3844-67-5
3844-67-5
Chemical Structure
(S)-Allantoin
- CAS No.: 3844-67-5
- Formula:C4H6N4O3
- Molecular Weight:158.12
IUPAC Name: (S)-1-(2,5-dioxoimidazolidin-4-yl)urea
InChIKey: POJWUDADGALRAB-SFOWXEAESA-N
SMILES: NC(N[C@H]1NC(NC1=O)=O)=O
Biological Activity: (S)-Allantoin is the S-isomer of Allantoin (HY-N0543). (S)-Allantoin binds selectively in the active site of urate oxidase. (S)-Allantoin can be converted to Allantoate by the action of allantoicase. (S)-Allantoin serves as a source of nitrogen in Arabidopsis thaliana[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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(S)-Allantoin | (S)-Allantoin is the S-isomer of Allantoin (HY-N0543). (S)-Allantoin binds selectively in the active site of urate oxidase. (S)-Allantoin can be converted to Allantoate by the action of allantoicase. (S)-Allantoin serves as a source of nitrogen in Arabidopsis thaliana. | |||||||||||||||||||||
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References
- [1]. Kim K, et al. Structural and functional basis for (S)-allantoin formation in the ureide pathway. J Biol Chem. 2007 Aug 10;282(32):23457-64. [Content Brief]
- [2]. Fahad S, et al. Suppressing photorespiration for the improvement in photosynthesis and crop yields: A review on the role of S-allantoin as a nitrogen source. J Environ Manage. 2019 May 1;237:644-651. [Content Brief]
Keywords
