Examples of 'compounds of examples' in a sentence
Meaning of "compounds of examples"
The phrase 'compounds of examples' is grammatically incorrect as it seems to combine the terms 'compounds' and 'examples' without a clear meaning. It is likely a typo or an incorrect use of language
How to use "compounds of examples" in a sentence
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compounds of examples
The compounds of Examples were duplicated at each concentration.
Pharmaceutical test examples with the compounds of Examples are described below.
Thus, the compounds of Examples are useful for osteoporosis.
With the proviso that, compounds of examples Nos.
The compounds of Examples 1 to 6 were metabolized to roflumilast by enzymes from human liver.
The Ki values of several compounds of Examples are shown in Tables below.
The compounds of Examples 1 to 3 relate to a particularly preferred embodiment of the present invention.
The structures and physicochemical data of the compounds of Examples are shown in Tables 9.
The compounds of Examples 1 to 5 were exposed to serial dilution and duplicated for each concentration.
These results indicate that the compounds of Examples 1 and 2 exhibit a mixed activity.
The Compounds of Examples tabulated below were all prepared using the following general method, -.
The two most sensitive compounds were the compounds of Examples 5 and 6 in all cases.
All compounds of Examples showed selective CB2 receptor affinity.
Delayed Release Fragrances stands in the following for compounds of Examples 2 and 3.
By a similar method the compounds of Examples 6 through 8 were prepared using the starting materials shown.
See also
Representative of the novel compounds of this invention are the compounds of examples 1-86 hereinafter.
The compounds of Examples 1 to 8 showed a nematocidal activity against Panagrellus silusiae.
These tests clearly show that the compounds of Examples 1 and 2 are indeed substance P antagonists.
Compounds of examples 1 to 3 have been prepared according to scheme 1.
Specific illustrative preparation of the compounds of Examples 1 and 3 are described after Table I.
Compounds of examples 1 and 2 were prepared according to this process.
Illustrative thereof are the compounds of examples 1 and 2b.
Particularly, the compounds of Examples of the present invention have high ACC2 selectivity.
Following the general method of example 1 the compounds of examples 2 to 37 were prepared.
Compounds of examples 1-6 were essentially stable under these conditions.
Physical properties of the compounds of Examples 9 to 81 are as follows.
The compounds of examples 1 to 4 have been obtained using synthetic method 1.
Pharmacological activity of the compounds of Examples 1 and 2.
All the compounds of examples 1 to 58 showed activity in the above test.
The product was identical to the compounds of Examples 5 and 8.
The following compounds of examples 2 to 6 can be prepared according to the same procedure,.
Preferred compounds of the invention include the compounds of Examples 1 to 68.
The compounds of examples 2-6 have advantageous pharmaceutical properties over a sustained period of time.
The structural formulas of the compounds of Examples are shown in Tables 1 to 3.
The compounds of Examples 9 to 12 were prepared in an analogous manner.
The antimicrobial activity of the compounds of Examples 1-5 was evaluated as follows.
The compounds of Examples 2 to 5 were prepared in the same manner.
Figure 2 shows the synthetic scheme of compounds of Examples 2 and 5.
The compounds of Examples 2-8 were prepared in the following manner.
Structures and physicochemical data of the compounds of Examples 1 to 16 are shown in Table 2.
The compounds of Examples 3 and 4 showed similar properties.
The most important activity was exhibited by the compounds of Examples 2 and 6.
The compounds of Examples 2 and 5 are dispersed in the aqueous phase.
Figure 2 is a schematic illustrating the preparation of the compounds of Examples 5 through 8.
The structures of the compounds of Examples 7 to 10 are shown below.
Compounds of Examples 2 to 33 were synthesized in similar manners to the method of Example 1.
The NMR chemical shifts of the compounds of examples 3 to 12 are described in the following,.
Scheme Ib illustrates but is not limited to the preparation of compounds of Examples 2 and 13.
The compounds of Examples 4 aind 5 have marked hypnotic power.
Compounds of the invention include the compounds of Examples 1 to 62 and salts thereof.
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