Chemical Formula: C9H9O4-

Chemical Formula C9H9O4-

Found 21 metabolite its formula value is C9H9O4-

(R+)-3-(4-hydroxyphenyl)lactate

(2R)-2-Hydroxy-3-(4-hydroxyphenyl)propanoic acid

C9H9O4- (181.0500814)


(r+)-3-(4-hydroxyphenyl)lactate, also known as (2r)-2-hydroxy-3-(4-hydroxyphenyl)propanoate or P-hydroxyphenyllactic acid, is a member of the class of compounds known as phenylpropanoic acids. Phenylpropanoic acids are compounds with a structure containing a benzene ring conjugated to a propanoic acid (r+)-3-(4-hydroxyphenyl)lactate is soluble (in water) and a weakly acidic compound (based on its pKa). (r+)-3-(4-hydroxyphenyl)lactate can be found in a number of food items such as muskmelon, coconut, lemon grass, and kohlrabi, which makes (r+)-3-(4-hydroxyphenyl)lactate a potential biomarker for the consumption of these food products.

   

3-(4-Hydroxyphenyl)lactate

3-(4-Hydroxyphenyl)lactate

C9H9O4- (181.0500814)


A 2-hydroxy carboxylate that is obtained by removal of a proton from the carboxylic acid group of 3-(4-hydroxyphenyl)lactic acid. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

3-(2,3-Dihydroxyphenyl)propanoate

3-(2,3-Dihydroxyphenyl)propanoate

C9H9O4- (181.0500814)


The conjugate base of 3-(2,3-dihydroxyphenyl)propanoic acid.

   

3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate

3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate

C9H9O4- (181.0500814)


3-(4-hydroxycyclohex-2-en-1-ylidene)pyruvate obtained by deprotonation of the carboxy group of 3-[(1E,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid; major species at pH 7.3.

   

3-(3,4-dihydroxyphenyl)propanoate

3-(3,4-dihydroxyphenyl)propanoate

C9H9O4- (181.0500814)


A monocarboxylic acid anion that is the conjugate base of 3-(3,4-dihydroxyphenyl)propanoic acid.

   

(4-Hydroxy-3-methoxyphenyl)acetate

(4-Hydroxy-3-methoxyphenyl)acetate

C9H9O4- (181.0500814)


   

(4R)-3,4-dihydro-4-hydroxyphenylpyruvate

(4R)-3,4-dihydro-4-hydroxyphenylpyruvate

C9H9O4- (181.0500814)


   

3-(cis-5,6-Dihydroxycyclohexa-1,3-dien-1-yl)prop-2-enoate

3-(cis-5,6-Dihydroxycyclohexa-1,3-dien-1-yl)prop-2-enoate

C9H9O4- (181.0500814)


   

methylphoracetophenone

methylphoracetophenone

C9H9O4- (181.0500814)


   

3,4-Dimethoxybenzoate

3,4-Dimethoxybenzoate

C9H9O4- (181.0500814)


   

2-Methoxymandelate

2-Methoxymandelate

C9H9O4- (181.0500814)


   

(R+)-3-(4-hydroxyphenyl)lactate

(R+)-3-(4-hydroxyphenyl)lactate

C9H9O4- (181.0500814)


   

3,5-Dimethoxybenzoate

3,5-Dimethoxybenzoate

C9H9O4- (181.0500814)


The conjugate base of 3,5-dimethoxybenzoic acid.

   

2,4-Dihydroxy-3,6-dimethylbenzoate

2,4-Dihydroxy-3,6-dimethylbenzoate

C9H9O4- (181.0500814)


   

3-(4-Hydroxycyclohex-2-en-1-ylidene)pyruvate

3-(4-Hydroxycyclohex-2-en-1-ylidene)pyruvate

C9H9O4- (181.0500814)


   

(E)-3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dienyl]acrylate

(E)-3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dienyl]acrylate

C9H9O4- (181.0500814)


   

5-Methylorsellinate

5-Methylorsellinate

C9H9O4- (181.0500814)


A dihydroxybenzoate that is the conjugate base of 5-methylorsellinic acid, obtained by the deprotonation of the carboxy group. It is the major species at pH 7.3.

   

3,4-Dihydro-4-hydroxyphenylpyruvate

3,4-Dihydro-4-hydroxyphenylpyruvate

C9H9O4- (181.0500814)


   

3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate

3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvate

C9H9O4- (181.0500814)


A 3-(4-hydroxycyclohex-2-en-1-ylidene)pyruvate obtained by deprotonation of the carboxy group of 3-[(1Z,4R)-4-hydroxycyclohex-2-en-1-ylidene]pyruvic acid; major species at pH 7.3.

   

4-(2-Carboxy-2-hydroxyethyl)phenolate

4-(2-Carboxy-2-hydroxyethyl)phenolate

C9H9O4- (181.0500814)


   

(R)-3-(4-Hydroxyphenyl)lactate

(R)-3-(4-Hydroxyphenyl)lactate

C9H9O4- (181.0500814)