MedKoo Cat#: 532609 | Name: S14506 HCl
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Description:

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

S 14506 is a highly potent selective 5-HT1A receptor full agonist (pKi values are 9.0, 6.6, 7.5, 6.6 and < 6.0 for 5-HT1A, 5-HT1B, 5-HT1C, 5-HT2 and 5-HT3 receptors respectively). It potentially binds between the agonist binding site and the G protein interaction switch site, affecting the activation mechanism, and may display positive cooperativity.

Chemical Structure

S14506 HCl
S14506 HCl
CAS#286369-38-8 (HCl)

Theoretical Analysis

MedKoo Cat#: 532609

Name: S14506 HCl

CAS#: 286369-38-8 (HCl)

Chemical Formula: C24H27ClFN3O2

Exact Mass: 0.0000

Molecular Weight: 443.95

Elemental Analysis: C, 64.93; H, 6.13; Cl, 7.99; F, 4.28; N, 9.47; O, 7.21

Price and Availability

Size Price Availability Quantity
50mg USD 550.00 2 Weeks
100mg USD 950.00 2 Weeks
200mg USD 1,650.00 2 Weeks
500mg USD 2,950.00 2 Weeks
1g USD 4,250.00 2 Weeks
2g USD 6,950.00 2 Weeks
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Related CAS #
135722-25-7 (free base) 286369-38-8 (HCl)
Synonym
S 14506 HCl; S14506HCl; S14506 HCl; S-14506.
IUPAC/Chemical Name
4-Fluoro-N-[2-[4-(7-methoxy-1-naphthalenyl)-1-piperazinyl]ethyl]benzamide hydrochloride
InChi Key
HWLZKPKZVOLFGK-UHFFFAOYSA-N
InChi Code
InChI=1S/C24H26FN3O2.ClH/c1-30-21-10-7-18-3-2-4-23(22(18)17-21)28-15-13-27(14-16-28)12-11-26-24(29)19-5-8-20(25)9-6-19;/h2-10,17H,11-16H2,1H3,(H,26,29);1H
SMILES Code
O=C(NCCN1CCN(C2=C3C=C(OC)C=CC3=CC=C2)CC1)C4=CC=C(F)C=C4.[H]Cl
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
>2 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

Preparing Stock Solutions

The following data is based on the product molecular weight 443.95 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
1: Walory J, Mielczarek L, Jarończyk M, Koronkiewicz M, Kossakowski J, Bugno R, Bojarski AJ, Chilmonczyk Z. Oncotoxic Properties of Serotonin Transporter Inhibitors and 5-HT1A Receptor Ligands. Int J Mol Sci. 2018 Oct 20;19(10):3260. doi: 10.3390/ijms19103260. PMID: 30347827; PMCID: PMC6214143. 2: Garrett TL, Joshi K, Rapp CM, Chapleau M, Cool DR, Schlager JJ, Lucot JB. The effects of 8-OH-DPAT on neuroinflammation after sarin exposure in mice. Toxicology. 2013 Aug 9;310:22-8. doi: 10.1016/j.tox.2013.05.005. Epub 2013 May 18. PMID: 23692952. 3: Lu S, Liow JS, Zoghbi SS, Hong J, Innis RB, Pike VW. Evaluation of [C]S14506 and [F]S14506 in rat and monkey as agonist PET radioligands for brain 5-HT(1A) receptors. Curr Radiopharm. 2010 Jan;3(1):9-18. doi: 10.2174/1874471011003010009. PMID: 20657759; PMCID: PMC2908029. 4: Cussac D, Palmier C, Finana F, De Vries L, Tardif S, Léger C, Bernois S, Heusler P. Mutant 5-hydroxytryptamine 1A receptor D116A is a receptor activated solely by synthetic ligands with a rich pharmacology. J Pharmacol Exp Ther. 2009 Oct;331(1):222-33. doi: 10.1124/jpet.109.156307. Epub 2009 Jul 15. PMID: 19605522. 5: Newman-Tancredi A, Rivet JM, Cussac D, Touzard M, Chaput C, Marini L, Millan MJ. Comparison of hippocampal G protein activation by 5-HT(1A) receptor agonists and the atypical antipsychotics clozapine and S16924. Naunyn Schmiedebergs Arch Pharmacol. 2003 Sep;368(3):188-99. doi: 10.1007/s00210-003-0788-2. Epub 2003 Aug 16. PMID: 12923612. 6: Newman-Tancredi A, Verrièle L, Millan MJ. Differential modulation by GTPgammaS of agonist and inverse agonist binding to h5-HT(1A) receptors revealed by [3H]-WAY100,635. Br J Pharmacol. 2001 Jan;132(2):518-24. doi: 10.1038/sj.bjp.0703832. PMID: 11159702; PMCID: PMC1572578. 7: Assié MB, Cosi C, Koek W. Correlation between low/high affinity ratios for 5-HT(1A) receptors and intrinsic activity. Eur J Pharmacol. 1999 Dec 10;386(1):97-103. doi: 10.1016/s0014-2999(99)00738-4. PMID: 10611469. 8: Goudie AJ, Smith JA, Taylor A, Taylor MA, Tricklebank MD. Discriminative stimulus properties of the atypical neuroleptic clozapine in rats: tests with subtype selective receptor ligands. Behav Pharmacol. 1998 Dec;9(8):699-710. doi: 10.1097/00008877-199812000-00006. PMID: 9890260. 9: Lima L, Laporte AM, Gaymard C, Spedding M, Mocaër E, Hamon M. Atypical in vitro and in vivo binding of [3H]S-14506 to brain 5-HT1A receptors. J Neural Transm (Vienna). 1997;104(10):1059-75. doi: 10.1007/BF01273319. PMID: 9503258. 10: Goudie AJ, Leathley MJ. Assessment of the dependence potential of the potent high-efficacy 5-HT1A agonist S-14506 in rats. J Psychopharmacol. 1994 Jan;8(4):213-21. doi: 10.1177/026988119400800404. PMID: 22298627.