Date published: 2026-4-30

1-800-457-3801

SCBT Portrait Logo
Seach Input

Indazole-3-carboxylic Acid (CAS 4498-67-3)

0.0(0)
Write a reviewAsk a question

See product citations (1)

Alternate Names:
1H-Indazole-3-carboxylic Acid; 3(1H)-Indazolecarboxylic Acid; 3-Carboxy-1H-indazole; 3-Carboxyindazole; NSC 520610
Application:
Indazole-3-carboxylic Acid is an antiinflammatory derivative of indole
CAS Number:
4498-67-3
Purity:
≥99%
Molecular Weight:
162.15
Molecular Formula:
C8H6N2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Derivative of indole that is useful in the treatment of pain and inflammation.


Indazole-3-carboxylic Acid (CAS 4498-67-3) References

  1. Characterization of the FAD-containing N-methyltryptophan oxidase from Escherichia coli.  |  Khanna, P. and Schuman Jorns, M. 2001. Biochemistry. 40: 1441-50. PMID: 11170472
  2. Structure-activity relationship study and discovery of indazole 3-carboxamides as calcium-release activated calcium channel blockers.  |  Bai, S., et al. 2017. Bioorg Med Chem Lett. 27: 393-397. PMID: 28057422
  3. Anti-cancer and anti-inflammatory activities of a new family of coordination compounds based on divalent transition metal ions and indazole-3-carboxylic acid.  |  García-Valdivia, AA., et al. 2021. J Inorg Biochem. 215: 111308. PMID: 33257004
  4. Structural and biochemical characterization of the prenylated flavin mononucleotide-dependent indole-3-carboxylic acid decarboxylase.  |  Gahloth, D., et al. 2022. J Biol Chem. 298: 101771. PMID: 35218772
  5. Indazoles as indole bioisosteres: synthesis and evaluation of the tropanyl ester and amide of indazole-3-carboxylate as antagonists at the serotonin 5HT3 receptor.  |  Fludzinski, P., et al. 1987. J Med Chem. 30: 1535-7. PMID: 3625701
  6. NIR and UV induced transformations of indazole-3-carboxylic acid isolated in low temperature matrices.  |  Pagacz-Kostrzewa, M., et al. 2023. Spectrochim Acta A Mol Biomol Spectrosc. 290: 122283. PMID: 36586171
  7. Effect of lonidamine derivatives on the inhibition of transformed cell area expansion.  |  Aoyama, M., et al. 2023. Biochem Biophys Rep. 34: 101480. PMID: 37180755
  8. Novel multi-target ligands of dopamine and serotonin receptors for the treatment of schizophrenia based on indazole and piperazine scaffolds-synthesis, biological activity, and structural evaluation.  |  Stępnicki, P., et al. 2023. J Enzyme Inhib Med Chem. 38: 2209828. PMID: 37184096
  9. Novel rhenium oxocomplexes of indazole-3-carboxylic acid – Synthesis, X-ray studies, spectroscopic characterization and DFT calculations  |  Machura, B., Świetlicka, A., Wolff, M., & Kruszynski, R. 2010. Polyhedron. 29(9): 2061-2069.
  10. Molecular modeling of indazole-3-carboxylic acid and its metal complexes (Zn, Ni, Co, Fe and Mn) as NO synthase inhibitors: DFT calculations, docking studies and molecular dynamics simulations  |  da Silva, T. U., da Silva, E. T., de Carvalho Pougy, K., da Silva Lima, C. H., & de Paula Machado, S. 2022. Inorganic Chemistry Communications. 135: 109120.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Indazole-3-carboxylic Acid, 2.5 g

sc-218595
2.5 g
$105.00