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製品番号: HY-114802

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O-1663

O-1663 is a full agonist of cannabinoid receptor 2 (CB2 receptor). O-1663 stimulates the production of ROS, downregulates Id1, and induces autophagy and apoptosis in breast cancer cells. O-1663 inhibits the proliferation, invasion and metastasis of breast cancer cells. O-1663 prolongs the survival of models with advanced metastatic breast cancer. O-1663 can be used for the research of metastatic breast cancer.

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: 468083-84-3
分子式: C₂₇H₃₈O₂
分子量:394.59

保管条件:

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

O-1663 構造式

CAS 番号: 468083-84-3

価格（税別）

Amount: USD 0.00

* アイテムを追加する前、数量をご選択ください

Use of MCE Products

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

生物活性
- 製品説明
- IC₅₀ & Target
- 体外実験
- 体内実験
化学情報
純度とドキュメンテーション
参考文献
Calculators
Help & FAQs
関連分類
Bioz

生物活性

製品説明

IC₅₀ & Target

^[1]

CB2

Cannabinoid Receptor アイソフォーム固有の製品をすべて表示 :

体外実験

Anti-cancerOxidative StressAutophagyApoptosis

Anti-cancer

Oxidative Stress

O-1663 (1-4 μM; 2 days) potently inhibits the proliferation/survival of human MDA-MB231 and 4T1 breast cancer cells, with IC₅₀ values of 0.85 μM and 0.83 μM, respectively. This effect is partially mediated by CB2 receptor activation and ROS production^[1].

Anti-cancer

O-1663 (1 μM; 3 days) potently inhibits the invasion of human MDA-MB231 breast cancer cells, with an IC₅₀ of 0.6 μM^[1].
O-1663 inhibits the proliferation and viability of human MDA-MB231-luc-D3H2LN breast cancer cells, with an IC₅₀ value of 1.0 μM^[1].

Autophagy

O-1663 (1-1.5 μM; 2-3 days) downregulates Id1 expression and upregulates Id2 expression in human MDA-MB231 and mouse 4T1 breast cancer cells, and also stimulates autophagy in MDA-MB231 cells by upregulating LC3-II expression to a level comparable to that of THC^[1].

Oxidative Stress

O-1663 (0.5-1.5 μM; 2 days) significantly induces ROS production in human MDA-MB231 breast cancer cells^[1].

Apoptosis

Anti-cancer

O-1663 (1.5 μM; 2 days) induces apoptosis in human MDA-MB231 breast cancer cells^[1].

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

Cell Proliferation Assay^[1]

Cell Line:

human MDA-MB231 breast cancer cells
Concentration:

1 μM; 4 μM
Incubation Time:

2 days
Result:

Inhibited MDA-MB231 cell proliferation/viability with an IC₅₀ of 0.85 μM.
Reversed inhibitory effect was observed with α-tocopherol and partially reversed by CB2 antagonist SR144528 (HY-13439), but not by CB1 antagonist SR141716A (HY-14137).

Cell Proliferation Assay^[1]

Cell Line:

mouse 4T1 breast cancer cells
Concentration:

1 μM; 4 μM
Incubation Time:

2 days
Result:

Inhibited 4T1 cell proliferation/viability with an IC₅₀ of 0.83 μM.
Reversed inhibitory effect was observed with α-tocopherol and partially reversed by CB2 antagonist SR144528, but not by CB1 antagonist SR141716A.

Cell Invasion Assay^[1]

Cell Line:

human MDA-MB231 breast cancer cells
Concentration:

1 μM
Incubation Time:

3 days
Result:

Inhibited MDA-MB231 cell invasion with an IC₅₀ of 0.6 μM, which was 1.7-fold more potent than CBD.
Partially reversed inhibitory effect was observed with CB2 antagonist SR144528.

Western Blot Analysis^[1]

Cell Line:

human MDA-MB231 breast cancer cells, mouse 4T1 breast cancer cells
Concentration:

1 μM; 1.5 μM
Incubation Time:

2 days (LC3-II); 3 days (Id1/Id2, LC3-II)
Result:

Almost completely down-regulated Id1 expression in both MDA-MB231 and 4T1 cells.
More potently up-regulated Id2 expression in 4T1 cells compared to CBD.
Up-regulated LC3-II expression to a similar extent as THC, producing a ~150% increase over vehicle control, which was significantly higher than the moderate increase induced by CBD.

