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Ahmed Al-Harrasi (1974-)

Chemiker

Name	Ahmed Al-Harrasi
Zeit	1974- (Lebensdaten)
Ort	Oman
Geschlecht	männlich
Akademischer Grad bzw. Titel	Prof. Dr.
Beruf	Chemiker (charakteristischer Beruf)
Variante	Ahmed Al- Harrasi Ahmed S. Al-Harrasi
Weitere Angaben	Diss. Fachbereich Chemie
Datensatztyp	Person
GND-Nummer	130650927
Datensatz-ID	130650927
Beteiligt an alle anzeigen Identification of new pharmacophore against SARS-CoV-2 spike protein by multi-fold computational and biochemical techniques Comparative study of the cytotoxicity, apoptotic, and epigenetic effects of Boswellic acid derivatives on breast cancer Hydroxyethylamide substituted triterpenoic acids hold good cytotoxicity for human tumor cells New synthetic 1H-1,2,3-triazole derivatives of 3-O-acetyl-β-boswellic acid and 3-O-acetyl-11-keto-β-boswellic acid from Boswellia sacra inhibit carbonic anhydrase II in vitro New amino acid clubbed Schiff bases inhibit carbonic anhydrase II, α-glucosidase, and urease enzymes: in silico and in vitro Apoptotic activity of substituted 3-O-acetyl-betulinic acid benzylamides The Presence of a Cyclohexyldiamine Moiety Confers Cytotoxicity to Pentacyclic Triterpenoids Total Synthesis of Surinamensinols A and B Platanic acid-derived methyl 20-amino-30-norlupan-28-oates are potent cytotoxic agents acting by apoptosis New transformations of enantiopure 3,6-dihydro-2H-1,2-oxazines : ring cleavages, ring enlargements and a novel approach to carbohydrate mimetics

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Ahmed Al-Harrasi (1974-)

Identification of new pharmacophore against SARS-CoV-2 spike protein by multi-fold computational and biochemical techniques

Comparative study of the cytotoxicity, apoptotic, and epigenetic effects of Boswellic acid derivatives on breast cancer

Hydroxyethylamide substituted triterpenoic acids hold good cytotoxicity for human tumor cells

New synthetic 1H-1,2,3-triazole derivatives of 3-O-acetyl-β-boswellic acid and 3-O-acetyl-11-keto-β-boswellic acid from Boswellia sacra inhibit carbonic anhydrase II in vitro

New amino acid clubbed Schiff bases inhibit carbonic anhydrase II, α-glucosidase, and urease enzymes: in silico and in vitro

Apoptotic activity of substituted 3-O-acetyl-betulinic acid benzylamides

The Presence of a Cyclohexyldiamine Moiety Confers Cytotoxicity to Pentacyclic Triterpenoids

Total Synthesis of Surinamensinols A and B

Platanic acid-derived methyl 20-amino-30-norlupan-28-oates are potent cytotoxic agents acting by apoptosis

New transformations of enantiopure 3,6-dihydro-2H-1,2-oxazines : ring cleavages, ring enlargements and a novel approach to carbohydrate mimetics