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M5255

Mycophenolsäure

from Penicillium brevicompactum, ≥98% (HPLC), powder, IMP dehydrogenase inhibitor

Synonym(e):

6-(1,3-Dihydro-7-hydroxy-5-methoxy-4-methyl-1-oxo-isobenzofuran-6-yl)-4-methyl-4-hexensäure

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Größe/SKUVerfügbarkeitPreis
50 mg
Warenkorb auf Verfügbarkeit prüfen
€ 89,70
250 mg
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€ 308,00

Über diesen Artikel

Empirische Formel (Hill-System):
C17H20O6
CAS-Nummer:
Molekulargewicht:
320.34
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
246-119-3
MDL number:
Beilstein/REAXYS Number:
1295848
Assay:
≥98%

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Produktname

Mycophenolsäure, ≥98%

biological source

Penicillium brevicompactum

Quality Segment

assay

≥98%

color

white to yellow-white

mp

<143.0 °C

solubility

methanol: 49.00-51.00 mg/mL, clear, colorless to faintly yellow

mode of action

enzyme | inhibits

originator

Novartis

storage temp.

2-8°C

SMILES string

COc1c(C)c2COC(=O)c2c(O)c1C\C=C(/C)CCC(O)=O

InChI

1S/C17H20O6/c1-9(5-7-13(18)19)4-6-11-15(20)14-12(8-23-17(14)21)10(2)16(11)22-3/h4,20H,5-8H2,1-3H3,(H,18,19)/b9-4+

InChI key

HPNSFSBZBAHARI-RUDMXATFSA-N

Gene Information

Application

Mycophenolic acid (MPA), produced by Penicillum brevi-compactum, is a selective inhibitor of inosine monphosphate dehydrogenase, thus inhibiting DNA synthesis in T and B lymphocytes. It has also been shown to act as an immunosuppressive agent, and as an inducer of monocyte differentiation and apoptosis in human lymphoid and monocytic cell lines. As a selection agent, MPA is used for transfected animal cells expressing the E. Coli gene for xanthine-guanine phosphoribosyl transferase, and is recommended for use at 25μg/mL.

Biochem/physiol Actions

Mode of Action: This product acts by suppressing the cytokine-induced nitric oxide production, inhibiting early stage biosynthesis of purine nucleotides and as a specific inhibitor of IMP dehydrogenase.

Features and Benefits

This compound was developed by Novartis. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Preparation Note

Mycophenolic acid is soluble in methanol at 50 mg/mL, yielding a colorless to faint yellow solution, as well as chloroform, dichloromethane, ethanol and .1 N NaOH. After reconstitution, the recommendation is to sterilize via filtration thorugh a 0.22 μm pore-size filter, aliquot, and freeze at -20°C.

Disclaimer

As supplied, this product should be stored desiccated at 2-8°C, and is stable for 5 years when stored properly.

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Dieser Artikel
89287M3536475913
description

≥98%

description

analytical standard

description

powder, BioReagent, suitable for cell culture

description

An immunosuppressive agent that inhibits de novo purine nucleotide synthesis via inhibition of inosine monophosphate dehydrogenase and prevents the formation of XMP and GMP.

assay

≥98%

assay

≥98.5% (HPLC)

assay

-

assay

≥95% (HPLC)

Quality Level

300

Quality Level

100

Quality Level

300

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

10-30°C

solubility

methanol: 49.00-51.00 mg/mL, clear, colorless to faintly yellow

solubility

-

solubility

methanol: 50 mg/mL

solubility

ethanol: soluble, 0.1 M NaOH: 10 mg/mL

originator

Novartis

originator

-

originator

-

originator

-

color

white to yellow-white

color

-

color

white to yellow-white

color

white to off-white


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Signalwort

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Muta. 2 - Repr. 1B - STOT RE 1 Oral

Zielorgane

Immune system

Lagerklasse

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Was ist los?

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

PSA (Persönliche Schutzausrüstung)

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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