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Sökning: onr:"swepub:oai:lup.lub.lu.se:885ca02d-dee0-4963-94d7-3b9929b320b2" > Natural Products as...

Natural Products as Leads for Pharmaceutically Active Compounds

Kahnberg, Pia (författare)
Lund University,Lunds universitet,Centrum för analys och syntes,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Centre for Analysis and Synthesis,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH
 (creator_code:org_t)
2001
Engelska 196 s.
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
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  • In the search for new pharmaceutically active compounds, it is recognized that Nature produces structurally different compounds in a great variety. By having the compounds or extracts tested in defined systems, new drugs or more often leads (a compound that has an interesting but moderate activity) can be found. When a lead is found, structurally similar compounds with modified functional groups are synthesized to find the structure-activity relationships (SAR:s). The secondary metabolite pterulone, isolated from the basidomycete Pterula species 82168 shows an selective and interesting antifungal activity, inhibiting Complex I in the respiration chain. Methods to synthesize pterulone has been developed and a number of analogues have been synthesized and tested on four different fungi, Mucor meihei, Paecilomyces variotii, Penicillium notatum, and Nematospora coryli. The structure-activity relationships were studied but no more efficient compounds than the natural product pterulone was obtained. Flavones belong to a substance class flavonoids present in virtually all plants. 6-Methylflavone shows a quite high affinity for the benzodiazepine site of the GABAA receptor with a K1 value of 125 nM. A number of flavones have been synthesized and the final product, 5'-bromo-2'-hydoxy-6-methylflavone has 250 times higher affinity for the binding site compared to 6-methylflavone. An existing pharmacophore model has been refined and used in the design of new flavones. The flavones were tested in vitro on rat cortical membranes and the pharmacophore model was confirmed and further refined by the structure-activity relationships observed. The pharmacophore model was also built in the database search program Catalyst™, to find new structural classes of substances, i.e scaffold hopping, that fits the model and may bind to the receptor. Databases from Maybridge, NCI and ACD were used for this purpose and a number of hits were obtained.

Ämnesord

NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)

Nyckelord

scaffold hopping
Catalyst
anxiety
benzodiazepine site
GABAA receptor
pharmacophore model
flavones
SAR
antifungal activity
Complex I
pterulone
Organic chemistry
Organisk kemi
Biochemical technology
Biokemisk teknik

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dok (ämneskategori)
vet (ämneskategori)

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Kahnberg, Pia
Om ämnet
NATURVETENSKAP
NATURVETENSKAP
och Kemi
och Organisk kemi
Av lärosätet
Lunds universitet

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