3-Indoleacetonitrile
Code | Size | Price |
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TAR-T8024-500mg | 500mg | £103.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. |
Quantity:
TAR-T8024-1mL | 1 mL * 10 mM (in DMSO) | £107.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
Images
Documents
Further Information
Bioactivity:
3-Indoleacetonitrile is a light-induced auxin-inhibitory substance that is isolated from light-grown cabbage shoots.
CAS:
771-51-7
Formula:
C10H8N2
Molecular Weight:
156.188
Pathway:
Metabolism;
Purity:
0.9973
SMILES:
N#CCc1c[nH]c2ccccc12
Target:
Endogenous Metabolite
References
Somei M , Kizu K , Kunimoto M , et al. ChemInform Abstract: The Chemistry of Indoles. Part 24. Syntheses of 3-Indoleacetic Acid and 3-Indoleacetonitrile Having a Halogeno Group and a Carbon Functional Group at the 4-Position.[J]. Chemischer Informationsdienst, 1986, 17(13).
Mahadevan S . Conversion of 3-indoleacetaldoxime to 3-indoleacetonitrile by plants[J]. Archives of Biochemistry & Biophysics, 1963, 100(3):557-558.