ACPT-I
ACPT-I Basic information
- Product Name:
- ACPT-I
- Synonyms:
-
- ACPT-I
- 4-AMINO-1BETA,2BETA,4BETA-CYCLOPENTANETRICARBOXYLIC ACID
- (1S,3R,4S)-1-AMINOCYCLOPENTANE-1,3,4-TRICARBOXYLIC ACID
- 1,2,4-Cyclopentanetricarboxylic acid, 4-amino-, (1α,2α,4β)-
- ACPT I,ACPTI
- CAS:
- 194918-76-8
- MF:
- C8H11NO6
- MW:
- 217.18
- Mol File:
- 194918-76-8.mol
ACPT-I Chemical Properties
- Boiling point:
- 440.4±45.0 °C(Predicted)
- Density
- 1.651±0.06 g/cm3(Predicted)
- storage temp.
- Desiccate at -20°C
- solubility
- Soluble to 10 mM in water and to 50 mM in 1.1eq. NaOH
- form
- Powder
- pka
- 1.85±0.60(Predicted)
- color
- White to off-white
ACPT-I Usage And Synthesis
Description
ACPT-I is an agonist of the group III metabotropic glutamate receptors (mGluRs) mGluR4a and mGluR8 (EC50s = 7.2 and 8.2 μM, respectively) that has no effect on mGluR1a or mGluR2. It has diverse biological activity, including neuroprotective, anticonvulsant, and anxiolytic-like effects. ACPT-I (1-200 μM) reduces cell death following oxygen-glucose deprivation in primary neuronal cultures and in a rat model of middle cerebral artery occlusion when used at a dose of 30 mg/kg. It is neuroprotective against excitotoxicity induced by kainite in vitro and in vivo and reduces the incidence of clonic seizures in various seizure models in mice and rats (ED50s = 0.08-49.3 nM, i.c.v.). ACPT-I also has anxiolytic-like effects in mice and rats, however, these effects can be blocked by WAY-100635 and flumazenil , indicating the involvement of the serotonin (5-HT) receptor subtype 5-HT1A and GABAA receptor.
Uses
ACPT-I is a competitive antagonist for metabotropic receptors (mGluRs).
Biological Activity
Agonist for group III mGlu receptors (EC 50 values are 7.2 and 8.2 μ M for mGlu 4a and mGlu 8 respectively). Anticonvulsant in mice.
storage
Desiccate at -20°C
References
[1] FRANCINE C. ACHER. Synthesis and Pharmacological Characterization of Aminocyclopentanetricarboxylic Acids: New Tools to Discriminate between Metabotropic Glutamate Receptor Subtypes[J]. Journal of Medicinal Chemistry, 1997, 40 19: 3119-3129. DOI: 10.1021/jm970207b
[2] HELENA DOMIN . Neuroprotective potential of the group III mGlu receptor agonist ACPT-I in animal models of ischemic stroke: In vitro and in vivo studies[J]. Neuropharmacology, 2016, 102: Pages 276-294. DOI: 10.1016/j.neuropharm.2015.11.025
[3] HELENA DOMIN. Group III mGlu receptor agonist, ACPT-I, exerts potential neuroprotective effects in vitro and in vivo.[J]. Neurotoxicity Research, 2014, 26 1: 99-113. DOI: 10.1007/s12640-013-9455-7
[4] ASTRID G CHAPMAN. Anticonvulsant activity of a mGlu4α receptor selective agonist, (1S,3R,4S)-1-aminocyclopentane-1,2,4-tricarboxylic acid[J]. European journal of pharmacology, 2001, 424 2: Pages 107-113. DOI: 10.1016/s0014-2999(01)01013-5
[5] K. STACHOWICZ . The group III mGlu receptor agonist ACPT-I exerts anxiolytic-like but not antidepressant-like effects, mediated by the serotonergic and GABA-ergic systems[J]. Neuropharmacology, 2009, 57 3: Pages 227-234. DOI: 10.1016/j.neuropharm.2009.06.005
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