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Thiazovivin

CAS No.
1226056-71-8
Chemical Name:
Thiazovivin
Synonyms
TZV;CS-1925;Thiazovivin;Thiazovivin (Tzv);Thiazovivin, >=98%;Thiazovivin USP/EP/BP;N-Benzyl-2-(pyrimidin-4-ylamino)thiazole-4-carboxamide;N-Benzyl-2-(4-pyrimidinylamino)-1,3-thiazole-4-carboxamide;N-(Phenylmethyl)-2-(4-pyrimidinylamino)-4-thiazolecarboxamide;4-Thiazolecarboxamide, N-(phenylmethyl)-2-(4-pyrimidinylamino)-
CBNumber:
CB92512070
Molecular Formula:
C15H13N5OS
Molecular Weight:
311.36
MDL Number:
MFCD16495823
MOL File:
1226056-71-8.mol
MSDS File:
SDS
Last updated:2023-07-12 16:54:15

Thiazovivin Properties

Density 1.379
storage temp. -20°C
solubility DMSO: soluble20mg/mL, clear
form powder
pka 13.87±0.46(Predicted)
color , white to beige to brown
Stability Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months.

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22
WGK Germany  3
HS Code  2934100090
NFPA 704
0
2 0

Thiazovivin price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML1045 Thiazovivin ≥98% (HPLC) 1226056-71-8 5mg $149 2024-03-01 Buy
Sigma-Aldrich SML1045 Thiazovivin ≥98% (HPLC) 1226056-71-8 25mg $476 2024-03-01 Buy
Cayman Chemical 14245 Thiazovivin ≥98% 1226056-71-8 1mg $40 2024-03-01 Buy
Cayman Chemical 14245 Thiazovivin ≥98% 1226056-71-8 5mg $79 2024-03-01 Buy
Cayman Chemical 14245 Thiazovivin ≥98% 1226056-71-8 10mg $139 2024-03-01 Buy
Product number Packaging Price Buy
SML1045 5mg $149 Buy
SML1045 25mg $476 Buy
14245 1mg $40 Buy
14245 5mg $79 Buy
14245 10mg $139 Buy

Thiazovivin Chemical Properties,Uses,Production

Description

Thiazovivin is a novel ROCK inhibitor with IC50 of 0.5 μM in a cell-free assay, promotes hESC survival after single-cell dissociation.

In vitro

Although displaying little impact on cell proliferation, Thiazovivin treatment significantly enhances the survival of human embryonic stem cells (hESCs) after enzymatic dissociation more than 30-fold, while homogenously maintaining pluripotency with the characteristic colony morphology, expression of typical pluripotency markers such as alkaline phosphatase (ALP), and normal karyotype. Dissociated hESCs treated with Thiazovivin display dramatically increased adhesion to matrigel-or laminin-coated plates but not to gelatin-coated plates within a few hours. Thiazovivin treatment increases cell-ECM adhesion-mediated β1 integrin activity, which synergizes with growth factors to promote cell survival. In addition to activating integrin, Thiazovivin but not Tyrintegin (Ptn) protects hESCs from death in the absence of ECM in suspension through E-cadherin-mediated cell-cell interaction. Thiazovivin treatment potently inhibits endocytosis of E-cadherin, consequently stabilizing E-cadherin on the cell surface and leading to reestablishment of cell-cell interaction, which is essential for hESC survival in ECM-free conditions. Thiazovivin but not Tyrintegin (Ptn) at 2 μM inhibits Rho-associated kinase (ROCK) activity and protects hESCs at a similar level as the widely used selective ROCK inhibitor Y-27632 at 10 μM, suggesting that Rho-ROCK signaling regulates cell-ECM and cell-cell adhesion. [1] Thiazovivin at 1 μM increases the reprogramming efficiency of CB mononuclear cells to induced pluripotent stem cells (iPSCs) by more than 10 times.

Description

Thiazovivin (1226056-71-8) dramatically improves (200-fold) the efficiency of induced pluripotent stem cell generation from human fibroblasts.1 Induces direct conversion of porcine embryonic fibroblasts into adipocytes.2?Cell permeable.

Uses

A compound that improves the survival of human embryonic stem cells (hESCs) upon trypsinization. In combination with ALK5 (TGFβ receptor) inhibitor SB-431542 and MEK inhibitor PD-0325901 (P217450), Thiazovivin promotes the transformation of fibroblasts into stem cells with a 200-fold efficiency over the classic method

Uses

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 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.

storage

-20°C

References

1) Lin et al. (2009), A chemical platform for improved induction of iPSC; Nature Methods, 6 805 2) Zhu et al. (2012), Direct conversion of porcine embryonic fibroblasts into adipocytes by chemical molecules; Cell Reprogram., 14 99

Thiazovivin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 139)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 967 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226 sales@hzclap.com CHINA 6313 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29627 58

View Lastest Price from Thiazovivin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Thiazovivin pictures 2019-07-06 Thiazovivin
1226056-71-8
US $2.00 / KG 1KG 99% customise Career Henan Chemical Co
  • Thiazovivin pictures
  • Thiazovivin
    1226056-71-8
  • US $2.00 / KG
  • 99%
  • Career Henan Chemical Co
N-(Phenylmethyl)-2-(4-pyrimidinylamino)-4-thiazolecarboxamide Thiazovivin Thiazovivin N-(Phenylmethyl)-2-(4-pyrimidinylamino)-4-thiazolecarboxamide Thiazovivin, >=98% N-Benzyl-2-(pyrimidin-4-ylamino)thiazole-4-carboxamide Thiazovivin N-(Phenylmethyl)-2-(4-pyrimidinylamino)-4-thiazolecarboxamide N-Benzyl-2-(4-pyrimidinylamino)-1,3-thiazole-4-carboxamide CS-1925 Thiazovivin (Tzv) 4-Thiazolecarboxamide, N-(phenylmethyl)-2-(4-pyrimidinylamino)- Thiazovivin USP/EP/BP TZV 1226056-71-8 226056-71-8 Inhibitors Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Sulfur & Selenium Compounds