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Article
In vivo arrhythmogenicity of the marine biotoxin azaspiracid-2 in rats
Azaspiracids (AZAs) are marine biotoxins produced by the dinoflagellate Azadinium spinosum that accumulate in several shellfish species. Azaspiracid poisoning episodes have been described in humans due to ingesti...
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Article
Asymmetric Synthesis of 3-Substituted 4-Oxoesters Using the SAMP-/RAMP-Hydrazone Method
Based on aldehydes 1a—f or ketone 1g, 3-substituted 4-oxo esters 6a—g were synthesized in three steps in moderate to good overall yield (12—50%) and in excellent enantiomeric excesses (ee >90—>95%) by an Umpolung...
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Article
Total synthesis of brevetoxin A
Brevetoxin A is the most potent neurotoxin secreted by Gymnodinium breve Davis, a marine organism often associated with harmful algal blooms known as ‘red tides’1,2,3. The compound, whose mechanism of action invo...
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Chapter
Ring-Closing Metathesis in the Synthesis of Epothilones and Polyether Natural Products
The increasing popularity of ring-closing metathesis (RCM) can be attributed to the development of transition metal complexes 1, 2 and 3 as initiators. These compounds efficiently promote the RCM process, are com...
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Article
Erratum: Synthesis of epothilones A and B in solid and solution phase
Nature 387, 268–272; (1997) We wish to add that, as well as a total synthesis of epothilone B, reference 19 includes biological data for compound 23 and other congeners similar to those reported in our Letter.
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Article
Synthesis of epothilones A and B in solid and solution phase
Epothilones A and B, two compounds that have been recently isolated1 from myxobacterium Sorangium cellulosum strain 90, have generated intense interest2–16 among chemists, biologists and clinicians owing to the s...
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Article
Chemical self-replication of palindromic duplex DNA
MOLECULAR replication, a fundamental process of life, has in recent years been the subject of laboratory investigations using simple chemical systems1–10. Whereas the work of Rebek's group4,5 has focused on molec...
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Article
Total synthesis of taxol
TAXOL1–4, a substance originally isolated from the Pacific yew tree (Taxus brevifolia) more than two decades ago, has recently been approved for the clinical treatment of cancer patients. Hailed as having provide...
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Article
Design, synthesis and biological activity of protaxols
TAXOL1–6 is a product isolated from the Pacific yew tree (Taxus brevifolia) and is a potent microtubule-stabilizing agent which has recently been approved for treatment of otherwise intractable ovarian cancer. De...
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Article
Pheromone blends of green stink bugs and possible parasitoid selection
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Article
Pharmacodynamics of lipoxin A4 in airway smooth muscle
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Article
Lipoxin A4 causes generation of thromboxane A2 in the guinea-pig lung
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Chapter and Conference Paper
Aspects of Eicosanoids in Inflammation
The microvascular system has a key role in host defence and expression of the inflammatory process which is indispensible for the elimination of foreign and noxious agents. Regardless of the nature of the init...
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Chapter
The Total Synthesis of the Lipoxins and Related Compounds
In 1984, a new class of arachidoníc acid derived products was discovered by Serhan et al.1–3 While studying lipoxygenase pathway interactions, these researchers isolated two major constituents from human leukocyt...
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Chapter
Actions of Lipoxin A4 and Related Compounds in Smooth Muscle Preparations and on the Microcirculation in Vivo
The present chapter summarizes our findings with lipoxins (LX) in spasmogenic assays and in the intact microvasculature of the hamster cheek pouch. The initial observations1,2 were made in experiments using lipox...
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Article
Thromboxane synthetase inhibitors differentially antagonize thromboxane receptors in vascular smooth muscle
A number of thromboxane (Tx) synthetase inhibitors have been found to prevent thromboxane release in acute cardiopulmonary disorders. However, little is known about Tx receptor antagonism by these substances. ...
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Article
A triple test for screening biological activity of prostacyclin analogues
6,9-Thiaprostacyclin was used as a representative of prostacyclin analogues with the aim to design the most convenient procedure for evaluation of vasodilator, anti-platelet and other biological properties wit...