ChemSpider 2D Image | BQ-788 | C34H50N5NaO7

BQ-788

  • Molecular FormulaC34H50N5NaO7
  • Average mass663.780 Da
  • Monoisotopic mass663.360779 Da
  • ChemSpider ID4470569
  • Charge - Charge

    defined stereocentres - 5 of 5 defined stereocentres


More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

BQ-788 [Wiki]
156161-89-6 [RN]
44OLL8XEJ4
BQ 788 sodium salt
BQ788
D-Norleucine, N-(((2R,6S)-2,6-dimethyl-1-piperidinyl)carbonyl)-4-methyl-L-leucyl-1-(methoxycarbonyl)-D-tryptophyl-, monosodium salt
D-Norleucine, N-((cis-2,6-dimethyl-1-piperidinyl)carbonyl)-4-methyl-L-leucyl-1-(methoxycarbonyl)-D-tryptophyl-, monosodium salt
D-Norleucine, N-[[(2R,6S)-2,6-dimethyl-1-piperidinyl]carbonyl]-4-methyl-L-leucyl-1-(methoxycarbonyl)-D-tryptophyl-, sodium salt (1:1) [ACD/Index Name]
N-{[(2R,6S)-2,6-Diméthyl-1-pipéridinyl]carbonyl}-4-méthyl-L-leucyl-N-[(1R)-1-carboxylatopentyl]-1-(méthoxycarbonyl)-D-tryptophaneamide de sodium [French] [ACD/IUPAC Name]
Natrium-N-{[(2R,6S)-2,6-dimethyl-1-piperidinyl]carbonyl}-4-methyl-L-leucyl-N-[(1R)-1-carboxylatopentyl]-1-(methoxycarbonyl)-D-tryptophanamid [German] [ACD/IUPAC Name]
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  • Experimental Physico-chemical Properties
  • Miscellaneous
    • Bio Activity:

      7-TM Receptors Tocris Bioscience 1500
      BQ-788 sodium salt is a potent, selective ETB receptor antagonist (IC50 = 1.2 nM for inhibition of ET-1 binding to human Girardi heart cells); poorly inhibited the binding to ET A receptors in human n euroblastoma cell line SK-N-MC cells (IC(50), 1300 nM). MedChem Express
      BQ-788 sodium salt is a potent, selective ETB receptor antagonist (IC50 = 1.2 nM for inhibition of ET-1 binding to human Girardi heart cells); poorly inhibited the binding to ET A receptors in human neuroblastoma cell line SK-N-MC cells (IC(50), 1300 nM).; IC50 value: 1.2 nM [1]; Target: ETB receptor; in vitro: BQ-788 potently and competitively inhibited (125)I-labeled ET-1 binding to ET(B) receptors in human Girrardi heart cells (hGH) with an IC(50) of 1.2 nM, but only poorly inhibited the binding to ET A receptors in human neuroblastoma cell line SK-N-MC cells (IC(50), 1300 nM). MedChem Express HY-15894
      BQ-788 sodium salt is a potent, selective ETB receptor antagonist (IC50 = 1.2 nM for inhibition of ET-1 binding to human Girardi heart cells); poorly inhibited the binding to ET A receptors in human neuroblastoma cell line SK-N-MC cells (IC(50), 1300 nM).;IC50 value: 1.2 nM [1];Target: ETB receptor;In vitro: BQ-788 potently and competitively inhibited (125)I-labeled ET-1 binding to ET(B) receptors in human Girrardi heart cells (hGH) with an IC(50) of 1.2 nM, but only poorly inhibited the binding to ET A receptors in human neuroblastoma cell line SK-N-MC cells (IC(50), 1300 nM). In isolated rabbit pulmonary arteries, BQ-788 showed no agonistic activity up to 10 microM and competitively inhibited the vasoconstriction induced by an ET(B)-selective agonist (pA(2), 8.4). BQ-788 also inhibited several bioactivities of ET-1, such as bronchoconstriction, cell proliferation, and clearance of perfused ET-1 [1]. In the rat aorta, BQ-788 antagonized the endothelium-dependent, ETB1 receptor-med MedChem Express HY-15894
      Endothelin Receptor MedChem Express HY-15894
      Endothelin Receptors Tocris Bioscience 1500
      GPCR/G protein MedChem Express HY-15894
      GPCR/G protein; MedChem Express HY-15894
      Peptide Receptors Tocris Bioscience 1500
      Potent, selective ETB receptor antagonist (IC50 = 1.2 nM for inhibition of ET-1 binding to human Girardi heart cells). Tocris Bioscience 1500
      Selective ETB antagonist Tocris Bioscience 1500

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module

No predicted properties have been calculated for this compound.

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