(Q72707235)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7922121%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

Rational design of high affinity tachykinin NK2 receptor antagonists (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7922121%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

author name string

S Boyle

1

1 reference

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28 October 2019

S Guard

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7922121%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

J Hodgson

3

1 reference

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28 October 2019

D C Horwell

4

1 reference

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28 October 2019

W Howson

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7922121%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

J Hughes

6

1 reference

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28 October 2019

A McKnight

7

1 reference

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28 October 2019

K Martin

8

1 reference

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28 October 2019

M C Pritchard

9

1 reference

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28 October 2019

K J Watling

10

1 reference

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28 October 2019

language of work or name

English

0 references

publication date

1 February 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7922121%20AND%20SRC:MED&resulttype=core&format=json

Bioorganic & Medicinal Chemistry

28 October 2019

published in

1 reference

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28 October 2019

volume

2

1 reference

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28 October 2019

issue

2

1 reference

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28 October 2019

page(s)

101-113

1 reference

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Formoterol and salbutamol inhibit bradykinin- and histamine-induced airway microvascular leakage in guinea-pig

28 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2982006-4

7 January 2021

Rationally designed "dipeptoid" analogues of CCK. alpha-Methyltryptophan derivatives as highly selective and orally active gastrin and CCK-B antagonists with potent anxiolytic properties.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2982006-4

7 January 2021

Chemical design of antagonists of substance P

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2982006-4

7 January 2021

Substance P--structure-activity studies and the development of antagonists.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2982006-4

7 January 2021

Analogues of substance P. Peptides containing D-amino acid residues in various positions of substance P and displaying agonist or receptor selective antagonist effects.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2982006-4

7 January 2021

Agonist and antagonist binding to tachykinin peptide NK-2 receptors.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2982006-4

7 January 2021

.alpha.-Methyl amino acids. Resolution and amino protection

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2800%2982006-4

7 January 2021

10.1016/S0968-0896(00)82006-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7922121%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference