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Umbelliferone–oxindole hybrids as novel apoptosis inducing agents
In furtherance of our endeavour towards the synthesis of novel bioactive agents, a panel of ( E )-3-((7-hydroxy-4-methyl-2-oxo-2 H -chromen-8-yl)methylene)indolin-2-one derivatives were synthesized using diverse 5-substituted oxindoles and 7-hydroxy-4-methyl-2-oxo-2 H -chromene-8-carbaldehyde ( 3a )...
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Published in: | New journal of chemistry 2017, Vol.41 (21), p.12604-12610 |
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container_end_page | 12610 |
container_issue | 21 |
container_start_page | 12604 |
container_title | New journal of chemistry |
container_volume | 41 |
creator | Nagarsenkar, Atulya Guntuku, Lalita Prajapti, Santosh Kumar Guggilapu, Sravanthi Devi Sonar, Rajkiran Vegi, Ganga Modi Naidu Babu, Bathini Nagendra |
description | In furtherance of our endeavour towards the synthesis of novel bioactive agents, a panel of (
E
)-3-((7-hydroxy-4-methyl-2-oxo-2
H
-chromen-8-yl)methylene)indolin-2-one derivatives were synthesized using diverse 5-substituted oxindoles and 7-hydroxy-4-methyl-2-oxo-2
H
-chromene-8-carbaldehyde (
3a
). These synthesized analogues were further evaluated for their
in vitro
cytotoxic activity against MDA-MB-231 (breast), MCF-7 (breast), DU145 (prostate), PC-3 (prostate) and A549 (lung) cancer cell lines by employing the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Among all the synthesized compounds, compounds
7q
(IC
50
= 9.52 and 9.9 μM) and
7r
(IC
50
= 15.3 and 11.7 μM) showed the most significant cytotoxicity towards DU145 and PC-3 cancer cell lines respectively. Compounds
7q
and
7r
were found to be comparatively safe towards normal human prostate epithelial (RWPE-1) cells. The apoptosis inducing effect of compounds
7q
and
7r
on PC-3 and DU145 cancer cells was further investigated using the annexin V-FITC/propidium iodide staining assay, which confirmed the increase in the percentage of early apoptotic cells. Moreover, the cell cycle analysis revealed cell cycle arrest particularly at the G0/G1 phase in the PC-3 and DU145 cells. In addition, the treatment with compounds
7q
and
7r
led to collapse of the mitochondrial membrane potential (DΨm) and increased levels of reactive oxygen species (ROS) in the PC-3 and DU145 cells. Western blotting was performed to examine the appearance of active forms of cytochrome
c
and cleaved PARP (Poly ADP ribose polymerase), indicator proteins of apoptosis in PC-3 cells; the study confirmed the triggering of the mitochondrial mediated apoptotic pathway upon exposure to compounds
7q
and
7r
. |
doi_str_mv | 10.1039/C7NJ02578E |
format | article |
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E
)-3-((7-hydroxy-4-methyl-2-oxo-2
H
-chromen-8-yl)methylene)indolin-2-one derivatives were synthesized using diverse 5-substituted oxindoles and 7-hydroxy-4-methyl-2-oxo-2
H
-chromene-8-carbaldehyde (
3a
). These synthesized analogues were further evaluated for their
in vitro
cytotoxic activity against MDA-MB-231 (breast), MCF-7 (breast), DU145 (prostate), PC-3 (prostate) and A549 (lung) cancer cell lines by employing the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Among all the synthesized compounds, compounds
7q
(IC
50
= 9.52 and 9.9 μM) and
7r
(IC
50
= 15.3 and 11.7 μM) showed the most significant cytotoxicity towards DU145 and PC-3 cancer cell lines respectively. Compounds
7q
and
7r
were found to be comparatively safe towards normal human prostate epithelial (RWPE-1) cells. The apoptosis inducing effect of compounds
7q
and
7r
on PC-3 and DU145 cancer cells was further investigated using the annexin V-FITC/propidium iodide staining assay, which confirmed the increase in the percentage of early apoptotic cells. Moreover, the cell cycle analysis revealed cell cycle arrest particularly at the G0/G1 phase in the PC-3 and DU145 cells. In addition, the treatment with compounds
