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  • DC Chemicals Limited
  • China
  • Product Name: MTOB
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/500mg
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

51828-97-8

51828-97-8 structure
51828-97-8 structure
  • Name: MTOB
  • Chemical Name: sodium,4-methylsulfanyl-2-oxobutanoate
  • CAS Number: 51828-97-8
  • Molecular Formula: C5H7NaO3S
  • Molecular Weight: 170.16200
  • Catalog: Research Areas Cancer
  • Create Date: 2018-05-14 08:00:00
  • Modify Date: 2024-01-02 13:19:26
  • MTOB sodium is a potent C-terminal binding protein (CtBP) inhibitor. MTOB sodium attenuates repetitive head injury-elicited neurologic dysfunction and neuroinflammation via inhibition of the transactivation activity of CtBP1 and CtBP2. MTOB sodium antagonizes the transcriptional regulatory activity of CtBP1 and CtBP2 by eviction from their target promoters in breast cancer cell lines[1][2].

Name sodium,4-methylsulfanyl-2-oxobutanoate
Synonyms KMBA
MFCD00010511
sodium 4-methylsulfanyl-2-oxo-butyrate
UNII-2EZY36W75U
Sodium 4-(methylthio)-2-oxobutanoate
sodium 4-methylthio-2-oxobutyrate
Fema No. 3881
4-Methylthio-2-oxobutanoic acid sodium salt
Description MTOB sodium is a potent C-terminal binding protein (CtBP) inhibitor. MTOB sodium attenuates repetitive head injury-elicited neurologic dysfunction and neuroinflammation via inhibition of the transactivation activity of CtBP1 and CtBP2. MTOB sodium antagonizes the transcriptional regulatory activity of CtBP1 and CtBP2 by eviction from their target promoters in breast cancer cell lines[1][2].
Related Catalog
Target

CtBP[1]

In Vitro MTOB sodium (10 mM) causes significant derepression (P<0.05) of 40% of CtBP target genes (including FGF9, CTNNB1, CEBPB, et al.) in MCF-7 and 46% in MBA-MD-231; increases the pro-epithelial E-cadherin/Vimentin ratio while reducing the pro-mesenchymal CD44/CD24 ratio, with a more significant trend (P<0.05) in MCF-7[2].
In Vivo MTOB sodium (860 mg/kg; IP, at 1 h and 18 h after the first injury) effectively suppresses the increases duration of righting reflex, and significantly decreased neurological severity score (NSS) scores[1]. Animal Model: C57BL/6 mice (traumatic brain injury)[1] Dosage: 860 mg/kg Administration: IP, at 1 h and 18 h after the first injury Result: Effectively suppressed the increased duration of righting reflex, and significantly decreased NSS scores.
References

[1]. Li H, et al. C-terminal binding proteins 1 and 2 in traumatic brain injury-induced inflammation and their inhibition as an approach for anti-inflammatory treatment. Int J Biol Sci. 2020 Feb 4;16(7):1107-1120.

[2]. Di LJ, et al. Genome-wide profiles of CtBP link metabolism with genome stability and epithelial reprogramming in breast cancer. Nat Commun. 2013;4:1449.

Melting Point >300ºC(lit.)
Molecular Formula C5H7NaO3S
Molecular Weight 170.16200
Exact Mass 170.00100
PSA 82.50000
Storage condition 2-8°C
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases 36/37/38
Safety Phrases 26-36
RIDADR UN 3335
HS Code 2930909090
Precursor  0

DownStream  3

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%