CONSCRIPTING BETA-LACTAMASE FOR USE IN DRUG DELIVERY - SYNTHESIS AND BIOLOGICAL-ACTIVITY OF A CEPHALOSPORIN C10-ESTER OF AN ANTIBIOTIC DIPEPTIDE

被引：38

作者：

MOBASHERY, S

LERNER, SA

JOHNSTON, M

机构：

[1] UNIV CHICAGO,SEARLE CHEM LAB,DEPT CHEM,CHICAGO,IL 60637

[2] UNIV CHICAGO,SEARLE CHEM LAB,DEPT BIOCHEM & MOLEC BIOL,CHICAGO,IL 60637

[3] UNIV CHICAGO,DEPT MED & MICROBIOL,CHICAGO,IL 60637

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1986年 / 108卷 / 07期

关键词：

D O I：

10.1021/ja00267a045

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1685 / 1686

页数：2

共 23 条

[1] ELECTRONIC-STRUCTURES OF CEPHALOSPORINS AND PENICILLINS .9. DEPARTURE OF A LEAVING GROUP IN CEPHALOSPORINS
BOYD, DB
LUNN, WHW
[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1979, 22 (07) : 778 - 784
[2] ELECTRONIC-STRUCTURES OF CEPHALOSPORINS AND PENICILLINS .4. MODELING ACYLATION BY BETA-LACTAM RING
BOYD, DB
HERMANN, RB
PRESTI, DE
MARSH, MM
[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1975, 18 (04) : 408 - 417
[3] NATURALLY-OCCURRING BETA-LACTAMASE INHIBITORS WITH ANTIBACTERIAL ACTIVITY
BROWN, AG
BUTTERWORTH, D
COLE, M
HANSCOMB, G
HOOD, JD
READING, C
[J]. JOURNAL OF ANTIBIOTICS, 1976, 29 (06) : 668 - 669
[4] STRUCTURES OF OLIVANIC ACID-DERIVATIVES MM 4550 AND MM 13902 - 2 NEW, FUSED BETA-LACTAMS ISOLATED FROM STREPTOMYCES OLIVACEUS
BROWN, AG
CORBETT, DF
EGLINGTON, AJ
HOWARTH, TT
[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1977, (15) : 523 - 525
[5] SEMISYNTHETIC PENICILLINASE INACTIVATOR
CARTWRIGHT, SJ
COULSON, AFW
[J]. NATURE, 1979, 278 (5702) : 360 - 361
[6] Cheung K., UNPUB
[7] CHLOROALANYL AND PROPARGYLGLYCYL DIPEPTIDES - SUICIDE SUBSTRATE CONTAINING ANTIBACTERIALS
CHEUNG, KS
WASSERMAN, SA
DUDEK, E
LERNER, SA
JOHNSTON, M
[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1983, 26 (12) : 1733 - 1741
[8] DOYLE F. P., 1964, ADVANCE DRUG RES, V1, P1
[9] CP-45,899, A BETA-LACTAMASE INHIBITOR THAT EXTENDS ANTIBACTERIAL SPECTRUM OF BETA-LACTAMS - INITIAL BACTERIOLOGICAL CHARACTERIZATION
ENGLISH, AR
RETSEMA, JA
GIRARD, AE
LYNCH, JE
BARTH, WE
[J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1978, 14 (03) : 414 - 419
[10] ELIMINATION OF A GOOD LEAVING GROUP FROM THE 3'-POSITION OF A CEPHALOSPORIN NEED NOT BE CONCERTED WITH BETA-LACTAM RING-OPENING - TEM-2 BETA-LACTAMASE-CATALYZED HYDROLYSIS OF PYRIDINE-2-AZO-4'-(N',N'-DIMETHYLANILINE) CEPHALOSPORIN (PADAC) AND OF CEPHALORIDINE
FARACI, WS
PRATT, RF
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (05) : 1489 - 1490

← 1 2 3 →