| Weight | 552.626 g/mol |
|---|---|
| Formula | C22H44N6O10 |
| Hydrogen Acceptors | 15 |
| Hydrogen Donors | 11 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 10 |
Arbekacin (51025-85-5)
Score:
#392 in Microbiology
,
#3063 in Biology
,
#3831 in Chemistry
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- In vitro activities of daptomycin, arbekacin, vancomycin, and gentamicin alone and/or in combination against glycopeptide intermediate-resistant Staphylococcus aureus in an infection model (Antimicrobial Agents and Chemotherapy, 2000)
- Comparative studies of the bactericidal, morphological and post-antibiotic effects of arbekacin and vancomycin against methicillin-resistant Staphylococcus aureus. (Journal of Antimicrobial Chemotherapy, 1997)
- Population Pharmacokinetics of Arbekacin, Vancomycin, and Panipenem in Neonates (Antimicrobial Agents and Chemotherapy, 2004)
- Clinical glycopeptide-intermediate staphylococci tested against arbekacin, daptomycin, and tigecycline (Diagnostic Microbiology and Infectious Disease, 2004)
- STRUCTURES OF ENZYMATICALLY MODIFIED PRODUCTS OF ARBEKACIN BY METHICILLIN-RESISTANT Staphylococcus aureus (The Journal of Antibiotics, 1993)
- Enzymatic 2'-N-Acetylation of Arbekacin and Antibiotic Activity of Its Product (The Journal of Antibiotics, 1996)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC(C(OC1CN)OC2C(CC(C(C2O)OC3C(C(C(C(O3)CO)O)N)O)NC(=O)C(CCN)O)N)N
-
InChIKeyMKKYBZZTJQGVCD-UHFFFAOYSA-N
- Pubchem - Arbekacin
- Wikipedia - arbekacin
Arbekacin (INN) is a semisynthetic aminoglycoside antibiotic. It is primarily used for the treatment of infections caused by multi-resistant bacteria including methicillin-resistant Staphylococcus aureus (MRSA). Arbekacin was originally synthesized from dibekacin in 1973.
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