Haloperidol hydrochloride
Tocris Bioscience, part of Bio-Techne | Catalog # 0931
Dopamine antagonist; displays some D2 selectivity
Key Product Details
Description
Dopamine antagonist; displays some D2 selectivity
Product Description
Haloperidol hydrochloride is a dopamine antagonist with selectivity for D2-like receptors (Ki values are 1.2, ~ 7, 2.3, ~ 80 and ~ 100 nM for D2, D3, D4, D1 and D5 receptors respectively). Subtype-selective NMDA antagonist. Identified as targeting human host proteins that interact with SARS-CoV-2.Product Specifications
Molecular Weight
412.33
Formula
C21H23ClFNO2.HCl
Storage
Store at RT
Purity
≥98% (HPLC)
Chemical Name
4-[4-(4-Chlorophenyl)-4-hydroxy-1-piperidinyl]-1-(4-fluorophenyl)-1-butanone hydrochloride
CAS Number
1511-16-6
PubChem ID
11495267
InChI Key
JMRYYMBDXNZQMH-UHFFFAOYSA-N
SMILES
Cl.OC1(CCN(CCCC(=O)C2=CC=C(F)C=C2)CC1)C1=CC=C(Cl)C=C1
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 10.31 | 25 with gentle warming |
Preparing Stock Solutions
for Haloperidol hydrochloride
The following data is based on the product molecular weight 412.33
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.25 mM | 9.70 mL | 48.50 mL | 97.01 mL |
| 1.25 mM | 1.94 mL | 9.70 mL | 19.40 mL |
| 2.5 mM | 0.97 mL | 4.85 mL | 9.70 mL |
| 12.5 mM | 0.19 mL | 0.97 mL | 1.94 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Gordon A SARS-CoV-2 protein-protein interaction map reveals drug targets and drug repurposing. Nature 2020 PMID: 32353859
- Seeman and Van Tol DA receptor pharmacology. TiPS 1994 PMID: 7940991
- IIyin Subtype-selective inhibition of N-MthD.-aspartate receptors by halope. Mol.Pharmacol. 1996 PMID: 8967976
- Lynch and Gallagher Inhibition of N-MthD.-aspartate receptors by haloperidol: development and pharmacological characterization in native and recombinant receptors. J.Pharmacol.Exp.Ther. 1996 PMID: 8858988
- Beresford and Ward Haloperidol decanoate. A preliminary review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in psychosis. Drugs 1987 PMID: 3545764
Product Specific Notices for Haloperidol hydrochloride
For research use only
⚠ WARNING: This product can expose you to chemicals including Haloperidol, which is known to the State of California to cause reproductive toxicity with developmental effects. For more information, go to www.P65Warnings.ca.gov
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