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3,4-Dichloro-N-(1-Methylbutyl)benza-Mide

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3,4-Dichloro-N-(1-Methylbutyl)benza-Mide Basic information

Product Name:
3,4-Dichloro-N-(1-Methylbutyl)benza-Mide
Synonyms:
  • 3,4-Dichloro-N-(1-Methylbutyl)benza-Mide
  • NSC 405020
  • 3,4-DICHLORO-N-(PENTAN-2-YL)BENZAMIDE
  • 3,4-Dichloro-N-(1-methylbutyl)-benzamide NSC405020
  • NSC 405020 3,4-Dichloro-N-(1-methylbutyl)-benzamide
  • NSC 405020, >=98%
  • NSC 405020, 7497-07-6
  • NSC 405020;NSC-405020
CAS:
7497-07-6
MF:
C12H15Cl2NO
MW:
260.16
EINECS:
804-136-9
Product Categories:
  • Inhibitors
Mol File:
7497-07-6.mol
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3,4-Dichloro-N-(1-Methylbutyl)benza-Mide Chemical Properties

Boiling point:
353.7±32.0 °C(Predicted)
Density 
1.182±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Soluble in DMSO (up to 25 mg/ml) or in Ethanol (up to 25 mg/ml).
form 
powder
pka
13.38±0.46(Predicted)
color 
white to beige
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26-24/25
RIDADR 
3077
WGK Germany 
3
HS Code 
29242990
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3,4-Dichloro-N-(1-Methylbutyl)benza-Mide Usage And Synthesis

Description

NSC-405020 (7497-07-6) is a membrane type-1 matrix metalloproteinase (MMP14 or MT1-MMP) inhibitor that prevents homodimerization and inhibits MMP14’s protumorigenic activity?in vivo. (IC50?> 100 μM). Inhibition is via interaction with the hemopexin domain (PEX) of MMP14. NSC-405020 does not interfere with the catalytic activity of MT1-MMP or MMP-2.? Suppresses bone erosion in a c-Fos-deficient mouse model.2?Decreases arsenic-mediated invasion of human squamous cell carcinoma HSC5 cells.3

Uses

NSC 405020 is a novel, selective, and noncatalytic membrane type-1 matrix metalloproteinase (MT1-MMP) inhibitor that directly interacts with the homopexin (PEX) domain of MT1-MMP.

storage

Store at RT

References

1) Remacle?et al.?(2012),?Novel MT1-MMP small-molecule inhibitors based on insights into hemopexin domain function in tumor growth;? Cancer Res.,?72?2339 2) Kittaka?et al.?(2018)?Cherubism Mice Also Deficient in c-Fos Exhibit Inflammatory Bone Destruction Executed by Macrophages That Express MMP14 Despite the Absence of TRAP+ Osteoclasts?; J. Bone Miner. Res.,?33?167 3) Thang?et al.?(2014)?Bidirectional functions of arsenic as a carcinogen and an anti-cancer agent in human squamous cell carcinoma; PLoS One,?9(5)?e96945

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