Chemical Formula: C6H11NO2S

Chemical Formula C6H11NO2S

Found 35 metabolite its formula value is C6H11NO2S

S-Allylcysteine

2-Amino-3-(prop-2-en-1-ylsulphanyl)propanoic acid

C6H11NO2S (161.051)


Occurs in garlic. Potential nutriceutical. S-Allylcysteine is found in garden onion, soft-necked garlic, and onion-family vegetables. S-Allylcysteine is found in garden onion. S-Allylcysteine occurs in garlic. Potential nutriceutica D000970 - Antineoplastic Agents S-Allyl-L-cysteine, one of the organosulfur compounds found in AGE, possess various biological effects including neurotrophic activity, anti-cancer activity, anti-inflammatory activity. S-Allyl-L-cysteine, one of the organosulfur compounds found in AGE, possess various biological effects including neurotrophic activity, anti-cancer activity, anti-inflammatory activity.

   

Entadamide A

N-(2-Hydroxyethyl)-3-methylthiopropenamide

C6H11NO2S (161.051)


   

trans-S-(1-Propenyl)-L-cysteine

2-Amino-3-[(1Z)-prop-1-en-1-ylsulphanyl]propanoic acid

C6H11NO2S (161.051)


trans-S-(1-Propenyl)-L-cysteine is found in onion-family vegetables. trans-S-(1-Propenyl)-L-cysteine is a constituent of garlic

   

Allyl cysteine

2-[(prop-2-en-1-yl)amino]-3-sulfanylpropanoic acid

C6H11NO2S (161.051)


D000970 - Antineoplastic Agents

   

Cysteine allyl ester

prop-2-en-1-yl 2-amino-3-sulfanylpropanoate

C6H11NO2S (161.051)


   

S-Propenylcysteine

(2R)-2-amino-3-[(1E)-prop-1-en-1-ylsulfanyl]propanoic acid

C6H11NO2S (161.051)


S-propenylcysteine is a member of the class of compounds known as L-cysteine-s-conjugates. L-cysteine-s-conjugates are compounds containing L-cysteine where the thio-group is conjugated. S-propenylcysteine is soluble (in water) and a moderately acidic compound (based on its pKa). S-propenylcysteine can be found in soft-necked garlic, which makes S-propenylcysteine a potential biomarker for the consumption of this food product. 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. 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-Ethyl 2-acetylaminoethanethioate

N-[2-(Ethylsulphanyl)-2-oxoethyl]ethanimidic acid

C6H11NO2S (161.051)


It is used as a food additive .

   

4-aminothiane-4-carboxylic acid

4-aminothiane-4-carboxylic acid

C6H11NO2S (161.051)


   

S-Propenylcysteine

(2R)-2-amino-3-[(E)-prop-1-enyl]sulfanylpropanoic acid

C6H11NO2S (161.051)


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. 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-Allylcysteine

S-Allyl-L-cysteine, United States Pharmacopeia (USP) Reference Standard

C6H11NO2S (161.051)


An S-hydrocarbyl-L-cysteine that is L-cysteine in which the hydrogen attached to the sulphur is replaced by a prop-2-enyl group. It commonly occurs in garlic and has been found to exhibit antineoplastic activity. S-allylcysteine is an S-hydrocarbyl-L-cysteine that is L-cysteine in which the hydrogen attached to the sulphur is replaced by a prop-2-enyl group. It commonly occurs in garlic and has been found to exhibit antineoplastic activity. It has a role as a metabolite and an antineoplastic agent. It is a tautomer of a S-allylcysteine zwitterion. See also: Garlic (part of). C26170 - Protective Agent > C275 - Antioxidant D000970 - Antineoplastic Agents S-Allyl-L-cysteine, one of the organosulfur compounds found in AGE, possess various biological effects including neurotrophic activity, anti-cancer activity, anti-inflammatory activity. S-Allyl-L-cysteine, one of the organosulfur compounds found in AGE, possess various biological effects including neurotrophic activity, anti-cancer activity, anti-inflammatory activity.

