1. Immunology/Inflammation
  2. PD-1/PD-L1
  3. D5B

D5B is a potent and selective PD-L1 inhibitor. D5B has been modified by DBCO. The EC50 of D5B degrading PD-L1 in 4T1 and B16-F10 tumor cells are 5.4 μM and 6.2 μM, respectively. D5B can block PD-L1/PD-1 interaction and has anti-tumor activity.

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D5B

D5B 構造式

容量 価格(税別) 在庫状況 数量
5 mg $375 お問い合わせ 2 - 4 weeks 1 - 3 weeks 3 - 5 weeks 1 - 3 weeks
10 mg $600 お問い合わせ 2 - 4 weeks 1 - 3 weeks 3 - 5 weeks 1 - 3 weeks
25 mg $1100 お問い合わせ 2 - 4 weeks 1 - 3 weeks 3 - 5 weeks 1 - 3 weeks
50 mg $1750 お問い合わせ 2 - 4 weeks 1 - 3 weeks 3 - 5 weeks 1 - 3 weeks
100 mg $2650 お問い合わせ 2 - 4 weeks 1 - 3 weeks 3 - 5 weeks 1 - 3 weeks
200 mg   お問い合わせ  
500 mg   お問い合わせ  
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製品説明

D5B is a potent and selective PD-L1 inhibitor. D5B has been modified by DBCO. The EC50 of D5B degrading PD-L1 in 4T1 and B16-F10 tumor cells are 5.4 μM and 6.2 μM, respectively. D5B can block PD-L1/PD-1 interaction and has anti-tumor activity[1].

IC50 & Target

EC50: 5.4 μM (PD-L1 in 4T1 tumor cells)[1]
EC50: 6.2 μM (PD-L1 in B16-F10 tumor cells)[1]

体外実験

D5B (0-10 μM; 24 h) can degrade PD-L1 in 4T1 and B16-F10 tumor cells with EC50 of 5.4 μM and 6.2 μM, respectively[1].
D5B (0-5 μM; 48 h) significantly decreases the PD-L1 abundance on cell membrane surface in IFN-γ treated and azide-labeled 4T1 and B16-F10 tumor cells[1].

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

Western Blot Analysis[1]

Cell Line: IFN-γ treated and azide-labeled 4T1 and B16-F10 tumor cells
Concentration: 0, 1.25, 2.5 and 5.0 μM
Incubation Time: 48 h
Result: Significantly reduced the level of PD-L1.
体内実験

D5B (5 mg/kg; intravenous injection; single dose) has anti-tumor effects in mouse tumor models and is more effective in combination with radiotherapy. (D5B is in the form of PCPGd@D5B nanoparticles)[1]

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

Animal Model: 4T1 tumor-bearing mice with radiotherapy[1]
Dosage: 5 mg/kg (D5B is in the form of PCPGd@D5B nanoparticles)
Administration: Intraperitoneal injection (i.p.); Single dose
Result: Completely eradicated 50% of the tumor xenografts, with 60% of the tumor-bearing mice survived over 100 days.
Increased the percentage of tumor-infiltrating IFN-γ+CD8+ T cells.
Efficiently provoked an adaptive antitumor immune response for tumor regression.
Animal Model: B16-F10 tumor-bearing mice with radiotherapy[1]
Dosage: 5 mg/kg (D5B is in the form of PCPGd@D5B nanoparticles)
Administration: Intraperitoneal injection (i.p.); Single dose
Result: Suppressed 95% of tumor growth, with complete tumor elimination in 43% of the tumor-bearing mice and elongated survival time over 50 days.
Effectively suppressed PD-L1 expression on the surface of tumor cells and TAM membrane.
Promoted the increase of tumor infiltrating CD8+ T cells.
分子量

983.15

分子式

C58H66N2O12

SMILES

O=C(CCC(N1CC2=CC=CC=C2C#CC3=C1C=CC=C3)=O)OCCOCCOCCOCCOCCOC([C@H]4N(CC5=C(OC)C=C(OCC6=CC=CC(C7=CC=CC=C7)=C6C)C=C5OC)CCCC4)=O

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
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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製品名:
D5B
製品番号:
HY-169392
数量:
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