(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.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- CAS No.: 3844-67-5
- 화학식: C4H6N4O3
- 분자량:158.12
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| Caco-2 | Inhibition |
9.66 %
Compound: ALLANTOIN
|
Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of Caco-2 cells at 10 uM after 48 hours by high content imaging
Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of Caco-2 cells at 10 uM after 48 hours by high content imaging
|
10.21203/rs.3.rs-23951/v1 |
Chemical Information
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CAS No. 3844-67-5
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분자량 158.12
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화학식 C4H6N4O3
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SMILES
NC(N[C@H]1NC(NC1=O)=O)=O
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Structure Classification
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Initial Source
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
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]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)