AGX51 - 10mM in DMSO , CAS No.330834-54-3

CAS: 330834-54-3 Cat. No.: A654898 Summenformel: C27H29NO4 Molekulargewicht: 431.52
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GRADE & PURITY 10mM in DMSO
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Deutschland (EU)
USA*
Price
Qty
1ml
A654898-1ml
Auf Bestellung · 8–12 Wochen
535,31€
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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

AGX51 is a first-in-class pan- Id (inhibitors of DNA-binding/differentiation proteins) antagonist and degrader. AGX51 inhibits the Id1-E47 interaction, leading to ubiquitin-mediated degradation of Ids, cell growth arrest, and reduces viability. AGX51 inhibits the TNBC cell lines with IC 50 s of nearly 25 μM. AGX51 can be used for the research of cancer

In Vitro

AGX51 (0-80 μM; 24 h) decreases ID1 protein levels in 4T1 cells. ?\nAGX51 (40 μM; 0-72 h) decreases ID1 levels protein with a 40 μM concentratio in 4T1 cells. ?\nAGX51 (40 μM; 24 h) influences 4T1 cells , ER+, HER2+, TNBC and three breast cancer PDX cell ines. ?\nAGX51 (0-80 μM; 24-48 h) influences cell cycle of 4T1 cells. ?\nAGX51 (40 μM; 4-24 h) influences phospho-histone H3 levels in 4T1 cells. ?\nAGX51 (40 μM; 24 h) influences ROS levels in 4T1 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: 4T1 cells Concentration: 0, 5, 10, 20, 40 and 80 μM Incubation Time: 24 hours Result: Decreased ID1 protein levels starting at a concentration of 40 μM in 4T1 cells. Western Blot AnalysisCell Line: 4T1 cells Concentration: 40 μM Incubation Time: 0, 2, 4, 8 , 12, 24, 48 and 72 hours Result: Decreased ID1 protein levels starting at 4 h, while until 24 h ID1 protein completely loss. Cell Viability AssayCell Line: 4T1 cells, HMLE RAS Twist , MDA-MB-157, MDA-MB-436, MDA-MB-231, MDA-MB-453, BT-474, MDA-MB-361, SK-BR-3, MCF-7, T47-D, PDX-BR7, PDX-IBT and PDX-BR11 Concentration: 40 μM Incubation Time: 24 hours Result: Inhibited 4T1, HMLE RAS Twist , MDA-MB-157, MDA-MB-436, SK-BR-3, MCF-7, PDX-BR7, PDX-IBT and PDX-BR11 cell lines with IC 50 s of 26.66, 8.7, 22.28, 30.91, 36.55, 60, 10.89, 11.97 and 18.56 μM, respectively. Cell Cycle AnalysisCell Line: 4T1 cells Concentration: 40 μM Incubation Time: 24 and 48 hours Result: Affected cell cycle of 4T1 cells with a G0/G1 phase accumulation. Cell Viability AssayCell Line: 4T1 cells Concentration: 40 μM Incubation Time: 4 and 24 hours Result: Reduced phospho-histone H3 levels in 4T1 cells. Cell Viability AssayCell Line: 4T1 cells Concentration: 40 μM Incubation Time: 24 hours Result: Increased ROS level of 4T1 cells and indicated ROS production is a main mechanism of cell killing.

In Vivo

AGX51 (50 mg/kg; i.p. twice a day for 4 weeks) inhibits lung metastasis . ?\nAGX51 (15 mg/kg; i.p. twice a day for 3 weeks) exibits anti-tumor activity with autochronous cancer . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Balb/c mice with luciferase-labeled 4T1 cells Dosage: 50 mg/kg Administration: Intraperitoneal injection; 60 mg/kg twice a day; for 4 weeks Result: Inhibited lung metastasis development. Animal Model: A/J mice with AOM colon tumor model Dosage: 15 mg/kg Administration: Intraperitoneal injection; 15 mg/kg twice a day; for 3 weeks Result: Dreased the colon tumors and exhibited anti-tumor activity in AOM colon tumor mice.

IC50& Target:IC50: 26.66 μM (4T1), 8.7 μM (HMLE RAS Twist), 22.28 μM (MDA-MB-157), 30.91 μM (MDA-MB-436), 36.55 μM (SK-BR-3), 60 μM (MCF-7), 10.89 μM (PDX-BR7), 11.97 μM (PDX-IBT) , 18.56 μM (PDX-BR11)

Specifications

Spezifikationen & Reinheit
10mM in DMSO
Biochemische und physiologische Mechanismen
AGX51 is a first-in-class pan- Id (inhibitors of DNA-binding/differentiation proteins) antagonist and degrader. AGX51 inhibits the Id1-E47 interaction, leading to ubiquitin-mediated degradation of Ids, cell growth arrest, and reduces viability. AGX51 inhi
Storage
Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
ANTAGONIST
Namen und Kennungen
Molekulargewicht 431.52

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:
Lösungsrechner
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Häufig gestellte Fragen

How should this product be stored?
Store at ?80 °C. Ultra-low temperature storage is required to maintain the specified shelf life.
How is this product shipped?
This product ships frozen with dry ice and cold packs. Unpack on arrival and transfer it to the storage condition stated above; handle dry ice with insulated gloves in a ventilated area.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 330834-54-3, the molecular formula is C27H29NO4, and the molecular weight is 431.52 g/mol.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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