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Volumn 19, Issue 18, 2011, Pages 5679-5692
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Synthesis and glycosidase inhibitory profiles of functionalised morpholines and oxazepanes
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Author keywords
Carbohydrate synthesis; Glycosidase inhibitor; Reductive amination
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Indexed keywords
(4 N BENZYL METHOXY MORPHOLIN YL)METHANOL;
(HYDROXYMETHYL) METHOXY [1,4] OXAZEPAN OL;
(METHOXY MORPHOLIN YL)METHANOL;
2 (2 HYDROXYMETHYL 6 METHOXYMORPHOLIN 4 YL) 9 (4 HYDROXYPHENYL)PROPIONIC ACID METHYL ESTER;
2 (2 HYDROXYMETHYL 6 METHOXYMORPHOLIN 4 YL) 9 PHENYL PROPIONIC ACID METHYL ESTER;
2 (2 HYDROXYMETHYL 6 METHOXYMORPHOLIN 4 YL)PROPIONIC ACID METHYL ESTER;
2 (6 HYDROXY 2 HYDROXYMETHYL 7 METHOXY [1,4] OXAZEPAN 4 YL) 10 (4 HYDROXYPHENYL)PROPIONIC ACID METHYL ESTER;
2 (6 HYDROXY 2 HYDROXYMETHYL 7 METHOXY [1,4] OXAZEPAN 4 YL) 10 PHENYL PROPIONIC ACID METHYL ESTER;
2 HYDROXYMETHYL 6 METHOXY MORPHOLIN 4 OL;
2 HYDROXYMETHYL 6 METHOXYMORPHOLIN 4 YL ACETIC ACID METHYL ESTER;
2 HYDROXYMETHYL 7 METHOXY 4 OCTYL [1,4] OXAZEPAN 6 OL;
2 HYDROXYMETHYL 7 METHOXY 4 PROPYL [1,4] OXAZEPAN 6 OL;
2 HYDROXYMETHYL 7 METHOXY [1,4] OXAZEPAN 6 OLS;
4 BUTYL 2 HYDROXYMETHYL 7 METHOXY [1,4] OXAZEPAN 6 OL;
4 N BENZYL HYDROXYMETHYL METHOXY [1,4] OXAZEPAN OL;
6 HYDROXY 2 HYDROXYMETHYL 7 METHOXY [1,4] OXAZEPAN 4 YL ACETIC ACID METHYL ESTER;
6 METHOXY 4 BUTYLMORPHOLIN 2 YL METHANOL;
6 METHOXY 4 METHYL MORPHOLIN 2 YL METHANOL;
6 METHOXY 4 OCTYLMORPHOLIN 2 YL METHANOL;
6 METHOXY 4 PROPYL MORPHOLIN 2 YL METHANOL;
GLYCOSIDASE INHIBITOR;
METHYL 2,3,4 TRI O BENZYL 6 DEOXY 6 (BENZYLOXYMETHYL BENZYLOXY METHOXY [1,4] OXAZEPAN 4 YL) ALPHA DEXTRO GLUCOPYRANOSIDE;
METHYL 2,3,4 TRI O BENZYL 6 DEOXY 6 (METHOXY HYDROXYMETHYL MORPHOLIN 4 YL) ALPHA DEXTRO GLUCOPYRANOSIDE;
METHYL 2,6 DI O BENZYL ALPHA DEXTRO GLUCOPYRANOSIDE;
METHYL 6 DEOXY 6 (M ETHOXY HYDROXYMETHYL MORPHOLIN 4 YL) ALPHA DEXTRO GLUCOPYRANOSIDE;
METHYL 6 DEOXY 6 AMINO 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOPYRANOSIDE;
METHYL 6 DEOXY 6 AZIDO 2,3,4 TRI O BENZYL ALPHA DEXTRO GLUCOPYRANOSIDE;
MORPHOLINE DERIVATIVE;
OXAZEPINE DERIVATIVE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
AMINATION;
ARTICLE;
CARBOHYDRATE SYNTHESIS;
CHEMICAL REACTION;
DEPROTECTION REACTION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HYDROGENATION;
MICHAELIS MENTEN KINETICS;
STRUCTURE ACTIVITY RELATION;
DOSE-RESPONSE RELATIONSHIP, DRUG;
ENZYME INHIBITORS;
GLYCOSIDE HYDROLASES;
MOLECULAR STRUCTURE;
MORPHOLINES;
OXAZEPINES;
SMALL MOLECULE LIBRARIES;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
BOVINAE;
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EID: 80052565467
PISSN: 09680896
EISSN: 14643391
Source Type: Journal
DOI: 10.1016/j.bmc.2011.07.019 Document Type: Article |
Times cited : (32)
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References (78)
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