Search Results - "Nazir, Majid"

Synthesis of Bi-heterocyclic Sulfonamides as Tyrosinase Inhibitors: Lineweaver-Burk Plot Evaluation and Computational Ascriptions by Abbasi, Muhammad Athar, Rehman, Zia-Ur, Rehman, Aziz-Ur, Siddiqui, Sabahat Zahra, Nazir, Majid, Hassan, Mubashir, Raza, Hussain, Shah, Syed Adnan Ali, Seo, Sung-Yum

“…The designed bi-heterocyclic sulfonamides were synthesized through a two-step protocol and their structures were ascertained by spectral techniques including…”
Get full text

Multi-step synthesis, kinetics and in silico explorations of indole-Phenyl-1,2,4-triazole Bi-heterocyclic hybrids unified with 3-substituted benzamides as elastase inhibitors by Shakila, Abbasi, Muhammad Athar, Aziz-ur-Rehman, Siddiqui, Sabahat Zahra, Nazir, Majid, Muhammad, Shabbir, Raza, Hussain, Shah, Syed Adnan Ali, Shahid, Muhammad, Chaudhry, Aijaz Rasool, Kim, Song Ja

“…•Designing of Indole-Phenyl-1,2,4-Triazole Bi-Heterocyclic.•Determining of In-vitro elastase inhibitory potential and kinetics.•Establishing the…”
Get full text

Convergent synthesis, kinetics and computational attributions of indole-N-phenyltriazole hybrids bearing N-(aryl)butanamides as alkaline phosphatase inhibitors by Shakila, Abbasi, Muhammad Athar, Aziz-ur-Rehman, Siddiqui, Sabahat Zahra, Nazir, Majid, Raza, Hussain, Shah, Syed Adnan Ali, Ayine-Tora, Daniel Moscoh, Shahid, Muhammad, Kim, Song Ja

“…•Designing of indole-N-phenyltriazole hybrids.•Determining of In-vitro Alkaline phosphatase inhibitory potential and kinetics.•Establishing the…”
Get full text

New indole based hybrid oxadiazole scaffolds with N-substituted acetamides: As potent anti-diabetic agents by Nazir, Majid, Abbasi, Muhammad Athar, Aziz-ur-Rehman, Siddiqui, Sabahat Zahra, Khan, Khalid Mohammed, Kanwal, Salar, Uzma, Shahid, Muhammad, Ashraf, Muhammad, Arif Lodhi, Muhammad, Ali Khan, Farman

“…[Display omitted] •Synthesis of new indole based hybrid oxadiazole scaffolds with N-substituted acetamides by multiple chemical transformations.•Structural…”
Get full text

Multi-step synthesis of indole-N-ethyltriazole hybrids amalgamated with N-arylated ethanamides: structure-activity relationship and mechanistic explorations through tyrosinase inhibition, kinetics and computational ascriptions by Shakila, Abbasi, Muhammad A., Aziz-ur-Rehman, Siddiqui, Sabahat Z., Nazir, Majid, Raza, Hussain, Zafar, Ayesha, Shah, Syed A.A., Shahid, Muhammad, Seo, Sung-Yum

“…•Designing of indole-N-ethyltriazole hybrids amalgamated with N-arylated ethanamides as tyrosinase inhibitors•Ascertaining of in vitro inhibitory potential,…”
Get full text

Synthesis of promising antibacterial and antifungal agents: 2-[[acetamides by Abbasi, Muhammad Athar, Irshad, Misbah, Aziz-ur-Rehman, Siddiqui, Sabahat Zahra, Nazir, Majid, Shah, Syed Adnan Ali, Shahid, Muhammad

“…In the presented work, 2,3-dihydro-l,4-benzodioxin-6-amine (1) was reacted with 4-chlorobenzenesulfonyl chloride (2) in presence of aqueous basic aqueous…”
Get full text

REPORT - Synthesis of promising antibacterial and antifungal agents: 2-[[(4-Chlorophenyl)sulfonyl](2,3-dihydro-1,4-benzodioxin-6-yl)amino]-N-(un/substituted-phenyl)acetamides by Abbasi, Muhammad Athar, Irshad, Misbah, Aziz-Ur-Rehman, -, Siddiqui, Sabahat Zahra, Nazir, Majid, Ali Shah, Syed Adnan, Shahid, Muhammad

