Farediah Ahmad
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Farediah Ahmad has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Wan Mohd Nuzul Hakimi Wan Salleh
Department of Chemistry, Faculty of Science and Mathematics, Universiti Pendidikan Sultan Idris
10 shared publications - Heng Yen Khong
Universiti Teknologi MARA
8 shared publications - Hasnah Mohd Sirat
Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310, Skudai, Johor, Malaysia
3 shared publications Razauden Mohamed Zulkifli
Department of Bioscience and Health Sciences, Faculty of Biosciences and Medical Engineering, University Teknologi Malaysia (UTM), 81310 Skudai, Johor, Malaysia
3 shared publicationsMuhammad Sum Idris
Department of Chemistry Faculty of Science UTM 81310
2 shared publications- Muhammad Taher
International Islamic University Malaysia
2 shared publications
Latest Publications
- 2 January 2017
- Published by Taylor & Francis in Journal of Essential Oil Bearing Plants
- Vol. 20 (1) , 223-232
In vitroAntioxidant, Antityrosinase, Antibacterial and Cytotoxicity Activities of the Leaf and Stem Essential Oil fromPiper magnibaccumC. DC.
The chemical composition of essential oils obtained from two parts of Piper magnibaccum C.DC. were analyzed by gas chromatography with a flame ionization detector (GC-FID) and gas chromatography-mass spectrometry (GC-MS). 25 components representing 93.5% of the essential oil were characterized from the leaf of P. magnibaccum. The essential oil was dominated by germacrene D (40.8%), β-caryophyllene (8.5%) and α-cadinol (6.1%). A total of 33 components, representing 87.6% of the total oil were identified from the stem of P. magnibaccum. The major constituents were β-caryophyllene (19.7%), germacrene D (10.7%), and α- cadinol (8.2%). The antioxidant potential of the leaf and stem essential oils of P. magnibaccum were determined on the basis of phenolic content and scavenging activity of the stable 1,1-diphenyl-2-picrylhydrazyl (DPPH) (IC50 20.5, 17.5 μg/mL) and 2,2′-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid (ABTS) (IC50 11.7, 12.9 μg/ mL) free radicals. Antityrosinase activity of the leaf and stem were also screened using mushroom tyrosinase assay (I %= 49.50±0.6, 57.01±0.8). The essential oil of P. magnibaccum leaf showed a moderate antibacterial activity with MIC value of 250 μg/mL against P. aeruginosa. None of the essential oils exhibited acute cytotoxicity against MCF-7 and A-549 cells proliferation.
- 2 January 2017
- Published by Taylor & Francis in Journal of Essential Oil Bearing Plants
- Vol. 20 (1) , 223-232
In vitroAntioxidant, Antityrosinase, Antibacterial and Cytotoxicity Activities of the Leaf and Stem Essential Oil fromPiper magnibaccumC. DC.
The chemical composition of essential oils obtained from two parts of Piper magnibaccum C.DC. were analyzed by gas chromatography with a flame ionization detector (GC-FID) and gas chromatography-mass spectrometry (GC-MS). 25 components representing 93.5% of the essential oil were characterized from the leaf of P. magnibaccum. The essential oil was dominated by germacrene D (40.8%), β-caryophyllene (8.5%) and α-cadinol (6.1%). A total of 33 components, representing 87.6% of the total oil were identified from the stem of P. magnibaccum. The major constituents were β-caryophyllene (19.7%), germacrene D (10.7%), and α- cadinol (8.2%). The antioxidant potential of the leaf and stem essential oils of P. magnibaccum were determined on the basis of phenolic content and scavenging activity of the stable 1,1-diphenyl-2-picrylhydrazyl (DPPH) (IC50 20.5, 17.5 μg/mL) and 2,2′-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid (ABTS) (IC50 11.7, 12.9 μg/ mL) free radicals. Antityrosinase activity of the leaf and stem were also screened using mushroom tyrosinase assay (I %= 49.50±0.6, 57.01±0.8). The essential oil of P. magnibaccum leaf showed a moderate antibacterial activity with MIC value of 250 μg/mL against P. aeruginosa. None of the essential oils exhibited acute cytotoxicity against MCF-7 and A-549 cells proliferation.
