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Merck
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17778

Millipore

Ticarcillin Supplement

suitable for microbiology

Synonyme(s) :

Ticarcillin

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About This Item

Formule empirique (notation de Hill):
C15H16N2O6S2
Numéro CAS:
34787-01-4
Poids moléculaire :
384.43
Numéro CE :
252-213-5
Numéro MDL:
MFCD00864998
Code UNSPSC :
41171614
ID de substance PubChem :
329751566
Nomenclature NACRES :
NA.85

Agence

according to ISO 10273:2017

Niveau de qualité

200

Stérilité

sterile

Forme

powder

Durée de conservation

limited shelf life, expiry date on the label

Application(s)

agriculture
environmental
food and beverages
microbiology

Température de stockage

2-8°C

Adéquation

Yersinia spp.

Chaîne SMILES 

CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](C(O)=O)c3ccsc3)C(=O)N2[C@H]1C(O)=O

InChI

1S/C15H16N2O6S2/c1-15(2)9(14(22)23)17-11(19)8(12(17)25-15)16-10(18)7(13(20)21)6-3-4-24-5-6/h3-5,7-9,12H,1-2H3,(H,16,18)(H,20,21)(H,22,23)/t7-,8-,9+,12-/m1/s1

Clé InChI

OHKOGUYZJXTSFX-KZFFXBSXSA-N

Catégories apparentées

Application

An antibiotic supplement recommended for the selective enrichment of Yersinia enterocolitica.

Composants

Composition (per vial; sufficient for 1000 mL medium): Ticarcillin 1.00 mg

Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Danger

Mentions de danger

H317,H334

Classification des risques

Resp. Sens. 1 - Skin Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCJ2997
BCCF7766
BCCC7238
BCCB4463
BCBW8163

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Consulter la Bibliothèque de documents

Pierre-François Laterre et al.
The Journal of antimicrobial chemotherapy, 70(3), 891-898 (2014-11-30)
The growing incidence of infections caused by Enterobacteriaceae producing ESBLs has led to increased use of carbapenems. Temocillin, which resists most β-lactamases, may be a useful alternative. The aim of this study was to assess the pharmacokinetics and target attainment
Yu-Ting Liao et al.
Antimicrobial agents and chemotherapy, 58(7), 3983-3990 (2014-05-07)
The role of carbapenem-resistant Acinetobacter baumannii (CRAb) in polymicrobial infection remains elusive. Having observed the ability of CRAb to shelter other susceptible bacteria from carbapenem killing, we sought to determine the factors contributing to this sheltering effect by transforming different
Anita Umerska et al.
Biomolecules, 8(4) (2018-10-27)
The worldwide occurrence of resistance to standard antibiotics and lack of new antibacterial drugs demand new strategies to treat complicated infections. Hence, the aim of this study was to examine the antibacterial activities of an antimicrobial peptide, arenicin-3 derivative AA230
Farid El Garch et al.
Antimicrobial agents and chemotherapy, 55(10), 4828-4833 (2011-07-27)
A carbapenem-resistant Pseudomonas aeruginosa strain (PA41437) susceptible to expanded-spectrum cephalosporins was recovered from several consecutive lower-respiratory-tract specimens of a patient who developed a ventilator-associated pneumonia while hospitalized in an intensive care unit. Cloning experiments identified OXA-198, a new class D
A B Bennett et al.
Australian veterinary journal, 91(5), 171-178 (2013-04-26)
To investigate in vitro susceptibilities of canine and feline Escherichia coli and canine Pseudomonas spp. isolates to ticarcillin and ticarcillin-clavulanic acid (T/C). In vitro susceptibility testing of bacterial isolates collected from infections. We tested 148 (83 canine and 65 feline)
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