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PB 28 dihydrochloride

CAS# 172907-03-8

PB 28 dihydrochloride

Catalog No. BCC7411----Order now to get a substantial discount!

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PB 28 dihydrochloride: 5mg $92 In Stock
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Quality Control of PB 28 dihydrochloride

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Chemical structure

PB 28 dihydrochloride

3D structure

Chemical Properties of PB 28 dihydrochloride

Cas No. 172907-03-8 SDF Download SDF
PubChem ID 123773276 Appearance Powder
Formula C24H38N2O.2HCl M.Wt 443.5
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble to 20 mM in water with gentle warming
Chemical Name (3E)-3-[1-(2-aminoanilino)ethylidene]-1-hydroxy-4-methylpyridine-2,6-dione;dihydrochloride
SMILES CC1=CC(=O)N(C(=O)C1=C(C)NC2=CC=CC=C2N)O.Cl.Cl
Standard InChIKey FKMUQHJGHGZYLC-IGUOPLJTSA-N
Standard InChI InChI=1S/C14H15N3O3.2ClH/c1-8-7-12(18)17(20)14(19)13(8)9(2)16-11-6-4-3-5-10(11)15;;/h3-7,16,20H,15H2,1-2H3;2*1H/b13-9+;;
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 PB 28 dihydrochloride

DescriptionHigh affinity σ2 receptor agonist (Ki values are 0.8 and 15.2 nM for σ2 and σ1 receptors respectively) that displays minimal affinity at other receptors. Inhibits electrically evoked twitch in guinea pig bladder and ileum (EC50 values are 2.62 and 3.96 μM respectively). Displays antiproliferative and cytotoxic effects in SK-N-SH neuroblastoma and C6 glioma cells.

PB 28 dihydrochloride Dilution Calculator

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PB 28 dihydrochloride Molarity Calculator

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Preparing Stock Solutions of PB 28 dihydrochloride

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.2548 mL 11.274 mL 22.5479 mL 45.0958 mL 56.3698 mL
5 mM 0.451 mL 2.2548 mL 4.5096 mL 9.0192 mL 11.274 mL
10 mM 0.2255 mL 1.1274 mL 2.2548 mL 4.5096 mL 5.637 mL
50 mM 0.0451 mL 0.2255 mL 0.451 mL 0.9019 mL 1.1274 mL
100 mM 0.0225 mL 0.1127 mL 0.2255 mL 0.451 mL 0.5637 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 PB 28 dihydrochloride

New sigma and 5-HT1A receptor ligands: omega-(tetralin-1-yl)-n-alkylamine derivatives.[Pubmed:8568804]

J Med Chem. 1996 Jan 5;39(1):176-82.

Two series of compounds that are structurally related to benzomorphans, derived by structural modification of arylpiperazines with high 5-HT1A affinity and moderate sigma affinity, were prepared in order to increase sigma affinity and selectivity. All new compounds are N-substituted-omega-(1,2,3,4-tetrahydronaphthalen-1-yl)- or -omega-(1,2-dihydronaphthalen-4-yl)-n-alkylamines with, in some cases, a methoxy group on the tetralin moiety. They were tested in radioligand binding assays on sigma ([3H]DTG and [3H]-(+)-pentazocine), D-2 dopaminergic, 5-HT1A and 5-HT2 serotonergic, and PCP (phencyclidine) receptors. A first set of compounds bearing a 4-(1-substituted)piperazine moiety as terminal fragment on the alkyl chain showed moderate to high sigma affinity (Ki = 5.3-139 nM), the most active and selective being 1-cyclohexyl-4-[3-(5-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)-n- propyl ]piperazine (14), with probable pronounced sigma 2 affinity (Ki = 5.3 nM on [3H]DTG and Ki = 71 nM on [3H]-(+)-pentazocine). Moreover, compound 13, a 1-benzylpiperazine analogue of 14, preserved a dual high 5-HT1A and sigma affinity (Ki = 3.6 nM on [3H]-5-HT and Ki = 7.0 nM on [3H]DTG). The second set of compounds includes some N-phenylalkyl derivatives of 3-(5-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)- n-propylamine that can be considered to be open-chain derivatives of 4-substituted-1-arylpiperazines. Among these compounds that had a lower activity toward sigma binding sites, a high 5-HT1A affinity was found for the N-(3-phenylpropyl) derivative 21 (Ki = 4.4 nM) which demonstrated very good selectivity.

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