NSC 95397
NSC 95397 Basic information
- Product Name:
- NSC 95397
- Synonyms:
-
- 2,3-BIS(2-HYDROXYETHYLTHIO)-1,4-NAPHTHALENEDIONE
- 2,3-BIS[(2-HYDROXYETHYL)THIO]-1,4-NAPHTHOQUINONE
- 2,3-BIS[(2-HYDROXYETHYL)THIOL]-1,4-NAPHTHOQUINONE
- 1,4-Naphthalenedione, 2,3-bis[(2-hydroxyethyl)thio]-
- Cdc25 Inhibitor IV, NSC 95397
- NSC 95397
- Cdc25 Inhibitor IV, NSC 95397 - CAS 93718-83-3 - Calbiochem
- Apoptosis,NSC-95397,Inhibitor,NSC 95397,inhibit,NSC95397,Phosphatase
- CAS:
- 93718-83-3
- MF:
- C14H14O4S2
- MW:
- 310.39
- Product Categories:
-
- Protein Phosphatase
- Mol File:
- 93718-83-3.mol
NSC 95397 Chemical Properties
- storage temp.
- -20°C
- solubility
- DMSO: 16 mg/mL
- form
- Orange solid
- color
- orange, solid
- Stability:
- Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
Safety Information
- Hazard Codes
- Xi
- WGK Germany
- 3
- HazardClass
- IRRITANT
MSDS
- Language:English Provider:SigmaAldrich
NSC 95397 Usage And Synthesis
Description
NSC 95397 (93718-83-3) is a potent and selective inhibitor of Cdc25 phosphatase (Ki? = 32, 96 and 40 nM for Cdc25A, B and C respectively). NSC-95397 inhibits the growth of several human tumor cell lines and blocks G2/M cell cycle transition.1 Induces cell cycle arrest, phosphorylation of EGFR and activation of ERK-1 and -2.2 Inhibits carboxyl-terminal binding protein a transcriptional corepressor that suppresses multiple pro-apoptotic and epithelial genes.3 Induces eryptosis in human erythrocytes.4
Uses
NSC 95397 is a quinone-based Cdc25 inhibitor, caspase-3 activator, ERK activator, and MKP inhibitor.
Definition
ChEBI: 2,3-bis(2-hydroxyethylthio)naphthalene-1,4-dione is a member of 1,4-naphthoquinones.
Biological Activity
Potent and selective irreversible inhibitor of Cdc25 dual specificity phosphatases (K i values are 32, 96 and 40 nM for inhibition of Cdc25A, -B and -C respectively). Displays 125-180-fold selectivity over VH1-related dual-specificity phosphatase and protein tyrosine phosphatase 1b. Inhibits carcinoma cell growth and blocks G 2 /M phase transition in vitro .
Biochem/physiol Actions
Irreversible Cdc25 dual specificity phosphatase inhibitor.
storage
Desiccate at -20°C
References
[1] J. LAZO. Identification of a potent and selective pharmacophore for Cdc25 dual specificity phosphatase inhibitors.[J]. Molecular Pharmacology, 2002, 61 4 1: 720-728. DOI:10.1124/mol.61.4.720
[2] IRA MELCHHEIER. Quinone-induced Cdc25A inhibition causes ERK-dependent connexin phosphorylation[J]. Biochemical and biophysical research communications, 2005, 327 4: Pages 1016-1023. DOI:10.1016/j.bbrc.2004.12.107
[3] MELANIE A. BLEVINS . Small Molecule, NSC95397, Inhibits the CtBP1-Protein Partner Interaction and CtBP1-Mediated Transcriptional Repression[J]. SLAS Discovery, 2015, 20 5: Pages 663-672. DOI:10.1177/1087057114561400
[4] MOHAMED JEMAÀ. Stimulation of Suicidal Erythrocyte Death by the CDC25 Inhibitor NSC-95397[J]. Cellular Physiology and Biochemistry, 2016, 40 1: 597-607. DOI:10.1159/000452573
NSC 95397Supplier
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