1. Karma
Yeshi, Darren Crayn, Edita Ritmejeryte and Phurpa Wangchuk. Plant Secondary
Metabolites Produced in Response to Abiotic Stresses Has Potential Application
in Pharmaceutical Product Development;Molecules 2022, 27, 313. https://doi.org/10.3390/molecules27010313.
2. Abdel
Razek MMM, Moussa AY, Elshanawany MM, Singab AN (2019) Comparative chemical and
biological study of roots and aerial parts of Halocnemum strobilaceum
growing wildly in Egypt. J Pharm Sci Res 11(2019):3289â3296.
3. Alanzi
A, Elhawary EA, Ashour ML, Moussa AY (2023) Aspergillus co-cultures: a
recent insight into their secondary metabolites and microbial interactions.
Arch Pharm Res 46(4):273â298. https://doi.org/10.1007/s12272-023-01442-5.
4. AbdelRazek
MMM, Elissawy AM, Mostafa NM, Moussa AY, Elanany MA, Elshanawany MA, Singab ANB
(2023) Chemical and Biological Review of Endophytic Fungi Associated with Morus
sp. (Moraceae) and in silico study of their antidiabetic potential. Molecules
28:4.
5. Pillay
LC, Nekati L, Makhwitine PJ, Ndlovu SI (2022) Epigenetic activation of silent
biosynthetic gene clusters in endophytic fungi using small molecular modifiers.
Front Microbiol 13:815008. https://doi.org/10.3389/fmicb.2022.815008.
6. Singh,
V.K., Kumar, A. (2023). Secondary Metabolites from Endophytic Fungi:
Production, Methods of Analysis, and Diverse Pharmaceutical Potential.
Symbiosis. https://doi.org/10.1007/s13199-023-00925-9.
7. Zhgun
AA (2023) Fungal BGCs for production of secondary metabolites: main types.
Central Roles in Strain Improvement, and Regulation According to the Piano Principle
24(13):11184â11184. https://doi.org/10.3390/ijms241311184.
8. Lv
H, Li W, Xu P, Tang J, Zheng Y, Wan Y, Lin Y, Wang H, Li X (2024) Structural
diversity of microbial secondary metabolites based on chemical epigenetic
manipulation. Bioorg Chem. https://doi.org/10.1016/j.bioorg.2023.107093.
9. Rani
N, Rani S, Patel H, Yadav S, Saini M, Rawat S, Saini K (2023) Characterization
and investigation of antioxidant and antimicrobial activity of zinc oxide
nanoparticles prepared using leaves extract of Nyctanthes arbor-tristis.
Inorg Chem Commun 150:110516.https://doi.org/10.1016/j.inoche.2023.110516.
10. Acharya
S (2011) Prediction of rainfall variation through flowering phenology of
night-flowering jasmine (Nyctanthes arbor-tristis L.; Verbenaceae) in
Tripura. Indian J TraditKnowl 10:96â101.
11. Hussain
A, Ramteke A (2012) Flower extract of Nyctanthes arbor-tristis modulates
glutathione level in hydrogen peroxide-treated lymphocytes. Pharmacogn Res
4:230.https://doi.org/10.4103/0974-8490.102272.
12. T.
K. Patle, K. Shrivas, R. Kurrey, S. Upadhyay, R. Jangde, and R. Chauhan,
âPhytochemical screening and determination of phenolics and flavonoids in Dilleniapentagyna
using UV-vis and FTIR spectroscopy,â Spectrochimica Acta Part A: Molecular and
Biomolecular Spectroscopy, vol. 242, Article ID 118717, 2020.
13. Panda
D, Dash BP, Manickam S, Boczkaj G (2021) Recent advancements in LC-MS based
analysis of biotoxins: Present and future challenges. Mass Spectrom Rev
41(5):766â803. https://doi.org/10.1002/mas.21689.
14. Munshi,
M., et al. (2021). Evaluation of bioactivity and phytochemical screening of
endophytic fungi isolated from Ceriopsdecandra (Griff.) W. Theob, a
mangrove plant in Bangladesh. Clinical Phytoscience, 7(1), 1â10.
15. Surendra
K. Gond, Ashish Mishra, Vijay K. Sharma, Satish K. Verma, Jitendra Kumar,
Ravindra N. Kharwar, Anuj Kumar; Diversity and antimicrobial activity of
endophytic fungi isolated from Nyctanthes arbor-tristis, a well-known
medicinal plant of India. Mycoscience (2012) 53:113â121; DOI 10.1007/s10267-011-0146-z.
16. Karpagasundari
C, Kulothungan S. Analysis of bioactive compounds in Physalisminima
leaves using GC MS, HPLC, UV-VIS and FTIR techniques. J. Pharmacogn. Phytochem.
2014; 3(4):196-201.
17. S.
Muruganantham, G. Anbalagan, N. Ramamurthy. FT-IR and Sem-Eds Comparative
Analysis of Medicinal Plants, Ecliptaalba
Hassk and Eclipta Prostrata
Linn. Romanian J. Biophys., Vol. 19, No. 4, P. 285â294, Bucharest, 2009.
18. Mamta
Gokhale, Monika Verma, Rumana Faraz and Diwyansh Raj; Bioactive Molecules
(GC-MS) of Endophytic Fungi, Xylaria from Nyctanthes arbor-tristis
(Linn). JAM 3(1) 2017 pp 43 â 53.
