Grundinformationen
- Standard-SMILES
NC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H](N)C[C@@H]2N)[C@H](O)[C@@H](O)[C@@H]1O.O=S(=O)(O)O- InChIKey
OOYGSFOGFJDDHP-KMCOLRRFSA-N- Summenformel
- C18H38N4O15S
- Durchschnittliche Molmasse
- 582,6 g/mol
- Monoisotopische Masse
- 582,20543769
Namen und Bezeichner
- Bevorzugter Name
- Kanamycin A Sulfate
- IUPAC
- (2R,3S,4S,5R,6R)-2-(aminomethyl)-6-[(1R,2R,3S,4R,6S)-4,6-diamino-3-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triol;sulfuric acid
- Lokaler Name
- Kanamycinsulfat
- Englischer Name
- Kanamycin sulfate
- Summenformel
- C18H38N4O15S
- Molmasse
- 582.58
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
25389-94-0、3847-27-6、64013-70-3- PubChem CID
- 441374
- DTXSID
DTXSID1047524- ChEMBL
CHEMBL1446- ChEBI
CHEBI:6109- UNII
- J80EX28SMQ
- EC Number
- 223-347-1、613-414-7
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 366 Ų
- H-Brücken-Donoren
- 13
- H-Brücken-Akzeptoren
- 19
- Frei drehbare Bindungen
- 6
- Schwere Atome
- 38
- Formalladung
- 0
- Komplexität
- 720
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 250 °C · 250°C
- Dichte
- 1.3619 · 1.3619 (rough estimate)
- Brechungsindex
- 117.5 ° · 117.5 ° (C=1, H2O)
- storage temp.
- 2 · 2-8°C
- Löslichkeit
- 2 O: · H2O: 10-50 mg/mL As a stock solution. Stock solutions should be stored at 2-8°C. Stable at 37°C for 5 days.
- Aggregatzustand
- powder
- Farbe
- white to off-white
- Biologische Quelle
- Streptomyces kanamyceticus
- Wasserlöslichkeit
- 10 mg/ml · Soluble in water at 10mg/ml
- Merck
- 14 · 14,5281
- Major Application
- pharmaceutical (small molecule)
- InChIKey
- OOYGSFOGFJDDHP-KMCOLRRFSA-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]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 1% (1 of 96) of reports.
Danger
H360 (69.8%): May damage fertility or the unborn child [Danger Reproductive toxicity];H372 (29.2%): Causes damage to organs through prolonged or repeated exposure [Danger Specific target organ toxicity, repeated exposure];H400 (29.2%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard];H410 (29.2%): Very toxic to aquatic life with long lasting effects [Warning Hazardous to the aquatic environment, long-term hazard]
P203, P260, P264, P270, P273, P280, P318, P319, P391, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 96 reports by companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Reported as not meeting GHS hazard criteria per 1 of 96 reports by companies.;There are 9 notifications provided by 95 of 96 reports by companies with hazard statement code(s).;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Gefahrenhinweise
Hazard Classes and Categories
Repr. 1B (69.8%);STOT RE 1 (29.2%);Aquatic Acute 1 (29.2%);Aquatic Chronic 1 (29.2%)
Repr. 1B (100%)
Sicherheitsdaten
- wgk
- 3
- hs_code
- 29419020
- RTECS-Nr.
- NZ3225030
- risk_code
- 61
- Toxizität
- LD50 in mice: 20.7 g/kg orally; 1450 mg/kg i.p. (Zel'tser)
- hazard_code
- T
- safety_code
- 22-24/25-45-53
- Speicherklasse
- 6.1D - Non-combustible acute toxic Cat.3toxic hazardous materials or hazardous materials causing chronic effects
- Hazard Classifications
- Repr. 1B
Chemie und Industrie
Verwendung und Herstellung
Anwendungen
BeschreibungKanamycin was found by Umezawa et al. in the culture broth of Streptomyces kanamyceticus in 1957. It is produced with other components, kanamycins B (bekanamycin) and C, which are also separated during the purification. The compound shows much lower toxicity than the earlier aminoglycosides, streptomycin and neomycin, and strong activity against a wide range of gram-positive and gram-negative bacteria, including Mycobacterium. Kanamycin has been used clinically for treatment of such serious infections as dysentery, salmonellosis, and tuberculosis.
VerwendenKanamycin sulfate is an antibacterial agent similar to neomycin.
Vor- und nachgelagerte Produkte
Vorgelagerte Rohstoffe
Anbieter50 Anbieter
Ergänzende Hinweise
DefinitionA broadspectrum antibiotic.
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