- 15 August 2016
- Published by Marmara University in Marmara Pharmaceutical Journal
- Vol. 21 (24530) , 127-131
Cytotoxicity of triterpenes from the leaves of Garcinia prainiana King (Guttiferae)
Garcinia prainiana yapraklarını konu alan fitokimyasal araştırmalar sonucunda triterpen yapısında beş bileşik izole edilmiştir; skualen 1, friedelin 2, lupeol 3, 3β-hidroksiöfa- 5,22-dien 4, and 3β-asetoksiöfa-5,22-dien 5. İzole edilen bileşiklerin yapıları spektroskopik yöntemler kullanılarak aydınlatılmış ve elde edilen sonuçlar yukarıda belirtilen bileşiklere ait spektroskopik verilerle karşılaştırılmıştır. Tüm bileşiklerin, H1299 ve A549 akciğer kanseri hücre hatları üzerindeki sitotoksik etkileri MTT yöntemiyle çalışılmıştır. 3β-Asetoksiöfa-5,22-dien 5, H1299 ve A549 hücre hatlarına karşı sırasıyla IC50 = 18.0 μg/ml ve IC50= 36.3 μg/ml derişimde etki göstererek serisindeki en etkili bileşik olarak öne çıkmıştır.
- 15 August 2016
- Published by Marmara University in Marmara Pharmaceutical Journal
- Vol. 21 (24530) , 127-131
Cytotoxicity of triterpenes from the leaves of Garcinia prainiana King (Guttiferae)
Garcinia prainiana yapraklarını konu alan fitokimyasal araştırmalar sonucunda triterpen yapısında beş bileşik izole edilmiştir; skualen 1, friedelin 2, lupeol 3, 3β-hidroksiöfa- 5,22-dien 4, and 3β-asetoksiöfa-5,22-dien 5. İzole edilen bileşiklerin yapıları spektroskopik yöntemler kullanılarak aydınlatılmış ve elde edilen sonuçlar yukarıda belirtilen bileşiklere ait spektroskopik verilerle karşılaştırılmıştır. Tüm bileşiklerin, H1299 ve A549 akciğer kanseri hücre hatları üzerindeki sitotoksik etkileri MTT yöntemiyle çalışılmıştır. 3β-Asetoksiöfa-5,22-dien 5, H1299 ve A549 hücre hatlarına karşı sırasıyla IC50 = 18.0 μg/ml ve IC50= 36.3 μg/ml derişimde etki göstererek serisindeki en etkili bileşik olarak öne çıkmıştır.
- Open Access
- 28 June 2016
- Published by Bangladesh Academy of Sciences in Dhaka University Journal of Pharmaceutical Sciences
- Vol. 14 (2) , 125-132
Evaluation of Antioxidant, Anticholinesterase and Antityrosinase Activities of Malaysian Cinnamomum Species
The extracts of the leaves and bark of five Cinnamomum species (C. altissimum, C. griffithii, C. javanicum, C. macrocarpum, and C. velutinum) were screened to evaluate their antioxidant, anticholinesterase, and antityrosinase activities. The bark of C. altissimum showed the highest phenolic content (130.1 mg GA/g), free radical scavenging by DPPH (IC50 126.2 ?g/mL) and ferric reducing antioxidant power (FRAP) assays (341.2 mg AA/g). All of the extracts inhibited linoleic acid peroxidation by greater than 70%, with the leaves of C. altissimum exhibiting the highest inhibition of 87.7%. The leaves of C. javanicum revealed the highest inhibition on anticholinesterase (AChE 30.8%) and butyrylcholinesterase (BChE 46.8%) enzymes. The leaves and bark of C. altissimum and C. velutinum exhibited greater than 20% tyrosinase inhibition, with the leaves of C. altissimum having the highest percentage of inhibition (34.6%). These bioactivities indicate that some Cinnamomum species have therapeutic potential in medicinal research and development of new drugs candidates.Dhaka Univ. J. Pharm. Sci. 14(2): 125-132, 2015 (December)
- 28 June 2016
- Published by Bangladesh Academy of Sciences in Dhaka University Journal of Pharmaceutical Sciences
- Vol. 14 (2) , 125-132
Open AccessEvaluation of Antioxidant, Anticholinesterase and Antityrosinase Activities of Malaysian Cinnamomum Species
The extracts of the leaves and bark of five Cinnamomum species (C. altissimum, C. griffithii, C. javanicum, C. macrocarpum, and C. velutinum) were screened to evaluate their antioxidant, anticholinesterase, and antityrosinase activities. The bark of C. altissimum showed the highest phenolic content (130.1 mg GA/g), free radical scavenging by DPPH (IC50 126.2 ?g/mL) and ferric reducing antioxidant power (FRAP) assays (341.2 mg AA/g). All of the extracts inhibited linoleic acid peroxidation by greater than 70%, with the leaves of C. altissimum exhibiting the highest inhibition of 87.7%. The leaves of C. javanicum revealed the highest inhibition on anticholinesterase (AChE 30.8%) and butyrylcholinesterase (BChE 46.8%) enzymes. The leaves and bark of C. altissimum and C. velutinum exhibited greater than 20% tyrosinase inhibition, with the leaves of C. altissimum having the highest percentage of inhibition (34.6%). These bioactivities indicate that some Cinnamomum species have therapeutic potential in medicinal research and development of new drugs candidates.Dhaka Univ. J. Pharm. Sci. 14(2): 125-132, 2015 (December)
