scholarly journals The possibility of using cell test-systems for screening for anti-inflammatory activity of novel 5(S)-menthyloxy derivatives of 2(5H)-furanone

2017 ◽  
Vol 98 (2) ◽  
pp. 211-217
Author(s):  
H H Cong ◽  
R R Sibgatullina ◽  
A M Khabibrakhmanova ◽  
A R Kurbangalieva ◽  
L E Ziganshina

Aim. Study of the possibility of using cell experimental models (erythrocytes hemolysis and platelet aggregation) for screening for anti-inflammatory activity of novel synthesized 5(S)-menthyloxy derivatives of 2(5Н)-furanone (compounds R1-R6). Methods. Evaluation of membrane-stabilizing activity of the test compounds was performed by means of models of erythrocyte hemolysis induced by hypotonic environment (osmotic hemolysis) and free radicals. Antiplatelet effect of the compounds was studied by inducing platelet aggregation by 1 mM arachidonic acid. Study of anti-inflammatory activity of novel potential anti-inflammatory molecules was performed with the use of the model of carrageenan-induced paw edema in mice. Results. Compounds R1, R2, R3, and R4 increase the degree of osmotic hemolysis. Compounds R5, R6 decrease the intensity of hemolysis at different concentrations. Compounds R1, R2, R4 and R6 promote free-radical erythrocyte membrane damage at all tested concentrations. Compound R3 protects erythrocytes at low concentrations and promotes erythrocyte damage with increasing concentration. Compound R5 protects erythrocytes at concentrations 3×10-9 и 3×10-5 М. Compounds R1, R2, R4 enhance platelet aggregation at different concentrations. Compound R3 inhibits platelet aggregation at concentration 10-6 М, and at concentrations 10-8 and 10-5 М it induces platelet aggregation. Compound R5 does not affect platelet aggregation. Compound R6 inhibits platelet aggregation at all tested concentrations. On the basis of the results obtained from in vitro test systems compound R6 was selected for further studies of anti-inflammatory activity as it demonstrated maximum effect based on two out of three evaluation criteria. Compound R6 posseses anti-inflammatory activity in the model of inflammation. Conclusion. The novel derivative of 2(5Н)-furanone bearing l-menthol moiety (compound R6) protects erythrocyte membrane from damaging action of hypotonic environment, inhibits platelet aggregation and demonstrates anti-inflammatory activity; cell experimental models can be used for the first phase of screening of novel chemical compounds for anti-inflammatory activity.

Author(s):  
Monther F. Mahdi ◽  
Noor H. Naser ◽  
Nethal H. Hammud

Objective: The objective of this search was to synthesize a new naproxen analogues having a 1,2,4-triazole-3-thiol heterocyclic ring, and preliminary pharmacological assessment of the anti-inflammatory activity of the synthesized compounds. Methods: The synthesis of naproxen analogues that having 1,2,4-triazole-3-thiol heterocyclic ring occur through esterification of naproxen, and then its reaction with hydrazine hydrate, and carbon disulfide, finally different aromatic aldehydes reacted with triazole derivatives of naproxen containing amino group to produce schiff bases.Results: In vivo acute anti-inflammatory activity of the synthesize compounds (Va-Vd) was evaluated in rats using egg-white induced edema model of inflammation in a dose equivalent to (50 mg/kg) of naproxen. All tested compounds were produced a significant reduction in paw edema with respect to the effect of propylene glycol 50% v/v (control group). Compound Vd produced superior anti-inflammatory activity compared to naproxen.Conclusion: The results obtained in this work give evidence about the valid synthesis of 1,2,4 triazole-3-thiol derivatives of naproxen, which reacted with different aldehydes to yield several schiff bases. The incorporation of benzaldehyde possess para-electron donating group (para-hydroxyl benzaldehyde) will increase the anti-inflammatory activity of naproxen.


2021 ◽  
Vol 7 (12) ◽  
pp. 25-33
Author(s):  
A. Chiriapkin ◽  
I. Kodonidi ◽  
A. Ivchenko ◽  
L. Smirnova

The article presents a modified method for the synthesis of 2-substituted 5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidine-4(3H)-one and the predict of their anti-inflammatory activity. The proposed method for obtaining tetrahydrothienopyrimidine derivatives is preparatively effective and simple. Their synthesis was carried out by heterocyclization of azomethine derivatives of 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide in the medium of glacial acetic acid with the catalytic addition of dimethyl sulfoxide. Preliminary prognosis of anti-inflammatory activity in silico method allowed us to identify the most promising compounds. Of these, the 4b structure containing a 2-hydroxyphenyl fragment in the second position of pyrimidine-4(3H)-one may be of the greatest interest. It seems appropriate to further study the spectrum of biological activity of the studied compounds.


Author(s):  
Inayat Kabir ◽  
Imtiyaz Ansari

The article emphasizes the anti-inflammatory effects of herbal extracts on different experimental models that are repeatedly used to test the in vivo anti-inflammatory activity of herbal components. Edema, granuloma and arthritis models are used to test the anti-inflammatory activity of plant extracts whereas formalin or acetic acid-induced writhing test and hot plate methods are the most repeatedly used to evaluate anti-nociceptive potentials of the herbal extracts. Although adjuvant-induced and collagen-induced arthritis models are also quite efficient, they have been used seldom to evaluate anti-inflammatory tendencies of the herbs. Here, we suggest a double positive reference model using both steroid and nonsteroidal anti-inflammatory drugs at the same time, instead of using only one of them either.


Author(s):  
Muralidharan V. ◽  
Asha Deepti C. ◽  
Raja S.

The pyrazoline ring is a ubiquitous structural feature of many natural and synthetic compounds with potent anti-inflammatory activity. The creation of novel pyrazoline derivatives and examination of their chemical and biological behaviour have gained additional focus in the current decade. Pyrazolines and its fused heterocyclic derivatives tested with anti-inflammatory activity constitute a significant class of compounds for novel drug evolution. Pyrazoline nucleus when linked with different substituents like alkyl, aromatic, heterocyclic rings and many other groups at different positions on the ring shows considerable to more effective anti-inflammatory activity. This article presents a comprehensive review of the anti-inflammatory activity of some novel derivatives of pyrazoline ring.


2020 ◽  
Vol 56 (4) ◽  
pp. 473-481 ◽  
Author(s):  
Nail S. Akhmadiev ◽  
Ekaterina S. Mescheryakova ◽  
Veronika R. Khairullina ◽  
Vnira R. Akhmetova ◽  
Askhat G. Ibragimov

2015 ◽  
Vol 41 (1) ◽  
pp. 83-86 ◽  
Author(s):  
S. F. Vasilevsky ◽  
D. S. Baranov ◽  
A. I. Govdi ◽  
I. V. Sorokina ◽  
T. G. Tolstikova

2013 ◽  
Vol 6 (2) ◽  
pp. 315-320 ◽  
Author(s):  
SHOBHA KAMBLE ◽  
Md. ZUBAIR AHMED ◽  
S. RAMABHIMAIAHA ◽  
PRABHAKAR PATIL

2017 ◽  
Vol 220 ◽  
pp. 20-33 ◽  
Author(s):  
Michal Markiewicz ◽  
Tadeusz Librowski ◽  
Anna Lipkowska ◽  
Pawel Serda ◽  
Krzysztof Baczynski ◽  
...  

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