CYPMPO structure
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Common Name | CYPMPO | ||
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CAS Number | 934182-09-9 | Molecular Weight | 247.23 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C10H18NO4P | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of CYPMPOCYPMPO is a spin-trapping reagent. CYPMPO, a cyclic DEPMPO-type nitrone, is evaluated for spin-trapping capabilities toward hydroxyl and superoxide radicals. anti-oxidant and anti-tumor activity[1]. |
Name | 2-(5,5-Dimethyl-2-oxido-1,3,2-dioxaphosphinan-2-yl)-1-hydroxy-2-methyl-3,4-dihydro-2H-1λ5-pyrrol-1-yl |
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Synonym | More Synonyms |
Description | CYPMPO is a spin-trapping reagent. CYPMPO, a cyclic DEPMPO-type nitrone, is evaluated for spin-trapping capabilities toward hydroxyl and superoxide radicals. anti-oxidant and anti-tumor activity[1]. |
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Related Catalog | |
In Vitro | "DMPO is often used as a spin trapping agent to detect oxygen-centered radicals. CYPMPO has a larger reaction rate constant with superoxide anion than DMPO and the superoxide adduct of CYPMPO is more stable than that of DMPO. CYPMPO (2.5 mM) acts as a spin-trap agent[2]. CYPMPO, a spin-trap, a cyclic DEPMPO-like nitrone trap, may provide new free radical information when used with mitochondria. CYPMPO has the preferential quality of having minimal mitochondrial toxicity at concentrations required for radical detection[3]. " |
References |
Molecular Formula | C10H18NO4P |
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Molecular Weight | 247.23 |
Exact Mass | 248.10500 |
PSA | 68.81000 |
LogP | 2.26700 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
RIDADR | NONH for all modes of transport |
~53% CYPMPO CAS#:934182-09-9 |
Literature: Gosset, Gaelle; Clement, Jean-Louis; Culcasi, Marcel; Rockenbauer, Antal; Pietri, Sylvia Bioorganic and Medicinal Chemistry, 2011 , vol. 19, # 7 p. 2218 - 2230 |
~% CYPMPO CAS#:934182-09-9 |
Literature: Gosset, Gaelle; Clement, Jean-Louis; Culcasi, Marcel; Rockenbauer, Antal; Pietri, Sylvia Bioorganic and Medicinal Chemistry, 2011 , vol. 19, # 7 p. 2218 - 2230 |
Precursor 1 | |
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DownStream 0 |
Serum hydroxyl radical scavenging capacity as quantified with iron-free hydroxyl radical source.
J. Clin. Biochem. Nutr. 45 , 193-201, (2009) We have developed a simple ESR spin trapping based method for hydroxyl (OH) radical scavenging-capacity determination, using iron-free OH radical source. Instead of the widely used Fenton reaction, a ... |
5-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)-1-METHYL-1H-PYRAZOLE |
2H-Pyrrol-1-yl, 2-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphorinan-2-yl)-1,1,3,4-tetrahydro-1-hydroxy-2-methyl- |
5-(5,5-dimethyl-2-oxo-1,3,2-dioxaphosphinan-2-yl)-5-methyl-1-pyrroline-N-oxide |
2-(5,5-Dimethyl-2-oxido-1,3,2-dioxaphosphinan-2-yl)-1-hydroxy-2-methyl-3,4-dihydro-2H-1λ-pyrrol-1-yl |
2-methyl-2-(5,5-dimethyl-2-oxo-1,3,2-dioxaphosphinan-2-yl)-3,4-dihydro-2H-pyrrole 1-oxide |
1-Methyl-1H-pyrazole-5-boronic acid,neopentyl glycol ester |
5-(2,2-dimethyl-1,3-propoxycyclophosphoryl)-5-methyl-1-pyrroline N-oxide |