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Synthesis antimicrobial and anticancer activity of N′-arylmethylidene-piperazine-1-carbothiohydrazide
Ten newly synthesized thiosemicarbazones of piperazine ( 3a – 3j ) were evaluated for their antibacterial and antifungal activity against non-pathogenic strains of Escherichia coli (NCIM 2068), Klebsiella pneumonia (NCIM 2957), Staphylococcus aureus (NCIM 2079), and Bacillus subtilis (NCIM 2921); pa...
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Published in: | Medicinal chemistry research 2013-06, Vol.22 (6), p.2802-2808 |
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container_start_page | 2802 |
container_title | Medicinal chemistry research |
container_volume | 22 |
creator | Kulandaivelu, Umasankar Shireesha, Boyapati Mahesh, Chidara Vidyasagar, Jannu Vincent Rao, Tadikonda Rama Jayaveera, K. N. Saiko, Philipp Graser, Geraldine Szekeres, Thomas Jayaprakash, Venkatesan |
description | Ten newly synthesized thiosemicarbazones of piperazine (
3a
–
3j
) were evaluated for their antibacterial and antifungal activity against non-pathogenic strains of Escherichia coli (NCIM 2068),
Klebsiella pneumonia
(NCIM 2957),
Staphylococcus aureus
(NCIM 2079), and
Bacillus subtilis
(NCIM 2921); pathogenic strains of
Vibrio cholerae
,
protease
,
Candida albicans
and
Aspergillus niger.
All the 10 compounds (
3a
–
3j
) were found to be better than Ciprofloxacin against
B. subtilis
and four molecules (
3c
,
3d, 3e,
and
3h)
against
S. aureus.
Compound
3j,
a derivative of benzophenone, has been identified as a potent and promising candidate against
C. albicans.
The compounds were also evaluated for their anticancer activity against HBL-100 and HL60 cell lines. Compound
3a,
a
p
-hydroxy benzaldehyde derivative, has been identified as a potent and promising candidate. |
doi_str_mv | 10.1007/s00044-012-0279-4 |
format | article |
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3a
–
3j
) were evaluated for their antibacterial and antifungal activity against non-pathogenic strains of Escherichia coli (NCIM 2068),
Klebsiella pneumonia
(NCIM 2957),
Staphylococcus aureus
(NCIM 2079), and
Bacillus subtilis
(NCIM 2921); pathogenic strains of
Vibrio cholerae
,
protease
,
Candida albicans
and
Aspergillus niger.
All the 10 compounds (
3a
–
3j
) were found to be better than Ciprofloxacin against
B. subtilis
and four molecules (
3c
,
3d, 3e,
and
3h)
against
S. aureus.
Compound
3j,
a derivative of benzophenone, has been identified as a potent and promising candidate against
C. albicans.
The compounds were also evaluated for their anticancer activity against HBL-100 and HL60 cell lines. Compound
3a,
a
p
-hydroxy benzaldehyde derivative, has been identified as a potent and promising candidate.</description><identifier>ISSN: 1054-2523</identifier><identifier>EISSN: 1554-8120</identifier><identifier>DOI: 10.1007/s00044-012-0279-4</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Original Research ; Pharmacology/Toxicology</subject><ispartof>Medicinal chemistry research, 2013-06, Vol.22 (6), p.2802-2808</ispartof><rights>Springer Science+Business Media New York 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c288t-3563d49948966130e2cb43156cb4967e4d4a9ee0f7869ccbf6996dcd3c62173e3</citedby><cites>FETCH-LOGICAL-c288t-3563d49948966130e2cb43156cb4967e4d4a9ee0f7869ccbf6996dcd3c62173e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Kulandaivelu, Umasankar</creatorcontrib><creatorcontrib>Shireesha, Boyapati</creatorcontrib><creatorcontrib>Mahesh, Chidara</creatorcontrib><creatorcontrib>Vidyasagar, Jannu Vincent</creatorcontrib><creatorcontrib>Rao, Tadikonda Rama</creatorcontrib><creatorcontrib>Jayaveera, K. N.</creatorcontrib><creatorcontrib>Saiko, Philipp</creatorcontrib><creatorcontrib>Graser, Geraldine</creatorcontrib><creatorcontrib>Szekeres, Thomas</creatorcontrib><creatorcontrib>Jayaprakash, Venkatesan</creatorcontrib><title>Synthesis antimicrobial and anticancer activity of N′-arylmethylidene-piperazine-1-carbothiohydrazide</title><title>Medicinal chemistry research</title><addtitle>Med Chem Res</addtitle><description>Ten newly synthesized thiosemicarbazones of piperazine (
3a
–
3j
) were evaluated for their antibacterial and antifungal activity against non-pathogenic strains of Escherichia coli (NCIM 2068),
Klebsiella pneumonia
(NCIM 2957),
Staphylococcus aureus
(NCIM 2079), and
Bacillus subtilis
(NCIM 2921); pathogenic strains of
Vibrio cholerae
,
protease
,
Candida albicans
and
Aspergillus niger.
