Exact Mass: 185.0322

Exact Mass Matches: 185.0322

Found 22 metabolites which its exact mass value is equals to given mass value 185.0322, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

2-Amino-3-carboxymuconic acid semialdehyde

(2Z)-2-amino-3-[(1Z)-3-oxoprop-1-en-1-yl]but-2-enedioic acid

C7H7NO5 (185.0324)


2-Amino-3-carboxymuconic acid semialdehyde (CAS: 16597-58-3) is an intermediate metabolite of the tryptophan-niacin catabolic pathway. Current interest in the degradation of tryptophan is mostly due to the role of quinolinate and other metabolites in several neuropathological conditions. Quinolinate is a neurotoxin formed nonenzymatically from 2-amino-3-carboxymuconic semialdehyde in mammalian tissues. 2-Amino-3-carboxymuconic acid semialdehyde is enzymatically converted into 2-aminomuconate via 2-aminomuconic semialdehyde (PMID: 10510494, 16267312, 14275129). 2-amino-3-carboxymuconic acid semialdehyde is an intermediate metabolite of the tryptophan-niacin catabolic pathway. Current interest in the degradation of tryptophan is mostly due to the role of quinolinate and other metabolites in several neuropathological conditions. Quinolinate is a neurotoxin formed nonenzymatically from 2-amino-3-carboxymuconic semialdehyde in mammalian tissues. 2-Amino-3-carboxymuconic semialdehyde is enzymatically converted to 2-aminomuconate via 2-aminomuconic semialdehyde. (PMID: 10510494, 16267312, 14275129) [HMDB]

   

ACMC-20mzul

(2Z,4E)-4-amino-6-oxohepta-2,4-dienedioic acid

C7H7NO5 (185.0324)


   

(4S)-4-hydroxy-2,3,4,5-tetrahydro-(2S)-dipicolinate

(2S,4S)-4-hydroxy-2,3,4,5-tetrahydropyridine-2,6-dicarboxylate

C7H7NO5 (185.0324)


(4s)-4-hydroxy-2,3,4,5-tetrahydro-(2s)-dipicolinate belongs to alpha amino acids and derivatives class of compounds. Those are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof (4s)-4-hydroxy-2,3,4,5-tetrahydro-(2s)-dipicolinate is soluble (in water) and a weakly acidic compound (based on its pKa). (4s)-4-hydroxy-2,3,4,5-tetrahydro-(2s)-dipicolinate can be found in a number of food items such as mamey sapote, red bell pepper, burbot, and kelp, which makes (4s)-4-hydroxy-2,3,4,5-tetrahydro-(2s)-dipicolinate a potential biomarker for the consumption of these food products.

   

L-alpha-amino-epsilon-keto-pimelate

(1,5-dicarboxylato-5-oxopentyl)azaniumyl

C7H7NO5 (185.0324)


L-alpha-amino-epsilon-keto-pimelate belongs to alpha amino acids and derivatives class of compounds. Those are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. L-alpha-amino-epsilon-keto-pimelate is slightly soluble (in water) and a moderately acidic compound (based on its pKa). L-alpha-amino-epsilon-keto-pimelate can be found in a number of food items such as star fruit, cottonseed, black-eyed pea, and longan, which makes L-alpha-amino-epsilon-keto-pimelate a potential biomarker for the consumption of these food products.

   

Enaminomycin C

2,5-dihydroxy-4-imino-7-oxabicyclo[4.1.0]hept-2-ene-3-carboxylic acid

C7H7NO5 (185.0324)


Enaminomycin C is a metabolite that has been isolated from Streptomyces species, which are a group of bacteria known for their ability to produce a wide array of secondary metabolites with diverse biological activities. Enaminomycin C is one such compound that has been identified and characterized from these bacteria. It belongs to the enediyne antibiotic class, which are complex natural products known for their potent antibacterial activity, particularly against Gram-positive bacteria. Enaminomycin C, like other enediyne antibiotics, is believed to exert its antibacterial effects by targeting the bacterial ribosome and forming a complex with the RNA, leading to the inhibition of protein synthesis and ultimately cell death. The structural features of Enaminomycin C contribute to its unique biological properties. It possesses an enediyne core, which is a key structural element responsible for its antibacterial activity. Additionally, it may have other functional groups or substituents that can influence its pharmacological properties, such as absorption, distribution, metabolism, and excretion. As a natural product with potential antimicrobial activity, Enaminomycin C and other related compounds have been of interest in the field of drug discovery and development. Researchers are interested in understanding their mechanisms of action, as well as exploring the potential for modifying these compounds to improve their therapeutic profiles, such as increasing potency, reducing toxicity, or expanding the spectrum of activity against drug-resistant bacteria. However, it is important to note that while Enaminomycin C has been identified and characterized from Streptomyces species, it may not have been extensively studied or developed into a therapeutic agent. Further research is needed to fully understand its potential as a novel antimicrobial agent and to address any challenges associated with its development, such as synthesis, scalability, and clinical trials.

