1. Karimian, S., Nikeghbali, N., Nahaei, A., Kabiri, M., Poustforoosh, A., Sakhteman, A., Khoshneviszadeh, M 1H-benzo[f]chromene-2-carboxylate derivatives: synthesis, computational investigations (docking, MD, and DFT), and in vitro biological evaluation as tyrosinase inhibitors.
2. Hassani, B., Jafari, A., Tavakkoli, M., Moosavi, F., Firuzi, O Olaparib has synergistic effects with DNA damaging agents in pancreatic ductal adenocarcinoma.
3. Khanehzar, E., Shams, F., Jafari, A The golden touch: a comprehensive network pharmacology-guided review of synergy between curcumin and PARP inhibitors.
4. Mortazavi, M., Edraki, N., Tavakkoli, M., Karimian, S., Saso, L., Firuzi, O Study of di- (thiophene-2-yl)-1,2,4-triazine derivatives as multikinase inhibitors and anticancer agents
5. Benabbes, M., El Moutaouakil Ala Allah, A., Ziraoui, O., Poustforoosh, A., El-Guourrami, O., Akhazzane, M., Tüzün, B., El Harti, J., Lamsaouri, J Design, synthesis, and biological evaluation of pyrazole-based schiff bases as dual α-amylase and α-glucosidase inhibitors with antioxidant potential
6. Jafari, A., Fathi, Sh., Moosavi, F., Firuzi, O, Expanding the therapeutic applications of PARP inhibitors in cancer by targeting receptor tyrosine kinases
7. İSPİR, Ü., Tüzün, B., KIRICI, M., Poustforoosh, A., YONAR, M., YONAR, S., ŞEKER, E. Biochemical effects and theoretical study of a metformin in the carp (Cyprinus carpio) fry
8. Mansouri, M., Ataollahi, E., Khabnadideh, S., Heidarneghad, K., Sedigh, M., Poustforoosh, A., Emami, M., Rezaei, Z . Design, synthesis, and evaluation of novel quinazoline-4-one derivatives as potential EGFR-targeting anticancer agents: integrated computational and biological insights
9. Aghanour Ashtiani, M., Karimian, S., Iraji, A., Dastyafteh, N., Mohammadi-Khanaposhtani, M., Larijani, B., Mahdavi, M., Salehi, P. Development of new coumarin-piperazine-N-phenylacetamid derivatives as potent tyrosinase inhibitors: In vitro and in silico evaluations
10. Moheimanian, N., Mirkhani, H., Edraki, N., Poustforoosh, A., Nabipour, I., El-Seedi, H., Sohrabipour, J., Jassbi, A . Bioassay-guided purification of swartzchromone, a novel chromone, as an α-glucosidase inhibitor from Sargassum swartzii C. Agardh (Sargassaceae, brown seaweed)
11.Bostancı, H., Yıldırım, E., Çetin, F., Kaplan, D., Koçyiğit, Ü., Poustforoosh, A., Tüzün, B., Kelebekli, L. Investigation of Carbonic Anhydrase Inhibition, Antioxidant Properties, and Selective Anticancer Activity of Methyl-Substituted Halogenated and Methoxy Conduritols
12. Parchenko, V., Poustforoosh, A., Karpenko, Y., Kyrychko, B., Tüzün, B., Kyrychko, E., Chetvertak, T., Kul, İ. The development and theoretical examination of hplc-ms determination method for a novel veterinary drug tryfuzol-neo 1% in meat and animal organs
13. Zakeri Khatir, Z., Alipour, A., Mortazavi, M., Tavakkoli, M., Irannejad, H., Foroumadi, A., Firuzi, O., Valipour,M. Design, synthesis, and bioactivity assessment of highly potent isatin-based small-molecules bearing 3-hydrazineyl-6-aryl-1,2,4-triazine moieties as potential c-MET targeting anticancer agents
14. Poustforoosh, A., Elyasi, M. Leveraging Scaffold Hopping and Machine Learning for the Innovative Design and Assessment of Pyridine Derivatives as c-Met Inhibitors Using Amide-based Bioisosteres
15. Kirici, M., Tüzün, B., Yonar, M., Poustforoosh, A., Mişe Yonar, S., Şeker, E., İspir, Ü. Change of micronucleus frequencies, antioxidant parameters and in silico in carp (Cyprinus carpio) fry exposed to ibuprofen
16. Khanehzar, E., Shams, F., Jafari, A., Poustforoosh, A . Next-generation AI-assisted drug design against cancer: large language models meet conventional in silico methods.
17. Khanehzar, E., Shams, F., Jafari, A., Poustforoosh, A., Abedi, M., Jafarinia, S. A novel framework for assessing large language models in computational drug design: Targeting AXL receptor tyrosine kinase for cancer therapy
18. Ashooriha, M., Alizadeh, S., Khoshneviszadeh, M., Ansari, M., Kabiri, M., Mahdavi, M., Talebi, M., Mohammadi-Khanaposhtani, M., Tahmasebi, E., Amanlou, M., Emami, S. Synthesis, in vitro evaluation and molecular docking of amino-kojic acid derivatives as potent tyrosinase and urease inhibitors
19.Ahmadnasr, M., Zarandi, B., Panjehshahin, M., Purkhosrow, A., Bahadoori, Sh. Sex Differences in the Effects of L-Menthol on Nociception in the Hot Plate Test and Acetic Acid Writhing Test in BALB/c Mice
