D-AP7

CAS# 81338-23-0

D-AP7

Catalog No. BCC6559----Order now to get a substantial discount!

Product Name & Size Price Stock
D-AP7:10mg $234.00 In stock
D-AP7:20mg $398.00 In stock
D-AP7:50mg $936.00 In stock
D-AP7:100mg $1638.00 In stock
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Chemical structure

D-AP7

3D structure

Chemical Properties of D-AP7

Cas No. 81338-23-0 SDF Download SDF
PubChem ID 1617430 Appearance Powder
Formula C7H16NO5P M.Wt 225.18
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble to 100 mM in 1eq. NaOH
Chemical Name (2R)-2-amino-7-phosphonoheptanoic acid
SMILES C(CCC(C(=O)O)N)CCP(=O)(O)O
Standard InChIKey MYDMWESTDPJANS-ZCFIWIBFSA-N
Standard InChI InChI=1S/C7H16NO5P/c8-6(7(9)10)4-2-1-3-5-14(11,12)13/h6H,1-5,8H2,(H,9,10)(H2,11,12,13)/t6-/m1/s1
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Biological Activity of D-AP7

DescriptionMore active form of AP7. DL Mixture also available.

D-AP7 Dilution Calculator

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D-AP7 Molarity Calculator

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Preparing Stock Solutions of D-AP7

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4409 mL 22.2045 mL 44.4089 mL 88.8178 mL 111.0223 mL
5 mM 0.8882 mL 4.4409 mL 8.8818 mL 17.7636 mL 22.2045 mL
10 mM 0.4441 mL 2.2204 mL 4.4409 mL 8.8818 mL 11.1022 mL
50 mM 0.0888 mL 0.4441 mL 0.8882 mL 1.7764 mL 2.2204 mL
100 mM 0.0444 mL 0.222 mL 0.4441 mL 0.8882 mL 1.1102 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on D-AP7

Behavioral effects of D-AP7 in rats subjected to experimental hypoxia.[Pubmed:14506312]

Pol J Pharmacol. 2003 May-Jun;55(3):337-44.

We investigated the effects of D-AP7 [D-(-)-2-amino-7-phosphonoheptanoic acid], a specific, potent antagonist of NMDA receptor on certain forms of behavior in control groups of rats and in rats submitted to hypoxia. D-AP7 given intracerebroventrically (icv) at a dose of 5 nmol was tested in the open field test, passive avoidance test and in elevated plus maze test. D-AP7 did not significantly change the locomotor and exploratory activity, but it exhibited a tendency to enhance motility of rats in the open field test. It impaired the acquisition and did not influence the consolidation and retrieval in the passive avoidance situation. D-AP7 did not produce any significant effects in the elevated plus maze in rats which did not undergo hypoxia. Short-term hypoxia (about 3 min) decreased the crossings, rearings and bar approaches in the open field test and impaired acquisition, consolidation and retrieval processes. It did not evoke any changes in elevated plus maze. In hypoxia-treated groups of rats, D-AP7 enhanced locomotor and exploratory activity and it did not change the acquisition and retrieval processes. D-AP7 administrated before hypoxia impaired the consolidation in the passive avoidance test vs. D-AP7-treated group of rats. D-AP7 shortened the time spent in open arms and decreased the number of entries in open arms in hypoxia-treated groups of rats. In conclusion, in hypoxia-treated groups of rats, D-AP7 enhanced motility, exhibited anxiogenic-like effect and impaired consolidation in passive avoidance.

Cortically evoked excitatory synaptic transmission in the cat red nucleus is antagonised by D-AP5 but not by D-AP7.[Pubmed:1361408]

Brain Res. 1992 Oct 23;594(1):176-80.

Extracellular recordings were made from magnocellular red nucleus neurons (mRN) in alpha-chloralose (50 mg/kg, iv.) anaesthetised cats. Iontophoretically applied N-methyl-D-aspartate (NMDA) excited the neuronal firing which was antagonised by 4 selective NMDA receptor antagonists: 2-amino-5-phosphonopentanoate (AP5), 2-amino-7-phosphonoheptanoate (AP7), RS-4-(phosphonomethyl) piperazine-2-carboxylic acid (PMPC) and R-4-(3-phosphonopropyl) piperazine-2-carboxylic acid (CPP), whereas AMPA responses were uneffected. Monosynaptic excitatory responses were produced by stimulation of the sensorimotor cortex. These responses were reduced and often abolished by AP5 and PMPC but not by AP7 or CPP. It is postulated that two NMDA receptor subtypes exist on mRN neurones.

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