- Open Access
- 1 January 2016
- Published by The Korean Society of Pharmacognosy in Natural Product Sciences
- Vol. 22 (4) , 225-230
Anticholinesterase and Anti-inflammatory Constituents fromBeilschmiedia pulverulentaKosterm
- 1 January 2016
- Published by The Korean Society of Pharmacognosy in Natural Product Sciences
- Vol. 22 (4) , 225-230
Open AccessAnticholinesterase and Anti-inflammatory Constituents fromBeilschmiedia pulverulentaKosterm
- Open Access
- 8 December 2015
- Published by African Journals Online (AJOL) in Tropical Journal of Pharmaceutical Research
- Vol. 14 (11) , 2139
A Review on Chemical Constituents and Biological Activities of the Genus Beilschmiedia (Lauraceae)
A Review on Chemical Constituents and Biological Activities of the Genus Beilschmiedia (Lauraceae)
- 8 December 2015
- Published by African Journals Online (AJOL) in Tropical Journal of Pharmaceutical Research
- Vol. 14 (11) , 2139
Open AccessA Review on Chemical Constituents and Biological Activities of the Genus Beilschmiedia (Lauraceae)
A Review on Chemical Constituents and Biological Activities of the Genus Beilschmiedia (Lauraceae)
- 30 September 2015
- Published by Oxford University Press (OUP) in International Journal of Food Science and Technology
- Vol. 51 (1) , 240-249
Comparative study of the essential oils of three Beilschmiedia species and their biological activities
Summary: This study was designed to examine the chemical compositions of the essential oils from three Beilschmiedia species and antioxidant, antimicrobial, antityrosinase, acetylcholinesterase and anti‐inflammatory activities. The essential oils of B. kunstleri, B. maingayi, B. penangiana gave β‐caryophyllene (10.6–12.1%), β‐eudesmol (17.5–24.1%) and δ‐cadinene (17.5–28.7%) as the most abundant components respectively. The bark oil of B. maingayi showed the highest activity in β‐carotene/linoleic acid (125.9%) and phenolic content (288.2 mg GA g−1), while B. penangiana bark oil was found to have strong activity in DPPH (IC50 84.7 μg mL−1) and ABTS (IC50 108.3 μg mL−1). The essential oils of B. penangiana showed the best activity against Candida glabrata with MIC value 31.3 μg mL−1. The bark oil of B. penangiana gave 82.5% tyrosinase inhibiton. The leaf oil of B. maingayi gave the highest inhibition in AChE (66.6%) and lipoxygenase (77.0%) assay. Our findings demonstrate that the essential oils have great potential for applications in pharmaceutical and food industries.
- 30 September 2015
- Published by Oxford University Press (OUP) in International Journal of Food Science and Technology
- Vol. 51 (1) , 240-249
Comparative study of the essential oils of three Beilschmiedia species and their biological activities
Summary: This study was designed to examine the chemical compositions of the essential oils from three Beilschmiedia species and antioxidant, antimicrobial, antityrosinase, acetylcholinesterase and anti‐inflammatory activities. The essential oils of B. kunstleri, B. maingayi, B. penangiana gave β‐caryophyllene (10.6–12.1%), β‐eudesmol (17.5–24.1%) and δ‐cadinene (17.5–28.7%) as the most abundant components respectively. The bark oil of B. maingayi showed the highest activity in β‐carotene/linoleic acid (125.9%) and phenolic content (288.2 mg GA g−1), while B. penangiana bark oil was found to have strong activity in DPPH (IC50 84.7 μg mL−1) and ABTS (IC50 108.3 μg mL−1). The essential oils of B. penangiana showed the best activity against Candida glabrata with MIC value 31.3 μg mL−1. The bark oil of B. penangiana gave 82.5% tyrosinase inhibiton. The leaf oil of B. maingayi gave the highest inhibition in AChE (66.6%) and lipoxygenase (77.0%) assay. Our findings demonstrate that the essential oils have great potential for applications in pharmaceutical and food industries.
