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Merck

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567020

Simvastatin

≥98% (HPLC), solid, HMG-CoA reductase inhibitor, Calbiochem®

Synonim(y):

Simvastatin, MK-733, L-Type Calcium Channel Blocker VI

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Do Państwa/SKUDostępnośćCena netto
50 mg

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

1190,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C25H38O5
Numer CAS:
Masa cząsteczkowa:
418.57
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
solid
Storage condition:
OK to freeze

1190,00 zł


Dostępne do wysyłki DZISIAJSzczegóły


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Nazwa produktu

Simvastatin, A lipophilic 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor that blocks Ras function through inhibition of farnesylation.

Quality Segment

description

Merck USA index - 14, 8539

assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

color

off-white

solubility

soluble (DMSO or Ethanol (50 mg/ml). Dissolve 50 mg in 1 ml in ethanol and add 0.813 ml of 1N NaOH. Adjust the pH to 7.2 by adding small quantities of 1N HCl before use.)

cation traces

heavy metals: ≤20 ppm, heavy metals: <20 ppm

shipped in

ambient

storage temp.

2-8°C

SMILES string

O1[C@@H](C[C@H](CC1=O)O)CC[C@@H]2[C@H]3[C@H](C[C@H](C=C3C=C[C@@H]2C)C)OC(=O)C(CC)(C)C

InChI

1S/C25H38O5/c1-6-25(4,5)24(28)30-21-12-15(2)11-17-8-7-16(3)20(23(17)21)10-9-19-13-18(26)14-22(27)29-19/h7-8,11,15-16,18-21,23,26H,6,9-10,12-14H2,1-5H3/t15-,16-,18+,19+,20-,21-,23-/m0/s1

InChI key

RYMZZMVNJRMUDD-HGQWONQESA-N

General description

A lipophilic 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor that blocks Ras function through inhibition of farnesylation. Also inhibits glucose-induced Ca2+-signaling and insulin secretion by blocking L-type Ca2+ channels in rat islet β-cells. Inhibits cell proliferation of human smooth muscle cells. Note: This product is supplied in an inactive form and requires treatment with NaOH in ethanol followed by neutralization to pH 7.2 for activation.

Biochem/physiol Actions

Cell permeable: no
Primary Target
farnesylation
Product does not compete with ATP.
Reversible: no

Preparation Note

Dissolve 50 mg in 1 ml in ethanol and add 0.813 ml of 1N NaOH. Adjust the pH to 7.2 by adding small quantities of 1N HCl before use.
Following reconstitution in ethanol-NaOH, aliquot and freeze (-20°C) Ethanol-NaOH solutions are stable for up to 1 month at -20°C. Neutralized solutions should be used immediately.

Other Notes

Yada, T., et al. 1999. Br. J. Pharmacol. 126, 1205.
Clutterbuck, R.D., et al. 1998. Br. J. Haematol. 102, 522.
Yokoyama, K., et al. 1998. Mol. Biochem. Parasitol. 94, 87.
Negre-Aminou, P., et al. 1997. Biochim. Biophys. Acta 1345, 259.
Vrtovsnik, F., et al. 1997. Kidney Int. 52, 1016.
Keyomarsi, K., et al. 1991. Cancer Res.51, 3602.

Legal Information

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

Disclaimer

Toxicity: Standard Handling (A)
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Ta pozycja
PHR14381612700S6196
Simvastatin United States Pharmacopeia (USP) Reference Standard

USP

1612700

Simvastatin

assay

≥98% (HPLC)

assay

-

assay

-

assay

≥97% (HPLC)

form

solid

form

-

form

-

form

solid

Quality Level

100

Quality Level

300

Quality Level

-

Quality Level

100

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

USP

manufacturer/tradename

-

storage temp.

2-8°C

storage temp.

-10 to -25°C

storage temp.

-

storage temp.

2-8°C

storage condition

OK to freeze

storage condition

-

storage condition

-

storage condition

-


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pictograms

Health hazard

signalword

Warning

hcodes

Hazard Classifications

Repr. 2

Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



Certyfikaty analizy (CoA)

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Questions

  1. Can I dissolve Simvastatin powder in DMSO and then activate it through NaOH treatment?

    1 answer
    1. This product is soluble in DMSO or ethanol at a concentration of 50 mg/mL. Treatment with NaOH in ethanol is required, followed by neutralization to pH 7.2 for activation.

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