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Merck

M9066

Sigma-Aldrich

Microsomes from Liver, Pooled

from rat(Sprague-Dawley), male

Sinónimos:

Liver microsome preparation

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About This Item

UNSPSC Code:
12161501
NACRES:
NA.47
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biological source

rat (Sprague-Dawley)

Quality Level

form

liquid

packaging

vial of ~10 mg

shipped in

dry ice

storage temp.

−70°C

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General description

Microsomes are the fraction of "submicroscopic” particles isolated from homogenates of liver and other tissues. Microsomes are rich in ribonucleic acid (RNA).[1]

Application

Microsomes from Liver, Pooled has been used in following studies:
  • inhibition of microsomal lipid peroxidation.[2]
  • hydroxylation of isorhynchophylline (ISOR) in rats.[3]

Biochem/physiol Actions

Liver microsomes are subcellular particles derived from the endoplasmic reticulum of hepatic cells. These microsomes are a rich source of drug metabolizing enzymes, including cytochrome P-450. Microsome pools from various sources are useful in the study of xenobiotic metabolism and drug interactions.
Microsomes might act as cell organelles and are actively involved in protein synthesis.[1] Carbon monoxide-binding pigment of microsomes, named P-450, is an integral element of mixed function oxidase systems involved in the oxidative demethylation and hydroxylation of drugs and steroids.[4] Murine liver microsomes plays a crucial role in degradation of small antimicrobial β2,2-amino acid derivatives.[3]
Source of drug metabolizing enzymes, including cytochrome P-450.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Visite la Librería de documentos

Xiaofei Zhang et al.
ACS chemical neuroscience, 8(9), 1937-1948 (2017-06-02)
Metabotropic glutamate 2 receptors (mGlu
Gengyang Yuan et al.
Journal of medicinal chemistry, 63(20), 12060-12072 (2020-09-29)
Three benzimidazole derivatives (13-15) have been synthetized as potential positron emission tomography (PET) imaging ligands for mGluR2 in the brain. Of these compounds, 13 exhibits potent binding affinity (IC50 = 7.6 ± 0.9 nM), positive allosteric modulator (PAM) activity (EC50
Isoquercitrin Esters with Mono- or Dicarboxylic Acids: Enzymatic Preparation and Properties.
Vavrikova E
International Journal of Molecular Sciences, 17(6) (2016)
Metabolism of isorhynchophylline in rats detected by LC-MS.
Wang W
J. Pharm. Pharm. Sci., 13(1), 27-37 (2010)
Liver microsomes; an integrated morphological and biochemical study.
PALADE GE
The Journal of Biophysical and Biochemical Cytology, 2(2), 171-200 (1956)

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