7q
and
7r
led to collapse of the mitochondrial membrane potential (DΨm) and increased levels of reactive oxygen species (ROS) in the PC-3 and DU145 cells. Western blotting was performed to examine the appearance of active forms of cytochrome
c
and cleaved PARP (Poly ADP ribose polymerase), indicator proteins of apoptosis in PC-3 cells; the study confirmed the triggering of the mitochondrial mediated apoptotic pathway upon exposure to compounds
7q
and
7r
.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/C7NJ02578E</identifier><language>eng</language><ispartof>New journal of chemistry, 2017, Vol.41 (21), p.12604-12610</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c231t-5d3692f046e3f5e6bf5dd2e96d6730400c9579061235858b295aeb8258c0bd5b3</citedby><cites>FETCH-LOGICAL-c231t-5d3692f046e3f5e6bf5dd2e96d6730400c9579061235858b295aeb8258c0bd5b3</cites><orcidid>0000-0001-7339-6067 ; 0000-0001-7378-0878</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4022,27922,27923,27924</link.rule.ids></links><search><creatorcontrib>Nagarsenkar, Atulya</creatorcontrib><creatorcontrib>Guntuku, Lalita</creatorcontrib><creatorcontrib>Prajapti, Santosh Kumar</creatorcontrib><creatorcontrib>Guggilapu, Sravanthi Devi</creatorcontrib><creatorcontrib>Sonar, Rajkiran</creatorcontrib><creatorcontrib>Vegi, Ganga Modi Naidu</creatorcontrib><creatorcontrib>Babu, Bathini Nagendra</creatorcontrib><title>Umbelliferone–oxindole hybrids as novel apoptosis inducing agents</title><title>New journal of chemistry</title><description>In furtherance of our endeavour towards the synthesis of novel bioactive agents, a panel of (
E
)-3-((7-hydroxy-4-methyl-2-oxo-2
H
-chromen-8-yl)methylene)indolin-2-one derivatives were synthesized using diverse 5-substituted oxindoles and 7-hydroxy-4-methyl-2-oxo-2
H
-chromene-8-carbaldehyde (
3a
). These synthesized analogues were further evaluated for their
in vitro
cytotoxic activity against MDA-MB-231 (breast), MCF-7 (breast), DU145 (prostate), PC-3 (prostate) and A549 (lung) cancer cell lines by employing the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Among all the synthesized compounds, compounds
7q
(IC
50
= 9.52 and 9.9 μM) and
7r
(IC
50
= 15.3 and 11.7 μM) showed the most significant cytotoxicity towards DU145 and PC-3 cancer cell lines respectively. Compounds
7q
and
7r
were found to be comparatively safe towards normal human prostate epithelial (RWPE-1) cells. The apoptosis inducing effect of compounds
7q
and
7r
on PC-3 and DU145 cancer cells was further investigated using the annexin V-FITC/propidium iodide staining assay, which confirmed the increase in the percentage of early apoptotic cells. Moreover, the cell cycle analysis revealed cell cycle arrest particularly at the G0/G1 phase in the PC-3 and DU145 cells. In addition, the treatment with compounds
7q
and
7r
led to collapse of the mitochondrial membrane potential (DΨm) and increased levels of reactive oxygen species (ROS) in the PC-3 and DU145 cells. Western blotting was performed to examine the appearance of active forms of cytochrome
c
and cleaved PARP (Poly ADP ribose polymerase), indicator proteins of apoptosis in PC-3 cells; the study confirmed the triggering of the mitochondrial mediated apoptotic pathway upon exposure to compounds
7q
and
7r
