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438187

Lovastatin, Sodium Salt

InSolution ≥95%

Synonim(y):

InSolution Lovastatin, Sodium Salt

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Rozmiar/SKUDostępnośćCena netto
5 mg

Dostępne do wysyłki DZISIAJzKuehne + Nagel Sp. z o.o.

1180,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C24H37O6 · Na
Masa cząsteczkowa:
444.54
NACRES:
NA.77
UNSPSC Code:
51111800
Assay:
≥95% (HPLC)
Form:
liquid
Storage condition:
OK to freeze, avoid repeated freeze/thaw cycles, protect from light

1180,00 zł


Dostępne do wysyłki DZISIAJSzczegóły


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Quality Segment

assay

≥95% (HPLC)

form

liquid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, avoid repeated freeze/thaw cycles, protect from light

shipped in

dry ice

storage temp.

−70°C

General description

Carboxylate form of Lovastatin (Cat. No. 438185) that is active in whole cells and cell-free assays. Lovastatin is reported to be an anti-hypercholesterolemic agent that acts as a reversible competitive inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase and blocks a series of biological events including activation of p21ras by insulin in 3T3-L1 fibroblasts and 3T3-L1 adipocytes, farnesylation of p21ras, which decreases the pool of intracellular Ras available for subsequent activation by growth factors (including insulin), and N-ras-induced neuronal differentiation. Causes cell cycle arrest in the late G1 phase. Shown to inhibit the stimulation of MAP kinase by insulin in HIRcB cells and block the transcription of the type-I SCR gene in THP-1-derived macrophages. Also blocks PDGF receptor tyrosine phosphorylation and MAP kinase activation by PDGF.

Biochem/physiol Actions

Cell permeable: yes
Primary Target
HMG-CoA reductase
Reversible: yes

Packaging

Packaged under inert gas

Physical form

A 10 mM (5 mg/1.13 ml) solution of Lovastatin, Sodium Salt (Cat. No. 438186) in H₂O.

Preparation Note

Following initial thaw, aliquot and freeze (-70°C). Aliquots are stable for up to 6 months at -70°C.

Other Notes

Rao, S., et al. 1999. Proc. Natl. Acad. Sci. USA96, 7197.
Carel, K., et al. 1996. J. Biol. Chem.271, 30625.
McGuire, T.F., et al. 1996. J. Biol. Chem.271, 27402.
Umetani, N., et al. 1996. Biochim. Biophys. Acta1303, 199.
Xu, X.Q., et al. 1996. Arch. Biochem. Biophys.326, 233.
Reusch, J.E.-B., et al. 1995. J. Biol. Chem.270, 2036.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Harmful (C)
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Ta pozycja
438185438186PHR1285
description

InSolution ≥95%

description

Lovastatin, CAS 75330-75-5, is an anti-hypercholesterolemic agent that inhibits the activity of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase.

description

Carboxylate form of Lovastatin that is active in whole cells and cell-free assays.

description

Pharmaceutical Secondary Standard; Certified Reference Material

assay

≥95% (HPLC)

assay

≥95% (HPLC)

assay

≥95% (HPLC)

assay

-

form

liquid

form

powder

form

solid

form

-

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

300

storage temp.

−70°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

-10 to -25°C

storage condition

avoid repeated freeze/thaw cycles, OK to freeze, protect from light

storage condition

protect from light, OK to freeze

storage condition

OK to freeze, desiccated (hygroscopic)

storage condition

-


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Klasa składowania

12 - Non Combustible Liquids

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