trans-4-Aminocyclohexanol

Molecular beacons with JOE dye: Influence of linker and 3' couple quencher.[Pubmed:27720907]

Mol Cell Probes. 2016 Oct;30(5):285-290.

Molecular beacons carrying JOE dye (4',5'-dichloro-2',7'-dimethoxy-6-carboxyfluorescein) on a rigid or flexible linker and one or two BHQ1 quenchers have been prepared and tested in real-time PCR using Fusarium avenaceum elongation factor 1alpha DNA template. The probes were different in their structures (loop size and stem length), linkers for dye attachment (6-aminohexanol or trans-4-Aminocyclohexanol), quencher composition (single and double BHQ1) to elucidate the influence of all these features. Fluorogenic properties of the probes were studied and compared to those of FAM (fluorescein)-based probes. All the factors - stem length, JOE vs FAM, rigid vs flexible linker, single vs double quencher - appeared to play a considerable role in the probe's fluorescent properties and determine the usability of the probe at two different temperatures of fluorescence detection (55 degrees capital ES, Cyrillic and 64 degrees capital ES, Cyrillic).

Novel dihydroquinoline-based MABAs; clues to the identity of LAS-190792: evaluation of WO20111411802.[Pubmed:22251094]

Expert Opin Ther Pat. 2012 Feb;22(2):185-92.

Bifunctional aromatic compounds are claimed to contain a beta(2) agonist pharmacophore linked by a flexible lipophilic spacer incorporating a trans-4-Aminocyclohexanol group to a muscarinic antagonist pharmacophore. The compounds display nanomolar affinity at both beta(2) and M(3) receptors and a prolonged duration of action in animal models. This application is the first from Almirall claiming such compounds although it has recently disclosed that LAS-190792 is progressing toward clinical development.

From 0D dimer to 2D network-supramolecular assembly of organic derivatized polyoxometalates with remote hydroxyl via hydrogen bonding.[Pubmed:19719087]

Inorg Chem. 2009 Oct 5;48(19):9222-35.

A series of remote hydroxyl functionalized organoimido derivatives of hexamolybdate, (Bu(4)N)(2)[Mo(6)O(18)(Cres)] (1) (Cres = 4-amino-m-cresol), (Bu(4)N)(2)[Mo(6)O(17)(Cres)(2)] x H(2)O (2), (Bu(4)N)(2)[Mo(6)O(18)(Phen)] x i-PrOH (Phen = p-aminophenol)(3), (Bu(4)N)(2)[Mo(6)O(18)(Phen)] x EtOH (4), (Bu(4)N)(2)[Mo(6)O(17)(Phen)(2)] (5), (Bu(4)N)(2)[Mo(6)O(18)(Naph)] (Naph = 5-amino-1-napheynyl) (6), and (Bu(4)N)(2)[Mo(6)O(18)(Chex)] x 1.5 H(2)O (Chex = trans-4-Aminocyclohexanol) (7) were synthesized and characterized by single crystal X-ray diffraction, FT-IR spectra, UV-vis spectra, elemental analysis, (1)H NMR, and cyclic voltammetry. X-ray structural study reveals that intermolecular and intramolecular hydrogen bonding plays an important role in their supramolecular assembly; it is found that (i) bridged oxo ligands of hexamolybdate cluster are more inclined to form hydrogen bonds as acceptors than terminal oxo ligands in this system; (ii) small solvent molecules with hydrogen bonding donor and acceptor, such as water, i-PrOH, and EtOH, usually act as hydrogen bonding bridge in their supramolecular assembly; (iii) hydrogen bonding has an important influence on their anion conformation besides cell packing; (iv) the hydrogen bonding supramolecular assembly of compounds 1-7 demonstrate an interesting change from dimer (3), to 1D infinite single chain (4), to 1D infinite double chain (2), and to 2D network (1, 5, 6, and 7) owing to the alteration of the grafting organic ligand, the substituted number, and the crystallized solvent molecule. To explore their potential application in conductivity, the optical band gap of compounds 1-7 were determined upon their solid state reflectance spectra. Our current study not only surveys systematically hydrogen bonding interaction and supramolecular assembly of remote hydroxyl functionalized organoimido-derivatized hexamolybdates but also provides some available precursors for further modification including esterification.