Examples of 'halofuginone' in a sentence
Meaning of "halofuginone"
halofuginone (noun) - A compound with pharmaceutical properties, used in medical research and potentially in the development of medications
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- A coccidiostat used in veterinary medicine; a synthetic halogenated derivative of febrifugine.
How to use "halofuginone" in a sentence
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halofuginone
The exact way halofuginone works is unknown.
Halofuginone was shown to induce apoptosis of tumors in vivo.
A suitable inhibitor of extracellular matrix synthesis is halofuginone.
The use of halofuginone in feedingstuffs for turkeys.
This increase was almost completely prevented by halofuginone treatment.
Halofuginone is a coccidiostat used in veterinary medicine.
The present invention relates to compositions containing halofuginone.
The use of halofuginone in feedingstuffs for poultry third report.
The method makes it possible to determine the level of halofuginone in feed.
Halofuginone base as lactate salt.
Determination of halofuginone.
No effect of halofuginone on the collagen content was observed in the tibialis muscle.
Premixtures for use in feed in which the use of halofuginone hydrobromide is not authorised.
Use of halofuginone for the manufacture of a medicament for attenuating neovascularization.
A blank feed shall be analysed to check that neither halofuginone nor interfering substances are present.
See also
Halofuginone as the free base is unstable in alkaline and ethyl acetate solutions.
An extension of the use of halofuginone under the following conditions has been proposed.
Halofuginone is a small molecule that can be obtained from the hydrangea root.
The presence of residues of halofuginone in soil therefore presents no risk for the crops.
This effect was also shown to be reversible upon removal of Halofuginone.
Use of halofuginone for the manufacture of a medicament for inhibiting proliferation of human tumour cells.
A murine corneal angiogenesis model was used to evaluate the inhibitory effect of Halofuginone in vivo.
Unchanged Halofuginone is the major component in the tissues.
Kriptazen contains the active substance halofuginone and is a ‘ generic medicine '.
Halofuginone hydrobromide Stenorol.
The data also demonstrate that Halofuginone is able to induce apoptosis of tumor cells.
C halofuginone concentration of the sample solution in μg/ml.
Is a characteristic curve demonstrating the effect of halofuginone on sulfate incorporation into the subendothelial ECM.
Halofuginone is to date the only known collagen type-specific inhibitor on the transcriptional level.
Notably, the in vitro action of halofuginone does not always predict its in vivo effects.
The use is permitted in feed containing the permitted coccidiostats: diclazuril, halofuginone and robenidine.
These effects of Halofuginone have not been demonstrated before.
Furthermore, the prior art does not teach the use of halofuginone in regeneration of muscle.
First, Halofuginone is synthesized in accordance with good pharmaceutical manufacturing practice.
In this study, the researchers hoped to find that halofuginone would suppress the differentiation process.
Furthermore, Halofuginone has been found to inhibit angiogenesis and tumor growth.
FIG . 4 is a bar chart illustrating muscle regeneration after halofuginone treatment.
The active substance in Halocur, halofuginone lactate, prevents the growth of Cryptosporidium parvum.
These results clearly illustrate the dose-dependence of the effect of Halofuginone against malignancies.
The active substance in Kriptazen, halofuginone lactate, prevents the growth of Cryptosporidium parvum.
Anti-sclerosing agents include, without limitation, collagenases and halofuginone.
However, the in vitro action of Halofuginone does not always predict its in vivo effects.
Thus, Halofuginone can be differentiated from currently available therapies for cancer which are actively cytotoxic.
Pharmacotherapeutic group, Other antiprotozoal agents, halofuginone.
Thus, the finding that Halofuginone can inhibit such angiogenesis is both novel and non-obvious.
An almost complete inhibition of microvessel formation was obtained at 100 ng / ml Halofuginone.
The content of halofuginone w (mg/kg) of the sample is given by the following formula.
The only substance, known as the PRS inhibitor, is halofuginone.
In addition, Halofuginone was administered i . p.
Figure 11 shows this effect quantitatively, at increasing doses of Halofuginone.
