The Crystal Structures of Three Rhodanine-3-Carboxylic Acids

被引:10
作者
Tejchman, Waldemar [1 ]
Skorska-Stania, Agnieszka [2 ]
Zeslawska, Ewa [1 ]
机构
[1] Pedag Univ, Inst Biol, Dept Chem, Podchorazych 2, PL-30084 Krakow, Poland
[2] Jagiellonian Univ, Fac Chem, Ingardena 3, PL-30060 Krakow, Poland
关键词
Rhodanine-3-acetic acid; N-(carboxyalkyl)rhodanine; X-ray crystal structure; Intermolecular interactions; Thiazolidine ring; RHODANINE DERIVATIVES; ANTIFUNGAL ACTIVITY; ACETIC ACID; AGENTS; EPALRESTAT; DATABASE; BEARING;
D O I
10.1007/s10870-016-0644-0
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The rhodanine derivatives show various pharmacological activities. Rhodanine-3-carboxylic acids can be used as the substrates in various synthesis of compounds containing rhodanine-3-carboxyalkyl moiety. In this paper new crystal structures of rhodanine-3-acetic acid and its two homologues, i.e. rhodanine-3-propionic acid and rhodanine-3-butyric acid, are reported. The relationship between the length of the alkyl chain and the geometry of these molecules was studied. The crystal network is dominated by strong hydrogen bonds O-H center dot center dot center dot O formed by the carboxyl groups. Additionally, weak C-H center dot center dot center dot O and C-H center dot center dot center dot S contacts are observed. To study the difference in intermolecular interactions of rhodanine-3-carboxylic acid, three crystal structures were determined by X-ray diffraction method. The crystal network in all studied structures is built of homosynthons and stabilized by weak C-H center dot center dot center dot O and C-H center dot center dot center dot S contacts.
引用
收藏
页码:181 / 187
页数:7
相关论文
共 28 条
[1]   The Cambridge Structural Database: a quarter of a million crystal structures and rising [J].
Allen, FH .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 2002, 58 (3 PART 1) :380-388
[2]   2H-chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents [J].
Azizmohammadi, Mohammad ;
Khoobi, Mehdi ;
Ramazani, Ali ;
Emami, Saeed ;
Zarrin, Abdolhossein ;
Firuzi, Omidreza ;
Miri, Ramin ;
Shafiee, Abbas .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2013, 59 :15-22
[3]   PATTERNS IN HYDROGEN BONDING - FUNCTIONALITY AND GRAPH SET ANALYSIS IN CRYSTALS [J].
BERNSTEIN, J ;
DAVIS, RE ;
SHIMONI, L ;
CHANG, NL .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1995, 34 (15) :1555-1573
[4]  
Bue-Valleskey JM, 1998, [No title captured], Patent No. [US 5716975 A, 5716975]
[5]  
Celestina SK, 2015, RES J PHARM BIOL CHE, V6, P1965
[6]   Discovery of a new class of dithiocarbamates and rhodanine scaffolds as potent antifungal agents: synthesis, biology and molecular docking [J].
Chauhan, Kuldeep ;
Sharma, Moni ;
Singh, Pratiksha ;
Kumar, Vikash ;
Shukla, Praveen K. ;
Siddiqi, Mohammad Imran ;
Chauhan, Prem. M. S. .
MEDCHEMCOMM, 2012, 3 (09) :1104-1110
[7]   Rhodanineacetic Acid Derivatives as Potential Drugs: Preparation, Hydrophobic Properties and Antifungal Activity of (5-Arylalkylidene-4-oxo-2-thioxo-1,3-thiazolidin-3-yl)acetic Acids [J].
Dolezel, Jan ;
Hirsova, Petra ;
Opletalova, Veronika ;
Dohnal, Jiri ;
Marcela, Vejsova ;
Kunes, Jiri ;
Jampilek, Josef .
MOLECULES, 2009, 14 (10) :4197-4212
[8]  
Farrugia L.J., 1997, J. Appl. Crystallogr., V30, P565, DOI DOI 10.1107/S0021889897003117
[9]   The Cambridge Structural Database in Retrospect and Prospect [J].
Groom, Colin R. ;
Allen, Frank H. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (03) :662-671
[10]   Synthesis and biological evaluation of rhodanine derivatives bearing a quinoline moiety as potent antimicrobial agents [J].
Guo, Meng ;
Zheng, Chang-Ji ;
Song, Ming-Xia ;
Wu, Yan ;
Sun, Liang-Peng ;
Li, Yin-Jing ;
Liu, Yi ;
Piao, Hu-Ri .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (15) :4358-4361