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trans-ACPD

Catalog No. T3484   CAS 67684-64-4
Synonyms: Trans-(±)-ACP, 1-amino-1,3-dicarboxycyclopentane, (±)-trans-ACPD

trans-ACPD ((±)-trans-ACPD) is an equimolecular mixture of (1S, 3R)- and (1R, 3S)-ACPD. trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

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trans-ACPD Chemical Structure
trans-ACPD, CAS 67684-64-4
Pack Size Availability Price/USD Quantity
1 mg In stock $ 41.00
2 mg In stock $ 57.00
5 mg In stock $ 91.00
10 mg In stock $ 150.00
25 mg In stock $ 293.00
50 mg In stock $ 531.00
100 mg In stock $ 768.00
1 mL * 10 mM (in DMSO) In stock $ 68.00
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Purity: 99.53%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description trans-ACPD ((±)-trans-ACPD) is an equimolecular mixture of (1S, 3R)- and (1R, 3S)-ACPD. trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).
Targets&IC50 mGluR4:800 μM(EC50), mGluR5:23μM(EC50), mGluR1:15μM(EC50), mGluR2:2μM(EC50)
In vitro Excitatory amino acid (EAA) analogues activate receptors that are coupled to the increased hydrolysis of phosphoinositides (PIs). Hippocampal slices are prepared from neonatal rats (6-11 days old) to characterize the effects of EAA analogues on these receptors in these studies. The concentration of trans-ACPD required to evoke half-maximal stimulation (EC50 value) is 51 μM. DL-2-Amino-3-phosphonopropionate (DL-AP3) is also equipotent as an inhibitor of PI hydrolysis stimulated by ibotenate, quisqualate, and trans-ACPD (IC50 values are 480-850 μM)[2].
In vivo Intrathecal administration of NMDA, kainate, and trans-ACPD, along with the pro-inflammatory cytokines TNF-α or IL-1β, markedly increases biting behavior in mice, a paradigm shift from the control group receiving saline. Pre-systemic intervention with GM at a dosage of 100 mg/kg intraperitoneally notably decreases biting behavior in comparison to saline treatment (10 mL/kg, i.p.), with statistical significance (p<0.001). The efficacy of GM is particularly pronounced against pro-inflammatory cytokines and NMDA, exhibiting inhibition rates of TNF-α (92±7%), IL-1β (91±5%), NMDA (69±1%), and trans-ACPD (71±12%). Conversely, kainate-induced biting responses remain unaffected by GM at the same concentration.
Synonyms Trans-(±)-ACP, 1-amino-1,3-dicarboxycyclopentane, (±)-trans-ACPD
Molecular Weight 173.17
Formula C7H11NO4
CAS No. 67684-64-4

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

1eq. NaOH: 50 mM

H2O: 5 mM, Heating is recommended.

TargetMolReferences and Literature

1. Linden DJ, et al. Trans-ACPD, a metabotropic receptor agonist, produces calcium mobilization and an inward current in cultured cerebellar Purkinje neurons. J Neurophysiol. 1994 May;71(5):1992-8. 2. Littman L, et al. Multiple mechanisms for inhibition of excitatory amino acid receptors coupled to phosphoinositide hydrolysis. J Neurochem. 1992 Nov;59(5):1893-904. 3. Córdova, M., Martins, D., Silva, M., Baggio, C., Carbonero, E., & Ruthes, A. et al. (2013). Polysaccharide glucomannan isolated from Heterodermia obscurata attenuates acute and chronic pain in mice. Carbohydrate Polymers, 92(2), 2058-2064. doi: 10.1016/j.carbpol.2012.11.041

Related compound libraries

This product is contained In the following compound libraries:
Anti-Neurodegenerative Disease Compound Library Membrane Protein-targeted Compound Library Neurotransmitter Receptor Compound Library NO PAINS Compound Library Bioactive Compounds Library Max Bioactive Compound Library Neuronal Signaling Compound Library Anti-Alzheimer's Disease Compound Library

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Keywords

trans-ACPD 67684-64-4 Neuroscience GluR Trans-(±)-ACP transACPD 1-amino-1,3-dicarboxycyclopentane Trans-ACP Metabotropic glutamate receptors (±)-trans-ACPD trans ACPD mGluR Inhibitor inhibit inhibitor

 

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