Thiazovivin

Modify Date: 2024-01-02 19:15:22

Thiazovivin Structure
Thiazovivin structure
Common Name Thiazovivin
CAS Number 1226056-71-8 Molecular Weight 311.362
Density 1.4±0.1 g/cm3 Boiling Point N/A
Molecular Formula C15H13N5OS Melting Point N/A
MSDS Chinese USA Flash Point N/A
Symbol GHS07
GHS07
Signal Word Warning

 Use of Thiazovivin


Thiazovivin is a potent ROCK inhibitor, which can protect human embryonic stem cells.

 Names

Name N-Benzyl-2-(pyrimidin-4-ylamino)thiazole-4-carboxamide
Synonym More Synonyms

 Thiazovivin Biological Activity

Description Thiazovivin is a potent ROCK inhibitor, which can protect human embryonic stem cells.
Related Catalog
Target

ROCK

In Vitro Thiazovivin is a ROCK inhibitor. Thiazovivin (2 μM) inhibits ROCK activity and protects human embryonic stem cells (hESCs). Thiazovivin significantly increases the survival of hESCs after dissociation while maintaining pluripotency. Thiazovivin enhances cell-ECM adhesion-mediated integrin signaling. Thiazovivin also stabilizes E-cadherin after cell dissociation to protect hESCs from death under ECM-free conditions[1]. Thiazovivin increases cellular attachment of embryo-derived stem-like cells (eSLCs) of cattle and formation of primary colonies on the feeder layer. Thiazovivin reinforces putative colony outgrowth and supports the expansion of eSLC cultures during the subculture for passaging. Furthermore, Thiazovivin causes greater expression of ectodermal lineage-specific genes in eSLCs of cattle[2].
Cell Assay For cell proliferation assays, embryo-derived stem-like cells (eSLCs) are newly passaged and cultured in 3i system for 48 h on the feeder-free condition to prevent contamination of the BrdU-positive feeder cells. Cells are fixed with 4% paraformaldehyde in PBS (pH 7.4) at 37°C for 2 h, acid-treated with 2 N HCl in PBS for 30 min at 45°C, equilibrated with 0.1 M borate buffer (pH 8.5), and finally incubated with blocking buffer (20% Calf serum; 0.1% Triton X-100; 1% DMSO in PBS) for 2 h. Fixed cells are immunostained with antibodies against anti-BrdU mouse monoclonal antibody IgG followed by incubation with the secondary antibodies FITC conjugated goat anti-mouse IgG. The treated cells are covered with slow-fade anti-fade with DAPI for nuclear staining and covered with a glass coverslip. Images are captured with the fluorescence microscope[2].
References

[1]. Xu Y, et al. Revealing a core signaling regulatory mechanism for pluripotent stem cell survival and self-renewal by small molecules. Proc Natl Acad Sci U S A. 2010 May 4;107(18):8129-34.

[2]. Park S, et al. Thiazovivin, a Rho kinase inhibitor, improves stemness maintenance of embryo-derived stem-like cells under chemically defined culture conditions in cattle. Anim Reprod Sci. 2015 Oct;161:47-57.

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Molecular Formula C15H13N5OS
Molecular Weight 311.362
Exact Mass 311.084076
PSA 108.04000
LogP 2.00
Appearance of Characters , white to beige to brown
Index of Refraction 1.691
Storage condition Store at -20°C
Water Solubility DMSO: soluble20mg/mL, clear

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Hazard Codes Xn
Risk Phrases 22
RIDADR NONH for all modes of transport
HS Code 2934100090

 Precursor & DownStream

Precursor  1

DownStream  0

 Customs

HS Code 2934100090
Summary 2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 Synonyms

Thiazovivin
4-Thiazolecarboxamide, N-(phenylmethyl)-2-(4-pyrimidinylamino)-
N-Benzyl-2-(pyrimidin-4-ylamino)-1,3-thiazole-4-carboxamide
N-Benzyl-2-(4-pyrimidinylamino)-1,3-thiazole-4-carboxamide
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