Thiazovivin (Synonyms: Tzv) |
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Catalog No.GC11181
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Thiazovivin es un inhibidor selectivo de la quinasa asociada a Rho (ROCK)
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1226056-71-8
Sample solution is provided at 25 µL, 10mM.
Thiazovivin es un inhibidor selectivo de la quinasa asociada a Rho (ROCK) [1]. Thiazovivin inhibe selectivamente la vías de señalización ROCK, reduce la tensión citoesquelética, reduce la apoptosis celular inducida por el estrés, promueve la adhesión y propagación celular y, por lo tanto, mejora la supervivencia celular en un estado unicelular [2-3]. Thiazovivin se utiliza a menudo en la investigación de células madre y la ingeniería celular [4].
En las células endoteliales corneales humanas (HCEC), Thiazovivin (2µM, 4µM, 6µM; 24h, 48h) mejora la morfología de la HCEC, las uniones celulares y la expresión del transportador de iones al inhibir EndMT/EMT [5]. En las células madre embrionarias humanas el tratamiento con Thiazovivin (2µM; 24h) mejora el mantenimiento del tallo en poblaciones putativas de células madre de ganado al promover la expresión de los genes marcadores de pluripotencia, así como mejorar la expresión del gen E-cadherin, lo que resulta en un aumento en la adhensión celular [1]. En las células endoteliales corneales humanas, el tratamiento con Thiazovivin (2µM, 4µM, 6µM; 24h) mejoró la morfología, conectividad y función celular, e inhibió significativamente la expresión de la proteína ROCK[6]. En embriones bovinos, el tratamiento con Thiazovivin (2µM; 96h) mejora la supervivencia embrionaria y las tasas de eclosión [7]. En las células musculares lisas humanas, Thiazovivin (2µM; 2h) revierte la fosforilación inducida por AngII de MYPT1 y MLC [8].
References:
[1]. Park S, Kim D, Jung YG, et al. Thiazovivin, a Rho kinase inhibitor, improves stemness maintenance of embryo-derived stem-like cells under chemically defined culture conditions in cattle. Animal reproduction science. 2015 Oct 1; 161: 47-57.
[2]. Mohseni R, Shoae‐Hassani A, Verdi J. Reprogramming of endometrial adult stromal cells in the presence of a ROCK inhibitor, thiazovivin, could obtain more efficient iPSCs. Cell biology international. 2015 May; 39(5): 515-518.
[3]. Laowtammathron C, Chingsuwanrote P, Srisook P, et al. The novel combination of small-molecule inhibitors increases the survival and colony formation capacity of human induced pluripotent stem cells after single-cell dissociation. Science Progress. 2025 Apr; 108(2): 00368504251330956.
[4]. Rizzino A. Stimulating progress in regenerative medicine: improving the cloning and recovery of cryopreserved human pluripotent stem cells with ROCK inhibitors. Regenerative medicine. 2010 Sep 1; 5(5): 799-807.
[5]. Wu Q, Ouyang C, Xie L, et al. The ROCK inhibitor, thiazovivin, inhibits human corneal endothelial‑to‑mesenchymal transition/epithelial‑to‑mesenchymal transition and increases ionic transporter expression. International journal of molecular medicine. 2017 Oct 1; 40(4): 1009-1018.
[6]. Wu QN, Ling YZ, Ouyang C, et al. Effect of a new ROCK inhibitor thiazovivin on the morphology and function of human corneal endothelial cells. [Zhonghua yan ke za Zhi] Chinese Journal of Ophthalmology. 2016 Sep 1; 52(9): 686-692.
[7]. Kim D, Sul H, Jung YG, et al. Holding of bovine blastocysts at suprazero temperatures using small molecules. Scientific Reports. 2017 Aug 25; 7(1): 9490.
[8]. Cao X, Luo T, Luo X, et al. Resveratrol prevents AngII-induced hypertension via AMPK activation and RhoA/ROCK suppression in mice. Hypertension Research. 2014 Sep; 37(9): 803-810.
| Experimentos celulares [1]: | |
Líneas celulares | Células endoteliales corneales humanas (HCEC) |
Método de preparación | Las HCEC primarias y de paso se cultivaron, y las células se identificaron observando la morfología celular bajo un microscopio de luz y a través de experimentos de tinción de inmunofluorescencia NSE. Cuando la confluencia de células primarias estaba cerca del 70%-80%, se añadió un 0,25% de tripsina-EDTA (1X) para la digestión. Después de la centrifugación, las células fueron subcultivadas (1-3 generaciones). Los HCEC primarios y de paso se cultivaron en placas de cultivo de cámara de 8 pozos. Cuando la confluencia celular alcanzó aproximadamente el 80 %, se añadieron varias concentraciones de tiazovina (2, 4 y 6 µM), DMSO al 0,6 % o 10 µM Y-27632. |
Condiciones de reacción | 2 µM, 4µM, 6µM; 24h, 48h |
Áreas de aplicación | La tiazovivina mejora la morfología de la HCEC, las uniones celulares y la expresión del transportador iónico inhibiendo EndMT/EMT. |
References: | |
| Cas No. | 1226056-71-8 | SDF | |
| Sinónimos | Tzv | ||
| Chemical Name | N-benzyl-2-(pyrimidin-4-ylamino)-1,3-thiazole-4-carboxamide | ||
| Canonical SMILES | C1=CC=C(C=C1)CNC(=O)C2=CSC(=N2)NC3=NC=NC=C3 | ||
| Formula | C15H13N5OS | M.Wt | 311.36 |
| Solubility | ≥ 15.55mg/mL in DMSO | Storage | Store at -20°C |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 3.2117 mL | 16.0586 mL | 32.1172 mL |
| 5 mM | 642.3 μL | 3.2117 mL | 6.4234 mL |
| 10 mM | 321.2 μL | 1.6059 mL | 3.2117 mL |
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Quality Control & SDS
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- Purity: >98.00% Appearance: A solid
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Average Rating: 5 (Based on Reviews and 24 reference(s) in Google Scholar.)