All the 10 compounds (
3a
–
3j
) were found to be better than Ciprofloxacin against
B. subtilis
and four molecules (
3c
,
3d, 3e,
and
3h)
against
S. aureus.
Compound
3j,
a derivative of benzophenone, has been identified as a potent and promising candidate against
C. albicans.
The compounds were also evaluated for their anticancer activity against HBL-100 and HL60 cell lines. Compound
3a,
a
p
-hydroxy benzaldehyde derivative, has been identified as a potent and promising candidate.</description><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Original Research</subject><subject>Pharmacology/Toxicology</subject><issn>1054-2523</issn><issn>1554-8120</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9UMtOwzAQtBBIlMcHcMsPGNaPOPERVbykCg7A2XLsTeOqTSo7IIUT38Qn8SW4lDOnmR3trGaHkAsGlwygukoAICUFxinwSlN5QGasLCWtGYfDzCFzXnJxTE5SWgGICmQ5I8vnqR87TCEVth_DJrg4NMGu8-R_FWd7h7GwbgzvYZyKoS0evz-_qI3TeoNjN62Dxx7pNmwx2o-QKaPOxmYYuzB0k9-JHs_IUWvXCc__8JS83t68zO_p4unuYX69oI7X9UhFqYSXWstaK8UEIHeNFKxUGbSqUHppNSK0Va20c02rtFbeeeEUZ5VAcUrY_m7-I6WIrdnGsMlhDQOza8rsmzK5KbNrysjs4XtPyrv9EqNZDW-xzzH_Mf0A5CRu7Q</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Kulandaivelu, Umasankar</creator><creator>Shireesha, Boyapati</creator><creator>Mahesh, Chidara</creator><creator>Vidyasagar, Jannu Vincent</creator><creator>Rao, Tadikonda Rama</creator><creator>Jayaveera, K. N.</creator><creator>Saiko, Philipp</creator><creator>Graser, Geraldine</creator><creator>Szekeres, Thomas</creator><creator>Jayaprakash, Venkatesan</creator><general>Springer-Verlag</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20130601</creationdate><title>Synthesis antimicrobial and anticancer activity of N′-arylmethylidene-piperazine-1-carbothiohydrazide</title><author>Kulandaivelu, Umasankar ; Shireesha, Boyapati ; Mahesh, Chidara ; Vidyasagar, Jannu Vincent ; Rao, Tadikonda Rama ; Jayaveera, K. N. ; Saiko, Philipp ; Graser, Geraldine ; Szekeres, Thomas ; Jayaprakash, Venkatesan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-3563d49948966130e2cb43156cb4967e4d4a9ee0f7869ccbf6996dcd3c62173e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Biology</topic><topic>Original Research</topic><topic>Pharmacology/Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kulandaivelu, Umasankar</creatorcontrib><creatorcontrib>Shireesha, Boyapati</creatorcontrib><creatorcontrib>Mahesh, Chidara</creatorcontrib><creatorcontrib>Vidyasagar, Jannu Vincent</creatorcontrib><creatorcontrib>Rao, Tadikonda Rama</creatorcontrib><creatorcontrib>Jayaveera, K. N.</creatorcontrib><creatorcontrib>Saiko, Philipp</creatorcontrib><creatorcontrib>Graser, Geraldine</creatorcontrib><creatorcontrib>Szekeres, Thomas</creatorcontrib><creatorcontrib>Jayaprakash, Venkatesan</creatorcontrib><collection>CrossRef</collection><jtitle>Medicinal chemistry research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kulandaivelu, Umasankar</au><au>Shireesha, Boyapati</au><au>Mahesh, Chidara</au><au>Vidyasagar, Jannu Vincent</au><au>Rao, Tadikonda Rama</au><au>Jayaveera, K. N.</au><au>Saiko, Philipp</au><au>Graser, Geraldine</au><au>Szekeres, Thomas</au><au>Jayaprakash, Venkatesan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis antimicrobial and anticancer activity of N′-arylmethylidene-piperazine-1-carbothiohydrazide</atitle><jtitle>Medicinal chemistry research</jtitle><stitle>Med Chem Res</stitle><date>2013-06-01</date><risdate>2013</risdate><volume>22</volume><issue>6</issue><spage>2802</spage><epage>2808</epage><pages>2802-2808</pages><issn>1054-2523</issn><eissn>1554-8120</eissn><abstract>Ten newly synthesized thiosemicarbazones of piperazine (
3a
–
3j
) were evaluated for their antibacterial and antifungal activity against non-pathogenic strains of Escherichia coli (NCIM 2068),
Klebsiella pneumonia
(NCIM 2957),
Staphylococcus aureus
(NCIM 2079), and
Bacillus subtilis
(NCIM 2921); pathogenic strains of
Vibrio cholerae
,
protease
,
Candida albicans
and
Aspergillus niger.
All the 10 compounds (
3a
–
3j
) were found to be better than Ciprofloxacin against
B. subtilis
and four molecules (
3c
,
3d, 3e,
and
3h)
against
S. aureus.
Compound
3j,
a derivative of benzophenone, has been identified as a potent and promising candidate against
C. albicans.
The compounds were also evaluated for their anticancer activity against HBL-100 and HL60 cell lines. Compound
3a,
a
p
-hydroxy benzaldehyde derivative, has been identified as a potent and promising candidate.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><doi>10.1007/s00044-012-0279-4</doi><tpages>7</tpages></addata></record> |
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issn | 1054-2523 1554-8120 |
language | eng |
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source | Springer Nature |
subjects | Biochemistry Biomedical and Life Sciences Biomedicine Cell Biology Original Research Pharmacology/Toxicology |
title | Synthesis antimicrobial and anticancer activity of N′-arylmethylidene-piperazine-1-carbothiohydrazide |
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