5-nitro-furan-2-carboxylic acid-(4-chloro-anilide)

Modify Date: 2024-01-11 14:54:06

5-nitro-furan-2-carboxylic acid-(4-chloro-anilide) Structure
5-nitro-furan-2-carboxylic acid-(4-chloro-anilide) structure
Common Name 5-nitro-furan-2-carboxylic acid-(4-chloro-anilide)
CAS Number 109844-92-0 Molecular Weight 266.63700
Density N/A Boiling Point N/A
Molecular Formula C11H7ClN2O4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of 5-nitro-furan-2-carboxylic acid-(4-chloro-anilide)


LCS3 inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) (IC50=3.3 µM and 3.8 µM, respectively) synergistically. LCS3 shows anti-tumor activity, and induces apoptosis. LCS3 can be used in lung adenocarcinoma (LUAD) research[1].

 Names

Name 5-nitro-furan-2-carboxylic acid-(4-chloro-anilide)
Synonym More Synonyms

  Biological Activity

Description LCS3 inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) (IC50=3.3 µM and 3.8 µM, respectively) synergistically. LCS3 shows anti-tumor activity, and induces apoptosis. LCS3 can be used in lung adenocarcinoma (LUAD) research[1].
Related Catalog
In Vitro LCS3 (5 nM-10 µM; 96 h) inhibits lung cancer cell lines, but not non-transformed lung cells[1]. LCS3 (3 µM; 96 h) selectively kills lung adenocarcinoma (LUAD) cell lines, in part through the induction of apoptosis[1]. LCS3 induces ROS and NRF2 pathway activation in sensitive lung adenocarcinoma (LUAD) cells[1]. Cell Viability Assay[1] Cell Line: Non-small cell lung cancer (NSCLC) cells and non-transformed lung cells Concentration: 5 nM-10 µM Incubation Time: 96 hours Result: Inhibited the growth of 24/25 NSCLC cell lines at low micromolar concentrations (IC50<5 µM), both of the non-transformed lung cell lines were relatively insensitive (IC50>10 µM). Apoptosis Analysis[1] Cell Line: lung adenocarcinoma (LUAD) cells Concentration: 3 µM Incubation Time: 96 hours Result: Increased cleavage of caspase 3, caspase 7 and/or PARP1 in all LCS3-sensitive LUAD cell lines. Cell Viability Assay[1] Cell Line: H23 and H1650 cells Concentration: 3 µM Incubation Time: 3, 6, and 12 hours Result: Responded to LCS3 by accumulating ROS and activating the NRF2 transcription program.
References

[1]. Fraser D Johnson, et al. Characterization of a small molecule inhibitor of disulfide reductases that induces oxidative stress and lethality in lung cancer cells. Cell Rep. 2022 Feb 8;38(6):110343.

 Chemical & Physical Properties

Molecular Formula C11H7ClN2O4
Molecular Weight 266.63700
Exact Mass 266.00900
PSA 88.06000
LogP 3.68970

 Synonyms

5-nitro-furan-2-carboxylic acid (4-chloro-phenyl)-amide
SKI-98698
5-Nitro-furan-2-carbonsaeure-(4-chlor-anilid)
5-Nitro-furan-2-carboxylic acid (4-chloro-phenyl)-amide
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