Thiazovivin
SIGMA/SML1045 - ≥98% (HPLC)
Synonym: N-
CAS Number: 1226056-71-8
Empirical Formula (Hill Notation): C15H13N5OS
Molecular Weight: 311.36
Linear Formula: C15H13N5OS
Product Type: Chemical
assay | ≥98% (HPLC) |
color | , white to beige to brown |
form | powder |
InChI | 1S/C15H13N5OS/c21-14(17-8 |
InChI key | DOBKQCZBPPCLEG-UHFFFAOYSA |
Quality Level | 100 |
solubility | DMSO: 20 mg/mL, clear |
storage temp. | −20°C |
Application: | Thiazovivin has been used in the generation of induced pluripotent stem cells (iPSCs) and induced neural stem cells (iNSCs) from human urine cells. It has also been used to study the the effect of pro-fibrotic inhibition on cardiac reprogramming. |
Biochem/physiol Actions: | Thiazovivin is a Rho Kinase (ROCK) inhibitor that promotes the transformation of fibroblasts into stem cells with a 200-fold efficiency over the classic method when used in combination with ALK5 inhibitor SB-431542 (S4317) and MEK inhibitor PD-0325901 (PZ0162). Thiazovivin stabilizes E-cadherin on the cell surface, necessary for human embryonic stem cell survival in culture. When human embryonic stem cells are cut out from the colony, this key protein is disrupted and then internalized within the cell. Without e-cadherin on the cell surface, cell signaling between the cells and their environment is disrupted and the cells quickly die. |
Biochem/physiol Actions: | Thiazovivin is an inhibitor of Rho associated coiled-coil containing protein kinase (ROCK). In vitro studies prove that thiazovivin is efficient in stimulating better morphology, expression of ionic transporter and protein involved in cell adhesion. |
Other Notes: | 2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research |
Packaging: | 5, 25 mg in glass bottle |
Hazard Codes | Xn |
Risk Statements | 22 |
RIDADR | NONH for all modes of transport |
WGK Germany | WGK 3 |
Flash Point(F) | Not applicable |
Flash Point(C) | Not applicable |
Purity | ≥98% (HPLC) |
Storage Temp. | −20°C |
UNSPSC | 12352200 |