Lyser

Andrew M Lyser, age 84, Newark, NY View Details

Cities: Newark NY, Chatham NY, Hilliard OH Possible Relatives: Andrew M Delyser, Corrine D Veith, David W Delyser

Brenda L Lyser, age 57, Webster, NY View Details

Cities: Newark NY, Chatham NY, Hilliard OH Possible Relatives: Andrew M Delyser, Corrine D Veith, David W Delyser

Aaron T Lyser, age 49, Aurora, CO View Details

Cities: Newark NY, Chatham NY, Hilliard OH Possible Relatives: Andrew M Delyser, Corrine D Veith, David W Delyser

Dawn Lyser, age 67, Clifford, ND View Details

Cities: Newark NY, Chatham NY, Hilliard OH Possible Relatives: Andrew M Delyser, Corrine D Veith, David W Delyser

Robert James Delyser, age 62, Pittsburgh, PA View Details

Locations: Elizabeth CO, Oviedo FL, Titusville FL Possible Relatives: Thomas R Delyser, Tina Y Delyser

Hansueli N Ryser, age 61, Durango, CO View Details

Locations: Elizabeth CO, Oviedo FL, Titusville FL Possible Relatives: Thomas R Delyser, Tina Y Delyser

Ronald W Leyser, age 59, Solon, OH View Details

Locations: Elizabeth CO, Oviedo FL, Titusville FL Possible Relatives: Thomas R Delyser, Tina Y Delyser

Bridgett M Kyser, age 55, Indianapolis, IN View Details

Locations: Elizabeth CO, Oviedo FL, Titusville FL Possible Relatives: Thomas R Delyser, Tina Y Delyser

Sparrow M Baranyai, age 52, Coeur D Alene, ID View Details

Locations: Elizabeth CO, Oviedo FL, Titusville FL Possible Relatives: Thomas R Delyser, Tina Y Delyser

Joseph Lysek, age 50, Simpsonville, SC View Details

Locations: Elizabeth CO, Oviedo FL, Titusville FL Possible Relatives: Thomas R Delyser, Tina Y Delyser

Aaron Thomas Delyser, age 40, Aurora, CO View Details

Locations: Elizabeth CO, Oviedo FL, Titusville FL Possible Relatives: Thomas R Delyser, Tina Y Delyser

Lysergic acid 2,4-dimethylazetidide

Lysergic acid 2,4-dimethylazetidide is an analog of LSD developed by the team led by David E. Nichols at Purdue University. It was developed as a rigid analog of LSD with the diethylamide group constrread more...ained into an azetidine ring in order to map the binding site at the 5-HT2A receptor. There are three possible stereoisomers around the azetidine ring, with the (S,S)-(+) isomer being the most active, slightly more potent than LSD itself in drug discrimination tests using trained rats.read less...

Lysergic acid hydroxyethylamide

D-Lysergic acid α-hydroxyethylamide, also known as D-lysergic acid methyl carbinolamide, is an alkaloid of the ergoline family, believed to be present in small amounts in various species in the Convoread more...lvulaceae, as well as some species of fungi.read less...

Lysergol

Lysergol is an alkaloid of the ergoline family that occurs as a minor constituent in some species of fungi, and in the morning glory family of plants (Convolvulaceae), including the hallucinogenic seeread more...ds of Rivea corymbosa (ololiuhqui), Argyreia nervosa and Ipomoea violacea. Lysergol is not a controlled substance in the USA. Its possession and sale is also legal under the U.S. Federal Analog Act because it does not have a known pharmacological action or a precursor relationship to LSD, which is a controlled substance. However, lysergol is an intermediate in the manufacture of some ergoloid medicines.read less...

Lysergic acid methyl ester

=Lysergic acid methyl ester is an analogue of lysergic acid diethylamide (LSD). It is a member of the tryptamine family and is extremely uncommon. It acts on the 5-HT receptors in the brain, as do mosread more...t tryptamines.read less...

Lysergic acid 2-butyl amide

Lysergic acid 2-butyl amide (2-Butyllysergamide, LSB) is an analogue of LSD originally developed by Richard Pioch at Eli Lilly in the 1950s, but mostly publicised through research conducted by the tearead more...m led by David E. Nichols at Purdue University. It is a structural isomer of LSD, with the two ethyl groups on the amide nitrogen having been replaced by a single sec-butyl group, joined at the 2-position. It is one of the few lysergamide derivatives to exceed the potency of LSD in animal drug discrimination assays, with the (R) isomer having an ED50 of 33nmol/kg for producing drug-appropriate responding, vs 48nmol/kg for LSD itself. The corresponding (R)-2-pentyl analogue has higher binding affinity for the 5-HT1A and 5-HT2A receptors, but is less potent in producing drug-appropriate responding, suggesting that the butyl compound has a higher efficacy at the receptor target. The drug discrimination assay for LSD in rats involves both 5-HT1A and 5-HT2A mediated components, and while lysergic acid 2-butyl amide is more potent than LSD as a 5-HT1A agonist, it is slightly less potent as a 5-HT2A agonist, and so would probably be slightly less potent than LSD as a hallucinogen in humans. The main use for this drug has been in studies of the binding site at the 5-HT2A receptor through which LSD exerts most of its pharmacological effects, with the stereoselective activity of these unsymmetric monoalkyl lysergamides foreshadowing the subsequent development of compounds such as lysergic acid 2,4-dimethylazetidide (LSZ).read less...

Lysergic Emanations

Lysergic Emanations is the debut studio album by the American band The Fuzztones, released in 1985.