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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Samorodov, A.V.</author>
     <author>Yi, W.</author>
     <author>Kudlay, D.A.</author>
     <author>Smolyarchuk, E.A.</author>
     <author>Dobrynin, A.B.</author>
     <author>Khamatgalimov, A.R.</author>
     <author>Shchebneva, K.</author>
     <author>Kadomtseva, M.</author>
     <author>Komunarova, D.</author>
     <author>Strelnik, A.G.</author>
    </authors>
   </contributors>
   <titles>
    <title>Phosphorus-Derived Isatin Hydrazones: Synthesis, Structure, Thromboelastography, Antiplatelet, and Anticoagulation Activity Evaluation</title>
   </titles>
   <keywords>
    <keyword>isatin</keyword>
    <keyword>phosphorus</keyword>
    <keyword>hydrazones</keyword>
    <keyword>crystal structure</keyword>
    <keyword>hemostasis</keyword>
    <keyword>antithrombotic&#13;
activity</keyword>
    <keyword>Scopus</keyword>
    <keyword>Web of Science</keyword>
    <keyword>Белый список</keyword>
   </keywords>
   <dates>
    <year>2025</year>
    <pub-dates>
     <date>2026-05-21</date>
    </pub-dates>
   </dates>
   <doi>10.3390/ijms26136147</doi>
   <journal>INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES</journal>
   <abstract>A series of new isatin hydrazones bearing phosphorus-containing moiety was synthesized through a simple, high-yield and easy work-up reaction of phosphine oxide&#13;
(Phosenazide) or phosphinate (2-chloroethyl (4-(dimethylamino)phenyl)(2-hydrazinyl-2-&#13;
oxoethyl)phosphinate, CAPAH) hydrazides with aryl-substituted isatins. The 31P NMR&#13;
technique showed that, in most cases, out of 12 examples in solution, the ratio of the&#13;
two spatial isomers varied from 1:1 to 1:3. Quantum chemical calculations confirmed the&#13;
predominance of Z,syn form both in the gas phase and in solution. According to X-ray&#13;
analysis data in crystals, they exist only in Z,syn form too. Most of the phosphine oxide&#13;
derivatives and 5-methoxy- and 5-bromoaryl phosphinate analogs exhibit anti-aggregant&#13;
activity at the level of acetylsalicylic acid but inhibit platelet activation processes more effectively. The 5-chloro type phosphinate derivative exhibits anti-aggregant properties more&#13;
effectively than acetylsalicylic acid under the conditions of the tissue factor (TF)-activated&#13;
thromboelastography (TEG) model, the ex vivo thrombosis model. Thus, all the obtained&#13;
results can become the basis for future pharmaceutical developments to create effective&#13;
anti-aggregation drugs with broad antithrombotic potential.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/5381</url>
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    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/5574</url>
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