“…In the presented work, 2,3-dihydro-1,4-benzodioxin-6-amine (1) was reacted with 4-chlorobenzenesulfonyl chloride (2) in presence of aqueous basic aqueous…”
Get full text

Novel indole based hybrid oxadiazole scaffolds with N -(substituted-phenyl)butanamides: synthesis, lineweaver-burk plot evaluation and binding analysis of potent urease inhibitors by Nazir, Majid, Abbasi, Muhammad Athar, Aziz-Ur-Rehman, Siddiqui, Sabahat Zahra, Raza, Hussain, Hassan, Mubashir, Ali Shah, Syed Adnan, Shahid, Muhammad, Seo, Sung-Yum

“…In the study presented herein, 4-(1 -indol-3-yl)butanoic acid (1) was sequentially transformed in the first phase into ethyl 4-(1 -indol-3-yl)butanoate (2),…”
Get full text

Convergent synthesis, free radical scavenging, Lineweaver‐Burk plot exploration, hemolysis and in silico study of novel indole‐phenyltriazole hybrid bearing acetamides as potent urease inhibitors by Khan, Wajiha, Abbasi, Muhammad A., Rehman, Aziz‐ur, Siddiqui, Sabahat Z., Nazir, Majid, Ali Shah, Syed A., Raza, Hussain, Hassan, Mubashir, Shahid, Muhammad, Seo, Sung Y.

“…In the current paper, through a convergent multi‐step approach, a library of novel indole‐phenyltriazole hybrids containing an amide moiety (9a‐k) was…”
Get full text

Synthesis, Antioxidant and In-Silico Studies of Potent Urease Inhibitors: N-(4-{[(4-Methoxyphenethyl)-(substituted)amino]sulfonyl}phenyl)acetamides by Abbasi, Muhammad Athar, Raza, Hussain, Rehman, Aziz Ur, Siddiqui, Sahahat Zahra, Nazir, Majid, Mumtaz, Ayesha, Shah, Syed Adnan Ali, Seo, Sung-Yum, Hassan, Mubashir

“…In this study, a new series of sulfonamides derivatives was synthesized and their inhibitory effects on DPPH and jack bean urease were evaluated. The in silico…”
Get more information

Bi‐heterocyclic benzamides as alkaline phosphatase inhibitors: Mechanistic comprehensions through kinetics and computational approaches by Abbasi, Muhammad A., Nazir, Majid, ur‐Rehman, Aziz, Siddiqui, Sabahat Z., Hassan, Mubashir, Raza, Hussain, Shah, Syed A. A., Shahid, Muhammad, Seo, Sung‐Yum

“…Novel bi‐heterocyclic benzamides were synthesized by sequentially converting 4‐(1H‐indol‐3‐yl)butanoic acid (1) into ethyl 4‐(1H‐indol‐3‐yl)butanoate (2),…”
Get full text

Synthesis of new S-substituted derivatives of 5-[3-(1H-indol-3-yl)propyl]-1,3,4-oxadiazol-2-ylhydrosulfide as suitable antibacterial and anticancer agents with moderate cytotoxicity by Nazir, Majid, Abbasi, Muhammad Athar, Aziz-Ur-Rehman, -, Siddiqui, Sabahat Zahra, Ali Shah, Syed Adnan, Shahid, M, Fatima, H, Iftikhar, Sunniya, Zaib Saleem, Rahman Shah

“…In the study presented here, the nucleophilic substitution reaction of 5-[3-(1H-indol-3-yl)propyl]-1,3,4-oxadiazol-2-ylhydrosulfide was carried out with…”
Get full text

Novel indole based hybrid oxadiazole scaffolds with N-(substituted-phenyl)butanamides: synthesis, lineweaver-burk plot evaluation and binding analysis of potent urease inhibitorsElectronic supplementary information (ESI) available. See DOI: 10.1039/c8ra04987d by Nazir, Majid, Abbasi, Muhammad Athar, Aziz-ur-Rehman, Siddiqui, Sabahat Zahra, Raza, Hussain, Hassan, Mubashir, Ali Shah, Syed Adnan, Shahid, Muhammad, Seo, Sung-Yum

“…In the study presented herein, 4-(1 H -indol-3-yl)butanoic acid ( 1 ) was sequentially transformed in the first phase into ethyl 4-(1 H -indol-3-yl)butanoate (…”
Get full text