Date published: 2026-4-30

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tert-Butyl β-Carboline-3-carboxylate (CAS 93835-05-3)

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CAS Number:
93835-05-3
Molecular Weight:
268.31
Molecular Formula:
C16H16N2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tert-Butyl β-Carboline-3-carboxylate is a significant regulator of cell adhesion, which plays a role in diverse cellular processes such as cell polarity and cell cycle control, as well as transcriptional regulation. As a multifaceted protein, tert-Butyl β-Carboline-3-carboxylate partakes in a range of biological processes like embryonic development, maintenance of tissue homeostasis, and tumorigenesis. It′s part of the catenin family of proteins, which contribute to the formation of cell-cell junctions and controlling gene expression. Tert-Butyl β-Carboline-3-carboxylate is pivotal to the operation of the Wnt signaling pathway, a critical process for tissue development and upkeep. Extensive scientific research has used tert-Butyl β-Carboline-3-carboxylate to study a variety of concepts, including embryonic development, tissue homeostasis, and tumorigenesis, as well as cell adhesion, cell polarity, and cell cycle control. Tert-Butyl β-Carboline-3-carboxylate interaction with cadherin molecules, proteins that form cell-cell junctions, leads to a clustering of these molecules which activates the Wnt signaling pathway. This activation, in turn, triggers the transcription of genes associated with cell proliferation, differentiation, and migration.


tert-Butyl β-Carboline-3-carboxylate (CAS 93835-05-3) References

  1. Novel N-(arylalkyl)indol-3-ylglyoxylylamides targeted as ligands of the benzodiazepine receptor: synthesis, biological evaluation, and molecular modeling analysis of the structure-activity relationships.  |  Primofiore, G., et al. 2001. J Med Chem. 44: 2286-97. PMID: 11428922
  2. GABAA Receptors Expressed in Oligodendrocytes Cultured from the Neonatal Rat Contain α3 and γ1 Subunits and Present Differential Functional and Pharmacological Properties.  |  Ordaz, RP., et al. 2021. Mol Pharmacol. 99: 133-146. PMID: 33288547
  3. Recent advances for the C–C and C–N bond formation in the synthesis of 1-phenethyl-tetrahydroisoquinoline, aporphine, homoaporphine, and β-carboline alkaloids  |  Galvis, C. E. P., & Kouznetsov, V. V. 2017. Synthesis. 49(20): 4535-4561.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

tert-Butyl β-Carboline-3-carboxylate, 10 mg

sc-504388
10 mg
$398.00