{"id":696,"date":"2018-07-03T07:07:15","date_gmt":"2018-07-03T04:07:15","guid":{"rendered":""},"modified":"2023-09-12T23:43:58","modified_gmt":"2023-09-12T20:43:58","slug":"%d9%81%d8%b1%d8%b9-%d8%a7%d9%84%d9%83%d9%8a%d9%85%d9%8a%d8%a7%d8%a1-%d8%a7%d9%84%d8%b5%d9%8a%d8%af%d9%84%d8%a7%d9%86%d9%8a%d8%a9-%d8%a8%d8%ad%d9%88%d8%ab-%d8%aa%d8%ae%d8%b1%d8%ac-%d8%a7%d9%84%d9%85","status":"publish","type":"post","link":"https:\/\/copharm.uobaghdad.edu.iq\/?p=696","title":{"rendered":"\u0641\u0631\u0639 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0635\u064a\u062f\u0644\u0627\u0646\u064a\u0629 \u0628\u062d\u0648\u062b \u062a\u062e\u0631\u062c \u0627\u0644\u0645\u0631\u062d\u0644\u0629 \u0627\u0644\u062e\u0627\u0645\u0633\u0629 \u0627\u0644\u0639\u0627\u0645 \u0627\u0644\u062f\u0631\u0627\u0633\u064a 2018-2017"},"content":{"rendered":"
\n

\u00a0 \u00a0 \u00a0\u0641\u0631\u0639 \u0627\u0644\u0643\u064a\u0645\u064a\u0627\u0621 \u0627\u0644\u0635\u064a\u062f\u0644\u0627\u0646\u064a\u0629\u00a0 \u0628\u062d\u0648\u062b \u062a\u062e\u0631\u062c\u00a0 \u0627\u0644\u0645\u0631\u062d\u0644\u0629 \u0627\u0644\u062e\u0627\u0645\u0633\u0629<\/p>\n

\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
\n

\u062a<\/span><\/p>\n<\/td>\n

\n

\u0623\u0633\u0645 \u0627\u0644\u062a\u062f\u0631\u064a\u0633\u0649<\/span><\/p>\n<\/td>\n

\n

\u0623\u0633\u0645 \u0627\u0644\u0637\u0627\u0644\u0628<\/span><\/p>\n<\/td>\n

\n

\u0639\u0646\u0648\u0627\u0646 \u0627\u0644\u0628\u062d\u062b<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

1<\/span><\/p>\n<\/td>\n

\n

\n

\u0623.\u0645. \u062f. \u0645\u062d\u0645\u062f \u062d\u0633\u0646<\/span><\/p>\n<\/td>\n

\n

\u062a\u0628\u0627\u0631\u0643 \u0639\u0644\u064a \u062c\u0645\u064a\u0644<\/span><\/p>\n<\/td>\n

\n

Prodrugs of 5-fluorouracil <\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0638\u0627\u0647\u0631 \u063a\u0627\u0646\u0645 \u0638\u0627\u0647\u0631 \u062d\u0633\u0646<\/span><\/p>\n<\/td>\n

\n

Hydrogen sulfide donor<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

2<\/span><\/p>\n<\/td>\n

\n

\n

\u0623.\u0645. \u062f.\u0639\u0645\u0627\u0631 \u0639\u0628\u062f \u0627\u0644\u0631\u0632\u0627\u0642<\/span><\/p>\n<\/td>\n

\n

\u0632\u064a\u0646\u0628 \u0645\u062d\u0645\u0648\u062f \u0635\u0628\u062d<\/span><\/p>\n<\/td>\n

\n

Enapril new derivatives<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0633\u0646\u0627\u0631 \u0639\u062f\u0646\u0627\u0646 \u062f\u0644\u0641<\/span><\/p>\n<\/td>\n

\n

NSAIDs as anticancer drugs<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0633\u064a\u0641 \u0635\u0644\u0627\u062d \u0647\u0648\u064a\u062f\u064a<\/span><\/p>\n<\/td>\n

\n

Gene therapy<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

3<\/span><\/p>\n<\/td>\n

\n

\n

\u0623.\u0645. \u062a\u063a\u0631\u064a\u062f \u0646\u0638\u0627\u0645 \u0627\u0644\u062f\u064a\u0646<\/span><\/p>\n<\/td>\n

\n

\u0633\u0627\u0631\u0647 \u0639\u0644\u064a \u062c\u0628\u0627\u0631<\/span><\/p>\n<\/td>\n

\n

Schiff base-pharmaceutical application.<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0637\u064a\u0628\u0629 \u062e\u0627\u0644\u062f \u0633\u0627\u0644\u0645<\/span><\/p>\n<\/td>\n

