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Luzindole (CAS 117946-91-5)

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Alternate Names:
N-Acetyl-2-benzyltryptamine; N-[2-[2-(Phenylmethyl)-1H-indol-3-yl]ethyl]acetamide
Application:
Luzindole is a selective antagonist of MEL-1B-R (melatonin receptor)
CAS Number:
117946-91-5
Purity:
≥96%
Molecular Weight:
292.37
Molecular Formula:
C19H20N2O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Luzindole is a synthetic compound structured as an indole derivative. In the realm of research, it is used as a tool compound to understand the function of specific receptors, not as a therapeutic agent but as a means to dissect receptor-mediated signaling pathways. In biochemical assays to characterize the binding affinity and selectivity of receptor-ligand interactions. Luzindole is also applied in the investigation of cellular communication processes, helping to elucidate the role of receptors in various cellular responses. It is also often employed as a reference compound in the development of detection and quantification methods for similar indole-based structures.


Luzindole (CAS 117946-91-5) References

  1. Pharmacological characterization of human recombinant melatonin mt(1) and MT(2) receptors.  |  Browning, C., et al. 2000. Br J Pharmacol. 129: 877-86. PMID: 10696085
  2. Selective MT(2) melatonin receptor antagonist blocks melatonin-induced antinociception in rats.  |  Yu, CX., et al. 2000. Neurosci Lett. 282: 161-4. PMID: 10717416
  3. Luzindole, a melatonin receptor antagonist, inhibits the transient outward K+ current in rat cerebellar granule cells.  |  Zhou, MO., et al. 2003. Brain Res. 970: 169-77. PMID: 12706258
  4. Pharmacology and function of melatonin receptors.  |  Dubocovich, ML. 1988. FASEB J. 2: 2765-73. PMID: 2842214
  5. Luzindole (N-0774): a novel melatonin receptor antagonist.  |  Dubocovich, ML. 1988. J Pharmacol Exp Ther. 246: 902-10. PMID: 2843633
  6. The melatonin receptor antagonist luzindole induces Ca2+ mobilization, reactive oxygen species generation and impairs trypsin secretion in mouse pancreatic acinar cells.  |  Estaras, M., et al. 2019. Biochim Biophys Acta Gen Subj. 1863: 129407. PMID: 31381958
  7. Luzindole attenuates LPS/d-galactosamine-induced acute hepatitis in mice.  |  Luo, Y., et al. 2020. Innate Immun. 26: 319-327. PMID: 31779498
  8. The melatonin receptor antagonist luzindole induces the activation of cellular stress responses and decreases viability of rat pancreatic stellate cells.  |  Estaras, M., et al. 2020. J Appl Toxicol. 40: 1554-1565. PMID: 32567733
  9. Melatonin promotes cardiomyocyte proliferation and heart repair in mice with myocardial infarction via miR-143-3p/Yap/Ctnnd1 signaling pathway.  |  Ma, WY., et al. 2021. Acta Pharmacol Sin. 42: 921-931. PMID: 32839503
  10. Luzindole and 4P-PDOT block the effect of melatonin on bovine granulosa cell apoptosis and cell cycle depending on its concentration.  |  Wang, S., et al. 2021. PeerJ. 9: e10627. PMID: 33732541
  11. Acute blockade of endogenous melatonin by Luzindole, with or without peripheral LPS injection, induces jejunal inflammation and morphological alterations in Swiss mice.  |  Matos, RS., et al. 2021. Braz J Med Biol Res. 54: e11215. PMID: 34431873
  12. Melatonin receptors: are there multiple subtypes?  |  Dubocovich, ML. 1995. Trends Pharmacol Sci. 16: 50-6. PMID: 7762083
  13. Luzindole, a melatonin receptor antagonist, suppresses experimental autoimmune encephalomyelitis.  |  Constantinescu, CS., et al. 1997. Pathobiology. 65: 190-4. PMID: 9396042
  14. Selective MT2 melatonin receptor antagonists block melatonin-mediated phase advances of circadian rhythms.  |  Dubocovich, ML., et al. 1998. FASEB J. 12: 1211-20. PMID: 9737724
  15. The melatonin antagonist luzindole protects retinal photoreceptors from light damage in the rat.  |  Sugawara, T., et al. 1998. Invest Ophthalmol Vis Sci. 39: 2458-65. PMID: 9804154

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Luzindole, 5 mg

sc-202700
5 mg
$104.00

Luzindole, 25 mg

sc-202700A
25 mg
$283.00

Luzindole, 100 mg

sc-202700B
100 mg
$567.00

Luzindole, 250 mg

sc-202700C
250 mg
$861.00

Luzindole, 2.5 g

sc-202700D
2.5 g
$4692.00

Can this product be used for plant research? I did not find the relevant literature. All literature is for animal research。 这个产品能用于植物研究么?我没有找到相关的文献。所有的文献都是用于动物研究。

Asked by: 高山流水
Thank you for your question. It would be helpful if you could call us, allowing for a more interactive discussion of this and other related questions.
Answered by: Technical Support
Date published: 2021-07-23

Is this product soluble in water?

Asked by: hawkeye11
Thank you for your question. This chemical is not very soluble in water. First it should be dissolved in an organic solvent such as methanol (50 mg/mL) or ethanol (30 mg/mL) and then diluted down with water. It is approximately soluble in a 1:1 ethanol:water solution at 0.5 mg/mL. Also, water greatly affects the stability of this compound so it should not be stored long term in water solutions. Please contact Technical Service if you have further questions concerning this product.
Answered by: Tech Service 9
Date published: 2017-01-25
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Rated 5 out of 5 by from Roy et alRoy et al. (PubMed ID 11684691) found that Luzindole, a melatonin receptor antagonist, blocked the melatonin-mediated, forskolin-induced accumulation of cAMP and inhibition of GnRH secretion in GT1-7 cells. -SCBT Publication Review
Date published: 2015-03-03
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Luzindole is rated 5.0 out of 5 by 1.
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