scholarly journals Evaluation of cytotoxic activity from Temurui (Murraya koenigii [Linn.] Spreng) leaf extracts against HeLa cell line using MTT assay

Author(s):  
Ulil Amna ◽  
Halimatussakdiah ◽  
Puji Wahyuningsih ◽  
Nurdin Saidi ◽  
Rosnani Nasution
2014 ◽  
Vol 9 (12) ◽  
pp. 1934578X1400901
Author(s):  
Uppuluri V. Mallavadhani ◽  
Banita Pattnaik ◽  
Nitasha Suri ◽  
Ajit K. Saxena

Ursolic acid (1), a natural pentacyclic triterpenic acid, afforded a variety of ring-C transformed products (5–11) when treated with N-bromosuccinimide under the influence of a range of protective groups and solvents. The synthesized compounds have been evaluated for cytotoxic activity against prostate PC 3, leukemia THP 1, cervical Hela and lung A-549 cancer cell lines. Among the tested analogs, compounds 5, 8, 9 and 10 showed potent activity against PC 3, THP 1 and Hela cell lines. Especially, compound 10 showed enhanced activity against the Hela cell line than the parent compound. Compounds 5, 8 and 9 showed comparable activities against PC 3 and THP 1 cell lines.


Molbank ◽  
10.3390/m1307 ◽  
2021 ◽  
Vol 2022 (1) ◽  
pp. M1307
Author(s):  
Dmitrii A. Aksenov ◽  
Alexander V. Aksenov ◽  
Lidiya A. Prityko ◽  
Nicolai A. Aksenov ◽  
Liliya V. Frolova ◽  
...  

2-Aryl-2-(3-indolyl)acetohydroxamic acids demonstrate promising antitumor activity, but quickly metabolize in vivo via glucuronidation of hydroxamic acid residue. In an attempt to improve their pharmacokinetics, methyl esters were synthesized via a newly developed protocol for chemoselective mono-methylation of hydroxamic acids. The cytotoxicity of these derivatives against the HeLa cell line was evaluated and found to be inferior compared to the parent lead compounds.


Author(s):  
Qing-Yun Lu ◽  
Jia-Hui Zhang ◽  
Ying-Yao Li ◽  
Xue-Xue Pu ◽  
Cui-Shan Zhang ◽  
...  

AbstractOne new Daphniphyllum alkaloid, daphnioldhanol A (1), together with three known ones, were isolated from the stem part of Daphniphyllum angustifolium Hutch. Their structures were elucidated by spectroscopic methods and comparing with the literature data. Compound 2 is a new natural product, but known by synthesis as a racemate. Compound 1 exhibited week cytotoxic activity against Hela cell line with IC50 of 31.9 μM. Graphic Abstract


2020 ◽  
Vol 1 (2) ◽  
Author(s):  
Adisty Ridha Damasuri ◽  
Eti Nurwening Sholikhah ◽  
Mustofa

In our previous study, some amino chalcone derivatives have been synthesized and evaluated their cytotoxicity against breast cancer cell line T47D. Among 11 amino chalcone derivatives, ((E)-1-(4-aminophenyl)-3-phenylprop-2-en-1-one)) exhibited the most active compound.This study aimed to investigate cytotoxic activity of the ((E)-1-(4-aminophenyl)-3-phenylprop-2-en-1-one)) against cervical cell line (HeLa). The cytotoxic activitywas determined using the MTT colorimetric assay. Cisplatin was used as positive control. From this MTT method, inhibitory concentration 50% (IC50) values were determined by probit analysis based on the relationship between log concentrations versus the percentage of cells growth inhibition.The results showed that the IC50 of ((E)-1-(4-aminophenyl)-3-phenylprop-2-en-1-one)) and cisplatinwere 22.75 ± 19.13 μg/mL and 14.96±1.08 μg/mL, respectively. In conclusion, the ((E)-1-(4-aminophenyl)-3-phenylprop-2-en-1-one)) has moderate cytotoxic activity against HeLa cell line based on National Cancer Institute (NCI) criteria.


2018 ◽  
Vol 2 (3) ◽  
pp. 122-125 ◽  
Author(s):  
Gujjula Nishitha ◽  
◽  
Gurram Asha Latha ◽  
Lagadapati Tejaswini ◽  
Amrutha Mounica ◽  
...  

2019 ◽  
Vol 8 (2S8) ◽  
pp. 1715-1718

Approval of the helpful restorative properties of different indigenous plants has increased monstrous significance as they can be utilized as an elective wellspring of lead mixes in pharmacological ventures to handle numerous advanced issues, for example, tranquilize obstruction in microorganisms and nonparticularity in chemotherapeutic operators. Cissusquadrangularis Linn.is one such plant which has been generally utilized for therapeutic purposes in customary frameworks of prescription. Thus this work looks to approve the anticancer property of methanolic and ethanolic concentrates of the plant against HeLa cell line. The IC50 fixation was recorded at 62.5 ug/ml for methanolic separate and 125ug/ml for ethanolic remove. The outcomes unmistakably uncovered that the methanolic concentrate of Cissusquadrangularis was progressively powerful on HeLa cell line when contrasted with ethanolic extricate.


2016 ◽  
Vol 4 (5) ◽  
pp. 1258-1267 ◽  
Author(s):  
Shivangi Mathur ◽  
◽  
Rinkal Mulani ◽  
L.B. George ◽  
Chiranjivi Barot ◽  
...  

2010 ◽  
Vol 10 (2) ◽  
pp. 240-244 ◽  
Author(s):  
Heny Ekowati ◽  
Indwiani Astuti ◽  
Mustofa Mustofa

Calanone (coumarin derivate compound), isolated from Calophyllum sp. had been shown to have cytotoxic activity on leukemia L1210 cell line with IC50 = 59.40 mg/mL. Calanone presumed have anticancer activity on HeLa cervical carcinoma cell. This study was conducted to investigate the cytotoxic and apoptotic activity of calanone and its effect to p53 and p21 expression on HeLa cervical carcinoma cell. Cytotoxic assay of calanone was performed on HeLa cell line, using MTT assay. Apoptotic assay was performed on HeLa cell line incubated with calanone for 24 h, by immunofluororescence method, using fluorochromes ethidium bromide and acridine orange. Expression of p53 was examined on HeLa cell line, by PCR with p53 wild-type primer. Expression of p21 was examined on HeLa cell line, by immunohistochemistry method. 5-fluorourasil was used as positive control in cytotoxic, apoptotic assay, and p53 expression. The result showed that calanone has cytotoxic activity on HeLa cell line, with IC50 = 22.887 mg/mL, caused cytotoxicity through apoptotic mechanism, increase p53 tumor suppressor gene expression, while the p21 expression test showed a negative result.   Keywords: Calanone, cytotoxic, HeLa cell line


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