SX 3228

    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 585127

CAS#: 156364-04-4

Description: SX 3228 is a selective ligand for the BZ1 receptor and potent hypnotic when given to the rat during the dark period of the light-dark cycle.

Chemical Structure

img
SX 3228
CAS# 156364-04-4
Instruction

Theoretical Analysis

MedKoo Cat#: 585127
Name: SX 3228
CAS#: 156364-04-4
Chemical Formula: C18H18N4O3
Exact Mass: 338.14
Molecular Weight: 338.367
Elemental Analysis: C, 63.89; H, 5.36; N, 16.56; O, 14.18

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: SX 3228; SX-3228; SX3228

IUPAC/Chemical Name: 1,6-Naphthyridin-2(1H)-one, 5,6,7,8-tetrahydro-3-(5-methoxy-1,3,4-oxadiazol-2-yl)-6-(phenylmethyl)-

InChi Key: BZLLVTYOOJNQIF-UHFFFAOYSA-N

InChi Code: InChI=1S/C18H18N4O3/c1-24-18-21-20-17(25-18)14-9-13-11-22(8-7-15(13)19-16(14)23)10-12-5-3-2-4-6-12/h2-6,9H,7-8,10-11H2,1H3,(H,19,23)

SMILES Code: O=C1NC2=C(CN(CC3=CC=CC=C3)CC2)C=C1C4=NN=C(OC)O4

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 338.37 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.
=
x
x
g/mol

*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

=
÷

Dilution Calculator

Calculate the dilution required to prepare a stock solution.
x
=
x

1: Alvariño F, Monti JM, Jantos H, Monti D. Effect of SX-3228, a selective ligand for the BZ1 receptor, on sleep and waking during the light-dark cycle in the rat. Braz J Med Biol Res. 1999 Aug;32(8):1007-14. PubMed PMID: 10454763.

2: Griebel G, Perrault G, Sanger DJ. Limited anxiolytic-like effects of non-benzodiazepine hypnotics in rodents. J Psychopharmacol. 1998;12(4):356-65. PubMed PMID: 10065909.

3: Griebel G, Perrault G, Tan S, Schoemaker H, Sanger DJ. Comparison of the pharmacological properties of classical and novel BZ-omega receptor ligands. Behav Pharmacol. 1999 Sep;10(5):483-95. PubMed PMID: 10780255.

4: Sanger DJ. The effects of new hypnotic drugs in rats trained to discriminate ethanol. Behav Pharmacol. 1997 Aug;8(4):287-92. PubMed PMID: 9832988.

5: Fujita M, Himi S, Handa T. Effects of compression and grinding on chemical stability of a benzodiazepine receptor agonist. Chem Pharm Bull (Tokyo). 2010 Jan;58(1):51-5. PubMed PMID: 20045966.

6: Fujita M, Himi S, Iwata M. Stabilization study on a wet-granule tableting method for a compression-sensitive benzodiazepine receptor agonist. Chem Pharm Bull (Tokyo). 2010 Mar;58(3):359-62. PubMed PMID: 20190441.

7: Ohta T. [Recent progress in development of psychotropic drugs (5)--Hypnotics]. Nihon Shinkei Seishin Yakurigaku Zasshi. 1996 Oct;16(5):161-70. Review. Japanese. PubMed PMID: 8962434.