.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpFj8FKxDAURYMoOI5u_IKshepL0qTNUsroKINunHVJmpcx0mlKUsXZ-Q_-oV_iiIKrexeXwz2EnDO4ZCD0VVM93AOXVb04IDMmlC40V-xw31lZFiBLdUxOcn4BYKxSbEaa9dZi3wePKQ749fEZ38PgYo_0eWdTcJmaTIf4hj01YxynmEOm-8VrF4YNNRscpnxKjrzpM5795ZysbxZPzbJYPd7eNderouOCTYV0-z_cQ6lQeInKeukcR62cqgSUAJ2WlQbFuJC1rC3X0qCtuaw7sE5aMScXv9wuxZwT-nZMYWvSrmXQ_ui3__riGyukTic</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Nagarsenkar, Atulya</creator><creator>Guntuku, Lalita</creator><creator>Prajapti, Santosh Kumar</creator><creator>Guggilapu, Sravanthi Devi</creator><creator>Sonar, Rajkiran</creator><creator>Vegi, Ganga Modi Naidu</creator><creator>Babu, Bathini Nagendra</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-7339-6067</orcidid><orcidid>https://orcid.org/0000-0001-7378-0878</orcidid></search><sort><creationdate>2017</creationdate><title>Umbelliferone–oxindole hybrids as novel apoptosis inducing agents</title><author>Nagarsenkar, Atulya ; Guntuku, Lalita ; Prajapti, Santosh Kumar ; Guggilapu, Sravanthi Devi ; Sonar, Rajkiran ; Vegi, Ganga Modi Naidu ; Babu, Bathini Nagendra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c231t-5d3692f046e3f5e6bf5dd2e96d6730400c9579061235858b295aeb8258c0bd5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagarsenkar, Atulya</creatorcontrib><creatorcontrib>Guntuku, Lalita</creatorcontrib><creatorcontrib>Prajapti, Santosh Kumar</creatorcontrib><creatorcontrib>Guggilapu, Sravanthi Devi</creatorcontrib><creatorcontrib>Sonar, Rajkiran</creatorcontrib><creatorcontrib>Vegi, Ganga Modi Naidu</creatorcontrib><creatorcontrib>Babu, Bathini Nagendra</creatorcontrib><collection>CrossRef</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagarsenkar, Atulya</au><au>Guntuku, Lalita</au><au>Prajapti, Santosh Kumar</au><au>Guggilapu, Sravanthi Devi</au><au>Sonar, Rajkiran</au><au>Vegi, Ganga Modi Naidu</au><au>Babu, Bathini Nagendra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Umbelliferone–oxindole hybrids as novel apoptosis inducing agents</atitle><jtitle>New journal of chemistry</jtitle><date>2017</date><risdate>2017</risdate><volume>41</volume><issue>21</issue><spage>12604</spage><epage>12610</epage><pages>12604-12610</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>In furtherance of our endeavour towards the synthesis of novel bioactive agents, a panel of (
E
)-3-((7-hydroxy-4-methyl-2-oxo-2
H
-chromen-8-yl)methylene)indolin-2-one derivatives were synthesized using diverse 5-substituted oxindoles and 7-hydroxy-4-methyl-2-oxo-2
H
-chromene-8-carbaldehyde (
3a
). These synthesized analogues were further evaluated for their
in vitro
cytotoxic activity against MDA-MB-231 (breast), MCF-7 (breast), DU145 (prostate), PC-3 (prostate) and A549 (lung) cancer cell lines by employing the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Among all the synthesized compounds, compounds
7q
(IC
50
= 9.52 and 9.9 μM) and
7r
(IC
50
= 15.3 and 11.7 μM) showed the most significant cytotoxicity towards DU145 and PC-3 cancer cell lines respectively. Compounds
7q
and
7r
were found to be comparatively safe towards normal human prostate epithelial (RWPE-1) cells. The apoptosis inducing effect of compounds
7q
and
7r
on PC-3 and DU145 cancer cells was further investigated using the annexin V-FITC/propidium iodide staining assay, which confirmed the increase in the percentage of early apoptotic cells. Moreover, the cell cycle analysis revealed cell cycle arrest particularly at the G0/G1 phase in the PC-3 and DU145 cells. In addition, the treatment with compounds
7q
and
7r
led to collapse of the mitochondrial membrane potential (DΨm) and increased levels of reactive oxygen species (ROS) in the PC-3 and DU145 cells. Western blotting was performed to examine the appearance of active forms of cytochrome
c
and cleaved PARP (Poly ADP ribose polymerase), indicator proteins of apoptosis in PC-3 cells; the study confirmed the triggering of the mitochondrial mediated apoptotic pathway upon exposure to compounds
7q
and
7r
.</abstract><doi>10.1039/C7NJ02578E</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7339-6067</orcidid><orcidid>https://orcid.org/0000-0001-7378-0878</orcidid></addata></record> |
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title | Umbelliferone–oxindole hybrids as novel apoptosis inducing agents |
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