CPP

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

CPP is a selective, high-affinity competitive NMDA receptor antagonist. The R(D) isomer, which is the active form, binds to the glutamate binding site of the NR2 subunit of the NMDA receptor complex. CPP is used solely as a laboratory research tool. © 2007

Original languageEnglish (US)
Title of host publicationxPharm
Subtitle of host publicationThe Comprehensive Pharmacology Reference
PublisherElsevier Inc.
Pages1-6
Number of pages6
ISBN (Print)9780080552323
DOIs
StatePublished - Jan 1 2007

Fingerprint

N-Methyl-D-Aspartate Receptors
Glutamic Acid
Binding Sites
Research
3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid

ASJC Scopus subject areas

  • Pharmacology, Toxicology and Pharmaceutics(all)

Cite this

Monaghan, D. T. (2007). CPP. In xPharm: The Comprehensive Pharmacology Reference (pp. 1-6). Elsevier Inc.. https://doi.org/10.1016/B978-008055232-3.61520-X

CPP. / Monaghan, Daniel T.

xPharm: The Comprehensive Pharmacology Reference. Elsevier Inc., 2007. p. 1-6.

Research output: Chapter in Book/Report/Conference proceedingChapter

Monaghan, DT 2007, CPP. in xPharm: The Comprehensive Pharmacology Reference. Elsevier Inc., pp. 1-6. https://doi.org/10.1016/B978-008055232-3.61520-X
Monaghan DT. CPP. In xPharm: The Comprehensive Pharmacology Reference. Elsevier Inc. 2007. p. 1-6 https://doi.org/10.1016/B978-008055232-3.61520-X
Monaghan, Daniel T. / CPP. xPharm: The Comprehensive Pharmacology Reference. Elsevier Inc., 2007. pp. 1-6
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