1. Antibody-drug Conjugate/ADC Related Apoptosis
  2. Antibody-Drug Conjugates (ADCs) Apoptosis TNF Receptor
  3. Brentuximab vedotin

Brentuximab vedotin  (Synonyms: 维布妥昔单抗;本妥昔单抗)

目录号: HY-P99107 纯度: 98.00%
COA 产品使用指南

Brentuximab vedotin (cAC10-vcMMAE) 是一种抗体-活性分子偶联物 (ADC),由抗 CD30 抗体和 Monomethyl auristatin E (MMAE) 组成。Brentuximab vedotin 抑制 CD30 阳性细胞,其 IC50 值为 2.5 ng/mL。Brentuximab vedotin 可用于复发难治性霍奇金淋巴瘤的研究。

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Brentuximab vedotin Chemical Structure

Brentuximab vedotin Chemical Structure

CAS No. : 914088-09-8

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Other Forms of Brentuximab vedotin:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Brentuximab vedotin (cAC10-vcMMAE) is an antibody-drug conjugate (ADC) comprising an anti-CD30 antibody and the cytotoxic agent Monomethyl auristatin E (MMAE). Brentuximab vedotin inhibits CD30-positive cells with an IC50 of 2.5 ng/mL. Brentuximab vedotin can be used for the research of relapsed and refractory Hodgkin lymphoma[1][2].

IC50 & Target

IC50: 2.5 ng/mL (CD30)[2]

体外研究
(In Vitro)

Brentuximab vedotin (cAC10-vcMMAE) (1 μg/mL;96 h) 在 Karpas 299 细胞中显示出对 CD30+ 的细胞毒性[2]
Brentuximab vedotin (CAC10-VCMMAE) (1 μg/mL;12,24 和 48 h) 选择性诱导 G2/M 期生长停滞,然后导致细胞凋亡[2]

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

Cell Cytotoxicity Assay[2]

Cell Line: Karpas 299 cells
Concentration: 1 μg/mL
Incubation Time: 96 h
Result: Showed cytotoxicity to CD30+ Karpas 299 cells with an IC50 value of 2.5 ng/mL.

Cell Cycle Analysis[2]

Cell Line: L540 cells
Concentration: 1 μg/mL
Incubation Time: 12, 24, and 48 h
Result: Selectively induced growth arrest in G2/M phase to apoptotic cell death.
体内研究
(In Vivo)

Brentuximab vedotin (cAC10-vcMMAE) (10-120 mg/kg;腹腔注射 3 周) 最大耐受剂量 (MTD) 在 30 和 40 mg/kg 之间[2]
Brentuximab vedotin (cAC10-vcMMAE) (0.3、1 mg/kg;侧腹注射;每 4 天一次,总共 4 剂 1 mg/kg) 诱导肿瘤 CD30 消退[2]

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

Animal Model: SCID mice[2]
Dosage: 10 to 120 mg/kg
Administration: Intravenous injection; 10 to 120 mg/kg; for 3 weeks
Result: Showed an maximum tolerated dose between 30 and 40 mg/kg.
Animal Model: SCID mice[2]
Dosage: 0.3 and 1 mg/kg
Administration: Flanks injection; 1 mg/kg every 4 days for a total of 4 doses; 0.3 mg/kg every 4 days for a total of 4 doses
Result: Induced complete and durable tumor regression, but 0.3 mg/kg provided lower therapy than 1 mg/kg dose.
Clinical Trial
CAS 号
性状

固体

颜色

White to off-white

中文名称

维布妥昔单抗;本妥昔单抗

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture and light

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

纯度 & 产品资料

纯度: 98.00%

参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

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

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
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:
Brentuximab vedotin
目录号:
HY-P99107
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