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Q: How would a molecule that mimics cyclic AMP affect an olfactory receptor?
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How would a molecule that blocks adenyl cyclase affect the sense of olfaction?

Blocking adenyl cyclase would decrease the production of cyclic AMP (cAMP), which is a second messenger involved in signal transduction in olfactory receptor neurons. As a result, the sense of olfaction would be impaired, as the signaling pathway that allows for the detection and discrimination of different odors would be disrupted.


What does C in the test CRP stands for?

Cyclic AMP Receptor Protein


What does a ring do for chemistry?

A ring is a cyclic molecule as benzene.


What are cyclic and acyclic organic molecule?

An acyclic organic molecule is an open chain compound, for example alkanes and acyclic aliphatic compounds. A cyclic organic molecule is a molecule in which a series of atoms connect to form a loop or ring.


What is the the role of cyclic AMP in cell proliferation?

It is a secondary signaling molecule.


What type of molecule is androstenedione?

Androstenedione is a steroidic hormone with a cyclic structure.


What type of bond does camphor have?

Camphor is an organic cyclic molecule, so it is covalent compound.


Both cyclic and noncyclic electron flow generate the high-energy ATP molecule?

true


Does Cyclic vomiting syndrome affect all races?

CVS appears to affect all races equally


What is yellow sulfur?

Most allotropes of sulfur are yellow. The most common form is the cyclic molecule S8


Is camphor a covalent bond or an ionic bond?

Camphor is an organic cyclic molecule so it is covalent compound.


Is acetic acid aromatic?

No. There are two molecular requirements that must be met to indicate aromaticity. In order to be aromatic a molecule must: 1) have a ring of pi electrons above and below the molecule. This means: a. The molecule must be cyclic. b. All atoms in the ring must be sp2 hybridized c. The molecule must be planar. 2) have an odd number of pairs of pi electrons. Since acetic acid is not cyclic, it cannot meet the first requirement and therefore cannot be aromatic. There are, however, delocalized electrons that increase the stability of the compound.