   

trans-S-(1-Propenyl)-L-cysteine

2-amino-3-[(1Z)-prop-1-en-1-ylsulfanyl]propanoic acid

C6H11NO2S (161.051)


   

(R)-5,5-Dimethyl-1,3-thiazolidine-4-carboxylic acid

(R)-5,5-Dimethyl-1,3-thiazolidine-4-carboxylic acid

C6H11NO2S (161.051)


   

4-Aminotetrahydro-2H-thiopyran-4-carboxylic acid

2H-Thiopyran-4-carboxylicacid, 4-aminotetrahydro-

C6H11NO2S (161.051)


   

2,2-dimethylthiazolidine-4-carboxylic acid

2,2-Dimethyl-1,3-thiazolidine-4-carboxylic acid

C6H11NO2S (161.051)


   

tert-Butylsulfonylacetonitrile

tert-Butylsulfonylacetonitrile

C6H11NO2S (161.051)


   

Thiomorpholine, 4-acetyl-, 1-oxide (9CI)

Thiomorpholine, 4-acetyl-, 1-oxide (9CI)

C6H11NO2S (161.051)


   

N-(ETHOXYCARBONYL)THIOPROPIONAMIDE

N-(ETHOXYCARBONYL)THIOPROPIONAMIDE

C6H11NO2S (161.051)


   

2-(tert-butylsulfonyl)acetonitrile

2-(tert-butylsulfonyl)acetonitrile

C6H11NO2S (161.051)


   

N,S-Diacetylcysteamine

N,S-Diacetylcysteamine

C6H11NO2S (161.051)


   

2-thiomorpholin-4-ylacetic acid

2-thiomorpholin-4-ylacetic acid

C6H11NO2S (161.051)


   

3-AMINOTETRAHYDRO-2H-THIOPYRAN-3-CARBOXYLIC ACID

3-AMINOTETRAHYDRO-2H-THIOPYRAN-3-CARBOXYLIC ACID

C6H11NO2S (161.051)


   

(4S,2RS)-2-ETHYLTHIAZOLIDINE-4-CARBOXYLIC ACID

(4S,2RS)-2-ETHYLTHIAZOLIDINE-4-CARBOXYLIC ACID

C6H11NO2S (161.051)


   

Thiocarbamoylameisensaeure-tert.-butylester

Thiocarbamoylameisensaeure-tert.-butylester

C6H11NO2S (161.051)


   

ethyl thiazolidine-4-carboxylate

ethyl thiazolidine-4-carboxylate

C6H11NO2S (161.051)


   

(4R)-2,2-Dimethyl-1,3-thiazolidine-4-carboxylic acid

(4R)-2,2-Dimethyl-1,3-thiazolidine-4-carboxylic acid

C6H11NO2S (161.051)


   

5,5-Dimethylthiazolidine-4-carboxylic acid

5,5-Dimethylthiazolidine-4-carboxylic acid

C6H11NO2S (161.051)


   

trans-S-(1-Propenyl)-L-cysteine

2-Amino-3-[(1Z)-prop-1-en-1-ylsulphanyl]propanoic acid

C6H11NO2S (161.051)


Trans-s-(1-propenyl)-l-cysteine belongs to cysteine and derivatives class of compounds. Those are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Trans-s-(1-propenyl)-l-cysteine is soluble (in water) and a moderately acidic compound (based on its pKa). Trans-s-(1-propenyl)-l-cysteine can be found in onion-family vegetables, which makes trans-s-(1-propenyl)-l-cysteine a potential biomarker for the consumption of this food product. trans-S-(1-Propenyl)-L-cysteine is found in onion-family vegetables. trans-S-(1-Propenyl)-L-cysteine is a constituent of garlic 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. 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].

   

(2R)-2-azaniumyl-3-[(prop-2-en-1-yl)sulfanyl]propanoate

(2R)-2-azaniumyl-3-[(prop-2-en-1-yl)sulfanyl]propanoate

C6H11NO2S (161.051)


   

S-trans-1-propenyl-L-cysteine

S-trans-1-propenyl-L-cysteine

C6H11NO2S (161.051)


   

N-Acetylthioglycine S-ethyl ester

N-Acetylthioglycine S-ethyl ester

C6H11NO2S (161.051)


   

allyl cysteine

allyl cysteine

C6H11NO2S (161.051)


D000970 - Antineoplastic Agents

   

N-(2-Hydroxyethyl)-3-methylthiopropenamide

N-(2-Hydroxyethyl)-3-methylthiopropenamide

C6H11NO2S (161.051)


   

S-allylcysteine zwitterion

S-allylcysteine zwitterion

C6H11NO2S (161.051)


An L-alpha-amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of S-allylcysteine. Major species at pH 7.3.

   

(2e)-n-(2-hydroxyethyl)-3-(methylsulfanyl)prop-2-enimidic acid

(2e)-n-(2-hydroxyethyl)-3-(methylsulfanyl)prop-2-enimidic acid

C6H11NO2S (161.051)


   

n-(2-hydroxyethyl)-3-(methylsulfanyl)prop-2-enimidic acid

n-(2-hydroxyethyl)-3-(methylsulfanyl)prop-2-enimidic acid

C6H11NO2S (161.051)