Results 111 to 120 of about 2,729,303 (155)
Changes in the proteomics and metabolomics profiles of Cormus Domestica (L.) fruits during the ripening process. [PDF]
Tartaglia M +8 more
europepmc +1 more source
Harnessing Photochemistry in Natural Product Synthesis: From Strategy to Applications. [PDF]
Taskinen EK, König B.
europepmc +1 more source
Uncovering the unique characteristics of different groups of 5-HT5AR ligands with reference to their interaction with the target protein. [PDF]
Kordylewski SK +3 more
europepmc +1 more source
Semi-synthesis in the exploration of opioid-targeting natural products.
Riley AP.
europepmc +1 more source
Independent Evolution of a Lysergic Acid Amide in Aspergillus Species. [PDF]
Lysergic acid derivatives are specialized metabolites with historical, agricultural, and medical significance and were known heretofore only from fungi in one family, the Clavicipitaceae. Our data show that several Aspergillus species, representing a different family of fungi, also produce lysergic acid derivatives ...
Daniel Panaccione, Chey R Steen
exaly +5 more sources
Here is a theoretical synthesis for a cinnamaldehyde adduct formation of a hypothetically proposed lysergamide derivative named cinnamylidene-bislysergamide or lysergic acid biscinnamylidene amide (LSBC). This lysergamide name and abbreviation is in keeping with names of other lysergamide derivatives, such as d-lysergic acid amine (LSA), lysergic acid ...
Chiruta, Victor
exaly +3 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Behavioural Brain Research, 1995
Studies of the affinities for serotonin 5-HT2A and 5-HT1A receptor subtypes of lysergic acid amides prepared from chiral 2-aminoalkanes showed a stereoselective preference at both receptor types for the amides with alkyl groups containing the R configuration. The 5-HT2A receptor was less tolerant of long alkyl groups than was the 5-HT1A subtype.
David E. Nichols, D Marona-Lewicka
exaly +3 more sources
Studies of the affinities for serotonin 5-HT2A and 5-HT1A receptor subtypes of lysergic acid amides prepared from chiral 2-aminoalkanes showed a stereoselective preference at both receptor types for the amides with alkyl groups containing the R configuration. The 5-HT2A receptor was less tolerant of long alkyl groups than was the 5-HT1A subtype.
David E. Nichols, D Marona-Lewicka
exaly +3 more sources
Lysergic Acid Amide-Induced Posterior Reversible Encephalopathy Syndrome With Status Epilepticus
Neurocritical Care, 2008Posterior reversible encephalopathy syndrome (PRES) is known to occur in association with several substances. However, lysergic acid amide (LSA) is not among the previously reported causes of PRES.We report on a patient with PRES presenting as convulsive status epilepticus associated with hypertensive encephalopathy after LSA ingestion.
Fabrice Bruneel +2 more
exaly +3 more sources

