Cefminox sodium

Names

[ Name ]:
Cefminox sodium

[Synonym ]:
Sodium (6R,7S)-7-({[(2-amino-2-carboxyethyl)sulfanyl]acetyl}amino)-7-methoxy-3-{[(1-methyl-1H-tetrazol-5-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
CefMinox SodiuM Salt Heptahydrate
Meicelin Heptahydrate
CefMinox SodiuM Heptahydrate
Cefminox sodium
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[2-[(2-amino-2-carboxyethyl)thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, sodium salt, (6R,7S)- (1:1)
Cefminox Sodium Salt

Biological Activity

[Description]:

Cefminox sodium (MT-141) is a semisynthetic cephamycin, which exhibits a broad spectrum of antibacterial activity[1]. Cefminox sodium (MT-141) also acts as a dual agonist of prostacyclin receptor (IP) and PPARγ, upregulates cAMP production and PTEN expression and inhibits Akt/mTOR signaling. Cefminox sodium (MT-141) also prevents pulmonary arterial hypertension[2].

[Related Catalog]:

Research Areas >> Cardiovascular Disease

Research Areas >> Infection

Signaling Pathways >> GPCR/G Protein >> Prostaglandin Receptor

Signaling Pathways >> Cell Cycle/DNA Damage >> PPAR

Signaling Pathways >> Anti-infection >> Bacterial

[Target]

PPARγ

IP Receptor

Bacterial

[References]

[1]. Inouye S, et al. In vitro and in vivo antibacterial activities of MT-141, a new semisynthetic cephamycin, compared with those of five cephalosporins. Antimicrob Agents Chemother. 1984 Nov;26(5):722-9.

[2]. Xia J, et al. Cefminox, a Dual Agonist of Prostacyclin Receptor and Peroxisome Proliferator-Activated Receptor-Gamma Identified by Virtual Screening, Has Therapeutic Efficacy against Hypoxia-Induced Pulmonary Hypertension in Rats. Front Pharmacol. 2018 Feb 23;9:134.

Chemical & Physical Properties

[ Molecular Formula ]:
C₁₆H₂₀N₇NaO₇S₃

[ Molecular Weight ]:
541.557

[ Exact Mass ]:
541.048401

[ PSA ]:
281.59000

Safety Information

[ HS Code ]:
3003201900

Customs

[ HS Code ]: 3003201900