Results 141 to 150 of about 674 (175)
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ChemInform Abstract: Serotonergic Ergoline Derivatives.
ChemInform, 1998AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
S. MANTEGANI +6 more
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Neurochemical Effects of Ergoline Derivatives
1986Sermion (nicergoline) is an ergoline derivative clinically active in chronic cerebral vascular insufficiency [1] and in patients with senile dementia [2].
A. Moretti +7 more
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Synthetic entry into N(5)-ergolines
Journal of the Chemical Society, Chemical Communications, 1985The first synthesis of the N(5)-ergoline system has achieved via a hetero Diels–Alder reaction on readily accessible substituted phenyl butadiene.
Jack E. Baldwin +3 more
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Ergoline congeners as potential inhibitors of prolactin release 2
Journal of Medicinal Chemistry, 1976In our attempts to elucidate the prolactin release inhibiting pharmacophore within the ergoline structure, we have prepared one indolealkylamine and several 2-aminotetralin derivatives. These congeners have been evaluated for inhibition of prolactin release in vivo.
D B, Rusterholz +2 more
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Radioimmunoassay for the Synthetic Ergoline Derivative Cabergoline in Biological Fluids
Journal of Immunoassay, 1992An antiserum against cabergoline, a powerful dopamine-agonist under clinical trials for the treatment of Parkinson's disease and hyperprolactinemia, has been raised in rabbits by immunization with an immunogen produced by conjugation of cabergoline to bovine serum albumin. The antiserum was able to bind a derivative of cabergoline labelled with tritium
S, Persiani +4 more
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Initial treatment of parkinsonism with 8‐alpha‐amino‐ergoline
Neurology, 1985We treated 12 patients with Parkinson's disease with an 8-alpha-amino-ergoline derivative, CU 32-085. The daily dosage was increased slowly to 7 mg over 9 weeks, held constant for 8 weeks, then replaced by placebo for 4 weeks. We found statistically significant benefit over placebo or pretreatment disability.
H, Teräväinen +2 more
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Sequential Aminodiene Diels−Alder Approach to the Ergoline Skeleton
The Journal of Organic Chemistry, 2005Through a novel sequence of aminodiene Diels-Alder reactions, several substituted amidofurans were readily converted to tricyclic ketones in good yield. The formation of the tricyclic ketone system is the result of a ring opening and dehydration of a transient oxabicyclic adduct formed by an intramolecular Diels-Alder cycloaddition of an amidofuran ...
Albert, Padwa +2 more
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Synthesis and in vitro and in vivo evaluation of dopaminergic ergoline derivatives
Il Farmaco, 1998A series of ergoline-amides was synthesised in the discovery of new dopaminomimetic agents. Several compounds exhibited in vivo high prolactin lowering activity (indirectly measured by the nidation test) in rats. For the most active, the potential anti-Parkinson activity was evaluated by observation of the contralateral turning behaviour in 6-OH-DA ...
S, Mantegani +7 more
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[Ergoline-induced retroperitoneal fibrosis].
Ugeskrift for laeger, 2006A 69-year-old man presented with anaemia, swelling of the legs and scrotum, weight gain and fatigue. MR scan and laboratory findings initiated a search for cancer, but eventually retroperitoneal fibrosis (RF) was suspected. A medical review revealed that an ergoline-based drug known to be associated with RF had been used for eight years.
Lars, Munksgaard +3 more
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Antiulcer and antisecretory ergoline derivatives.
Farmaco (Societa chimica italiana : 1989), 1989New ergoline derivatives exhibiting antiulcer and antisecretory activities were synthesized and tested. Stereochemical modification of the ergoline skeleton was found to influence the selective activity of the compounds.
D, Ruggieri +4 more
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