(R)-CPP , CAS No.126453-07-4

Item Number
C274632
Grouped product items
SKUSizeAvailabilityPrice Qty
C274632-1ml
1ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$472.90

Potent NMDA antagonist. 1 ml water soluble pack.

Basic Description

Synonyms(R)-CPP | 126453-07-4 | (2R)-4-(3-phosphonopropyl)piperazine-2-carboxylic acid | (R)-4-(3-phosphonopropyl)piperazine-2-carboxylic acid | 2-Piperazinecarboxylic acid, 4-(3-phosphonopropyl)-, (2R)- | A3QV2VT7SN | CHEMBL47277 | CPP, (R)- | CPP, (-)- | 3-((R)-2-Carboxypiperazi
Biochemical and Physiological MechanismsHighly potent, competitive NMDA antagonist; more active enantiomer of ( RS )-CPP. (K i values are 0.04, 0.3, 0.6 and 2.0 μM at NR1/NR2A, NR1/NR2B, NR1/NR2C and NR1/NR2D, respectively).
Storage TempRoom temperature,Desiccated
Shipped InNormal
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Store at Room Temperature. Store under desiccating conditions. The product can be stored for up to 12 months.

Associated Targets(Human)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate [NMDA] receptor (933 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Grin1 Glutamate NMDA receptor (6467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gria2 Glutamate receptor ionotropic, AMPA (2103 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor; Grin1/Grin2b (1028 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor; Grin1/Grin2a (798 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor; Grin1/Grin2c (1127 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

IUPAC Name (2R)-4-(3-phosphonopropyl)piperazine-2-carboxylic acid
INCHI InChI=1S/C8H17N2O5P/c11-8(12)7-6-10(4-2-9-7)3-1-5-16(13,14)15/h7,9H,1-6H2,(H,11,12)(H2,13,14,15)/t7-/m1/s1
InChi Key CUVGUPIVTLGRGI-SSDOTTSWSA-N
Canonical SMILES C1CN(CC(N1)C(=O)O)CCCP(=O)(O)O
Isomeric SMILES C1CN(C[C@@H](N1)C(=O)O)CCCP(=O)(O)O
PubChem CID 6603754
Molecular Weight 252.21

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble in 1 ml water to give specified mM/ml concentration

Related Documents

References

1. Pugh JR & Jahr CE.  (2011)  Axonal GABAA receptors increase cerebellar granule cell excitability and synaptic activity..  J Neurosci,  31  (2): (565-74).  [PMID:21228165]
2. Herman MA et al..  (2011)  Distribution of extracellular glutamate in the neuropil of hippocampus..  PLoS One,  (11): (e26501).  [PMID:22069455]
3. Chanda S & Xu-Friedman MA.  (2011)  Excitatory modulation in the cochlear nucleus through group I metabotropic glutamate receptor activation..  J Neurosci,  31  (20): (7450-5).  [PMID:21593328]
4. Bagnall MW et al..  (2009)  Glycinergic projection neurons of the cerebellum..  J Neurosci,  29  (32): (10104-10).  [PMID:19675244]
5. Apostolides PF & Trussell LO.  (2013)  Rapid, activity-independent turnover of vesicular transmitter content at a mixed glycine/GABA synapse..  J Neurosci,  33  (11): (4768-81).  [PMID:23486948]
6. Bock R et al..  (2013)  Strengthening the accumbal indirect pathway promotes resilience to compulsive cocaine use..  Nat Neurosci,  16  (5): (632-8).  [PMID:23542690]

Solution Calculators