RX-3117 - 10mM in DMSO , CAS No.865838-26-2

CAS: 865838-26-2 Cat. No.: R655689 Peso molecular: 257.22 PubChem CID: 11242315
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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
Estado
Price
Qty
1ml
R655689-1ml
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299,90US$
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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.

Descripción general

RX-3117 (TV-1360) is a potent and orally active anticancer and antimetabolite agent. RX-3117 inhibits DNA methyltransferase 1 (DNMT1). RX-3117 shows antiproliferative and anti-tumour activity. RX-3117 induces cell cycle arrest at S phase and apoptosis .

In Vitro

RX-3117 causes both inhibition of DNA and RNA synthesis. ?\nRX-3117 (11.7, 21 μM; 48 h) shows antiproliferative activity in A549, SW1573 cells. ?\nRX-3117 is activated by uridine-cytidine kinase 2 (UCK2). ?\nRX-3117 (1-25 μM; 72 h) inhibits the growth of HCT-116, MDA-MB-231, PANC-1, Caki-1, MCF7, A549, MKN45, U251 cells with IC 50 s of 0.39, 0.18, 0.62, 0.84, 0.34, 0.34, 0.50, 0.83 μM, respectively. ?\nRX-3117 (5, 10 μM; 4 days) induces cell cycle arrest at S phase and apoptosis. ?\nRX-3117 (1-5 μM; 24 h) decreases the cellular amount of DNMT1 in a dose-dependent manner in MDA-MB-231. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: A549, SW1573 cells Concentration: 11.7, 21 µM Incubation Time: 48 h Result: Showed antiproliferative activity in A549 (63.7% cell growth), SW1573 cells (59% cell growth). Apoptosis AnalysisCell Line: A549, SW1573 NSCLC cells Concentration: 5 µM for A549 cells, 10 µM for SW1573 cells Incubation Time: 4 days Result: Induced cell cycle arrest at S phase and apoptosis.

In Vivo

RX-3117 (2, 10 mg/kg; i.p.; three times per week for five weeks) shows anti-tumour activity in nude mice. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Nude mice (human colon carcinoma HCT116 xenograft model)Dosage: 2, 10 mg/kg Administration: I.p.; three times per week for five weeks Result: Caused significant inhibition of tumor growth at the doses of 2 and 10 mg/kg.

Specifications

Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
RX-3117 (TV-1360) is a potent and orally active anticancer and antimetabolite agent. RX-3117 inhibits DNA methyltransferase 1 (DNMT1) . RX-3117 shows antiproliferative and anti-tumour activity. RX-3117 induces cell cycle arrest at S phase and apoptosis [1
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Isómeros SMILES C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H](C(=C2F)CO)O)O
PubChem CID 11242315
Peso molecular 257.22

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Calculadoras de soluciones
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