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Thiazovivin

Thiazovivin Struktur
1226056-71-8
CAS-Nr.
1226056-71-8
Englisch Name:
Thiazovivin
Synonyma:
TZV;CS-1925;Thiazovivin;Thiazovivin (Tzv);Thiazovivin, >=98%;Thiazovivin USP/EP/BP;Thiazovivin, ROCK inhibitor;Thiazovivin (DMSO solution), Rho kinase inhibitor;N-Benzyl-2-(pyrimidin-4-ylamino)thiazole-4-carboxamide;N-Benzyl-2-(4-pyrimidinylamino)-1,3-thiazole-4-carboxamide
CBNumber:
CB92512070
Summenformel:
C15H13N5OS
Molgewicht:
311.36
MOL-Datei:
1226056-71-8.mol

Thiazovivin Eigenschaften

Dichte
1.379
storage temp. 
-20°C
L?slichkeit
DMSO: soluble20mg/mL, clear
Aggregatzustand
powder
pka
13.87±0.46(Predicted)
Farbe
, white to beige to brown
Stabilit?t:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months.
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn
R-S?tze: 22
WGK Germany  3
HS Code  2934100090
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.

Thiazovivin Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

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

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.

Thiazovivin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Thiazovivin Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 147)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806
sales@capot.com China 29793 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 32956 60
career henan chemical co
+86-0371-86658258 +8613203830695
sales@coreychem.com China 29880 58
Biochempartner
0086-13720134139
candy@biochempartner.com CHINA 965 58
BOC Sciences
+1-631-485-4226
inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873
sales@chemdad.com China 39894 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49374 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000
marketing@targetmol.com United States 32161 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226
sales@hzclap.com CHINA 6312 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250
1026@dideu.com China 22787 58

1226056-71-8()Verwandte Suche:


  • 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
  • Thiazovivin (DMSO solution), Rho kinase inhibitor
  • Thiazovivin, ROCK inhibitor
  • 1226056-71-8
  • 226056-71-8
  • Inhibitors
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Sulfur & Selenium Compounds
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