S-Allylmercaptocysteine

Modify Date: 2025-08-25 20:04:09

S-Allylmercaptocysteine Structure
S-Allylmercaptocysteine structure
Common Name S-Allylmercaptocysteine
CAS Number 2281-22-3 Molecular Weight 193.29
Density N/A Boiling Point N/A
Molecular Formula C6H11NO2S2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of S-Allylmercaptocysteine


S-allylmercaptocysteine, an organic sulfur compound extracted from garlic, has anti-inflammatory and anti-oxidative effects for various pulmonary diseases. S-allylmercaptocysteine achieves its anti-cancer effect through a variety of pathways such as inducing the apoptosis of cancer cells through the TGF-β signaling pathway, or reducing the NF-κB activity and up-regulating Nrf2 to achieve the effects of anti-inflammation and anti-oxidation[1][2][3].

 Names

Name S-Allylmercaptocysteine

 S-Allylmercaptocysteine Biological Activity

Description S-allylmercaptocysteine, an organic sulfur compound extracted from garlic, has anti-inflammatory and anti-oxidative effects for various pulmonary diseases. S-allylmercaptocysteine achieves its anti-cancer effect through a variety of pathways such as inducing the apoptosis of cancer cells through the TGF-β signaling pathway, or reducing the NF-κB activity and up-regulating Nrf2 to achieve the effects of anti-inflammation and anti-oxidation[1][2][3].
Related Catalog
In Vitro S-Allylmercaptocysteine attenuates cisplatin-induced nephrotoxicity through suppression of apoptosis, oxidative stress, and inflammation[2]. S-Allylmercaptocysteine (400 μM; 48 hours) induces apoptosis evaluated by detecting the activated caspase 3 and cleaved PARP in SW620, SW480, and Caco-2 cells. Both activated caspase 3 and cleaved PARP1 are found in the cells treated with SAMC while no activated PARP1 and caspase 3 are found in the untreated control cells[4].
In Vivo S-Allylmercaptocysteine (25 and 50 mg/kg; oral gavage) could significantly ameliorate the pathological structure, and decrease inflammatory cell infiltration and pro-inflammatory cytokines in bronchoalveolar lavage fluid (BALF) in BLM-induced pulmonary fibrosis mice. S-Allylmercaptocysteine shows an anti-fibrosis effect by increasing anti-oxidants like HO-1, GSH and SOD as well as decreasing hydroxyproline (HYP) in BLM-induced mice[1].
References

[1]. Tong D, et al. S-allylmercaptocysteine promotes MAPK inhibitor-induced apoptosis by activating the TGF-β signaling pathway in cancer cells. Oncol Rep. 2014;32(3):1124-1132.

[2]. Zhu X, et al. S-Allylmercaptocysteine Attenuates Cisplatin-Induced Nephrotoxicity through Suppression of Apoptosis, Oxidative Stress, and Inflammation. Nutrients. 2017;9(2):166. Published 2017 Feb 20.

[3]. Li C, et al. S-Allylmercaptocysteine attenuates Bleomycin-induced pulmonary fibrosis in mice via suppressing TGF-β1/Smad and oxidative stress pathways. Int Immunopharmacol. 2020;79:106110.

[4]. Liang D, et al. S-allylmercaptocysteine effectively inhibits the proliferation of colorectal cancer cells under in vitro and in vivo conditions. Cancer Lett. 2011;310(1):69-76.

 Chemical & Physical Properties

Molecular Formula C6H11NO2S2
Molecular Weight 193.29
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here


Get all suppliers and price by the below link:

S-Allylmercaptocysteine suppliers

S-Allylmercaptocysteine price

Related Compounds: More...
(S)-3-(BENZYLOXY)-2-(((TERT-BUTOXYCARBONYL)AMINO)METHYL)PROPANOIC ACID
865704-62-7
(S)-1-(Naphthalen-1-yl)propan-1-amine hydrochloride
873893-96-0
(S)-1-(p-tolyl)ethyl 2,3,4,5,6-pentafluorobenzoate
622852-35-1
(S)-1-(4-bromophenylsulfonyl)pyrrolidin-3-ol
1001334-19-5
S-[4-[2-(4-formamidophenyl)ethynyl]phenyl] ethanethioate
825615-32-5
(S)-2,4-dimethyl-docos-2t-enoic acid methyl ester
19789-09-4
(S)-N-(2,4-difluorobenzyl)-2'-ethyl-9'-hydroxy-1',8'-dioxo-1',2,2',4,4',5,6,8'-octahydrospiro[pyran-3,3'-pyrido[1,2-a]pyrazine]-7'-carboxamide
1799952-48-9
S-ethenyl N,N-dipropylcarbamothioate
101622-02-0
(S)-(-)-1,1-DIPHENYL-1,2-PROPANEDIOL
233772-38-8
N~4~-cyclopropyl-6-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide
1282100-29-1
N-isobutyl-6-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide
1282134-12-6
6-isopropyl-N~4~-(4-methoxybenzyl)-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide
1282116-96-4
N-(3,5-dimethoxyphenyl)-1,3-dimethyl-6-(propan-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxamide
1324084-05-0
N~4~-cyclopentyl-6-isopropyl-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide
1282116-99-7
1,3-dimethyl-6-(propan-2-yl)-N-(pyridin-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxamide
1282101-78-3
Ethyl 2-(6-bromo-8-methylimidazo[1,2-a]pyridin-2-yl)acetate
1239741-70-8
4-[4-(1-Hydroxy-ethyl)-5-methyl-thiazol-2-yl]-piperidine-1-carboxylic acid tert-butyl ester
1044136-48-2
4-(2-(Tetrahydrofuran-2-yl)-ethyl)-benzaldehyde
936343-92-9
4-(5-Chloromethyl-thiazol-2-yl)-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester
1044136-57-3