19. Eman,
A.E., Sanaa, M.M.S., Hanan, S.G., Mohamed, A.T., Emad, A.S., 2021. Evaluation
of antioxidant and anticancer activity of crude extract and different fractions
of Chlorellavulgaris axenic culture grown under various concentrations
of copper ions. BMC Complement. Med. Ther. 21, 51. https://doi.org/10.1186/s12906-020-03194-x.
20. Ukwubile,
C.A.; Ahmed, A.; Katsayal, U.A.; Yau, J.; Mejida, S. GC-MS analysis of
bioactive from Melastomastrumcapitatum Fern. Leaf methanol extract. An
anticancer plant. Sci. Afr. 2019, 3, 900e.
21. Singh,
S.; Nair, V.; Jain, S.; Gupta, Y.K. Evaluation of anti-inflammatory activity of
plant lipids containing α-linolenic acid. Indian. J. Exp. Bio. 2008, 46,
453â456.
22. Jegadeeswari,
P.; Nishanthini, N.; Muthukumarasamy, S.; Mohan, V.R. GC-MS analysis of
bioactive components of Aristolochiakrysagathra (Aristolochiaceae.). J.
Chem. Pharm Sci. 2012, 2, 226â232.
23. Ali,
A.; Alharthi, S.; Al-Shalan, N.H.; Santali, E.Y. Development of Narrow-Bore C18
Column for Fast Separation of Peptides and Proteins in High-Performance Liquid
Chromatography. Polymers. 2022,14, 2576.
24. A.A.
Ayoola1,D.A. Ekunseitan,S.B. Muhammad,M.A. Oguntoye and Y.A. Adejola.
Phytochemicals Analysis and GC-MS Determination of Ethanolic Extracts of Azadirachtaindica
and Mangiferaindica Stem Bark and their Biological Potentials. Volume
21. Number 1. May 2020 (Spring).
25. Gyula
Ujlaki, Tünde Kovács, András Vida, Endre Kókai, Boglára Rauch, Szandra
Schwarcz,Edit Mikó, Eszter Janka, Adrienn Sipos, Csaba Hegedus, Karen Uray ,
Péter Nagy and Peter Bai; Identification of BacterialMetabolitesModulating
Breast Cancer Cell Proliferation and Epithelial-Mesenchymal
Transition;Molecules 2023, 28, 5898. https://doi.org/10.3390/molecules28155898.
26. Antioxidant,
Anti-Cancer Activity and Phytochemicals Profiling of Kigelia pinnata Fruits KMA
Ramadan, HS El-Beltagi, HI Mohamed, TA Shalaby, A Galal, AT
Mansourâ¦Separations, 2022â¢mdpi.com.
27. Deepthi
Ramesh, Balaji Gowrivel Vijayakumar, Tharanikkarasu Kannan;Therapeutic
potential of uracil and its derivatives in countering pathogenic and physiological
disorders;DOI:10.1016/j.ejmech.2020.112801.
28. R
Doddapaneni, JD Tucker, PJ Lu, QL Lu;Metabolic Reprogramming by Ribitol Expands
the Therapeutic Window of BETi JQ1 against Breast Cancer; 2023 - mdpi.com.
29. SMFM
Begum, S Priya, R Sundararajan; Novel anti-cancerous compounds from Sargassum
wightii: In silico and in vitro approaches to test the antiproliferative
efficacy, S Hemalatha Journal of Advanced Pharmacy Education & Research|
Jul-Sep, 2017â¢academia.edu.
30. Boobalan
Bharath, Kantharaj Perinbam, Sandhanasamy Devanesan, Mohamad S AlSalhi and
Muthupandian Saravanan; Evaluation of the anticancer potential of Hexadecanoic
acid from brown algae Turbinaria ornata on HTâ29 colon cancer
cells;https://doi.org/10.1016/j.molstruc.2021.130229.
31. Mahender
Thatikayala, Pankaj Wadhwa, Paranjeet Kaur, Pankaj Kumar Singh, Ankit Yadav,
Monika Kaushik and Sanjeev Kumar Sahu;Beta-carboline as a promising
heterocyclic nucleus: Synthetic aspects, pharmacological potential and
structure activity relationship;https://doi.org/10.1016/j.ejmcr.2022.10009.
32. F.R
Yu, X.Z. Lian, H.Y. Guo, P.M. McGuire, R.D. Li, R. Wang, F.H. Yu; Isolation and
characterization of methyl esters and derivatives from Euphorbia kansui
(Euphorbiaceae) and their inhibitory effects on the human SGC-7901 cells;J.
Pharm. Pharm. Sci., 8 (2005), pp. 528-535.
33. M.
Yoshiyuki, T. Nobukazu, Y. Hisaaki, K. Takayoshi, O. Megumi, S. Hirokazu, et
al.Fatty acids selectively inhibit eukaryotic DNA polymerase activities in
vitroBiochimica et Biophysica Acta (BBA)-Gene Struct. Expr., 1308 (3)
(1996), pp. 256-262.
34. N
K Millaty, N Wijayanti, L Hidayati and T R Nuringtyas;Identification of
anticancer compounds in leaves extracts of agarwood (Aquilaria malaccensis(Lamk.));DOI
10.1088/1755-1315/457/1/012036; 2020.