Apoptosis Analysis^[1]

Cell Line:

human MDA-MB231 breast cancer cells
Concentration:

1.5 μM
Incubation Time:

2 days
Result:

Induced apoptosis in ~18% of MDA-MB231 cells, which was significantly higher than the minimal apoptosis induced by CBD and higher than the ~9% apoptosis induced by THC.

体内実験

Anti-cancer

O-1663 (0.1-1 mg/kg; i.p.; once daily; for 14 consecutive days) potently inhibits breast cancer metastasis in BALB/c mice^[1].
O-1663 (0.5-1 mg/kg; i.p.; daily administration; for 6 consecutive weeks) potently inhibits the metastasis of human MDA-MB231 breast cancer cells in athymic nu/nu mice^[1].

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

Animal Model:

BALB/c (6-8 week old female; i.v. injection of 2 × 10⁴ mouse 4T1 breast cancer cells)^[1]
Dosage:

0.1 mg/kg; 0.5 mg/kg; 1 mg/kg
Administration:

i.p.; daily; 14 days
Result:

Exhibited 2.3-fold more potency than CBD at inhibiting total metastasis, with an EC₅₀ of 0.13 mg/kg.
Showed 7.0-fold more potency than CBD at inhibiting lung metastatic foci ≥ 2 mm, with an EC₅₀ of 0.02 mg/kg.
Reduced total metastasis to ~15% relative to vehicle at 1 mg/kg.
Reduced lung metastatic foci ≥ 2 mm to near 0 at 1 mg/kg.
Had anti-metastatic activity partially reversed by co-administration with CB₂ receptor antagonist SR144528.

Animal Model:

BALB/c (6-8 week old female; i.v. injection of 2 × 10⁴ mouse 4T1 breast cancer cells, treatment initiated 7 days post-injection when lung metastatic foci were established)^[1]
Dosage:

0.5 mg/kg; 1 mg/kg
Administration:

i.p.; daily; 14 days
Result:

Reduced total metastasis to ~45% relative to vehicle at 0.5 mg/kg.
Reduced lung metastatic foci ≥2 mm to ~1 at 0.5 mg/kg.
Reduced total metastasis to ~30% relative to vehicle at 1 mg/kg.
Reduced lung metastatic foci ≥ 2 mm to near 0 at 1 mg/kg.
Produced a median survival increase of 30 days.
Allowed 50% of treated mice to remain alive with no disease progression at 2 months, with 20% having few visible lung metastatic foci.

Related Protocols :

化学情報

CAS 番号 468083-84-3
分子量 394.59
分子式 C₂₇H₃₈O₂
SMILES

OC1=CC(C(C)(CCCCCC)C)=CC(O)=C1C2CCC(CC2)C3=CC=CC=C3
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

取扱説明書 (2659 KB)

参考文献

[1]. Murase R, et al. Targeting multiple cannabinoid anti-tumour pathways with a resorcinol derivative leads to inhibition of advanced stages of breast cancer. British journal of pharmacology. 2014 Oct;171(19):4464-77. [Content Brief]

Calculators

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

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希釈計算機

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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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- IC₅₀ & Target
- 体外実験
- 体内実験
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O-1663

Cannabinoid Receptor アイソフォーム固有の製品をすべて表示

生物活性

製品説明

IC₅₀ & Target

体外実験

体内実験

化学情報

純度とドキュメンテーション

参考文献

Calculators

Help & FAQs

Bioz

Keywords

最近チェックした製品

O-1663

Cannabinoid Receptor アイソフォーム固有の製品をすべて表示

生物活性

製品説明

IC50 & Target

体外実験

体内実験

化学情報

純度とドキュメンテーション

参考文献

Calculators

Help & FAQs

O-1663 関連分類

HY-114802 関連分類

Bioz

Keywords

最近チェックした製品

IC₅₀ & Target