The indane (2,3-dihydro-1H-indene) ring system is an attractive scaffold for biologically active compounds due to the combination of aromatic and aliphatic properties fused together in one rigid system. This bicyclic structure provides a wide range of possibilities to incorporate specific substituents in different directionalities, thus being an attractive scaffold for medicinal chemists. Notably, many indane-based compounds are being used in the clinic to treat various diseases, such as indinavir, an HIV-1 protease inhibitor; indantadol, a potent Monoamine Oxidase (MAO)-inhibitor; the amine uptake inhibitor indatraline; and the ultra-long-acting β-adrenoceptor agonist indacaterol. Given the diversity of targets these drugs act on, one coul...
Rigidification of the isobutyl side chain of drug-like AT(2) receptor agonists and antagonists that ...
A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagoni...
Rigidification of the isobutyl side chain of drug-like AT(2) receptor agonists and antagonists that ...
Title compds. I [L1 = O, CO or SO2; L2 = NR8SO2 or SO2NR9; R1 = H, (un)substituted alkyl, cycloalkyl...
In quest of elucidating the diverse pharmacological properties of 1,3-indanedione derivatives, we ha...
The present invention relates to indane deriv. I [L1 = O, (CR5R6)m, OCR7R8, CR9R10O; L2 = NR11SO2 or...
The present invention relates to indane deriv. I [L1 = O, (CR5R6)m, OCR7R8, CR9R10O; L2 = NR11SO2 or...
A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagoni...
A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagoni...
The indanone core is ubiquitous to a host of isolated natural compounds that have shown significant ...
Recent reports document that α-tetralone (3,4-dihydro-2H-naphthalen-1-one) is an appropriate scaffol...
The indan ring system is present in several compounds with important pharmacological properties. In ...
A Privileged structureis a molecular scaffold that can provide potent and selective ligands for a ra...
International audienceIndenoindoles and their isomers cyclopentacarbazoles represent a wide class of...
Rigidification of the isobutyl side chain of drug-like AT(2) receptor agonists and antagonists that ...
Rigidification of the isobutyl side chain of drug-like AT(2) receptor agonists and antagonists that ...
A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagoni...
Rigidification of the isobutyl side chain of drug-like AT(2) receptor agonists and antagonists that ...
Title compds. I [L1 = O, CO or SO2; L2 = NR8SO2 or SO2NR9; R1 = H, (un)substituted alkyl, cycloalkyl...
In quest of elucidating the diverse pharmacological properties of 1,3-indanedione derivatives, we ha...
The present invention relates to indane deriv. I [L1 = O, (CR5R6)m, OCR7R8, CR9R10O; L2 = NR11SO2 or...
The present invention relates to indane deriv. I [L1 = O, (CR5R6)m, OCR7R8, CR9R10O; L2 = NR11SO2 or...
A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagoni...
A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagoni...
The indanone core is ubiquitous to a host of isolated natural compounds that have shown significant ...
Recent reports document that α-tetralone (3,4-dihydro-2H-naphthalen-1-one) is an appropriate scaffol...
The indan ring system is present in several compounds with important pharmacological properties. In ...
A Privileged structureis a molecular scaffold that can provide potent and selective ligands for a ra...
International audienceIndenoindoles and their isomers cyclopentacarbazoles represent a wide class of...
Rigidification of the isobutyl side chain of drug-like AT(2) receptor agonists and antagonists that ...
Rigidification of the isobutyl side chain of drug-like AT(2) receptor agonists and antagonists that ...
A high throughput screening campaign identified 5-(2-chlorophenyl)indazole compound 4 as an antagoni...
Rigidification of the isobutyl side chain of drug-like AT(2) receptor agonists and antagonists that ...