檢索結果 - "Bioorganic Chemistry" :: Updates@UiTM Library

1

The immunomodulation potential of the synthetic derivatives of benzothiazoles: Implications in immune system disorders through in vitro and in silico studies

由 Khan K.M.; Mesaik M.A.; Abdalla O.M.; Rahim F.; Soomro S.; Halim S.A.; Mustafa G.; Ambreen N.; Khalid A.S.; Taha M.; Perveen S.; Alam M.T.; Hameed A.; Ul-Haq Z.; Ullah H.; Rehman Z.U.; Siddiqui R.A.; Voelter W.
發表在 Bioorganic Chemistry (2016)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
2

Enhanced binding interaction and antibacterial inhibition for nanometal oxide particles activated with Aloe Vulgarize through one-pot ultrasonication techniques

由 Dzulkharnien N.S.F.; Rohani R.; Tan Kofli N.; Mohd Kasim N.A.; Abd. Muid S.; Patrick M.; Mohd Fauzi N.A.; Alias H.; Ahmad Radzuan H.
發表在 Bioorganic Chemistry (2024)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
3

Discovery of novel 1,8-naphthalimide piperazinamide based benzenesulfonamides derivatives as potent carbonic anhydrase IX inhibitors and ferroptosis inducers for the treatment of t...

由 2-s2.0-85197352734
發表在 Bioorganic Chemistry (2024)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
4

Evaluation and docking of indole sulfonamide as a potent inhibitor of α-glucosidase enzyme in streptozotocin –induced diabetic albino wistar rats

由 2-s2.0-85102849446
發表在 Bioorganic Chemistry (2021)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
5

Design, synthesis, in vitro evaluation, molecular docking and ADME properties studies of hybrid bis-coumarin with thiadiazole as a new inhibitor of Urease

由 2-s2.0-85071689548
發表在 Bioorganic Chemistry (2019)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
6

Synthesis, molecular docking, dynamic simulations, kinetic mechanism, cytotoxicity evaluation of N-(substituted-phenyl)-4-{(4-[(E)-3-phenyl-2-propenyl]-1-piperazinyl} butanamides a...

由 2-s2.0-85076239103
發表在 Bioorganic Chemistry (2020)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
7

Designing of promising medicinal scaffolds for Alzheimer's disease through enzyme inhibition, lead optimization, molecular docking and dynamic simulation approaches

由 2-s2.0-85070881566
發表在 Bioorganic Chemistry (2019)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
8

Synthesis, in vitro alpha-glucosidase inhibitory potential of benzimidazole bearing bis-Schiff bases and their molecular docking study

由 2-s2.0-85074862203
發表在 Bioorganic Chemistry (2020)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
9

Synthesis of novel N-(1,3-thiazol-2-yl)benzamide clubbed oxadiazole scaffolds: Urease inhibition, Lipinski rule and molecular docking analyses

由 2-s2.0-85054810473
發表在 Bioorganic Chemistry (2019)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
10

Synthesis and structure-activity relationship of tyrosinase inhibiting novel bi-heterocyclic acetamides: Mechanistic insights through enzyme inhibition, kinetics and computational...

由 2-s2.0-85061452076
發表在 Bioorganic Chemistry (2019)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
11

Synthesis, in vitro α-glucosidase inhibitory potential and molecular docking study of thiadiazole analogs

由 2-s2.0-85044438335
發表在 Bioorganic Chemistry (2018)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
12

Synthesis, α-glucosidase inhibition and molecular docking study of coumarin based derivatives

由 2-s2.0-85042298379
發表在 Bioorganic Chemistry (2018)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
13

Molecular hybridization conceded exceptionally potent quinolinyl-oxadiazole hybrids through phenyl linked thiosemicarbazide antileishmanial scaffolds: In silico validation and SAR...

由 2-s2.0-85013078177
發表在 Bioorganic Chemistry (2017)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
14

Synthesis, α-glucosidase inhibitory activity and in silico study of tris-indole hybrid scaffold with oxadiazole ring: As potential leads for the management of type-II diabetes mell...

由 2-s2.0-85025127822
發表在 Bioorganic Chemistry (2017)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
15

Carbohydrazones as new class of carbonic anhydrase inhibitors: Synthesis, kinetics, and ligand docking studies

由 2-s2.0-85017101492
發表在 Bioorganic Chemistry (2017)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
16

5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes

由 2-s2.0-85016039331
發表在 Bioorganic Chemistry (2017)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
17

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives

由 2-s2.0-84984780886
發表在 Bioorganic Chemistry (2016)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
18

Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies

由 2-s2.0-84948649641
發表在 Bioorganic Chemistry (2016)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
19

Synthesis of 2-acylated and sulfonated 4-hydroxycoumarins: In vitro urease inhibition and molecular docking studies

由 2-s2.0-84964603375
發表在 Bioorganic Chemistry (2016)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code
20

Hybrid benzothiazole analogs as antiurease agent: Synthesis and molecular docking studies

由 2-s2.0-84962360234
發表在 Bioorganic Chemistry (2016)
期刊標題: “...Bioorganic Chemistry...”

獲取全文

Article

Show QR Code