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Том 53, № 1 (2019) Synthesis, Characterization and Biological Evaluations of New Imidazo[4,5-a]Acridines as Potential Antibacterial Agents PDF
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Том 52, № 11 (2019) Synthesis and Anti-Inflammatory Activity of Tyrosol and Its Structural Analogs PDF
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Özdemir Z., Başak-Türkmen N., Ayhan İ., Çiftçi O., Uysal M.
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Trineeva O., Safonova E., Slivkin A.
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Murzina E., Sofronov G., Simbirtsev A., Ishchenko A., Antipova T., Aksenova N., Veselova O., Zatsepin V.
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Gmiro V., Serdyuk S., Veselkina O.
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Ukrainets I., Mospanova E., Bereznyakova N., Davidenko A.
Том 52, № 10 (2019) Synthesis and Neurotropic Activity of New Condensed Pyrano[4,3-b]-Pyridines Derivatives PDF
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Dabaeva V., Bagdasaryan M., Dashyan S., Dzhagatspanyan I., Nazaryan I., Akopyan A., Paronikyan R.
Том 52, № 10 (2019) Validation of Methods and Procedures in Pharmacopoeial Monographs in the Framework of a Drug Standardization Program PDF
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Olefir Y., Sakanyan E., Luttseva A., Babeshina L., Shemeryankina T.
Том 52, № 10 (2019) Chemoprevention of Radiation-Induced Carcinogenesis Using Decoction of Meadowsweet (Filipendula Ulmaria) Flowers PDF
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Том 52, № 9 (2018) Synthesis and Biological Properties of a New Dipeptide Mimetic of Brain-Derived Neurotrophic Factor Loop 2** PDF
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Том 52, № 9 (2018) Influence of Various Disintegrants on the Quality of Microcrystalline Cellulose Tablets PDF
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Zyryanova I., Larionov L., Shadrina E., Ivanenko M., Khonina T.
Том 52, № 9 (2018) Unfractionated Heparin Activity Testing in Preparations and Substances PDF
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Berkovskii A., Sergeeva E., Suvorov A.
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Том 52, № 8 (2018) Influence of New Promising Analgesic Compounds on Locomotor Activity of Mice PDF
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Palikova Y., Skobtsova L., Zharmukhamedova T., Palikov V., Rudenko V., Khokhlova O., Lobanov A., Rzhevskii D., Slashcheva G., D’yachenko E., Belous G., Andreev Y., Logashina Y., Kozlov S., Yavorskii A., Elyakova E., D’yachenko I.
Том 52, № 8 (2018) Antioxidant and Antiradical Activity of Drugs Intended for Treating Ophthalmic Disorders PDF
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Том 52, № 8 (2018) Tissue-Level Dynamics and Redox State of Coenzyme Q10 in Rats After Intravenous Injection of Ubiquinol PDF
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Shevchenko K., Andreeva L., Nagaev I., Shevchenko V., Myasoedov N.
Том 52, № 8 (2018) Synthesis and Antimicrobial, Antiprotozoal, and Fungistatic Activity of [5-(Amino-, Acylamino-, and 2-Pyridylmethylamino)-1-Alkylbenzimidazol-2-yl]Diphenylmethanols PDF
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Koshchienko Y., Drobin Y., Zubenko A., Timoshevskii D., Fetisov L., Bodryakov A.
Том 52, № 8 (2018) Synthesis and Analgesic, Anthelmintic, and Insecticidal Activity of 3,3-Dialkyl-1-(2-Phenylamino-2-Thioxoethyl)-3,4-Dihydroisoquinolinium Chlorides PDF
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Том 52, № 8 (2018) Optimization of the First Step of Enoxaparin Synthesis by Hydrolytic Depolymerization of Unfractionated Heparin PDF
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Frumin L., Yur’eva K., Askretkov A., Prokhorov D., Matveev A., Zhavoronok E., Panov A., Shatalov D., Shnyak E., Kedik S.
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Том 52, № 8 (2018) Local Analgesic Activity of Hemantane Gel Dosage Forms Evaluated Using the Formalin Test in Rats PDF
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Ivanova E., Matyushkin A., Blynskaya E., Voronina T.
Том 52, № 8 (2018) Cytotoxic Activity and Kinetic Release Study of Lovastatin-Loaded Ph-Sensitive Polymersomes PDF
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Nosrati H., Alimohammadi N., Manjili H., Danafar H.
Том 52, № 7 (2018) Synthesis and some Pharmacological Properties of an Immunoactive Lysine-Containing Tetrapeptide PDF
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Kholnazarov B., Bobizoda G., Olefir Y., Prokof’ev A., Sapovskii M., Evteev V., Bunyatyan N.
Том 52, № 7 (2018) Synthesis, Structure, and Anticaries Activity of 2-Amino-4,6-Dihydroxypyrimidinium Hexafluorosilicate PDF
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Том 52, № 7 (2018) Bioactivity of Three Salvia Species in Relation to Their Total Phenolic and Flavonoid Contents PDF
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Sharopov F., Valiev A., Sobeh M., Arnold E., Winka M.
Том 52, № 7 (2018) Effects of Novel Potential Analgesic Compounds on the Cardiovascular and Respiratory Systems PDF
