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F0881

Fusidic acid sodium salt

≥98% (TLC), Bacterial protein synthesis inhibitor

Sinonimo/i:

Fucidin

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1 g
Per informazioni sulla disponibilità, contatta il Servizio Clienti.
369,00 €
5 g
Per informazioni sulla disponibilità, contatta il Servizio Clienti.
1.470,00 €
1.249,50 €

Informazioni su questo articolo

Formula condensata:
C31H47O6Na
Numero CAS:
Peso molecolare:
538.69
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
212-030-3
MDL number:
Assay:
≥98% (TLC)
Quality level:

369,00 €


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Nome del prodotto

Fusidic acid sodium salt, ≥98% (TLC)

Quality Level

assay

≥98% (TLC)

solubility

H2O: soluble

antibiotic activity spectrum

neoplastics

mode of action

protein synthesis | interferes

storage temp.

2-8°C

SMILES string

[Na+].C[C@@H]1[C@H](O)CC[C@@]2(C)C1CC[C@@]3(C)C2[C@H](O)CC4\C([C@H](C[C@]34C)OC(C)=O)=C(/CC\C=C(\C)C)C([O-])=O

InChI

1S/C31H48O6.Na/c1-17(2)9-8-10-20(28(35)36)26-22-15-24(34)27-29(5)13-12-23(33)18(3)21(29)11-14-30(27,6)31(22,7)16-25(26)37-19(4)32;/h9,18,21-25,27,33-34H,8,10-16H2,1-7H3,(H,35,36);/q;+1/p-1/b26-20-;/t18-,21-,22-,23+,24+,25-,27-,29-,30-,31-;/m0./s1

InChI key

HJHVQCXHVMGZNC-JCJNLNMISA-M

General description

Fusidic acid is an antibiotic substance, resembling the structure of a steroid. It belongs to the class of fusidanes.

Application

Fusidic acid sodium salt has been used to study the effects of three-drug combinations on the growth rate of a bacterium, wild-type Escherichia coli. It is also used to study the in vitro susceptibility of dog-derived European methicillin-resistant Staphylococcus pseudintermedius and Staphylococcus aureus strains and their methicillin-susceptible counterparts.

Biochem/physiol Actions

Suppresses nitric oxide lysis of pancreatic islet cells. Inhibits protein synthesis in prokaryotes by inhibiting the ribosome-dependent activity of G factor and translocation of peptidyl-tRNA.
Suppresses nitric oxide lysis of pancreatic islet cells; inhibits protein synthesis in prokaryotes.
Fusidic acid possesses antimicrobial action against skin pathogens. It is highly specific to Staphylococcus aureus. It is therefore used for treating infected traumatic wounds, folliculitis, furunculosis, impetigo, erythrasma and abscesses.

Features and Benefits

This compound is a featured product for Gene Regulation research. Click here to discover more featured Gene Regulation products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

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Questo articolo
F0756F6513Y0001394
Fusidic acid

Sigma-Aldrich

F0756

Fusidic acid

Fusaric acid from Gibberella fujikuroi

Sigma-Aldrich

F6513

Fusaric acid

assay

≥98% (TLC)

assay

-

assay

≥98% (TLC)

assay

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

solubility

H2O: soluble

solubility

-

solubility

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

solubility

-

mode of action

protein synthesis | interferes

mode of action

-

mode of action

enzyme | inhibits

mode of action

-

antibiotic activity spectrum

neoplastics

antibiotic activity spectrum

-

antibiotic activity spectrum

Gram-positive bacteria

antibiotic activity spectrum

-


Hazard Classifications

Acute Tox. 4 Oral

pictograms

Exclamation mark

signalword

Warning

hcodes

Classe di stoccaggio

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Articoli

We offer a variety of small molecule research tools, such as transcription factor modulators, inhibitors of chromatin modifying enzymes, and agonists/antagonists for target identification and validation in gene regulation research; a selection of these research tools is shown below.


Susceptibility in vitro of canine methicillin-resistant and-susceptible staphylococcal isolates to fusidic acid, chlorhexidine and miconazole: opportunities for topical therapy of canine superficial pyoderma
<BIG>Clark SM, et al. </BIG>
The Journal of Antimicrobial Chemotherapy, 2048-2052 (2015)
Fusidic acid in dermatology
British Journal of Dermatology, 37-40 (1998)
Enhanced identification of synergistic and antagonistic emergent interactions among three or more drugs
<BIG>Tekin E, et al.</BIG>
Journal of the Royal Society, Interface / the Royal Society, 20160332-20160332 (2016)



Numero articolo commerciale globale

SKUGTIN
F0881-5G04061833611432
F0881-1G04061835556793

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