\n

Amino acid as spacer in designing of prodrug<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0641\u0627\u0637\u0645\u0629 \u0627\u0644\u0632\u0647\u0631\u0627\u0621 \u0641\u0627\u0636\u0644<\/span><\/p>\n<\/td>\n

\n

Combinatorial chemistry<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u064a\u0642\u064a\u0646 \u0627\u0646\u0633 \u0639\u0628\u062f \u0627\u0644\u062c\u0644\u064a\u0644<\/span><\/p>\n<\/td>\n

\n

Quinoline derivatives as anti-inflammatory agents<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

4<\/span><\/p>\n<\/td>\n

\n

\n

\u0623.\u0645 . \u0645\u064a \u0645\u062d\u0645\u062f \u062c\u0648\u0627\u062f<\/span><\/p>\n<\/td>\n

\n

\u0627\u064a\u0629 \u0633\u0645\u064a\u0631 \u062d\u0633\u064a\u0646<\/span><\/p>\n<\/td>\n

\n

The amide prodrugs of most common NSAIDs<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0632\u064a\u0646\u0628 \u0645\u062b\u0646\u0649 \u0627\u0633\u0645\u0627\u0639\u064a\u0644<\/span><\/p>\n<\/td>\n

\n

Isatin derivatives with anti-inflammatory and analgesic activities<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

5<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u062f. \u0623\u062d\u0644\u0627\u0645 \u062c\u0645\u064a\u0644<\/span><\/p>\n<\/td>\n

\n

\u062d\u064a\u062f\u0631 \u0631\u0627\u0626\u062f<\/span><\/p>\n<\/td>\n

\n

Schiff base as antifungal agents<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0627\u062d\u0645\u062f \u062c\u0628\u0627\u0631<\/span><\/p>\n<\/td>\n

\n

Thiadiazole derivatives of <\/span>NSAIDs as anti-inflammatory agents<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0631\u0646\u062f \u0639\u0628\u062f \u0627\u0644\u0643\u0631\u064a\u0645<\/span><\/p>\n<\/td>\n

\n

NSAIDs derivatives with anti-cancer activity<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

6<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u062f. \u0633\u0648\u0632\u0627\u0646 \u0648\u062f\u064a\u0639<\/span><\/p>\n<\/td>\n

\n

\u062c\u0639\u0641\u0631 \u0633\u0627\u0645\u064a<\/span><\/p>\n<\/td>\n

\n

Carboxylic acid isosteres in drug design<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0627\u062d\u0645\u062f \u062c\u0645\u064a\u0644<\/span><\/p>\n<\/td>\n

\n

Synthesis & biological evaluation of 1,3,4-oxadiazole derivatives of NSAIDs<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0635\u0641\u0627 \u0632\u064a\u062f<\/span><\/p>\n<\/td>\n

\n

CNS-targeted drug delivery systems<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

7<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u062f.\u062f\u064a\u0627\u0631 \u0639\u0627\u0631\u0641<\/span><\/p>\n<\/td>\n

\n

\u0632\u0647\u0631\u0627\u0621 \u0627\u0643\u0631\u0645 \u062d\u0646\u0634<\/span><\/p>\n<\/td>\n

\n

New=nazal application of benzodiazepine<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0632\u064a\u0646\u0628 \u0646\u0639\u064a\u0645 \u0633\u0639\u064a\u062f<\/span><\/p>\n<\/td>\n

\n

Prodrug for oral delivary<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u063a\u0646\u0649 \u0645\u062d\u0645\u062f \u0645\u0646\u064a\u0631<\/span><\/p>\n<\/td>\n

\n

Payloronic acid-paclitaxal bioconjugation prodrugs<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

8<\/span><\/p>\n<\/td>\n

\n

\n

\u0645.\u062f. \u0645\u062b\u0646\u0649 \u0633\u0639\u062f\u064a<\/span><\/p>\n<\/td>\n

\n

\u0645\u062d\u0645\u062f \u0641\u0627\u0636\u0644 \u0639\u0628\u062f<\/span><\/p>\n<\/td>\n

\n

Cephalosporin shift base derivative <\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0627\u0641\u0631\u0627\u062d \u062d\u0633\u0646 \u0639\u0644\u064a<\/span><\/p>\n<\/td>\n

\n

Brain cancer targating<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0632\u0647\u0631\u0627\u0621 \u0648\u0644\u064a\u062f \u0641\u064a\u0635\u0644<\/span><\/p>\n<\/td>\n

\n

Anticancer folate targating<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

9<\/span><\/p>\n<\/td>\n

\n

\n

\u0645.\u062f.\u0645\u062d\u0645\u062f \u0643\u0627\u0645\u0644<\/span><\/p>\n<\/td>\n