- Open Access
- 31 December 2014
- Vol. 4, 527-531
Anticholinesterase and Antityrosinase Activities of Ten Piper Species from Malaysia
Purpose: The aim of this study was to investigate acetylcholinesterase (AChE), butyrylcholinesterase (BChE) and antityrosinase activities of extracts from ten Piper species namely; P. caninum, P. lanatum, P. abbreviatum, P. aborescens, P. porphyrophyllum, P. erecticaule, P. ribesioides, P. miniatum, P. stylosum, and P. majusculum.
- 31 December 2014
- Vol. 4, 527-531
Open AccessAnticholinesterase and Antityrosinase Activities of Ten Piper Species from Malaysia
Purpose: The aim of this study was to investigate acetylcholinesterase (AChE), butyrylcholinesterase (BChE) and antityrosinase activities of extracts from ten Piper species namely; P. caninum, P. lanatum, P. abbreviatum, P. aborescens, P. porphyrophyllum, P. erecticaule, P. ribesioides, P. miniatum, P. stylosum, and P. majusculum.
- 2 November 2014
- Published by Taylor & Francis in Journal of Essential Oil Bearing Plants
- Vol. 17 (6) , 1329-1334
Chemical Composition and Antimicrobial Activity of Essential Oil ofPiper muricatumBlume (Piperaceae)
The essential oil isolated by hydrodistillation from fresh whole plant parts of Piper muricatum Blume (Piperaceae) was analyzed by GC and GC-MS. Forty components were identified, representing 90.8 % of the total oil. The major components were aromadendrene (16.2 %), β-caryophyllene (8.8 %), germacrene D (7.9 %), γ-cadinene (7.9 %), elemol (5.4 %), γ-elemene (4.9 %) and bicyclogermacrene (4.4 %). The antimicrobial evaluation revealed that the essential oil had moderate activity towards Gram positive bacteria, Bacillus cereus and Streptococcus mutans each with MIC value of 250 µg/mL.
- 2 November 2014
- Published by Taylor & Francis in Journal of Essential Oil Bearing Plants
- Vol. 17 (6) , 1329-1334
Chemical Composition and Antimicrobial Activity of Essential Oil ofPiper muricatumBlume (Piperaceae)
The essential oil isolated by hydrodistillation from fresh whole plant parts of Piper muricatum Blume (Piperaceae) was analyzed by GC and GC-MS. Forty components were identified, representing 90.8 % of the total oil. The major components were aromadendrene (16.2 %), β-caryophyllene (8.8 %), germacrene D (7.9 %), γ-cadinene (7.9 %), elemol (5.4 %), γ-elemene (4.9 %) and bicyclogermacrene (4.4 %). The antimicrobial evaluation revealed that the essential oil had moderate activity towards Gram positive bacteria, Bacillus cereus and Streptococcus mutans each with MIC value of 250 µg/mL.
- 8 August 2014
- Published by Springer Nature in Archives of Pharmacal Research
- Vol. 38 (4) , 485-493
Chemical compositions and biological activities of the essential oils of Beilschmiedia madang Blume (Lauraceae)
The present study aimed to examine the chemical compositions of the essential oils of Beilschmiedia madang and their antioxidant, antibacterial, antifungal, anticholinesterase and anti-tyrosinase activities. The major constituents of the essential oils of leaf and bark of B. madang were δ-cadinene (17.0 and 20.5 %), β-caryophyllene (10.3 and 6.7 %), α-cubebene (11.3 and 15.6 %), and α-cadinol (5.8 and 10.6 %). The essential oils were screened for their antioxidant activities using 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical, β-carotene/linoleic acid bleaching, and total phenolic content. The bark oil showed the highest β-carotene/linoleic acid bleaching (90.3 % ± 0.2) and DPPH radical scavenging (IC50 212.0 µg/mL), while the highest phenolic content was exhibited by the leaf oil (94.5 % ± 0.3 mg GA/g). The antibacterial and antifungal activities were investigated by the disc diffusion and micro dilution method. The leaf and bark oils showed moderate activity towards Bacillus subtilis and Staphylococcus aureus with minimum inhibitory concentration (MIC) value 125 µg/mL. For antifungal assay, the bark oil showed strong activity towards Aspergillus niger and Aspergillus fumigatus with MIC value 62.5 µg/mL. Anticholinesterase and anti-tyrosinase activities were evaluated against Ellman method and mushroom tyrosinase, respectively. The results showed that leaf oil gave significant percentage inhibition (I%: acetylcholinesterase 55.2 %, butyrylcholinesterase 60.4 %, tyrosinase 53.1 %).
