90507-35-0Relevant academic research and scientific papers
4-[(4-(CARBOXYETHYL) PIPERIDINYL) METHYL] PYRROLIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY
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Page 33, (2010/02/07)
3-Substituted pyrrolidines having a 4-carboxypiperidinylmethyl substituent on the 4-position of the ring are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-3 and/or CCR-5.
4(SPIROPIPERIDINYL)METHYL SUBSTITUTED PYRROLIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY
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Page 42-43, (2010/02/07)
3-Substituted pyrrolidines having a spiropiperidinylmethyl substituent on the 4-position of the ring are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-3 and/or CCR-5.
Synthesis and cardiovascular properties of furazanyl-1,4-dihydropyridines and of furoxanyl analogues
Gasco,Fruttero,Sorba,Gasco,Budriesi,Chiarini
, p. 921 - 925 (2007/10/02)
A series of furazanyl- and furoxanyl-1,4-dihydropyridines has been synthesized and tested for their cardiovascular activity. The new compounds showed a modest activity in comparison with nifedipine and some selectivity for the myocardial muscle. The most active compound was diethyl 1,4-dihydro-2,6-dimethyl-4-(3-phenyl-4-furoxanyl)3,5-pyridine dicarboxylate, 4d.
Nonquaternary cholinesterase reactivators. II. α-Heteroaromatic aldoximes and thiohydroximates as reactivators of ethyl methylphosphonyl-acetylcholinesterase in vitro
Kenley,Bedford,Dailey Jr.,Howd,Miller
, p. 1201 - 1211 (2007/10/02)
We prepared six pairs of α-heteroaromatic aldoximes, RC(=NOH)H, and thiohydroximates, RC(=NOH)S(CH2)2N(C2H5)2, where R represents various oxadiazole and thiadiazole rings. Each compound was characteri