\n

\u0627\u0631\u064a\u062c \u0645\u062d\u0645\u062f \u0634\u0646\u064a\u0627\u0631<\/span><\/p>\n<\/td>\n

\n

Synthesis and biological activity of coumarin derivatives<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0632\u064a\u0646\u0629 \u0628\u0627\u0633\u0645 \u0639\u0628\u062f \u0627\u0644\u0627\u0645\u064a\u0631<\/span><\/p>\n<\/td>\n

\n

Selective COX-2 inhibitors :chemical classification ,side effect and their use in cancer.<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

10<\/span><\/p>\n<\/td>\n

\n

\n

\u0645.\u062f. \u0632\u064a\u0646\u0628 \u0639\u0628\u062f \u0627\u0644\u0647\u0627\u062f\u064a<\/span><\/p>\n<\/td>\n

\n

\u0635\u0628\u0627 \u0645\u062d\u0645\u062f \u0634\u0631\u064a\u0641 \u0645\u0635\u0637\u0641\u0649<\/span><\/p>\n<\/td>\n

\n

Synthesis of new sulfonyl urea der.s as antihyperglycemic agents.<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0627\u064a\u0629 \u0647\u0627\u0634\u0645 \u0639\u0628\u062f \u0627\u0644\u0631\u0632\u0627\u0642<\/span><\/p>\n<\/td>\n

\n

Synthesis of new quinoline der.s as anticancer agents.<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0634\u0647\u062f \u0639\u0627\u0645\u0631 \u0641\u064a\u0635\u0644<\/span><\/p>\n<\/td>\n

\n

Synthesis of new pyrazole der.s as antituberculosis agents.<\/span><\/p>\n

\n<\/td>\n<\/tr>\n

\n

\u062a<\/span><\/p>\n<\/td>\n

\n

\u0623\u0633\u0645 \u0627\u0644\u062a\u062f\u0631\u064a\u0633\u0649<\/span><\/p>\n<\/td>\n

\n

\u0623\u0633\u0645 \u0627\u0644\u0637\u0627\u0644\u0628<\/span><\/p>\n<\/td>\n

\n

\u0639\u0646\u0648\u0627\u0646 \u0627\u0644\u0628\u062d\u062b<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

11<\/span><\/p>\n<\/td>\n

\n

\n

\u0645.\u0627\u0645\u064a\u0631\u0629 \u0639\u0628\u0627\u0633<\/span><\/p>\n<\/td>\n

\n

\u0633\u0648\u0632\u0627\u0646 \u0633\u0639\u062f \u0633\u0639\u064a\u062f<\/span><\/p>\n<\/td>\n

\n

Macrolides antibiotic<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0646\u062c\u0627\u0629 \u0635\u0628\u062d\u064a<\/span><\/p>\n<\/td>\n

\n

NSAIDs as anti-cancer<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

1<\/span>2<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u0623\u0632\u0647\u0627\u0631 \u0645\u0647\u062f\u064a<\/span><\/p>\n<\/td>\n

\n

\u0632\u0647\u0631\u0627\u0621 \u062d\u0627\u0645\u062f<\/span><\/p>\n<\/td>\n

\n

Amide derivatives as potential prodrugs<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0627\u064a\u0629 \u0631\u0623\u0641\u062a<\/span><\/p>\n<\/td>\n

\n

synthesis of a new potential antifungal drugs<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

13<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u0645\u0639\u0627\u0630 \u0642\u0635\u064a<\/span><\/p>\n<\/td>\n

\n

\u0627\u0637\u064a\u0627\u0641 \u0628\u0627\u0633\u0645 \u0645\u0631\u0639\u064a<\/span><\/p>\n<\/td>\n

\n

Butyrephenones psychatry<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0641\u0631\u062d \u0637\u0644\u0627\u0644 \u0628\u0647\u0646\u0627\u0645<\/span><\/p>\n<\/td>\n

\n

Taxanes as chemotherapeutic agents<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

14<\/span><\/p>\n<\/td>\n

\n

\n

\u0645.\u0645.\u0633\u062d\u0631 \u0645\u062d\u0645\u062f \u0634\u0627\u0643\u0631<\/span><\/p>\n<\/td>\n

\n

\u0639\u0644\u064a \u0635\u0641\u0627\u0621 \u062c\u0648\u0627\u062f<\/span><\/p>\n<\/td>\n

\n

Development of cephalosporins antibiotics<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0631\u064a\u0627\u0645 \u0635\u0627\u062f\u0642 \u062c\u0639\u0641\u0631<\/span><\/p>\n<\/td>\n

\n

Protein kinases targeted anticancer drugs<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

