「PENICILLIN」の共起表現(1語左で並び替え)

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共起表現

「PENICILLIN」の共起表現一覧(1語左で並び替え)

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Propicillin is a	penicillin.
Sulbenicillin (INN) is a	penicillin antibiotic.
In enzymology, a	penicillin amidase (EC 3.5.1.11)
Bacampicillin (INN) is a	penicillin antibiotic.
Pheneticillin (or phenethicillin) is a	penicillin.
Metampicillin (INN) is a	penicillin antibiotic.
The ampicillin resistance gene is a	penicillin beta-lactamase.
lled Miracle Cures for Syphilis: Facts about	Penicillin & Syphilis, Complications and Treatment (194
It is used in medicine such as Calpol and	Penicillin.
sts of antibiotics including doxycycline and	penicillin for up to four weeks in the acute case.
lergy risk of 10% between cephalosporins and	penicillin, recent assessments have shown no increased
ing the molecular structures of morphine and	penicillin.
ming accidentally rediscovers the antibiotic	Penicillin, forgotten since Ernest Duchesne's original
to two or more of the following antibiotics:	penicillin, 2nd generation cephalosporins, e.g., cefuro
Thus, the two substrates of this enzyme are	penicillin and H2O, whereas its two products are carbox
The 3 substrates of this enzyme are	penicillin N, 2-oxoglutarate, and O2, whereas its 4 pro
emisynthetic antibiotic in the same class as	penicillin.
ave in the past yielded such useful drugs as	penicillin and streptomycin and plants use their antibi
thine phenoxymethylpenicillin (or benzathine	penicillin V) is a penicillin.
ension which 1.2 million units of benzathine	penicillin & 1.2 million units of procaine penicillin p
Benzyl	Penicillin Potassium
PBPs vary in their affinity for binding	penicillin or other beta-lactam antibiotics.
Because both	penicillin and para-aminohippurate compete for the same
s, they were replaced for this indication by	penicillin in the 1940s.
estern mores occurring after WWII, caused by	penicillin and the anti-baby pill, was rolled back effe
N, and H2O, whereas its 3 products are CoA,	penicillin G, and L-2-aminohexanedioate.
l engineer who designed the first commercial	penicillin production plant.
Other names in common use include DAOCS,	penicillin N expandase, and DAOC synthase.
s Hans Margreiter and Ernst Brandl developed	Penicillin V in Kundl and from this time on the drug co
f Oxford University scientists who developed	penicillin and was Regius Professor of Medicine at Oxfo
Alexander Fleming had first discovered	penicillin by accident in 1928, but at that time believ
with antibiotic properties, which he dubbed	penicillin.
Having only tried the extracted	penicillin on mice, Florey and colleagues were fearful
he rapid progression of the disease, however	penicillin is the drug of choice for treatment.
This enzyme participates in	penicillin and cephalosporin biosynthesis.
ssociated with angioedema and anaphylaxis in	penicillin allergic patients.
Other names in common use include	penicillin acylase, benzylpenicillin acylase, novozym 2
ailable are also important: Glucose inhibits	penicillin production, whereas lactose does not.
The systematic name of this enzyme class is	penicillin amidohydrolase.
Biochemicals) Limited, or DCBL, manufactured	penicillin in Speke, Liverpool, beginning in 1942.
muramoyl-N-acetyl-D-glucosaminyltransferase,	penicillin binding protein (3 or 1B), and peptidoglycan
isolate the active substance which he named	penicillin, but he was not the first to use its propert
Structure of	Penicillin V
Main article: History of	penicillin
zathine benzylpenicillin (rINN) is a form of	penicillin also known as benzathine penicillin.
terized by their affinity for and binding of	penicillin.
of macrolides is slightly wider than that of	penicillin, and, therefore, macrolides are a common sub
gested transferring the active ingredient of	penicillin back into water by changing its acidity, thi
rst patient to be treated with injections of	penicillin.
, who was responsible for the development of	penicillin.
The discovery of	penicillin is attributed to Scottish scientist and Nobe
as a skin test before the administration of	penicillin.
