GLPBio

Y-33075

Catalog No.: GC37947Purity:>98.00%Synonyms: RKI-983, SNJ-1656, Y-39983
Y-33075 ist ein selektiver ROCK-Inhibitor, abgeleitet von Y-27632, und mit einem IC50 von 3,6 nM wirksamer als Y-27632.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


Y-33075
Cas No.: 199433-58-4
10mM (in 1mL DMSO)In Stock
$54.00
1
5mgIn Stock
$49.00
1
10mgIn Stock
$81.00
1
25mgIn Stock
$168.00
1
50mgIn Stock
$270.00
1
100mgIn Stock
$420.00
1

Zitate (Citations)

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    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Y-33075 is a potent ROCK (Rho-associated protein kinase) inhibitor with an IC50 value of 3.6nM[1]. ROCK is a serine-threonine kinase belonging to the AGC (PKA/PKG/PKC) family of kinases and is present in mammals, zebrafish, Xenopus laevis, invertebrates, and chickens[2]. Y-33075 exhibits neuroprotective effects on retinal ganglion cells (RGCs)[3]. Treatment of Xenopus laevis with Y-33075 can disrupt the homeostasis of ciliated epithelial tissues, leading to abnormal epithelial growth at the tail margins[4].

In vitro, treatment of primary hepatic stellate cells (HSCs) isolated from FVB/NJ mice and the immortalized human hepatic stellate cell line (TWNT-4 cells) with Y-33075 (10nM-10µM) for 24h significantly reduced the contraction, fibrosis, and proliferation of activated mouse HSCs and TWNT-4 cells, while significantly increasing the migration of mouse HSCs[5]. Treatment of activated LX-2 cells with Y-33075 (10nM) downregulated the expression of ROCK and p-MLC and upregulated the expression of cAMP and PKA[6].

References:
[1] Vercammen H, Ondra M, Kotulova J, et al. “Keep on ROCKIn”: Repurposed ROCK inhibitors to boost corneal endothelial regeneration[J]. Biomedicine & Pharmacotherapy, 2024, 174: 116435.
[2] Amin F, Ahmed A, Feroz A, et al. An update on the association of protein kinases with cardiovascular diseases[J]. Current Pharmaceutical Design, 2019, 25(2): 174-183.
[3] Reboussin É, Bastelica P, Benmessabih I, et al. Evaluation of Rho kinase inhibitor effects on neuroprotection and neuroinflammation in an ex-vivo retinal explant model[J]. Acta Neuropathologica Communications, 2024, 12(1): 150.
[4] Khan F, Pitstick L, Lara J, et al. Rho-Associated protein kinase activity is required for tissue homeostasis in the Xenopus laevis ciliated epithelium[J]. Journal of Developmental Biology, 2024, 12(2): 17.
[5] Bachtler N, Torres S, Ortiz C, et al. The non-selective Rho-kinase inhibitors Y-27632 and Y-33075 decrease contraction but increase migration in murine and human hepatic stellate cells[J]. PLoS One, 2023, 18(1): e0270288.
[6] Zeng R, Guo Y, Qi J, et al. Dantao formula alleviates hepatic fibrosis and portal hypertension via modulation of the cAMP/PKA/ROCK signaling pathway in hepatic stellate cells[J]. Journal of Ethnopharmacology, 2025: 120650.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

Primary isolated HSC from FVB/NJ mice、the immortalized human HSC line TWNT-4

Preparation Method

Primary isolated HSC from FVB/NJ mice and the immortalized human HSC line TWNT-4 were culture-activated and incubated with Y-27632 and Y-33075 (10nM to 10μM) for 24h. Protein expression levels were analyzed by Western Blots and transcriptional levels of profibrotic markers and proliferative markers were evaluated using real-time qPCR. Migration was investigated by wound-healing assay. Proliferation was assessed by BrdU assay.

Reaction Conditions

10nM-10µM; 24h

Applications

Both Rho-kinase inhibitors, Y-27632 and Y-33075, reduced contraction, fibrogenesis and proliferation in activated primary mouse HSC (FVB/NJ) and human HSC line (TWNT-4) significantly. Y-33075 demonstrated a 10-times increased potency compared to Y-27632. Both inhibitors mediated a substantial and unexpected increase in migration of HSC in FVB/NJ.

References:
[1] Bachtler N, Torres S, Ortiz C, et al. The non-selective Rho-kinase inhibitors Y-27632 and Y-33075 decrease contraction but increase migration in murine and human hepatic stellate cells[J]. PLoS One, 2023, 18(1): e0270288.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
199433-58-4
Synonyme
RKI-983, SNJ-1656, Y-39983
SMILES
O=C(NC1=C2C(NC=C2)=NC=C1)C3=CC=C(C=C3)[C@H](N)C
Summenformel
C16H16N4O
Molekulargewicht
280.32
Löslichkeit
DMSO: 50 mg/mL (178.37 mM and warming); Water: < 0.1 mg/mL (insoluble)
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

Reviews

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