52438-09-2
52438-09-2
Chemical Structure
S-1-Propenyl-L-cysteine
- CAS No.: 52438-09-2
- Formula:C6H11NO2S
- Molecular Weight:161.22
IUPAC Name: (E)-S-(prop-1-en-1-yl)-L-cysteine
InChIKey: HYGGRRPFVXHQQW-HRJJCQLASA-N
SMILES: N[C@@H](CS/C=C/C)C(O)=O
Biological Activity: S-1-Propenyl-L-cysteine is a stereoisomer of S-allyl-l-cysteine, extracted from garlic, with immunomodulatory effects and reduces blood pressure in a hypertensive animal model[1]. S-1-Propenyl-L-cysteine exhibits antioxidative efficacy through a NO-dependent BACH1 signaling pathway[2]. S-1-Propenyl-L-cysteine is orally active.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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S-1-Propenyl-L-cysteine | 99.91% | S-1-Propenyl-L-cysteine is a stereoisomer of S-allyl-l-cysteine, extracted from garlic, with immunomodulatory effects and reduces blood pressure in a hypertensive animal model. S-1-Propenyl-L-cysteine exhibits antioxidative efficacy through a NO-dependent BACH1 signaling pathway. S-1-Propenyl-L-cysteine is orally active. | ||||||||||||||||||||
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S-1-Propenyl-L-cysteine (Standard) | ≥98% | S-1-Propenyl-L-cysteine (Standard) is the analytical standard of S-1-Propenyl-L-cysteine. This product is intended for research and analytical applications. S-1-Propenyl-L-cysteine is a stereoisomer of S-allyl-l-cysteine, extracted from garlic, with immunomodulatory effects and reduces blood pressure in a hypertensive animal model. S-1-Propenyl-L-cysteine exhibits antioxidative efficacy through a NO-dependent BACH1 signaling pathway. S-1-Propenyl-L-cysteine is orally active. | ||||||||||||||||||||
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References
- [1]. Kodera Y, et al. Chemical and Biological Properties of S-1-Propenyl-l-Cysteine in Aged Garlic Extract. Molecules. 2017 Mar 31;22(4). [Content Brief]
- [2]. Tsuneyoshi T, et al., S-1-Propenylcysteine augments BACH1 degradation and heme oxygenase 1 expression in a nitric oxide-dependent manner in endothelial cells. Nitric Oxide. 2019 Mar 1;84:22-29. [Content Brief]
