Examples of 'pharmacologically acceptable salt thereof' in a sentence
Meaning of "pharmacologically acceptable salt thereof"
pharmacologically acceptable salt thereof: This phrase is technical terminology used in pharmacology or chemistry to refer to a chemically acceptable salt form of a drug compound that can be used for pharmaceutical purposes
How to use "pharmacologically acceptable salt thereof" in a sentence
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pharmacologically acceptable salt thereof
Hydroxycitric acid or a pharmacologically acceptable salt thereof.
Represents a hydrogen atom or a methyl group, a pharmacologically acceptable ester thereof, or a pharmacologically acceptable salt thereof.
And a pharmacologically acceptable salt thereof.
A phosphonooxymethyl derivative of ravuconazole is preferably a solvate of a pharmacologically acceptable salt thereof.
Or a pharmacologically acceptable salt thereof.
The compound according to the present invention can be formed into a pharmacologically acceptable salt thereof.
Glycine, or a pharmacologically acceptable salt thereof.
The compound useful according to the present invention is Donepezil or a pharmacologically acceptable salt thereof.
A compound or pharmacologically acceptable salt thereof which is selected from the following group,.
The use of a phosphoric diester compound of the following Formula I or a pharmacologically acceptable salt thereof.
A compound of Claim 1 or a pharmacologically acceptable salt thereof for treating cancer.
The benzimidazole derivative according to claim 1 which is or a pharmacologically acceptable salt thereof.
A diazepinedione derivative or a pharmacologically acceptable salt thereof defined in claim 1, wherein W is tetrazole.
For example, an arylcarboxylic acid is added to a pyridonecarboxylic acid or a pharmacologically acceptable salt thereof.
A compound of Claim 1 or a pharmacologically acceptable salt thereof for treating or preventing a neurodegenerative disease.
See also
pharmacologically acceptable
pharmacologically acceptable salt
pharmacologically active
pharmacologically active compound
For example, a heterocyclic base is added to an arylcarboxylic acid or a pharmacologically acceptable salt thereof.
A penem derivative or a pharmacologically acceptable salt thereof according to Claim 1 for use in therapy.
An antispasmodic composition containing a compound of the formula ( I ) or a pharmacologically acceptable salt thereof.
The tocopherol derivative or pharmacologically acceptable salt thereof according to claim 1 wherein R ₃ is taurine.
A novel tetracyclic compound represented by general formula ( I ) or a pharmacologically acceptable salt thereof.
The tocopherol derivative or pharmacologically acceptable salt thereof according to claim 1 wherein R ₃ is cysteine.
An antiulcer composition containing a compound of the formula ( I ) or a pharmacologically acceptable salt thereof.
A compound of Claim 1 or a pharmacologically acceptable salt thereof for treating cellular proliferative disorders.
A combination consisting of ketanserin and L-carnitine or one pharmacologically acceptable salt thereof.
The tocopherol derivative or pharmacologically acceptable salt thereof according to claim 1 wherein R ₃ is glutathione.
The above-mentioned preparation contains an effective amount of compound ( I ) or a pharmacologically acceptable salt thereof.
The biphenylmethane derivative or a pharmacologically acceptable salt thereof as claimed in claim 1, wherein R ⁵ is carboxyl.
A pharmaceutical composition including the pyridine derivative according to ( 1 ) or ( 2 ) above or a pharmacologically acceptable salt thereof.
The inhibitor contains beraprost or a pharmacologically acceptable salt thereof as the active ingredient.
The present invention provides 2-fluoroneplanocin A or a pharmacologically acceptable salt thereof.
The tocopherol derivative or pharmacologically acceptable salt thereof according to claim 1 wherein R ₃ is aspartic acid.
The DMG component may be N, N-dimethylglycine or a pharmacologically acceptable salt thereof.
The tocopherol derivative or pharmacologically acceptable salt thereof according to claim 1 wherein R ₃ is glutamic acid.
Use according to claim 19, wherein the active ingredient is tolterodine or a pharmacologically acceptable salt thereof.
The tocopherol derivative or pharmacologically acceptable salt thereof according to claim 1 wherein R ₃ is Y - aminobutyric acid.
V represents CH or a nitrogen atom ; X represents a halogen atom, and, a pharmacologically acceptable salt thereof.
A cyclic ketone derivative or a pharmacologically acceptable salt thereof according to Claim 1, where X is O.
The agents can be a free acid or base, or a pharmacologically acceptable salt thereof.
The compound or pharmacologically acceptable salt thereof according to claim 1, which is,.
The present invention provides the compound defined below, a pharmacologically acceptable salt thereof or a hydrate thereof.
A compound or a pharmacologically acceptable salt thereof according to claim 1, selected from the following,.
A compound of Claim 1 selected from, or a pharmacologically acceptable salt thereof.
The compound or pharmacologically acceptable salt thereof of claim 1, wherein R3 and R4 are methyl groups.
A thiadiazoline derivative represented by formula ( 208 ), or a pharmacologically acceptable salt thereof.
A triazole compound or a pharmacologically acceptable salt thereof according to claims 2 to 17 wherein p is 0 or 1.
The amide derivative according to [ 1 ], wherein W is a bond, or a pharmacologically acceptable salt thereof.
The tocopherol derivative or pharmacologically acceptable salt thereof as defined under ( 1 ) wherein R ₃ is glutamic acid.
The compound of Claim 5 where J is C1-C6 alkoxy, or a pharmacologically acceptable salt thereof.
A compound of Claim 1 or a pharmacologically acceptable salt thereof for inhibiting PARP, VEGFR2, or MLK3 activity.
X represents a halogen atom, or a pharmacologically acceptable salt thereof.
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Uppers and parts thereof excluding stiffeners
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Those which are deemed acceptable are to be used as textbooks
Acceptable and sustainable resolution of defence property
Pooled testing is an acceptable approach in many situations
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These metabolites appear to be pharmacologically inactive in man