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  3. Zn-DPA-maytansinoid conjugate 1

Zn-DPA-maytansinoid conjugate 1 

目录号: HY-151559
产品使用指南

Zn-DPA-maytansinoid conjugate 1 是一种类美坦素偶联物,靶向小分子免疫检查点。Zn-DPA-maytansinoid conjugate 1 可诱导肿瘤生长持续消退,使肿瘤微环境 (TME) 恢复活力、变成“发炎热肿瘤”。

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Zn-DPA-maytansinoid conjugate 1 Chemical Structure

Zn-DPA-maytansinoid conjugate 1 Chemical Structure

CAS No. : 3034629-04-1

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Zn-DPA-maytansinoid conjugate 1 is a small molecule-based maytansinoid conjugate targeting immune checkpoint. Zn-DPA-maytansinoid conjugate 1 induces lasting regression of tumor growth and rejuvenates tumor microenvironment (TME) to an "inflamed hot tumor" [1].

体外研究
(In Vitro)

Zn-DPA-maytansinoid conjugate 1 (compound 40a) (0-20 mM; 72 h) inhibits the growth of human pancreatic cancer MIA PaCa2 cells and triple-negative breast cancer HCC1806 cells and displays no effect on normal fibroblast (Detroit 551)[1].
Zn-DPA-maytansinoid conjugate 1 increases CD8+ T cell infiltration significantly in the tumor mass that sensitized tumors from the intrinsic immune-suppressive TME[1].
Zn-DPA-maytansinoid conjugate 1 induces tumor inflammation-related mRNA expression such as STAT1, CXCL10, CCL5, and CCL2[1].
Zn-DPA-maytansinoid conjugate 1 leads to rejuvenation of TME with enhancement in T cell, macrophage, NK cell, chemokine, and cytokine functions[1].

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

Cell Viability Assay[1]

Cell Line: Detroit 551, human pancreatic cancer MIA PaCa2 cells and triple-negative breast cancer HCC1806 cells
Concentration: 0-20 mM
Incubation Time: 72 hours
Result: Inhibited cancer cells with IC50s of 676 nM (MIA PaCa2) and 39 nM (HCC1806), respectively.
Showed low cytotoxicity against Detroit 551 cells (IC50>20 mM).
体内研究
(In Vivo)

Zn-DPA-maytansinoid conjugate 1 (compound 40a) (1-2.5 mg/kg; i.v.; twice a week for 2 weeks) effectively shrank the growth of many solid tumors, exerts antipancreatic cancer, anti-triple-negative breast cancer and anti-sorafenib-resistant HCC tumor activities[1].

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

Animal Model: Nude mice bearing MIA PaCa-2, HCC1806 or sorafenib-resistant HCC xenograft tumors, respectively[1]
Dosage: 1 mg/kg, 2 mg/kg, 2.5 mg/kg
Administration: Intravenous injection; twice (day 1 and day 4) a week for 2 weeks; measured tumor twice weekly
Result: Resulted a lasting regression of tumor growth.
Animal Model: Male SD rats (8-week-old)[1]
Dosage: 1 mg/kg
Administration: Intravenous injection; once a week for 4 weeks (days 1, 8, 15, and 22); measured body weights daily
Result: Showed no effect on rats body weight.
Animal Model: Pharmacokinetic study in ICR mice (6-week-old) bearing HCC1806 tumors[1]
Dosage: 5 mg/kg (in 10% DMA/20% Cremophor EL/70% (5% dextrose))
Administration: Intravenous injection; single dose; collected blood samples at 0.003, 0.083, 0.25, 0.5, 1, 2, 4, 6, 8, and 24 h and collected tumor samples at 0.5, 2, 6, 24, 72, and 168 h
Result: CL (mL/min/kg)=0.9; Vss (L/kg)=0.12; AUC (0-24 h) (ng/mL·h)=105599.
分子量

2505.83

Formula

C115H145ClN18O31S2Zn2

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

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

纯度 & 产品资料
参考文献
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  • 稀释计算器

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Help & FAQs
  • 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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产品名称:
Zn-DPA-maytansinoid conjugate 1
目录号:
HY-151559
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