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Palikova Y., Skobtsova L., Palikov V., Belous G., Khokhlova O., Lobanov A., Slashcheva G., Rzhevskii D., Rudenko V., Kalabina E., Osipova G., Andreev Y., Logashina Y., Kozlov S., Yavorskii A., Elyakova G., D’yachenko I.
Том 52, № 7 (2018) Analytical Method Development and Validation for HPLC-ECD Determination of Moxifloxacin in Marketed Formulations PDF
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Phani Sekhar Reddy G., Navyasree K., Jagadish P., Bhat K.
Том 52, № 7 (2018) Preparation and In Vitro/In Vivo Evaluation of Antihistaminic Ocular Inserts PDF
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Shah S., Nawaz A., Javed H., Rafiq M., Riaz R., Sadaquat H., Akhtar M.
Том 52, № 7 (2018) Comparative Analysis of the Heavy Metal, Aluminum, and Arsenic Contents in Brown Algae of Various Origins PDF
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Shchukin V., Kuz’mina N., Erina A., Yashkir V., Merkulov V.
Том 52, № 7 (2018) Quantification of Sofosbuvir in Human Plasma: RP-HPLC Method Development and Validation PDF
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Rathod R., Navyasree K., Bhat K.
Том 52, № 7 (2018) Validation of a Method for Assay of Trifluoroacetates in the Pharmaceutical Substance Glatiramer Acetate by 19F NMR Spectroscopy PDF
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Moiseev S., Kuz’mina N., Krylov V., Yashkir V., Merkulov V.
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Lukashov O., Kazakov P., Mirzabekova N.
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Том 52, № 6 (2018) Structure and Analgesic Activity of 13-(N-Aryl(N,N-Diethyl)Aminocarbonyl)-9-Methyl-11-Thioxo-8-Oxa-10,12-Diazatricyclo [7.3.1.02,7]Trideca-2,4,6-Trienes and Their 10-N-Phenyl Derivatives PDF
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Gein V., Zamaraeva T., Buzmakova N., Rudakova I., Dmitriev M.
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Vlasov S., Kovalenko S., Osolodchenko T., Lenitskaya E., Chernykh V.
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Skachilova S., Zheltukhin N., Sergeev V., Davydova N.
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Gil’deeva G., Yurkov V.
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Singh S., Verma R., Kumar L.
Том 52, № 6 (2018) Synthesis and Antimicrobial Activity of 5-(Arylmethylidene)-2,4,6-Pyrimidine-2,4,6(1H,3H,5H)-Triones PDF
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Luzhnova S., Tyrkov A., Gabitova N., Yurtaeva E.
Том 52, № 6 (2018) Development and Validation of a Stability-Indicating Liquid Chromatographic Method with Mass-Spectrometric Detection for the Analysis of Apixaban and Determination of Production Related Impurities PDF
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Arous B., Al-Mardini M.
Том 52, № 6 (2018) Development and Validation of GC-MS Bioanalytical Method to Detect Organic Acidemia in Neonatal/Pediatric Urine Samples PDF
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Dhokade P., Mathew E., Nalini K., Rao P., Lewis L., Moorkoth S.
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Sakhno N., Gunar O., Roshchina M., Kolosova L., Grigor’eva V.
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Том 52, № 6 (2018) Bioequivalence of a Dosage form of the New Drug Mefebut PDF
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Smirnova L., Suchkov E., Ryabukha A., Kuznetsov K., Velikopol’skaya M., Tyurenkov I., Bakulin D., Stepanova É., Shevchenko A.
Том 52, № 5 (2018) Synthesis and Biological Activity of 1-Chloromethyl- and 1-Dichloromethyl-3,3-Dialkyl-3,4-Dihydroisoquinolinium Chlorides PDF
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Kirillov N., Makhmudov R., Kashkin P., Nikiforova E., Mardanova L.
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Ovsepyan T., Dilanyan S., Arsenyan F., Muradyan R., Minasyan N., Melik-Ohanjanyan R.
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Tallerova A., Povarnina P., Blynskaya E., Bueva V., Alekseev K., Gudasheva T., Seredenin S.
Том 52, № 5 (2018) Synthesis and Neuropsychotropic Activity of Indole-Containing Gamma-Aminobutyric Acid Derivatives PDF
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Berestovitskaya V., Vasil’eva O., Ostroglyadov E., Aleksandrova S., Tyurenkov I., Merkushenkova O., Bagmetova V.
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Arutyunyan G., Arutyunyan A., Gevorkyan K., Gasparyan S., Paronikyan R., Stepanyan G., Minasyan N.
Том 52, № 5 (2018) Microwave-Assisted Synthesis, In Vivo Anti-Inflammatory and In Vitro Anti-Oxidant Activities, and Molecular Docking Study of New Substituted Schiff Base Derivatives PDF
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Hanif M., Hassan M., Rafiq M., Abbas Q., Ishaq A., Shahzadi S., Seo S., Saleem M.
Том 52, № 5 (2018) Technological Aspects of Ensuring the Specific Safety of Human Immunoglobulin and Albumin Preparations PDF
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Kornilova O., Krivykh M., Kudasheva É., Borisevich I.
