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Volumn 12, Issue 10, 2002, Pages 1429-1433
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Solid-phase synthesis of FKBP12 inhibitors: N-sulfonyl and N-carbamoylprolyl/pipecolyl amides
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Author keywords
[No Author keywords available]
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Indexed keywords
1,2,3,6 TETRAHYDRO 1 METHYL 4 PHENYLPYRIDINE;
CYCLOPHILIN;
ENZYME FKBP12;
ENZYME INHIBITOR;
FKBP12 INHIBITOR;
UNCLASSIFIED DRUG;
ANIMAL MODEL;
ANIMAL TISSUE;
ARTICLE;
CONTROLLED STUDY;
CYCLIZATION;
DRUG ACTIVITY;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
ENZYME INHIBITION;
HYDROPHOBICITY;
IN VITRO STUDY;
IN VIVO STUDY;
MALE;
METHODOLOGY;
MOUSE;
NONHUMAN;
PARKINSON DISEASE;
SOLID;
1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE;
ANIMALS;
CARBAMATES;
COMBINATORIAL CHEMISTRY TECHNIQUES;
DRUG DESIGN;
ENZYME INHIBITORS;
MICE;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
PARKINSONIAN DISORDERS;
PIPECOLIC ACIDS;
STRUCTURE-ACTIVITY RELATIONSHIP;
SULFONIC ACIDS;
TACROLIMUS BINDING PROTEINS;
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EID: 18344393965
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/S0960-894X(02)00146-4 Document Type: Article |
Times cited : (14)
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References (9)
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