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Inhibition of dynamin mediated endocytosis by the dynoles : synthesis and functional activity of a family of indoles

Hill, Timothy A (author)
Gordon, Christopher P (author)
McGeachie, Andrew B (author)
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Venn-Brown, Barbara (author)
Odell, Luke R (author)
Uppsala universitet,Avdelningen för organisk farmaceutisk kemi
Chau, Ngoc (author)
Quan, Annie (author)
Mariana, Anna (author)
Sakoff, Jennette A (author)
Chircop, Megan (author)
Robinson, Phillip J (author)
McCluskey, Adam (author)
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 (creator_code:org_t)
2009-05-21
2009
English.
In: Journal of Medicinal Chemistry. - : American Chemical Society (ACS). - 0022-2623 .- 1520-4804. ; 52:12, s. 3762-3773
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Screening identified two bisindolylmaleimides as 100 microM inhibitors of the GTPase activity of dynamin I. Focused library approaches allowed development of indole-based dynamin inhibitors called dynoles. 100-Fold in vitro enhancement of potency was noted with the best inhibitor, 2-cyano-3-(1-(2-(dimethylamino)ethyl)-1H-indol-3-yl)-N-octylacrylamide (dynole 34-2), a 1.3 +/- 0.3 microM dynamin I inhibitor. Dynole 34-2 potently inhibited receptor mediated endocytosis (RME) internalization of Texas red-transferrin. The rank order of potency for a variety of dynole analogues on RME in U2OS cells matched their rank order for dynamin inhibition, suggesting that the mechanism of inhibition is via dynamin. Dynoles are the most active dynamin I inhibitors reported for in vitro or RME evaluations. Dynole 34-2 is 15-fold more active than dynasore against dynamin I and 6-fold more active against dynamin mediated RME (IC(50) approximately 15 microM; RME IC(50) approximately 80 microM). The dynoles represent a new series of tools to better probe endocytosis and dynamin-mediated trafficking events in a variety of cells.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

PHARMACY
FARMACI
Organic Pharmaceutical Chemistry
Organisk farmaceutisk kemi

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