(Q67942959)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1871039%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

title

Amine prodrugs which utilize hydroxy amide lactonization. II. A potential esterase-sensitive amide prodrug (English)

1 reference

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19 September 2019

author name string

K L Amsberry

series ordinal

1

1 reference

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19 September 2019

A E Gerstenberger

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1871039%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

R T Borchardt

series ordinal

3

1 reference

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19 September 2019

publication date

1 April 1991

1 reference

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19 September 2019

published in

Pharmaceutical Research

1 reference

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19 September 2019

volume

8

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19 September 2019

issue

4

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19 September 2019

page(s)

455-461

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Rationalization of the rate of the acylation step in chymotrypsin-catalyzed hydrolysis of amides

19 September 2019

cites work

1 reference

12 December 2020

Pro-drugs of amides, imides, and amines

1 reference

12 December 2020

REACTION OF FICIN WITH DIISOPROPYLPHOSPHOROFLUORIDATE. EVIDENCE FOR A CONTAMINATING INHIBITOR.

1 reference

12 December 2020

Stereopopulation control. I. Rate enhancement in the lactonizations of o-hydroxyhydrocinnamic acids

1 reference

12 December 2020

Rationale for Design of Biologically Reversible Drug Derivatives: Prodrugs

1 reference

12 December 2020

Stereopopulation control. II. Rate enhancement of intramolecular nucleophilic displacement

1 reference

12 December 2020

Stereopopulation control. 3. Facilitation of intramolecular conjugate addition of the carboxyl group

1 reference

12 December 2020

Human plasma prekallikrein. Studies of its activation by activated factor XII and of its inactivation by diisopropyl phosphofluoridate

1 reference

12 December 2020

Carboxylesterases in rat and human sera and their relationship of serum aryl acylamidases and cholinesterases.

1 reference

12 December 2020

Amine prodrugs which utilize hydroxy amide lactonization. I. A potential redox-sensitive amide prodrug

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1015890809507

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1871039%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

1 reference