131615-52-6

TISCH Chemical Structure
131615-52-6

Chemical Structure

TISCH

  • CAS No.: 131615-52-6
  • Formula:C17H17ClINO
  • Molecular Weight:413.68

IUPAC Name: (R)-8-chloro-5-(3-iodophenyl)-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-ol

InChIKey: DUTJKDUWCSYNLM-OAHLLOKOSA-N

SMILES: OC1=C(C=C2CCN(C[C@@H](C2=C1)C3=CC=CC(I)=C3)C)Cl

Biological Activity: TISCH is a potent and selective iodinated ligand with high affinity and selectivity for CNS D1 dopamine receptors. TISCH showed a Kd value of 0.205 nM in rat striatal tissue, indicating its effectiveness in biological activity. TISCH is able to easily cross the blood-brain barrier and show distribution in specific areas with D1 receptor density. TISCH is considered to be useful as a pharmacological tool for characterizing D1 dopamine receptors. When labeled with I-123, TISCH has the potential to be used as an in vivo imaging agent for CNS D1 dopamine receptors[1].

Cat. No. Product Name Purity Description Pricing
HY-116450
TISCH TISCH is a potent and selective iodinated ligand with high affinity and selectivity for CNS D1 dopamine receptors. TISCH showed a Kd value of 0.205 nM in rat striatal tissue, indicating its effectiveness in biological activity. TISCH is able to easily cross the blood-brain barrier and show distribution in specific areas with D1 receptor density. TISCH is considered to be useful as a pharmacological tool for characterizing D1 dopamine receptors. When labeled with I-123, TISCH has the potential to be used as an in vivo imaging agent for CNS D1 dopamine receptors.
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