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製品番号: HY-184394

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JD-13

JD-13 is a HPV-1 inhibitor and anti-proliferative agent against cancer cells. JD-13 downregulates the expression of HSV-1 DNA polymerase-related genes UL30 and UL42, and inhibits viral replication. JD-13 induces apoptosis (apoptosis) in colorectal cancer cells and suppresses their colony formation. JD-13 can be applied to the research of herpes simplex virus infection and related diseases including colorectal cancer, lung cancer, esophageal cancer and 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: 2969172-58-3
分子式: C₂₅H₃₂N₄O₃
分子量:436.55

保管条件:

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

JD-13 構造式

CAS 番号: 2969172-58-3

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

体外実験

JD-13 (0.125-0.5 μM; 72 h) potently inhibits acyclovir-resistant herpes simplex virus type 1 (HSV-1-153) infection in Vero cells, with near-complete inhibition at concentrations of 0.125, 0.25, and 0.5 μM^[1].
JD-13 (0.125-0.5 μM; 24 h) effectively reduces herpes simplex virus type 1 genomic DNA copy numbers in Vero cells, with stronger activity than acyclovir at concentrations of 0.125, 0.25, and 0.5 μM after 24 hours of incubation^[1].
JD-13 (0.5 μM) most potently inhibits herpes simplex virus type 1 protein expression in Vero cells when administered within the first 6 hours of infection^[1].
JD-13 (0.5 μM; 2-6 h) downregulates the expression of herpes simplex virus type 1 DNA polymerase-related genes UL30 and UL42 in Vero cells, with significant inhibition observed at 4 hours for UL42 and 6 hours for both UL30 and UL42^[1].
JD-13 (20-80 nM; 24 h) inhibits the colony formation ability of HCT116 and SW620 human colon cancer cells after a 24-hour treatment followed by 14 days of drug-free culture^[1].

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

Western Blot Analysis^[1]

Cell Line:

Vero cells
Concentration:

0.5 μM
Incubation Time:

24 h (added at 0 h post-infection); 21 h (added at 3 h post-infection); 18 h (added at 6 h post-infection); 15 h (added at 9 h post-infection); 12 h (added at 12 h post-infection)
Result:

Showed the strongest inhibitory effect on the expression of HSV-1 proteins gB and ICP0 when added within 6 hours post-infection.
Exhibited weakened inhibitory effect when added at 9 or 12 hours post-infection.

Real Time qPCR^[1]

Cell Line:

Vero cells
Concentration:

0.5 μM
Incubation Time:

2 h; 4 h; 6 h
Result:

Had no significant effect on the expression of UL30 and UL42 at 2 hours post-treatment.
Significantly downregulated UL42 expression at 4 hours post-treatment.
Significantly downregulated both UL30 and UL42 expression at 6 hours post-treatment.

Cell Viability Assay^[1]

Cell Line:

HCT116, SW620, A549, Eca109, MDA-MB-231
Concentration:

Variable concentrations
Incubation Time:

48 h
Result:

Inhibited the viability of HCT116, SW620, A549, Eca109, and MDA-MB-231 cells in a concentration-dependent manner.
Had IC₅₀ values of 35.49 nM for HCT116, 24.64 nM for SW620, 36.19 nM for A549, 35.82 nM for Eca109, and 52.14 nM for MDA-MB-231.
Showed significantly lower IC₅₀ values than the reference compound JD-02.

Cell Proliferation Assay^[1]

Cell Line:

HCT116, SW620
Concentration:

20-80 nM
Incubation Time:

24 h (followed by 14 days of drug-free culture)
Result:

Significantly reduced the size and number of cell colonies formed by HCT116 and SW620 cells compared to the control group.

Apoptosis Analysis^[1]

Cell Line:

HCT116, SW620
Concentration:

Low, medium, and high doses
Incubation Time:

48 h
Result:

Induced typical apoptotic characteristics including cell shrinkage, cytoplasmic condensation, highly condensed and marginalized nuclear chromatin, fragmented nuclei, and apoptotic bodies compared to the blank control group.
Increased the number of cells with strong blue fluorescent apoptotic nuclei in a concentration-dependent manner.

化学情報

CAS 番号 2969172-58-3
分子量 436.55
分子式 C₂₅H₃₂N₄O₃
SMILES

O=C(C1=CC=C(N2N=C(C)C3=C2CC(C)(C)CC3=O)C=C1NC45CCC(CC4)(CC5)O)N
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]. Liu Kaisheng, et al. Novel multi-effect benzamide compound and its preparation method, use method and application. CN116554105A. 2023-04-26.

[2]. Xiong Y, et al. Mechanical properties of T-joints of offshore floating photovoltaic structure in marine environment[J]. Journal of Constructional Steel Research, 2026, 245: 110509.

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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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Minimum order quantity

100 mg

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