Том 52, № 5 (2018) Development and Validation of a Liquid Chromatography Method for the Analysis of Rivaroxaban and Determination of Its Production Related Impurities PDF
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Arous B., Al-Mardini M., Karabet F., Daghestani M., Al-Lahham F., Al-Askar A.
Том 52, № 5 (2018) Synthesis and Antiproliferative Activity of Imidazole and Triazole Derivatives of Flavonoids PDF
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Sable P., Potey L.
Том 52, № 5 (2018) 3D-Modeling of the Influence of Isomalt, Glucose, and Compaction Pressure on the Quality of Ascorbic-Acid Tablets PDF
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Filimonova A., Tret’yakova Y., Gavrilov A.
Том 52, № 5 (2018) Alkaloid Content, Antioxidant and Cytotoxic Activities of Various Parts of Papaver somniferum PDF
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Sharopov F., Valiev A., Gulmurodov I., Sobeh M., Satyal P., Wink M.
Том 52, № 5 (2018) Synthesis, Antimicrobial Activity and QSAR Studies of Some New Sparfloxacin Derivatives PDF
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Kumar A., Grewal A., Singh V., Narang R., Pandita D., Lather V.
Том 52, № 4 (2018) Synthesis and Antimicrobial Activity of N-Decylpyridinium Salts with Inorganic Anions PDF
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Zhuravlev O., Voronchikhina L.
Том 52, № 4 (2018) Computer Analysis of the Structure–Activity Relationship for Immunoactive Thiazolo[3,2-a]Benzimidazole Derivatives PDF
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Dianov V., Alekhin E., Tyurina L., Aleksandrova E.
Том 52, № 4 (2018) Two New Antioxidative Geniposides (Ulmoside C, Ulmoside D) and 10-O-Acetylgeniposidic Acid from Eucommia Ulmoides PDF
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Xi Z., Khan S., Jichuan Z., Ullah H., Khan H., Zhang L.
Том 52, № 4 (2018) Synthesis and Antiproliferative Activity of Daunorubicin Conjugates with Sesquiterpene Lactones PDF
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Anikina L., Semakov A., Afanas’eva S., Pukhov S., Klochkov S.
Том 52, № 4 (2018) Synthesis and Tuberculostatic Activity of 2-Alkyl-5-Aryltetrazoles PDF
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Ishmetova R., Tolshchina S., Ignatenko N., Kravchenko M., Skornyakov S., Rusinov G., Charushin V.
Том 52, № 4 (2018) Water-Soluble Form of 1-Alkyl(Aryl)Imidazole-4,5-Dicarboxylic Acids. Structure and Anticonvulsant Activity of the Triethanolammonium Salt of 1-Propylimidazole-4,5-Dicarboxylic Acid PDF
(Eng)
Brusina M., Nikolaev D., Fundamenskii V., Gurzhii V., Zolotarev A., Selitrenikov A., Zevatskii Y., Potapkin A., Ramsh S., Piotrovskii L.
Том 52, № 4 (2018) Vasopressor Properties of Nitric Oxide Synthase Inhibitor T1059. Part I: Synthesis, Toxicity, NOS-Inhibition Activity, and Hemodynamic Effects Under Normotensive Conditions PDF
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Filimonova M., Shevchenko L., Makarchuk V., Chesnakova E., Surinova V., Shevchuk A., Filimonov A., Kryzhanovskii S., Shevchenko T., Bugrova A., Kalamkarov G.
Том 52, № 4 (2018) Antifungal Activity of Various Species and Strains of Turmeric (Curcuma SPP.) Against Fusarium Solani Sensu Lato PDF
(Eng)
Hou D., Akter J., Amzad Hossain M., Sano A., Takara K., Zahorul Islam M.
Том 52, № 4 (2018) Cytotoxic Effect of Fusarium Equiseti Fungus Metabolites Against N-Nitrosodiethylamine- and CCL4-Induced Hepatocarcinogenesis in Rats PDF
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Hawas U., Farrag A., Ahmed E., Abou El-Kassem L.
Том 52, № 4 (2018) A Stability-Indicating LC-MS Method for Determination of Perindopril and its Process Related Impurities PDF
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Kumar N., Sreenivasulu V., Ramachandra B., Asif M., Ibrahim A.
Том 52, № 4 (2018) Development of an HPLC-MS/MS Method for Quantitative Determination of Rivaroxaban in Human Blood Serum PDF
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Rodina T., Mel’nikov E., Aksenov A., Belkov S., Sokolov A., Prokof’ev A., Ramenskaya G.
Том 52, № 4 (2018) Granulation of Effervescent Ingredients for Optimization of Gastroretentive Properties of Floating Proroxan Prolonged-Release Tablets PDF
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Nifontova G., Krechetov S., Dolotova O., Buyukli S., Akhmetzyanova A., Krasnyuk I.
Том 52, № 4 (2018) Phytochemical Investigation, Antioxidant and Antimicrobial Assays of Algerian Plant Calamintha baborensis Batt. PDF
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Seraoui R., Benkiniouar R., Akkal S., Ros G., Nieto G.
Том 52, № 4 (2018) Development and Validation of an Express Technique for Isolation and Quantitative Determination of Water-Soluble Polysaccharides from Roots of Taraxacum Officinale Wigg. PDF
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D’yakova N., Slivkin A., Samylina I., Gaponov S., Myndra A., Shushunova T.
Том 52, № 3 (2018) Study on the Best Initial Processing Technology of Gastrodia Elata PDF
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Liu Y., Ran R., Huang G.
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Согласие на обработку персональных данных с помощью сервиса «Яндекс.Метрика»

