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LP 12 hydrochloride

5-HT7 agonist CAS# 1185136-22-4

LP 12 hydrochloride

Catalog No. BCC7517----Order now to get a substantial discount!

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LP 12 hydrochloride: 5mg $115 In Stock
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Chemical structure

LP 12 hydrochloride

3D structure

Chemical Properties of LP 12 hydrochloride

Cas No. 1185136-22-4 SDF Download SDF
PubChem ID 56972187 Appearance Powder
Formula C32H40ClN3O M.Wt 518.13
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble to 75 mM in DMSO and to 75 mM in ethanol
Chemical Name 6-[4-(2-phenylphenyl)piperazin-1-yl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)hexanamide;hydrochloride
SMILES C1CC(C2=CC=CC=C2C1)NC(=O)CCCCCN3CCN(CC3)C4=CC=CC=C4C5=CC=CC=C5.Cl
Standard InChIKey XNDUOTNYUWDFKR-UHFFFAOYSA-N
Standard InChI InChI=1S/C32H39N3O.ClH/c36-32(33-30-18-11-15-26-14-6-7-16-28(26)30)20-5-2-10-21-34-22-24-35(25-23-34)31-19-9-8-17-29(31)27-12-3-1-4-13-27;/h1,3-4,6-9,12-14,16-17,19,30H,2,5,10-11,15,18,20-25H2,(H,33,36);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 LP 12 hydrochloride

Description5-HT7 receptor agonist displaying selectivity over D2, 5-HT1A and 5-HT2A receptors (Ki values are 0.22, 7.3, 52.7 and 326 nM respectively). Induces relaxation of substance P-induced contractions in guinea pig ileum (EC50 = 1.77 μM).

LP 12 hydrochloride Dilution Calculator

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LP 12 hydrochloride Molarity Calculator

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Preparing Stock Solutions of LP 12 hydrochloride

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.93 mL 9.6501 mL 19.3002 mL 38.6004 mL 48.2504 mL
5 mM 0.386 mL 1.93 mL 3.86 mL 7.7201 mL 9.6501 mL
10 mM 0.193 mL 0.965 mL 1.93 mL 3.86 mL 4.825 mL
50 mM 0.0386 mL 0.193 mL 0.386 mL 0.772 mL 0.965 mL
100 mM 0.0193 mL 0.0965 mL 0.193 mL 0.386 mL 0.4825 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 LP 12 hydrochloride

Structure-activity relationship study on N-(1,2,3,4-tetrahydronaphthalen-1-yl)-4-aryl-1-piperazinehexanamides, a class of 5-HT7 receptor agents. 2.[Pubmed:17649988]

J Med Chem. 2007 Aug 23;50(17):4214-21.

Here we report the synthesis of N-(1,2,3,4-tetrahydronaphthalen-1-yl)-4-aryl-1-piperazinealkylamides 16-29 that were designed to elucidate both structure-affinity and -activity relationships for the 5-HT7 receptor, by targeting the substituent in 2-position of the aryl linked to the piperazine ring. The affinities of 16-29 for 5-HT7, 5-HT1A, 5-HT2A, and D2 receptors were assessed by radioligand binding assays. The intrinsic activities at the 5-HT7 receptor of the most potent compounds were determined. A series of substituents covering a wide range of electronic, steric, and polar properties was evaluated, revealing a key role on 5-HT7 receptor affinity and intrinsic activity. Certain lipophilic substituents (SCH3, CH(CH3)2, N(CH3)2, CH3, Ph) led to high-affinity agonists, whereas OH and NHCH3 substituents switched intrinsic activity toward antagonism. 4-[2-(1-Methylethyl)phenyl]-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-1-piperazinehex anamide (19), 4-(2-diphenyl)-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-1-piperazinehexanamide (21), and 4-(2-dimethylaminophenyl)-N-(1,2,3,4-tetrahydronaphthalen-1-yl)-1-piperazinehexan amide (22) were identified as potent 5-HT7 receptor agonists (Ki = 0.13-1.1 nM, EC50 = 0.90-1.77 microM), showing selectivity over 5-HT1A, 5-HT2A, and D2 receptors.

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