(Q42541961)

English

Trinitrophenyl-substituted nucleotides are potent antagonists selective for P2X1, P2X3, and heteromeric P2X2/3 receptors.

scientific article published on June 1998

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PubMed ID

9614197

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9614197%20AND%20SRC:MED&resulttype=core&format=json

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12 November 2019

title

Trinitrophenyl-substituted nucleotides are potent antagonists selective for P2X1, P2X3, and heteromeric P2X2/3 receptors (English)

1 reference

stated in

Europe PubMed Central

PubMed ID

9614197

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9614197%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 November 2019

author name string

Virginio C

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1

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PubMed ID

9614197

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9614197%20AND%20SRC:MED&resulttype=core&format=json

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12 November 2019

Robertson G

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2

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PubMed ID

9614197

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9614197%20AND%20SRC:MED&resulttype=core&format=json

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12 November 2019

Surprenant A

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3

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PubMed ID

9614197

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12 November 2019

North RA

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4

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PubMed ID

9614197

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12 November 2019

publication date

1 June 1998

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PubMed ID

9614197

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12 November 2019

published in

Molecular Pharmacology

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PubMed ID

9614197

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9614197%20AND%20SRC:MED&resulttype=core&format=json

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12 November 2019

volume

53

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PubMed ID

9614197

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9614197%20AND%20SRC:MED&resulttype=core&format=json

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12 November 2019

issue

6

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PubMed ID

9614197

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12 November 2019

page(s)

969-973

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PubMed ID

9614197

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12 November 2019

Identifiers

PubMed ID

9614197

1 reference

stated in

Europe PubMed Central

PubMed ID

9614197

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9614197%20AND%20SRC:MED&resulttype=core&format=json

(Q42541961)

Trinitrophenyl-substituted nucleotides are potent antagonists selective for P2X1, P2X3, and heteromeric P2X2/3 receptors.

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