Ribostamycin sulfate
Ribostamycin sulfate Basic information
- Product Name:
- Ribostamycin sulfate
- Synonyms:
-
- Rribostamycin sulfate
- Ribostamycin sulfate
- D-Streptamine, O-2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl-(1→4)-O-[β-D-ribofuranosyl-(1→5)]-2-deoxy-, sulfate (1:1)
- Ribose neoMycin sulfate
- Ribostamycin s
- DTDP-GLUCOSE, DISODIUM SALT
- landamycine
- o-2,6-diamino-2,6-dideoxy-alpha-d-glucopyranosyl-(1-4)-o-(beta-d-streptamin
- CAS:
- 53797-35-6
- MF:
- C17H36N4O14S
- MW:
- 552.55
- EINECS:
- 258-783-1
- Product Categories:
-
- Antibiotics
- AminoglycosidesAntibiotics
- Antibacterial
- Antibiotics A to
- Antibiotics by Application
- Antibiotics N-SAntibiotics
- Chemical Structure Class
- Genetic Marker SelectionAntibiotics
- Interferes with Protein SynthesisSpectrum of Activity
- L - Z
- Mechanism of Action
- Mol File:
- 53797-35-6.mol
Ribostamycin sulfate Chemical Properties
- Melting point:
- 175-180 C
- alpha
- D20 +39° (c = 1)
- Flash point:
- >110°(230°F)
- storage temp.
- Inert atmosphere,2-8°C
- solubility
- H2O: soluble50mg/mL
- form
- powder
- color
- White to Off-White
- Water Solubility
- Soluble in water
- Merck
- 14,8206
- Stability:
- Hygroscopic
- InChIKey
- RTCDDYYZMGGHOE-CARKYZAMNA-N
- SMILES
- OS(O)(=O)=O.NC[C@@H]1O[C@@H](O[C@H]2[C@H](N)C[C@H](N)[C@@H](O)[C@@H]2O[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)[C@@H](N)[C@H](O)[C@H]1O
Safety Information
- Hazard Codes
- T,Xi
- Risk Statements
- 61-20/21/22-36/38
- Safety Statements
- 53-22-36/37/39-45-37/39-26
- WGK Germany
- 3
- RTECS
- WK2300000
- HS Code
- 2941.90.1010
- Storage Class
- 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects - Hazard Classifications
- Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Repr. 1B - Toxicity
- LD50 i.v. in mice: 225 mg/kg (Shomura)
Ribostamycin sulfate Usage And Synthesis
Uses
Antibacterial;Ribosomal protein synthesis inhibitor
Uses
Ribostamycin is a broad-spectrum antimicrobial isolated from Streptomyces ribosifidicus. It is used in pharmacokinetic and nephrotoxicity studies.
Definition
ChEBI: An aminoglycoside sulfate salt resulting from the reaction of ribostamycin with sulfuric acid.
Biological Activity
Aminoglycosides, such as ribostamycin, bind to the bacterial 30S and 50S ribosomal subunit, which inhibits the translocation of the peptidyl-tRNA from the A-site to the P-site. This causes misreading of mRNA which makes bacteria unable to make essential proteins. It also inhibits the chaperone activity of protein disulfide isomerase (PDI).
Synthesis
Preparation of high-purity ribostamycin sulfate:
1. The resolving solution is acidified and diluted.
2. Loaded onto an ion-exchange column, washed with water.
3. Eluted with ammonia, collecting fractions before optical rotation reaches "0".
4. The eluate is concentrated by nanofiltration and then by steam thin-film evaporation.
5. The concentrate is treated with charcoal and spray-dried.
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Ribostamycin sulfate(53797-35-6)Related Product Information
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- Magnesium sulfate heptahydrate
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- Ribose
- Ribonucleic acid
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- Neomycin sulfate
- D-Ribose
- Ammonium sulfate
- Barium sulfate
- Kanamycin sulfate
- Aluminum sulfate
- MICRONOMICIN SULFATE
- sulfate
- 1,1,3,3-TETRAMETHYLBUTYL ISOCYANIDE