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Ming-Xia Song, Chang-Ji Zheng, Xian-Qing Deng, Qing Wang, Shao-Pu Hou, Ting-Ting Liu, Xiao-Lan Xing, Hu-Ri Piao*. Synthesis and bioactivity evaluation of rhodanine derivatives as potential anti-bacterial agents. Eur J Med Chem. 2012. 54: 403-12.
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1.






Novel arylhydrazone derivatives bearing a rhodanine moiety: synthesis and evaluation of their antibacterial activities

×÷Õß: Li, Wei; Zheng, Chang-Ji; Sun, Liang-Peng; µÈ.

ARCHIVES OF PHARMACAL RESEARCH  ¾í: 37   ÆÚ: 7   Ò³: 852-861   ³ö°æÄê: JUL 2014

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Synthesis and evaluation of the antimicrobial activities of 3-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)-2-thioxothiazolidin-4-one derivatives

×÷Õß: Liu, Jia-Chun; Zheng, Chang-Ji; Wang, Meng-Xiao; µÈ.

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY  ¾í: 74   Ò³: 405-410   ³ö°æÄê: MAR 3 2014

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Synthesis of 5-Benzylidine-3-alpha-carboxy Ethyl Rhodanines and Study of their Anticancer Activity Against HeLa Cell Lines and Antibacterial Activity Against MRSA

×÷Õß: Sundaram, Kaveri; Ravi, Subban

ASIAN JOURNAL OF CHEMISTRY  ¾í: 25   ÆÚ: 18   Ò³: 10353-10356   ×Ó¼­: B   ³ö°æÄê: DEC 2013





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Synthesis and biological evaluation of rhodanine derivatives bearing a quinoline moiety as potent antimicrobial agents

×÷Õß: Guo, Meng; Zheng, Chang-Ji; Song, Ming-Xia; µÈ.

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS  ¾í: 23   ÆÚ: 15   Ò³: 4358-4361   ³ö°æÄê: AUG 1 2013

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Synthesis and biological evaluation of a new class of 4-aminoquinoline-rhodanine hybrid as potent anti-infective agents

×÷Õß: Chauhan, Kuldeep; Sharma, Moni; Saxena, Juhi; µÈ.

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY  ¾í: 62   Ò³: 693-704   ³ö°æÄê: APR 2013

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A Simple and Green Procedure for the Synthesis of 5-Arylidenerhodanines Catalyzed by Diammonium Hydrogen Phosphate in Water

×÷Õß: Han, Liangliang; Wu, Tao; Zhou, Zhongqiang

SCIENTIFIC WORLD JOURNAL    ÎÄÏ׺Å: 543768   ³ö°æÄê: 2013

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Synthesis and biological evaluation of 5-aryloxypyrazole derivatives bearing a rhodanine-3-aromatic acid as potential antimicrobial agents

×÷Õß: Zheng, Chang-Ji; Song, Ming-Xia; Sun, Liang-Peng; µÈ.

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS  ¾í: 22   ÆÚ: 23   Ò³: 7024-7028   ³ö°æÄê: DEC 1 2012

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Discovery of a new class of dithiocarbamates and rhodanine scaffolds as potent antifungal agents: synthesis, biology and molecular docking

×÷Õß: Chauhan, Kuldeep; Sharma, Moni; Singh, Pratiksha; µÈ.

MEDCHEMCOMM  ¾í: 3   ÆÚ: 9   Ò³: 1104-1110   ³ö°æÄê: SEP 2012

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Synthesis and bioactivity evaluation of rhodanine derivatives as potential anti-bacterial agents


×÷Õß:Song, MX (Song, Ming-Xia)[ 1 ] ; Zheng, CJ (Zheng, Chang-Ji)[ 1 ] ; Deng, XQ (Deng, Xian-Qing)[ 1 ] ; Wang, Q (Wang, Qing)[ 1 ] ; Hou, SP (Hou, Shao-Pu)[ 1 ] ; Liu, TT (Liu, Ting-Ting)[ 1 ] ; Xing, XL (Xing, Xiao-Lan)[ 1 ] ; Piao, HR (Piao, Hu-Ri)[ 1 ]




EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY



¾í: 54

Ò³: 403-412

DOI: 10.1016/j.ejmech.2012.05.023

³ö°æÄê: AUG 2012

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Five series of (Z)-5-(4-(2-oxo-2-phenylethoxy)benzylidene)-2-thioxothiazolidin-4-one derivatives (I-V) were synthesized, characterized, and evaluated for their anti-bacterial activity. Most of the synthesized compounds showed potent inhibition against several Gram-positive bacteria (including multidrug-resistant clinical isolates) with MIC values in the range of 1-32 mu g/mL. Compounds IIIi, Vb and Vc presented the most potent activity, showing four-fold more potency than norfloxacin (MIC = 8 mu g/mL and 4 mu g/mL) and 64-fold more activity than oxacillin (MIC > 64 mu g/mL) against MRSA CCARM 3167 and 3506 strains with MIC values of 1 mu g/mL, and 64-fold more potency than norfloxacin (MIC > 64 mu g/mL) and comparable activity to oxacillin (MIC = 1 mu g/mL) against the QRSA CCARM 3505 and 3519 strains. None of the compounds exhibited any activity against the Gram-negative bacteria Escherichia coli 1356 at 64 mu g/mL. (C) 2012 Elsevier Masson SAS. All rights reserved.


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×÷Õ߹ؼü´Ê:Rhodanine; Propanoic acid; Acetic acid; Anti-bacterial activity

KeyWords Plus:ANTIFUNGAL; INHIBITORS; 4-THIAZOLIDINONE; ACID


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ͨѶ×÷ÕßµØÖ·: Piao, HR (ͨѶ×÷Õß)





Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Jilin Province, Peoples R China.





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[ 1 ] Yanbian Univ, Coll Pharm, Affiliated Minist Educ, Key Lab Nat Resources & Funct Mol Changbai Mt, Yanji 133002, Jilin Province, Peoples R China





µç×ÓÓʼþµØÖ·:piaohuri@yahoo.com.cn


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National Science Foundation of China


20962021

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ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER, 23 RUE LINOIS, 75724 PARIS, FRANCE


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Ñо¿·½Ïòharmacology & Pharmacy

Web of Science Àà±ð:Chemistry, Medicinal


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ÓïÖÖ:English

Èë²ØºÅ: WOS:000307920600042

ISSN: 0223-5234


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