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製品番号: HY-158197

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RC-106

RC-106 is a proteasome inhibitor (IC50: 35 μM) and Sigma receptor modulator with anticancer activity. RC-106 has antiproliferative activity against cancer cells including glioblastoma (GB) and multiple myeloma (MM).

商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。

CAS 番号: 1346216-50-9
分子式: C₂₆H₂₉N
分子量:355.52

保管条件:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (265 KB)

RC-106 構造式

CAS 番号: 1346216-50-9

容量

価格（税別）

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数量

Amount: USD 0.00

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

生物活性

製品説明

Sigma Receptor アイソフォーム固有の製品をすべて表示 :

Cellular Effect

Cell Line	Type	Value	Description	References
Capan-2	IC₅₀	52.6 μM Compound: 3	Cytotoxicity against human Capan2 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay Cytotoxicity against human Capan2 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay	[PMID: 27614411]
Capan-2	IC₅₀	9.61 μM Compound: 3	Cytotoxicity against human Capan2 cells assessed as reduction in cell viability after 24 hrs in absence of 10% fetal calf serum by MTS assay Cytotoxicity against human Capan2 cells assessed as reduction in cell viability after 24 hrs in absence of 10% fetal calf serum by MTS assay	[PMID: 27614411]
LNCaP	IC₅₀	61.1 μM Compound: 3	Cytotoxicity against human LNCAP cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay Cytotoxicity against human LNCAP cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay	[PMID: 27614411]
LNCaP	IC₅₀	9.58 μM Compound: 3	Cytotoxicity against human LNCAP cells assessed as reduction in cell viability after 24 hrs in absence of 10% fetal calf serum by MTS assay Cytotoxicity against human LNCAP cells assessed as reduction in cell viability after 24 hrs in absence of 10% fetal calf serum by MTS assay	[PMID: 27614411]
MDA-MB-231	IC₅₀	64.9 μM Compound: 3	Cytotoxicity against human MDA-MB-231 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay Cytotoxicity against human MDA-MB-231 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay	[PMID: 27614411]
PC-3	IC₅₀	50.6 μM Compound: 3	Cytotoxicity against human PC3 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay Cytotoxicity against human PC3 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay	[PMID: 27614411]
SUM-159-PT	IC₅₀	58.3 μM Compound: 3	Cytotoxicity against human SUM159 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay Cytotoxicity against human SUM159 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay	[PMID: 27614411]
U-87MG ATCC	IC₅₀	10.47 μM Compound: 3	Cytotoxicity against human U87 cells assessed as reduction in cell viability after 24 hrs in absence of 10% fetal calf serum by MTS assay Cytotoxicity against human U87 cells assessed as reduction in cell viability after 24 hrs in absence of 10% fetal calf serum by MTS assay	[PMID: 27614411]
U-87MG ATCC	IC₅₀	60.6 μM Compound: 3	Cytotoxicity against human U87 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay Cytotoxicity against human U87 cells assessed as reduction in cell viability after 24 hrs in presence of 10% fetal calf serum by MTS assay	[PMID: 27614411]

体外実験

RC-106 (60 μM; 24 h) inhibits cancer cell activity^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay^[1]

Cell Line:

U87-MG cells
Concentration:

40, 60 μM
Incubation Time:

24 h
Result:

Showed a moderate activity against U87-MG cells at 60 μM, reducing the cell viability to 34%。

化学情報

CAS 番号 1346216-50-9
分子量 355.52
分子式 C₂₆H₂₉N
SMILES

C/C(C1=CC2=C(C=CC=C2)C=C1)=C\CN3CCC(CC3)CC4=CC=CC=C4
輸送条件

Room temperature in continental US; may vary elsewhere.
保管条件

Please store the product under the recommended conditions in the Certificate of Analysis.

純度とドキュメンテーション

バッチを選択:

純度: 99.98%

Assay: 99.98%

ee.: 99.98%

データシート (265 KB)
COA (2659 KB)
元素分析報告書 (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
取扱説明書 (2659 KB)

参考文献

[1]. Listro R, et al. Exploring the RC-106 Chemical Space: Design and Synthesis of Novel (E)-1-(3-Arylbut-2-en-1-yl)-4-(Substituted) Piperazine Derivatives as Potential Anticancer Agents. Front Chem. 2020 Jun 30;8:495. [Content Brief]

Calculators

モル濃度計算機

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

濃度濃度

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分子量分子量

希釈計算機

濃度 _(開始) × 体積 _(開始) = 濃度 _(終了) × 体積 _(終了)

濃度 _(開始) 濃度 _(開始)

体積 _(開始) 体積 _(開始)

濃度 _(終了) 濃度 _(終了)

体積 _(終了) 体積 _(終了)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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MOQ

Minimum order quantity

100 mg

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生物活性
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- 体外実験
化学情報
純度とドキュメンテーション
参考文献

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RC-106

Sigma Receptor アイソフォーム固有の製品をすべて表示

生物活性

化学情報

純度とドキュメンテーション

参考文献

Calculators

Help & FAQs

RC-106 関連分類

HY-158197 関連分類