratt C
Acta Obstet Gynecol Scand
. 2024 Nov;
104(2):319-330.
PMID: 39611242
Introduction: Hypertensive disorders of pregnancy (HDP) or prepregnancy overweight/obesity are independently associated with the risk for certain neurodevelopmental and psychiatric disorders in offspring. These two conditions often co-exist but the...
5.
Aggarwal R, Kumar P, Hooda M, Singh R, Kumar P
Org Biomol Chem
. 2024 Nov;
23(1):213-225.
PMID: 39540780
Diabetes poses a significant global health challenge, driving the search for effective management strategies. In the past years, α-amylase inhibitors have emerged as promising candidates for regulating blood sugar levels....
6.
Lotfi S, Ahmadi S, Azimi A, Kumar P
Toxicol Mech Methods
. 2024 Oct;
35(3):305-317.
PMID: 39397353
The fast-increasing use of chemicals led to large numbers of chemical compounds entering the aquatic environment, raising concerns about their potential effects on ecosystems. Therefore, assessment of the ecotoxicological features...
7.
Chahal S, Rani P, Singh R, Joshi G, Kumar R, Kumar P, et al.
Future Med Chem
. 2024 Sep;
16(21):2231-2245.
PMID: 39301934
Elevated levels of amylase in the blood, known as hyperamylasemia, have been correlated with diabetes and cancer. To investigate the impact of hyperamylasemia on cellular proliferation, it is imperative to...
8.
Malik S, Jakhar K, Singh D, Hooda A, Redhu S, Dalal S, et al.
RSC Adv
. 2024 Jul;
14(31):22642-22655.
PMID: 39027040
Complexes of dysprosium(iii) ions with 1,1,1,5,5,5-hexafluoro-2,4-pentanedione featuring various mono and bi-dentate neutral ligands have been prepared and thoroughly investigated. The synthesized complexes exhibit an octa-coordinated environment, achieved by stoichiometrically combining...
9.
Malik S, Jakhar K, Singh D, Dalal S, Hooda A, Nehra K, et al.
Luminescence
. 2024 Jul;
39(7):e4810.
PMID: 38965929
Four eight-coordinated luminescent samarium complexes of type [Sm(hfpd)L] and [Sm(hfpd)L'] [where hfpd = 1,1,1,5,5,5-Hexafluoro-2,4-pentanedione L = tri-octyl-phosphine oxide (TOPO) and L' = 1,10-phenanthroline (phen), neocuproine (neoc) and bathocuproine (bathoc) were...
10.
Singh R, Sindhu J, Devi M, Kumar P, Lal S, Kumar A, et al.
Eur J Med Chem
. 2024 Jun;
275:116623.
PMID: 38943875
A new series of thiazolidine-2,4-dione tethered 1,2,3-triazole derivatives were designed, synthesized and screened for their α-amylase inhibitory potential employing in vitro and in silico approaches. The target compounds were synthesized...