Molecular structure of Imipramine N-β-D-Glucuronide
Imipramine N-β-D-Glucuronide (CAS 165602-94-8)
Alternate Names:
N-β-D-Glucopyranuronosyl-10,11-dihydro-N,N-dimethyl-5H-dibenz[b,f]azepine-5-propanaminium Inner Salt
CAS Number:
165602-94-8
Molecular Weight:
456.53
Molecular Formula:
C25H32N2O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Imipramine N-β-D-Glucuronide, derived from imipramine, is a metabolite that exhibits solubility in water and ethanol, while being insoluble in ether or chloroform. Through a click reaction, Imipramine N-β-D-glucuronide can be subjected to modification, enabling the introduction of fluorine atoms at specific locations within the sugar molecule. This chemical modification serves various purposes, including glycosylation studies and the fluorescent labeling of glycoconjugates, facilitating their use in imaging investigations.
Imipramine N-β-D-Glucuronide (CAS 165602-94-8) References
- In vitro selective inhibition of human UDP-glucuronosyltransferase (UGT) 1A4 by finasteride, and prediction of in vivo drug-drug interactions. | Lee, SJ., et al. 2015. Toxicol Lett. 232: 458-65. PMID: 25448279
- Glucuronidation of OTS167 in Humans Is Catalyzed by UDP-Glucuronosyltransferases UGT1A1, UGT1A3, UGT1A8, and UGT1A10. | Ramírez, J., et al. 2015. Drug Metab Dispos. 43: 928-35. PMID: 25870101
- In vitro stereoselective inhibition of ginsenosides toward UDP-glucuronosyltransferase (UGT) isoforms. | Kim, D., et al. 2016. Toxicol Lett. 259: 1-10. PMID: 27462006
- In Vitro Inhibition of Human UDP-Glucuronosyl-Transferase (UGT) Isoforms by Astaxanthin, β-Cryptoxanthin, Canthaxanthin, Lutein, and Zeaxanthin: Prediction of in Vivo Dietary Supplement-Drug Interactions. | Zheng, YF., et al. 2016. Molecules. 21: PMID: 27529203
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Imipramine N-β-D-Glucuronide, 1 mg | sc-471182 | 1 mg | $414.00 |