1. Я (далее – «Пользователь» или «Субъект персональных данных»), осуществляя использование сайта https://journals.rcsi.science/ (далее – «Сайт»), подтверждая свою полную дееспособность даю согласие на обработку персональных данных с использованием средств автоматизации Оператору - федеральному государственному бюджетному учреждению «Российский центр научной информации» (РЦНИ), далее – «Оператор», расположенному по адресу: 119991, г. Москва, Ленинский просп., д.32А, со следующими условиями.

2. Категории обрабатываемых данных: файлы «cookies» (куки-файлы). Файлы «cookie» – это небольшой текстовый файл, который веб-сервер может хранить в браузере Пользователя. Данные файлы веб-сервер загружает на устройство Пользователя при посещении им Сайта. При каждом следующем посещении Пользователем Сайта «cookie» файлы отправляются на Сайт Оператора. Данные файлы позволяют Сайту распознавать устройство Пользователя. Содержимое такого файла может как относиться, так и не относиться к персональным данным, в зависимости от того, содержит ли такой файл персональные данные или содержит обезличенные технические данные.

3. Цель обработки персональных данных: анализ пользовательской активности с помощью сервиса «Яндекс.Метрика».

4. Категории субъектов персональных данных: все Пользователи Сайта, которые дали согласие на обработку файлов «cookie».

5. Способы обработки: сбор, запись, систематизация, накопление, хранение, уточнение (обновление, изменение), извлечение, использование, передача (доступ, предоставление), блокирование, удаление, уничтожение персональных данных.

6. Срок обработки и хранения: до получения от Субъекта персональных данных требования о прекращении обработки/отзыва согласия.

7. Способ отзыва: заявление об отзыве в письменном виде путём его направления на адрес электронной почты Оператора: info@rcsi.science или путем письменного обращения по юридическому адресу: 119991, г. Москва, Ленинский просп., д.32А

8. Субъект персональных данных вправе запретить своему оборудованию прием этих данных или ограничить прием этих данных. При отказе от получения таких данных или при ограничении приема данных некоторые функции Сайта могут работать некорректно. Субъект персональных данных обязуется сам настроить свое оборудование таким способом, чтобы оно обеспечивало адекватный его желаниям режим работы и уровень защиты данных файлов «cookie», Оператор не предоставляет технологических и правовых консультаций на темы подобного характера.

9. Порядок уничтожения персональных данных при достижении цели их обработки или при наступлении иных законных оснований определяется Оператором в соответствии с законодательством Российской Федерации.

10. Я согласен/согласна квалифицировать в качестве своей простой электронной подписи под настоящим Согласием и под Политикой обработки персональных данных выполнение мною следующего действия на сайте: https://journals.rcsi.science/ нажатие мною на интерфейсе с текстом: «Сайт использует сервис «Яндекс.Метрика» (который использует файлы «cookie») на элемент с текстом «Принять и продолжить».