Others involved in the mass production of	penicillin include Ernst Chain, Howard Florey and Norma
or Merck & Co. to develop mass production of	penicillin.
y, Australian pathogist and co-discoverer of	penicillin, was a resident of the City of Tea Tree Gull
ated with a large intramuscular injection of	penicillin.
eems to have been to determine the effect of	penicillin in the prevention and treatment of venereal
ldren who did not need such large amounts of	penicillin, until their methods of production improved.
nd met the professor to give a final dose of	penicillin to two of the mice.
bitory action against at least 18 strains of	penicillin resistant Staphylococcus bacteria."
The last step in the biosynthesis of	penicillin G is the exchange of the side-chain group so
early 1951 for work on the mode of action of	penicillin.
ccredited with developing the application of	penicillin, and was awarded the Nobel prize for Medicin
The development of	penicillin for use as a medicine is attributed to the A
on's, but he also worked on the chemistry of	Penicillin during the war, and had interest in non-benz
Low levels of	penicillin and nalidixic acid are also present in LJ me
s for the stragically important materials of	penicillin and synthetic rubber.
s showing the in vivo bactericidal action of	penicillin.
of a group that published an early paper on	penicillin in 1943.
e for Physiology or Medicine for his work on	penicillin.
is a distinguished scientist, who worked on	penicillin with Alexander Fleming, and is noted especia
ol, with an antibiotic such as cephalexin or	penicillin and sometimes nicotinamide.
successful, despite producing the first oral	penicillin.
ein altering the side-chains on the original	penicillin molecule has increased the affinity of PBPs
As with any other	penicillin, convulsions can occur if very high doses ar
zylpenicillin (rINN), also known as procaine	penicillin, is a form of penicillin which is a combinat
Bacillus megaterium produces	penicillin amidase used for making penicillin.
DSM Anti-Infectives produces	penicillin G and penicillin intermediates (6-APA and 7-
Temocillin is a β-lactamase resistant	penicillin introduced by Beecham, marketed by Eumedica
For the Japanese band, see	Penicillin (band).
Ampicillin is a moderate spectrum	penicillin antibiotic with good cover against group A s
It stabilises	penicillin and prolongs its sojourn when injected into
Three of the most common are tetracycline,	penicillin and naladixic acid.
en shown to be 100 times more effective than	penicillin, killing over 99% of the pathogenic bacteria
He confirmed that	penicillin was neither an enzyme, as previously thought
icillin is a beta lactam antibiotic from the	penicillin family.
Both parts are members of the	penicillin family of antibiotics, and therefore should
They belong to the	penicillin family and comprise the members ampicillin,
arrow-spectrum beta-lactam antibiotic of the	penicillin class.
Tazobactam sodium is a derivative of the	penicillin nucleus and is a penicillanic acid sulfone.
arrow spectrum beta-lactam antibiotic of the	penicillin class.
uring this period, he became involved in the	penicillin project where he studied the effects of peni
cle growth, and to become a precursor in the	penicillin biosynthetic pathway.
It was Mohandas, after learning that the	penicillin had to be administered by injection every fo
Modifications of the	penicillin molecule so that it was resistant to being b
f insects to insecticides and of bacteria to	penicillin and related anti-bacterial drugs.
today and reserved for patients allergic to	penicillin or where bacteria has developed resistance.
1000 units/ml	Penicillin G
Unlike	penicillin, macrolides have been shown to be effective
This is similar to the fashion in which	penicillin quickly replaced mercurials, particularly ca
II, para-aminohippurate was given along with	penicillin in order to prolong the time penicillin circ
cetamol containing products, when taken with	Penicillin products can cause brief spells of unconscio
phalosporins, the cross-reactivity rate with	penicillin is much lower, having no significantly incre

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「PENICILLIN」の共起表現一覧(1語左で並び替え)