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43963

Millipore

Moxalactam Supplement

suitable for microbiology

Synonim(y):

Listeria MOX Supplement

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About This Item

Wzór empiryczny (zapis Hilla):
C20H20N6O9S
Numer CAS:
64952-97-2
Masa cząsteczkowa:
520.47
Numer WE:
265-287-9
Numer MDL:
MFCD00865991
Kod UNSPSC:
41171614
Identyfikator substancji w PubChem:
329756436
NACRES:
NA.85

sterylność

sterile

Poziom jakości

100

Postać

powder

okres trwałości

limited shelf life, expiry date on the label

Zastosowanie

environmental
food and beverages
microbiology

temp. przechowywania

2-8°C

przydatność

Listeria spp.

ciąg SMILES

CO[C@]2(NC(=O)C(C(O)=O)c1ccc(O)cc1)[C@H]3OCC(CSc4nnnn4C)=C(N3C2=O)C(O)=O

InChI

1S/C20H20N6O9S/c1-25-19(22-23-24-25)36-8-10-7-35-18-20(34-2,17(33)26(18)13(10)16(31)32)21-14(28)12(15(29)30)9-3-5-11(27)6-4-9/h3-6,12,18,27H,7-8H2,1-2H3,(H,21,28)(H,29,30)(H,31,32)/t12?,18-,20+/m1/s1

Klucz InChI

JWCSIUVGFCSJCK-CAVRMKNVSA-N

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Opis ogólny

An antibiotic supplement recommended for selective isolation and cultivation of Listeria monocytogenes.

Zastosowanie

for selective isolation and cultivation of Listeria monocytogenes

Komponenty

(per vial, sufficient for 1000 ml medium)
Moxalactam 20.0 mg

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certyfikaty analizy (CoA)

Lot/Batch Number
BCCL5467
BCCM4077
BCCJ8290
BCCG5972
BCCC3601

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Xiaojun Wang et al.
Proteins, 47(1), 86-96 (2002-03-01)
The class A beta-lactamase TEM-1 is a key bacterial resistance enzyme against beta-lactam antibiotics, but little is known about the energetic bases for complementarity between TEM-1 and its inhibitors. Most inhibitors form a covalent adduct with the catalytic Ser70, making
Lionel Vercheval et al.
The Biochemical journal, 432(3), 495-504 (2010-11-27)
The activity of class D β-lactamases is dependent on Lys70 carboxylation in the active site. Structural, kinetic and affinity studies show that this post-translational modification can be affected by the presence of a poor substrate such as moxalactam but also
James Spencer et al.
Journal of the American Chemical Society, 127(41), 14439-14444 (2005-10-13)
Metallo-beta-lactamases are zinc-dependent enzymes responsible for resistance to beta-lactam antibiotics in a variety of host bacteria, usually Gram-negative species that act as opportunist pathogens. They hydrolyze all classes of beta-lactam antibiotics, including carbapenems, and escape the action of available beta-lactamase
Julian R Garneau et al.
Journal of clinical microbiology, 57(5) (2019-02-15)
The epidemiology of Clostridioides difficile infection (CDI) has drastically changed since the emergence of the epidemic strain BI/NAP1/027, also known as ribotype 027 (R027). However, the relationship between the infecting C. difficile strain and clinical outcomes is still debated. We
Markus Fridén et al.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 30(1), 150-161 (2009-09-17)
A major challenge associated with the determination of the unbound brain-to-plasma concentration ratio of a drug (K(p,uu,brain)), is the error associated with correction for the drug in various vascular spaces of the brain, i.e., in residual blood. The apparent brain
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