15<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u0645. \u0639\u0628\u062f \u0627\u0644\u062d\u0641\u064a\u0638 \u062d\u0645\u064a\u062f<\/span><\/p>\n<\/td>\n

\n

\u063a\u0641\u0631\u0627\u0646 \u0627\u0628\u0631\u0627\u0647\u064a\u0645<\/span><\/p>\n<\/td>\n

\n

Peptides as targeting agents<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0627\u062d\u0645\u062f \u0633\u0639\u062f<\/span><\/p>\n<\/td>\n

\n

Drug containing indol moiety as anti-cancer agent<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

16<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u0645. \u0634\u064a\u0645\u0627\u0621 \u0644\u0624\u064a<\/span><\/p>\n<\/td>\n

\n

\u0645\u062d\u0645\u062f \u0646\u0635\u0631 \u0639\u0628\u0627\u0633<\/span><\/p>\n<\/td>\n

\n

Metal complexes acting as drugs <\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0637\u064a\u0628\u0629 \u0633\u0627\u0645\u064a \u0645\u062d\u0645\u062f<\/span><\/p>\n<\/td>\n

\n

Synthesis of benzimidazole derivatives with antimicrobial activity<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

17<\/span><\/p>\n<\/td>\n

\n

\n

\u0645.\u0645. \u0631\u0646\u0627 \u0639\u0627\u062f\u0644 \u0643\u0645\u0648\u0646<\/span><\/p>\n<\/td>\n

\n

\u0639\u0644\u064a \u0639\u0628\u062f \u0627\u0644\u0633\u0627\u062f\u0629 \u0641\u0632\u0639<\/span><\/p>\n<\/td>\n

\n

Derivatives of sulfonamide as <\/span>antimicrobial agent<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0627\u064a\u0629 \u0627\u064a\u0627\u062f \u0645\u062d\u0645\u0648\u062f<\/span><\/p>\n<\/td>\n

\n

NSAIDs<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

18<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u0645. \u0645\u062d\u0645\u062f \u0639\u0628\u062f \u0627\u0644\u0623\u0645\u064a\u0631<\/span><\/p>\n<\/td>\n

\n

\u0628\u062a\u0648\u0644 \u062f\u0627\u0648\u062f \u0633\u0644\u0645\u0627\u0646<\/span><\/p>\n<\/td>\n

\n

Recent developments in anti-cancer drug delivery using dual target drug<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0631\u0627\u0641\u0639 \u0635\u0644\u0627\u062d \u0641\u0627\u0644\u062d<\/span><\/p>\n<\/td>\n

\n

Investigation of 1,3,4diazolas potential anti-microbial agent<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

19<\/span><\/p>\n<\/td>\n

\n

\n

\u0645.\u0645.\u0633\u0627\u0631\u0627 \u0633\u062a\u0627\u0631<\/span><\/p>\n<\/td>\n

\n

\u0631\u0641\u0644 \u0639\u0644\u0627\u0621 \u0627\u0644\u062f\u064a\u0646 \u0634\u0627\u0643\u0631<\/span><\/p>\n<\/td>\n

\n

Chitosan derivatives as <\/span>anti-microbial agent<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0627\u062d\u0645\u062f \u0641\u0644\u0627\u062d \u0646\u062c\u0645<\/span><\/p>\n<\/td>\n

\n

1,3,4-oxadiazolo <\/span>derivatives as anti-microbial agent<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

20<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u0645.<\/span> \u0634\u0645\u0633 \u0639\u0648\u0627\u062f<\/span><\/p>\n<\/td>\n

\n

\u0627\u064a\u0629 \u0641\u0631\u0627\u0633<\/span><\/p>\n<\/td>\n

\n

synthesis of new anti-cancer drug<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0632\u064a\u0646\u0647 \u0645\u0627\u0644\u0643<\/span><\/p>\n<\/td>\n

\n

Anti-microbial activity of sulfanilamide<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\n

21<\/span><\/p>\n<\/td>\n

\n

\n

\u0645. \u0645. \u0639\u0644\u064a \u062d\u064a\u062f\u0631<\/span><\/p>\n<\/td>\n

\n

\u0627\u0633\u0631\u0627\u0621 \u0639\u0645\u0627\u062f \u0633\u0639\u064a\u062f<\/span><\/p>\n<\/td>\n

\n

Stratigies toward synthesis of 2\u0301-nucleoside analogues<\/span><\/p>\n

As potential inhibitors for HCV N S5B polymerase enzyme<\/span><\/p>\n<\/td>\n<\/tr>\n

\n

\u0642\u0627\u0633\u0645 \u0645\u062d\u0645\u062f \u062b\u0627\u0628\u062a<\/span><\/p>\n<\/td>\n

\n

NSAIDs<\/span><\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n

 <\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

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