Biological Activity
Potent 5-HT1A/1B and moderate 5-HT2C agonist that may also release 5-HT. Centrally active following systemic administration.
Technical Data
M. Wt | 287.34 |
Formula | C14H16N2O.½C4H6O4 |
Storage | Store at RT |
Purity | ≥99% (HPLC) |
CAS Number | 66611-27-6 |
PubChem ID | 3050530 |
InChI Key | BNYJLRQAWCQJOM-UHFFFAOYSA-N |
Smiles | OC(=O)CCC(O)=O.COC1=CC=C2NC=C(C2=C1)C1=CCNCC1.COC1=CC=C2NC=C(C2=C1)C1=CCNCC1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
DMSO | 14.37 | 50 | |
water | 8.62 | 30 |
Preparing Stock Solutions
The following data is based on the product molecular weight 287.34. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 3.48 mL | 17.4 mL | 34.8 mL |
5 mM | 0.7 mL | 3.48 mL | 6.96 mL |
10 mM | 0.35 mL | 1.74 mL | 3.48 mL |
50 mM | 0.07 mL | 0.35 mL | 0.7 mL |
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References
References are publications that support the products' biological activity.
Gudermann et al (1993) Human S31 serotonin receptor clone encodes a 5-hydroxytryptamine1E-like serotonin receptor. Mol.Pharmacol. 43 412 PMID: 8450834
Tomkins and O'Neill (2000) Effect of 5-HT1B receptor ligands on self-administration of ethanol in an operant procedure in rats. Pharmacol.Biochem.Behav. 66 129 PMID: 10837852
Guillaume et al (1987) Synthesis of 3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoles and study of their serotonergic and antidopaminergic properties. Eur.J.Med.Chem. 22 33 PMID:
Keywords: RU 24969 hemisuccinate, supplier, 5-HT1B/1A, agonists, Serotonin, Receptors, RU24969, hemisuccinate, C14H16N2O.0.5C4H6O4, 5-HT1A, Receptors, Tocris Bioscience