114943-19-0

LY 178210 Chemical Structure
114943-19-0

Chemical Structure

LY 178210

  • CAS No.: 114943-19-0
  • Formula:C18H25N3O
  • Molecular Weight:299.41

IUPAC Name: 4-(dipropylamino)-1,3,4,5-tetrahydrobenzo[cd]indole-6-carboxamide

InChIKey: YTOJFUORFUYGSV-UHFFFAOYSA-N

SMILES: O=C(C1=C2C3=C(NC=C3CC(N(CCC)CCC)C2)C=C1)N

Biological Activity: LY 178210 (Compound 24) is a selective partial agonist of the 5-HT1A receptor, with Ki values ​​of 0.67 and 380 nM for the 5-HT1A and 5-HT1D receptors, respectively. LY 178210 has almost no activity against α₂-adrenergic receptors, 5-HT₂, and other neurotransmitter receptors. LY 178210 inhibits Foscolin-stimulated cyclase activity, but its maximum potency is lower than that of the full agonist 8-OH-DPAT (HY-112061). LY 178210 significantly reduces 5-hydroxyindoleacetic acid (5-HIAA) levels in the greater hypothalamus and increases serum corticosterone concentrations[1][2].

Cat. No. Product Name Purity Description Pricing
HY-129481
LY 178210 LY 178210 (Compound 24) is a selective partial agonist of the 5-HT1A receptor, with Ki values ​​of 0.67 and 380 nM for the 5-HT1A and 5-HT1D receptors, respectively. LY 178210 has almost no activity against α₂-adrenergic receptors, 5-HT₂, and other neurotransmitter receptors. LY 178210 inhibits Foscolin-stimulated cyclase activity, but its maximum potency is lower than that of the full agonist 8-OH-DPAT (HY-112061). LY 178210 significantly reduces 5-hydroxyindoleacetic acid (5-HIAA) levels in the greater hypothalamus and increases serum corticosterone concentrations.
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