ArtNr |
HY-110024-100mg |
Hersteller |
MedChem Express
|
CAS-Nr. |
286369-38-8 |
Menge |
100 mg |
Quantity options |
100 mg
10 mM/1 mL
10 mg
1 ea
1 mg
25 mg
50 mg
5 mg
|
Kategorie |
|
Typ |
Chemicals |
Specific against |
other |
Purity |
99.92 |
Formula |
C24H27ClFN3O2 |
Citations |
[1]Francis C. Colpaert, et al. S 14506: A novel, potent, high-efficacy 5-HT1A agonist and potential anxiolytic agent. 1992, 21-48. [2]Protais P, et al. Dopamine receptor antagonist properties of S 14506, 8-OH-DPAT, raclopride and clozapine in rodents. Eur J Pharmacol. 1994 Dec 12;271(1):167-77. [3]Schreiber R, et al. The potent activity of the 5-HT1A receptor agonists, S 14506 and S 14671, in the rat forced swim test is blocked by novel 5-HT1A receptor antagonists. Eur J Pharmacol. 1994 Dec 27;271(2-3):537-41. [4]Assié MB, et al. Correlation between low/high affinity ratios for 5-HT(1A) receptors and intrinsic activity. Eur J Pharmacol. 1999 Dec 10;386(1):97-103. |
Smiles |
O=C(C1=CC=C(C=C1)F)NCCN2CCN(CC2)C3=C4C=C(C=CC4=CC=C3)OC.[H]Cl |
ECLASS 10.1 |
32160000 |
ECLASS 11.0 |
32160000 |
UNSPSC |
12000000 |
Versandbedingung |
Gekühlt |
Lieferbar |
|
Manufacturer - Type |
Reference compound |
Manufacturer - Applications |
Neuroscience-Neuromodulation |
Manufacturer - Targets |
5-HT Receptor; Dopamine Receptor |
Shipping Temperature |
Blue Ice |
Storage Conditions |
-20°C (Powder, sealed storage, away from moisture) |
Molecular Weight |
443.94 |
Product Description |
S-14506 hydrochloride is a potent 5-HT1A agonist, as well as 5-HT2A/2C antagonist. S-14506 hydrochloride displays dopamine antagonist properties by blocking dopamine D2 receptors. S-14506 hydrochloride inhibits the in vivo binding of [3H]raclopride in striatum and olfactory bulbs. S-14506 hydrochloride has the potential for the research of anxiolytic agent[1][2][3]. |
Manufacturer - Research Area |
Neurological Disease |
Solubility |
DMSO : 250 mg/mL (ultrasonic) |
Manufacturer - Pathway |
GPCR/G Protein; Neuronal Signaling |
Isoform |
5-HT1 Receptor; 5-HT2 Receptor; D2 Receptor |
Clinical information |
No Development Reported |
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