Ristomycin sulfate

Modify Date: 2024-01-06 19:30:22

Ristomycin sulfate Structure
Ristomycin sulfate structure
Common Name Ristomycin sulfate
CAS Number 11140-99-1 Molecular Weight 2165.996
Density N/A Boiling Point N/A
Molecular Formula C95H110N8O44.H2SO4 Melting Point N/A
MSDS Chinese USA Flash Point N/A

 Use of Ristomycin sulfate


Ristomycin sulfate is a glycopeptide antibiotic isolated from Nocardia lurida[1].

 Names

Name ristocetin sulfate salt
Synonym More Synonyms

 Ristomycin sulfate Biological Activity

Description Ristomycin sulfate is a glycopeptide antibiotic isolated from Nocardia lurida[1].
Related Catalog
References

[1]. M C Berndt, et al. Ristocetin-dependent reconstitution of binding of von Willebrand factor to purified human platelet membrane glycoprotein Ib-IX complex. Biochemistry. 1988 Jan 26;27(2):633-40.

 Chemical & Physical Properties

Molecular Formula C95H110N8O44.H2SO4
Molecular Weight 2165.996
Exact Mass 2164.628906
PSA 899.20000
Storage condition -20°C

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
VJ8650000
CHEMICAL NAME :
Ristomycin, sulfate
CAS REGISTRY NUMBER :
11140-99-1
LAST UPDATED :
198903

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
660 mg/kg
TOXIC EFFECTS :
Behavioral - tremor Behavioral - excitement Lungs, Thorax, or Respiration - other changes
REFERENCE :
AMBIEH Antibiotiki i Meditsinskaya Biotekhnologiya. Antibiotics and Medical Biotechnology. (V/O Mezhdunarodnaya Kniga, 113095 Moscow, USSR) V.30-V.32, 1985-1987 Volume(issue)/page/year: 32,910,1987

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Risk Phrases 36/38
Safety Phrases 22-24/25-37/39-26
RIDADR UN 3249
RTECS VJ8650000
Packaging Group III
Hazard Class 6.1(b)

 Articles5

More Articles
Overproduction of Ristomycin A by activation of a silent gene cluster in Amycolatopsis japonicum MG417-CF17.

Antimicrob. Agents Chemother. 58(10) , 6185-96, (2014)

The emergence of antibiotic-resistant pathogenic bacteria within the last decades is one reason for the urgent need for new antibacterial agents. A strategy to discover new anti-infective compounds is...

Jordan, D.C., D. Gottlieb and P. Shaw,, ed.

Antibiotics New York , (1967) 1 , 84

Ristocetin- and thrombin-induced platelet aggregation at physiological shear rates: differential roles for GPIb and GPIIb-IIIa receptor.

Thromb. Haemost. 80 , 428-436, (1998)

We recently reported that washed platelets (WP) activated with ADP and expressing surface-bound vWF aggregated in flow through small tubes or in a cylindrical couette device at physiological shear rat...

 Synonyms

RISTOCETIN A SULFATE
Methyl (1S,2R,18R,19R,22R,34S,37R,40R)-22-amino-2-[(3-amino-2,3,6-trideoxy-α-L-ribo-hexopyranosyl)oxy]-64-{[β-D-arabinopyranosyl-(1->2)-D-mannopyranosyl-(1->2)-[6-deoxy-α-L-mannopyranosyl-( 1->6)]-β-D-glucopyranosyl]oxy}-18,26,31,44,49-pentahydroxy-47-(β-D-mannopyranosyloxy)-30-methyl-21,35,38,54,56,59-hexaoxo-7,13,28-trioxa-20,36,39,53,55,58-hexaazaundecacyclo[38.14.2.2.2.2.1.1.1.1~41,
Ristocetin sulfate salt
RISTOMYCIN MONOSULFATE
RISTOCETINSULFATQ
Ristocetin A sulphate
RISTOCETIN SULFATE
RISTOMYCIN
SPONTIN
ristomycin,sulfate
RISTON
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