CAY10746 - ≥99% , CAS No.2247240-76-0

CAS: 2247240-76-0 Cat. No.: C651177 Summenformel: C26H23N3O5 Molekulargewicht: 457.48
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GRADE & PURITY ≥99%
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Deutschland (EU)
USA*
Price
Qty
1mg
C651177-1mg
Auf Bestellung · 8–12 Wochen
382,59€
5mg
C651177-5mg
Auf Bestellung · 8–12 Wochen
955,29€
10mg
C651177-10mg
Auf Bestellung · 8–12 Wochen
1.528,00€
25mg
C651177-25mg
Auf Bestellung · 8–12 Wochen
2.430,45€
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

CAY10746 is a selective Rho kinase (ROCK) inhibitor. CAY10746 has inhibitory activity for ROCK I , ROCK II with IC 50 values of 0.014 μM and 0.003 μM, respectively. CAY10746 can be used for the research of diabetic retinopathy (DR)

In Vitro

CAY10746 (compound 12j) has inhibitory activity for ROCK I, ROCK II with IC 50 values of 0.014 μM and 0.003 μM, respectively. CAY10746 (0.1, 1 and 10 μM; 0.25, 1, 2 and 4 h) inhibits ROCK kinase activity in SH-SY5Y cells. CAY10746 (1 μM; 24 h, 36 h) inhibits endothelial cell migration in vitro. CAY10746 (1 μM; 5 days) protects retinal neurons from high glucose-induced oxidative stress and apoptosis-mediated cell death. CAY10746 (1 μM; 5 days) suppresses the improper proliferation of Müller cells and promoted the regression of vascular vessels in retinal explants cultured in a high glucose microenvironment. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: SH-SY5Y cells Concentration: 0.1, 1 and 10 μM; 10 μM Incubation Time: 2 h; 0.25, 1, 2 and 4 h Result: Inhibited the phosphorylation of MYPT1 but did not impact the MYPT1 expression in dose-dependence and time- dependence. Cell Proliferation AssayCell Line: SH-SY5Y cells Concentration: 1 μM Incubation Time: 5 days Result: Significantly protected the cells from death. Cell Migration AssayCell Line: HUVEC cells Concentration: 1 μM Incubation Time: 24 h, 36 h Result: Significantly reduced migrating cell numbers and significantly reduce the rate of wound healing at 24 h and 36 h. Apoptosis AnalysisCell Line: ex vivo DR model Concentration: 1 μM Incubation Time: 5 days Result: Significantly protected neuronal cells from death.

Form:Solid

IC50& Target:IC50: 0.014 μM (ROCK I),0.003 μM (ROCK II)

Specifications

Spezifikationen & Reinheit
≥99%
Biochemische und physiologische Mechanismen
CAY10746 is a selective Rho kinase (ROCK) inhibitor. CAY10746 has inhibitory activity for ROCK I , ROCK II with IC 50 values of 0.014 μM and 0.003 μM, respectively. CAY10746 can be used for the research of diabetic retinopathy (DR).
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
INHIBITOR
Reinheit
≥99%
Namen und Kennungen
Molekulargewicht 457.48

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
LöslichkeitDMSO : 83.33 mg/mL (182.15 mM; ultrasonic and warming and heat to 60°C)
Lösungsrechner
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