1258955-93-9
1258955-93-9
Chemical Structure
Indole-3-carboxylic acid-d4
- CAS No.: 1258955-93-9
- Formula:C9H3D4NO2
- Molecular Weight:165.18
InChIKey: KMAKOBLIOCQGJP-RHQRLBAQSA-N
SMILES: OC(C1=CNC2=C([2H])C([2H])=C([2H])C([2H])=C12)=O
Biological Activity: Indole-3-carboxylic acid-d4 is deuterium labeled Indole-3-carboxylic acid. Indole-3-carboxylic acid is a normal urinary indolic tryptophan metabolite and has been found elevated in patients with liver diseases[1][2][1][2][3].
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Indole-3-carboxylic acid-d4 | Indole-3-carboxylic acid-d4 is deuterium labeled Indole-3-carboxylic acid. Indole-3-carboxylic acid is a normal urinary indolic tryptophan metabolite and has been found elevated in patients with liver diseases. | |||||||||||||||||||||
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Indole-3-carboxylic acid (Standard) | 99.58% | Indole-3-carboxylic acid (Standard) is the analytical standard of Indole-3-carboxylic acid. This product is intended for research and analytical applications. Indole-3-carboxylic acid is a normal urinary indolic tryptophan metabolite and has been found elevated in patients with liver diseases. | ||||||||||||||||||||
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Indole-3-carboxylic acid | 99.96% | Indole-3-carboxylic acid is an orally active urinary indolic tryptophan metabolite. Indole-3-carboxylic acid is a mediator of priming against Plectosphaerella cucumerina. Indole-3-carboxylic acid enhances the anti-colorectal cancer potency of Doxorubicin (HY-15142A) by inducing cell senescence. Indole-3-carboxylic acid can be used in liver disease research. | ||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [2]. Byrd DJ, et al. The analysis of indolic tryptophan metabolites in human urine. Thin-layer chromatography and in situ quantitation. J Chromatogr. 1974 Jul 17;94(0):85-106. [Content Brief]
- [3]. HARTMANN F, et al. [Indolepatterns in the urine of liver patients]. Klin Wochenschr. 1962 Jul 15;40:721-9. [Content Brief]
