MZ-1

Catalog No.S8889 Batch:S888902

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Technical Data

Formula

C49H60ClN9O8S2

Molecular Weight 1002.64 CAS No. 1797406-69-9
Solubility (25°C)* In vitro DMSO 100 mg/mL (99.73 mM)
Ethanol 100 mg/mL (99.73 mM)
Water Insoluble
In vivo (Add solvents to the product individually and in order)
5%DMSO 40%PEG300 5%Tween80 50%ddH2O
5.0mg/ml
5% DMSO 95% Corn oil
2.5mg/ml
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
* Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

Biological Activity

Description MZ-1 is a PROTAC degrader of bromodomain-containing protein 4 (BRD4). MZ-1 binds to the Brd bromodomain with Kd of 62 nM, 60 nM, 21 nM, 13 nM, 39 nM and 15 nM for Brd2BD1, Brd2BD2, Brd3BD1, Brd3BD2, Brd4BD1 and Brd4BD2.
Targets
Brd3(BD2) [1]
(Cell-free assay)
Brd4(BD2) [1]
(Cell-free assay)
Brd3(BD1) [1]
(Cell-free assay)
Brd4(BD1) [1]
(Cell-free assay)
Brd2(BD2) [1]
(Cell-free assay)
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13 nM(Kd) 15 nM(Kd) 21 nM(Kd) 39 nM(Kd) 60 nM(Kd)
In vitro

MZ-1 induces apoptosis of ovarian cancer cells and inhibits periostin-mediated ovarian cancer cell migration and invasion in vitro. MZ-1 specifically and efficiently inhibits the colony formation of periostin cells in soft agar, which clearly indicates a proproliferation role of periostin.[2]

In vivo

Our in vivo studies shows significant growth inhibition by MZ-1 on both subcutaneous and intraperitoneal (i.p.) tumors derived from the periostin-expressing ovarian cancer cell line A2780. In addition, MZ-1 treatment leads to a reduction of the metastatic potential of these A2780 i.p. tumors. The in vivo antitumor effects of MZ-1 are linked to its specific inhibition of anchorage-independent growth and survival of periostin-expressing cells, as well as its neutralizing effects on periostin-induced cancer cell migration and invasion.[2]

Protocol (from reference)

Cell Assay:

[2]

  • Cell lines

    A2780, OAW-42, SKOV-3, TOV-112D, ES2, SP2/0 cell line

  • Concentrations

    20 μM

  • Incubation Time

    2 and 4 days

  • Method

    In vitro apoptosis assay: Cells are grown in 24-well plates in serum-free medium (SFM) plus 1% BSA overnight to reach 50% to 60% confluency. A portion of 20 mg/mL of MZ-1 or control antibody is added into the wells. Cell apoptosis is analyzed 2 and 4 days later by using Annexin V-FITC Apoptosis Detection Kit. The cell flow cytometry is carried on Cell LabQuanta SC.

Animal Study:

[2]

  • Animal Models

    Female SCID beige mice (6-8 weeks old) with A2780/TOV-112D xenografts

  • Dosages

    20 mg/kg

  • Administration

    IH/SC, IP

Selleck's MZ-1 has been cited by 3 publications

Screening of an epigenetic compound library identifies BRD4 as a potential antiviral target for hepatitis B virus covalently closed circular DNA transcription [ Antiviral Res, 2023, 211:105552] PubMed: 36737008
Dual mechanism: Epigenetic inhibitor apabetalone reduces SARS-CoV-2 Delta and Omicron variant spike binding and attenuates SARS-CoV-2 RNA induced inflammation [ Int Immunopharmacol, 2023, 117:109929] PubMed: 36857935
Genomic Mapping of Splicing-Related Genes Identify Amplifications in LSM1, CLNS1A, and ILF2 in Luminal Breast Cancer [ Cancers (Basel), 2021, 13(16)4118] PubMed: 34439272

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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.

NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.