Benzeneacetic acid, a-hydroxy-a-phenyl-, (3-endo)-8-azabicyclo[3.2.1]oct-3-ylester

CAS: 16444-19-2

Ref. 3D-FB151764

Produktinformation

• Name: Benzeneacetic acid, a-hydroxy-a-phenyl-, (3-endo)-8-azabicyclo[3.2.1]oct-3-ylester
• Synonyme: 1aH,5aH-Nortropan-3a-ol Benzilate, 1α<span class="text-smallcaps">H</smallcap>,5α<smallcap>H</span>-Nortropan-3α-ol, benzilate (ester), 8-Azabicyclo[3.2.1]Oct-3-Yl Hydroxy(Diphenyl)Acetate, Benzeneacetic acid, α-hydroxy-α-phenyl-, (3-endo)-8-azabicyclo[3.2.1]oct-3-yl ester, Benzeneacetic acid, α-hydroxy-α-phenyl-, 8-azabicyclo[3.2.1]oct-3-yl ester, endo-, Benzilic acid, 1α<span class="text-smallcaps">H</smallcap>,5α<smallcap>H</span>-nortropan-3α-yl ester, N-Desmethyl Tropan-3a-yl-(2-hydroxy-2,2-diphenyl)acetate, Nortropinyl benzilate, a-Hydroxy-a-phenylbenzeneacetic Acid (3-endo)-8-Azabicyclo[3.2.1]oct-3-yl Ester, 1αH,5αH-Nortropan-3α-ol, benzilate (ester), Norglipin, Benzilic acid, 1αH,5αH-nortropan-3α-yl ester

Beschreibung

Research has shown that benzeneacetic acid, a-hydroxy-a-phenyl-, (3-endo)-8-azabicyclo[3.2.1]oct-3-ylester has affinity for muscarinic acetylcholine receptors in the brain and spinal cord. The affinity of this ligand for these receptors is higher than that of acetylcholine. This compound is able to bind to the same receptors as acetylcholine, but with a higher efficiency. These properties make it an interesting candidate as a ligand in the development of new drugs to treat diseases related to the nervous system, such as Alzheimer's disease or Parkinson's disease.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 337.41 g/mol
• Formel: C₂₁H₂₃NO₃
• Reinheit: Min. 95%
• InChl: InChI=1S/C21H23NO3/c23-20(25-19-13-17-11-12-18(14-19)22-17)21(24,15-7-3-1-4-8-15)16-9-5-2-6-10-16/h1-10,17-19,22,24H,11-14H2
• InChI Key: InChIKey=HIIVXBCWDPCZJA-UHFFFAOYSA-N
• SMILES: O=C(OC1CC2CCC(C1)N2)C(O)(c1ccccc1)c1ccccc1