Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Urooj Muqadar"'
Autor:
Fawad Ahmad, Aamer Saeed, Muhammad Faisal, Fayaz Ali Larik, Urooj Muqadar, Erum Dilshad, Bushra Mirza, Saira Khatoon, Haroon Mehfooz, Sajid Rashid, Shagufta Shafique, Salma Bilquees, Hammad Ismail, Pervaiz Ali Channar
Publikováno v:
Research on Chemical Intermediates. 46:2437-2456
Meldrum’s acid derivatives were facile synthesized by one-pot condensation process and characterized by NMR (1H, 13C, DEPT-90 and DEPT-135) and EI-MS. The synthesized compounds were screened for their potential to inhibit butyrylcholinesterase (BCh
Autor:
Aamer Saeed, Farukh Jabeen, Bushra Mirza, Hammad Ismail, Pervaiz Ali Channar, Erum Dilshad, Fayaz Ali Larik, Ulrich Flörke, Urooj Muqadar, Shomaila Saeed
Publikováno v:
Inorganica Chimica Acta. 464:204-213
A series of organotin esters has been synthesized using a diverse array of drugs containing carboxylic function with triphenyl/tributyltin. The synthesized derivatives were bioevaluated for antibacterial, antifungal and enzyme inhibition (α-amylase,
Autor:
Haroon Mehfooz, Pervaiz Ali Channar, Fayaz Ali Larik, Hesham R. El-Seedi, Urooj Muqadar, Muhammad Faisal, Aamer Saeed
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 192:490-502
This review, including 111 references, describes the applications of Lawesson's reagent (LR) [2,4-bis(p-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-dithione] for the total synthesis of macrocycl...
Publikováno v:
Journal of Sulfur Chemistry. 38:206-227
This review aims to illustrate the applications of Lawesson's reagent (LR) [2,4-bis(p-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide] in the synthesis of naturally occurring medicinally important alkaloids. LR is primarily used for thionati
Publikováno v:
Applied Organometallic Chemistry. 31
Autor:
Aamer Saeed, Mubashir Hassan, Pervaiz Ali Channar, Michael Bolte, Fayaz Ali Larik, Qamar Abbas, Sung-Yum Seo, Urooj Muqadar
Publikováno v:
European journal of medicinal chemistry. 141
A series of novel 1-pentanoyl-3-arylthioureas was designed as new mushroom tyrosinase inhibitors and free radical scavengers. The title compounds were obtained in excellent yield and characterized by FTIR, 1 H NMR, 13 C NMR and X-ray crystallography
Publikováno v:
Journal of Health & Medical Informatics.
It is believed that herbal medicines act in a holistic way, but been derived from nature they can be specific in response. Herein, we review herbal medicines which are used for the treatment of cardiovascular diseases (CVDs) and their interactions wi
Publikováno v:
Applied Organometallic Chemistry. 31:e3664
Ferrocene derivatives constitute an important class of organometallic compounds with not only an extensive range of biological activities but also diverse industrial as well as material science applications. These stimulating features of ferrocene de