3-CPMT

Dopamine uptake inhibitor CAS# 14008-79-8

3-CPMT

Catalog No. BCC6845----Order now to get a substantial discount!

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3-CPMT: 5mg $46 In Stock
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Chemical structure

3-CPMT

3D structure

Chemical Properties of 3-CPMT

Cas No. 14008-79-8 SDF Download SDF
PubChem ID 203135 Appearance Powder
Formula C21H25Cl2NO M.Wt 378.34
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble to 75 mM in DMSO
Chemical Name 3-[(4-chlorophenyl)-phenylmethoxy]-8-methyl-8-azabicyclo[3.2.1]octane;hydrochloride
SMILES CN1C2CCC1CC(C2)OC(C3=CC=CC=C3)C4=CC=C(C=C4)Cl.Cl
Standard InChIKey FXKCQWIUITUJFU-UHFFFAOYSA-N
Standard InChI InChI=1S/C21H24ClNO.ClH/c1-23-18-11-12-19(23)14-20(13-18)24-21(15-5-3-2-4-6-15)16-7-9-17(22)10-8-16;/h2-10,18-21H,11-14H2,1H3;1H
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 3-CPMT

DescriptionThis cocaine analog binds with high affinity to the dopamine transporter (Ki = 30 nM) and blocks re-uptake of dopamine. However, it is a weak psychomotor stimulant and does not substitute for cocaine in addicted rats.

3-CPMT Dilution Calculator

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3-CPMT Molarity Calculator

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Preparing Stock Solutions of 3-CPMT

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.6431 mL 13.2156 mL 26.4313 mL 52.8625 mL 66.0781 mL
5 mM 0.5286 mL 2.6431 mL 5.2863 mL 10.5725 mL 13.2156 mL
10 mM 0.2643 mL 1.3216 mL 2.6431 mL 5.2863 mL 6.6078 mL
50 mM 0.0529 mL 0.2643 mL 0.5286 mL 1.0573 mL 1.3216 mL
100 mM 0.0264 mL 0.1322 mL 0.2643 mL 0.5286 mL 0.6608 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 3-CPMT

Novel 4'-substituted and 4',4"-disubstituted 3 alpha-(diphenylmethoxy)tropane analogs as potent and selective dopamine uptake inhibitors.[Pubmed:7562926]

J Med Chem. 1995 Sep 29;38(20):3933-40.

A series of 4'-substituted and 4',4"-disubstituted 3 alpha-(diphenylmethoxy)tropane analogs were prepared as novel probes for the dopamine transporter. These compounds were evaluated in radiolabeled binding assays for the dopamine, norepinephrine, and serotonin transporters. All of these compounds monophasically displaced [3H]WIN 35,428 binding in rat caudate putamen with Ki values ranging from 11.8 to 2000 nM. The most potent compound in this series was 4',4"-difluoro 3 alpha-(diphenylmethoxy)tropane 7c with a Ki = 11.8 nM. All of the compounds inhibited dopamine uptake in rat caudate putamen (IC50 = 24-4456 nM) which correlated significantly (r = 0.907; p > 0.0001) with binding affinities at the dopamine transporter. None of the compounds demonstrated high-affinity binding at the norepinephrine (Ki > 4800 nM) or serotonin (Ki > 690 nM) transporters. Therefore, the most potent dopamine uptake inhibitors in this series were highly selective for the dopamine transporter. Preliminary behavioral studies of several of these analogs (7a-e) suggested that the compounds did not display a cocaine-like behavioral profile, despite their ability to inhibit dopamine uptake. The present data coupled with the observed differences from cocaine in structure-activity relationships suggested that the 3 alpha-(diphenylmethoxy)tropane analogs may be interacting at a different active site than cocaine on the dopamine transporter and that an additional binding domain might be exploited for the identification of potential therapeutics for the treatment of cocaine abuse.

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