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  • DC Chemicals Limited
  • China
  • Product Name: NSC 19630
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

72835-26-8

72835-26-8 structure
72835-26-8 structure
  • Name: MIRA-1
  • Chemical Name: (2,5-dioxopyrrol-1-yl)methyl propanoate
  • CAS Number: 72835-26-8
  • Molecular Formula: C8H9NO4
  • Molecular Weight: 183.16
  • Catalog: Signaling Pathways Apoptosis Apoptosis
  • Create Date: 2016-12-26 20:18:22
  • Modify Date: 2024-01-12 11:29:44
  • MIRA-1 is a maleimide analogue. MIRA-1 can induce apoptosis in mutant p53 cells via restoration of p53-dependent transcriptional transactivation. MIRA-1 has anticancer activity[1].

Name (2,5-dioxopyrrol-1-yl)methyl propanoate
Synonyms MIRA-1
N-propionyloxymethyl-maleimide
N-Propionyloxymethyl-maleinimid
NSC 19630
Description MIRA-1 is a maleimide analogue. MIRA-1 can induce apoptosis in mutant p53 cells via restoration of p53-dependent transcriptional transactivation. MIRA-1 has anticancer activity[1].
Related Catalog
Target

IC50: 10 μM (Saos-2 His273)[1]

In Vitro MIRA-1 suppresses growth of Saos-2-His273 cells expressing mutant p53[1]. MIRA-1 (25 μM; 48 hours) inhibits cell growth in a mutant p53-dependent manner[1]. MIRA-1 (5 μM; 14 days) dramatically reduces the number of colonies formed by His273-expressing Saos-2 cells, but is much less efficient in inhibiting p53-null Saos-2 cells[1]. MIRA-1 (10 μM; 48 hours) causes a substantial increase in the fraction of Saos-2 and Saos-2-His273 cells with a sub-G1 DNA content in the presence of mutant p53[1]. MIRA-1 (5 and 10 μM; 24 hours) induces EGFP expression, MDM2 and Bax in SKOV-His175 cells[1]. Cell Proliferation Assay Cell Line: Saos-2-His273, H1299-His175, SKOV-His175 and SKOV-His273[1] Concentration: 25 μM Incubation Time: 48 hours Result: Inhibited cell growth in a mutant p53-dependent manner, with survival rate of 18.5~39% in no doxycycline and 71.5~87.5% in doxycycline. Apoptosis Analysis Cell Line: Saos-2 and Saos-2-His273 cells[1] Concentration: 10 μM Incubation Time: 48 hours Result: Caused a substantial increase in the fraction of cells with a sub-G1 DNA content in the presence of mutant p53.
References

[1]. Bykov VJ, et al. Reactivation of mutant p53 and induction of apoptosis in human tumor cells by maleimide analogs [published correction appears in J Biol Chem. 2017 Dec 1;292(48):19607]. J Biol Chem. 2005;280(34):30384-30391.

Density 1.307g/cm3
Boiling Point 298.2ºC at 760 mmHg
Molecular Formula C8H9NO4
Molecular Weight 183.16
Flash Point 134.1ºC
Exact Mass 183.05300
PSA 63.68000
Index of Refraction 1.514
Storage condition 2-8°C

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72835-26-8 structure

72835-26-8

Literature: U.S.Rubber Co. Patent: US2790787 , 1953 ;
Precursor  2

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