- 8 August 2014
- Published by Springer Nature in Archives of Pharmacal Research
- Vol. 38 (4) , 485-493
Chemical compositions and biological activities of the essential oils of Beilschmiedia madang Blume (Lauraceae)
The present study aimed to examine the chemical compositions of the essential oils of Beilschmiedia madang and their antioxidant, antibacterial, antifungal, anticholinesterase and anti-tyrosinase activities. The major constituents of the essential oils of leaf and bark of B. madang were δ-cadinene (17.0 and 20.5 %), β-caryophyllene (10.3 and 6.7 %), α-cubebene (11.3 and 15.6 %), and α-cadinol (5.8 and 10.6 %). The essential oils were screened for their antioxidant activities using 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical, β-carotene/linoleic acid bleaching, and total phenolic content. The bark oil showed the highest β-carotene/linoleic acid bleaching (90.3 % ± 0.2) and DPPH radical scavenging (IC50 212.0 µg/mL), while the highest phenolic content was exhibited by the leaf oil (94.5 % ± 0.3 mg GA/g). The antibacterial and antifungal activities were investigated by the disc diffusion and micro dilution method. The leaf and bark oils showed moderate activity towards Bacillus subtilis and Staphylococcus aureus with minimum inhibitory concentration (MIC) value 125 µg/mL. For antifungal assay, the bark oil showed strong activity towards Aspergillus niger and Aspergillus fumigatus with MIC value 62.5 µg/mL. Anticholinesterase and anti-tyrosinase activities were evaluated against Ellman method and mushroom tyrosinase, respectively. The results showed that leaf oil gave significant percentage inhibition (I%: acetylcholinesterase 55.2 %, butyrylcholinesterase 60.4 %, tyrosinase 53.1 %).
- Open Access
- 20 July 2014
- Published by Penerbit UTM Press in Malaysian Journal of Fundamental and Applied Sciences
- Vol. 6 (1)
Synthesis of 4’,5,7-trihydroxyflavanone and 3’,4’,5,7-tetrahydroxyflavanone and antioxidant activity
Natural flavonoids, 4’,5,7-trihydroxyflavanone and 3’,4’,5,7-tetrahydroxyflavanone were synthesised via their respective chalcone. The initial step wasto synthesise derivatives of 2-hydroxyacetophenone and benzaldehyde by protecting the phenolic hydroxyl groups. The chalcone was synthesised byClaisen-Schmidt condensation. Acid hydrolysis and subsequent treatment with sodium acetate of 2’-hydroxy-4,4’-6’-tris(methoxymethyloxy)chalconeand 2’-hydroxy-3,4,4’,6’-tetrakis(methoxymethyloxy)chalcone, gave 4’,5,7-trihydroxyflavanone and 3’,4’,5,7-tetrahydroxyflavanone, respectively.3’,4’,5,7-Tetrahydroxyflavanone was found to be more potent as an antioxidant agent than 4’,5,7-trihydroxyflavanone with 83.11% inhibition and SC508.57 μg/mL in the radical scavenging activity by ESR method.
- 20 July 2014
- Published by Penerbit UTM Press in Malaysian Journal of Fundamental and Applied Sciences
- Vol. 6 (1)
Open AccessSynthesis of 4’,5,7-trihydroxyflavanone and 3’,4’,5,7-tetrahydroxyflavanone and antioxidant activity
Natural flavonoids, 4’,5,7-trihydroxyflavanone and 3’,4’,5,7-tetrahydroxyflavanone were synthesised via their respective chalcone. The initial step wasto synthesise derivatives of 2-hydroxyacetophenone and benzaldehyde by protecting the phenolic hydroxyl groups. The chalcone was synthesised byClaisen-Schmidt condensation. Acid hydrolysis and subsequent treatment with sodium acetate of 2’-hydroxy-4,4’-6’-tris(methoxymethyloxy)chalconeand 2’-hydroxy-3,4,4’,6’-tetrakis(methoxymethyloxy)chalcone, gave 4’,5,7-trihydroxyflavanone and 3’,4’,5,7-tetrahydroxyflavanone, respectively.3’,4’,5,7-Tetrahydroxyflavanone was found to be more potent as an antioxidant agent than 4’,5,7-trihydroxyflavanone with 83.11% inhibition and SC508.57 μg/mL in the radical scavenging activity by ESR method.