Ether lipid metabolism, GPI anchor biosynthesis, and signal transduction are putative targets for anti-leishmanial alkyl phospholipid analogues

Advances in Experimental Medicine and Biology

Volumn 416, Issue , 1997, Pages 201-211

  Lux, H ^a   Hart, D T ^a   Parker, P J ^b   Klenner, T ^c  

^a KING'S COLLEGE LONDON   (United Kingdom)

^b IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

^c ASTA MEDICA AG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANTILEISHMANIAL AGENT; EDELFOSINE; ETHER LIPID; ETHER PHOSPHOLIPID; GLYCOSYLPHOSPHATIDYLINOSITOL; MILTEFOSINE; PAROMOMYCIN; PENTAMIDINE; PHOSPHOLIPID DERIVATIVE; PROTEIN KINASE C; STIBOGLUCONATE SODIUM;

ANTINEOPLASTIC ACTIVITY; CELL FREE SYSTEM; CONTROLLED STUDY; CYTOTOXICITY; DRUG ACTIVITY; DRUG STRUCTURE; DRUG TARGETING; LD 50; LEISHMANIA MEXICANA; LIPID ANALYSIS; LIPID METABOLISM; NONHUMAN; PHOSPHOINOSITIDE METABOLISM; PRIORITY JOURNAL; PROMASTIGOTE; REVIEW; SIGNAL TRANSDUCTION;

ANIMALS; ANTIPROTOZOAL AGENTS; GLYCOSYLPHOSPHATIDYLINOSITOLS; ISOENZYMES; LEISHMANIA MEXICANA; LETHAL DOSE 50; LIPID METABOLISM; PHOSPHOLIPIDS; PROTEIN KINASE C; SIGNAL TRANSDUCTION;

LEISHMANIA MEXICANA;

EID: 0030995115     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Review

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