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286281 Aldrich

Indole-3-acetamide

98%

Synonym: 3-Indolylacetamide, NSC 1969

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Properties

Related Categories Building Blocks, C10, Chemical Synthesis, Heterocyclic Building Blocks, Indoles More...
InChI Key   ZOAMBXDOGPRZLP-UHFFFAOYSA-N
assay   98%
mp   148-150 °C(lit.)

Description

Packaging

1, 5 g in glass bottle

Application

Indole-3-acetamide was used in the synthesis of [5.5.6.6]diazafenestrane skeleton and indole-3-acetic acid.

Reactant for the synthesis of:
• PET agent for imaging of protein kinase C
• A potential agent against Prion Disease
• Protein kinase C (PKC) inhibitor bisindolylmaleimide IV
• Glycogen synthase kinase-3ß (GSK-3ß) inhibitors
• Inhibitors of CaMKIId
• A VEGF inhibitor
• JAK3 inhibitors
• Inhibitors of NAD+-Dependent Histone Deacetylases
• Inhibitors of human adipocyte fatty acid-binding protein
• Cyclin-dependent kinase inhibitors

General description

Indole-3-acetamide is an auxin precursor.

Other Notes

Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 286281.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

Price and Availability

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

MSMLS Online Plate Map

Metabolite descriptors included with the software download upon purchase of the product include: Name, Parent CID, molecular formula, molecular weight, CAS, ChEBI, HMDB ID, PubChem Compound and Subst...
Keywords: Mass spectrometry, Metabolites

Related Content

Indoles, Purines, and Their Isosteres

Substituted indoles and purines have frequently been referred to as “privileged structures” since they are capable of binding to multiple receptors with high affinity, and thus have applications acro...
Keywords: Building blocks, Medicinal chemistry

Peer-Reviewed Papers
15

References

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