   

4-hydroxy-5-methoxy-1-methylpyridine-2,3,6-trione

4-hydroxy-5-methoxy-1-methylpyridine-2,3,6-trione

C7H7NO5 (185.0324)


   

2-Amino-3-carboxymuconic acid 6-semialdehyde

2-Amino-3-carboxymuconic acid 6-semialdehyde

C7H7NO5 (185.0324)


   

2,4,-pyridinedicarboxylic acid monohydrate

2,4,-pyridinedicarboxylic acid monohydrate

C7H7NO5 (185.0324)


   

2-Furancarboxylic acid,5-nitro-, ethyl ester

2-Furancarboxylic acid,5-nitro-, ethyl ester

C7H7NO5 (185.0324)


   

Difluoromethionine

Difluoromethionine

C5H9F2NO2S (185.0322)


   

L-alpha-amino-epsilon-keto-pimelate

(1,5-dicarboxylato-5-oxopentyl)azaniumyl

C7H7NO5 (185.0324)


L-alpha-amino-epsilon-keto-pimelate belongs to alpha amino acids and derivatives class of compounds. Those are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. L-alpha-amino-epsilon-keto-pimelate is slightly soluble (in water) and a moderately acidic compound (based on its pKa). L-alpha-amino-epsilon-keto-pimelate can be found in a number of food items such as star fruit, cottonseed, black-eyed pea, and longan, which makes L-alpha-amino-epsilon-keto-pimelate a potential biomarker for the consumption of these food products. L-α-amino-ε-keto-pimelate belongs to alpha amino acids and derivatives class of compounds. Those are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. L-α-amino-ε-keto-pimelate is slightly soluble (in water) and a moderately acidic compound (based on its pKa). L-α-amino-ε-keto-pimelate can be found in a number of food items such as star fruit, cottonseed, black-eyed pea, and longan, which makes L-α-amino-ε-keto-pimelate a potential biomarker for the consumption of these food products.

   

(2S,4S)-4-Hydroxy-2,3,4,5-tetrahydrodipicolinate

(2S,4S)-4-Hydroxy-2,3,4,5-tetrahydrodipicolinate

C7H7NO5-2 (185.0324)


   

2-(Acetamidomethylene)succinate

2-(Acetamidomethylene)succinate

C7H7NO5-2 (185.0324)


   

(2e)-2-Amino-3-[(1e)-3-Oxoprop-1-En-1-Yl]but-2-Enedioic Acid

(2e)-2-Amino-3-[(1e)-3-Oxoprop-1-En-1-Yl]but-2-Enedioic Acid

C7H7NO5 (185.0324)


   

E-2-(acetamidomethylene)succinate

E-2-(acetamidomethylene)succinate

C7H7NO5-2 (185.0324)


   

(E,2E)-2-(hydroxymethylidene)-5-iminohex-3-enedioic acid

(E,2E)-2-(hydroxymethylidene)-5-iminohex-3-enedioic acid

C7H7NO5 (185.0324)


   

(E)-2-((N-methylformamido) methylene)succinate

(E)-2-((N-methylformamido) methylene)succinate

C7H7NO5-2 (185.0324)


   

2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid

2-Amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid

C7H7NO5 (185.0324)


An oxo dicarboxylic acid that is but-2-enedioic acid substituted by an amino group at position 2 and a 3-oxoprop-1-enyl group at position 3.

   

2-amino-3-(3-oxoprop-1-en-1-yl)but-2-enedioic acid

cis,cis-2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid

C7H7NO5 (185.0324)


The cis,cis-isomer of 2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid.

   

(2Z,4E)-4-amino-6-oxohepta-2,4-dienedioic acid

(2Z,4E)-4-amino-6-oxohepta-2,4-dienedioic acid

C7H7NO5 (185.0324)


   

Aminocarboxymuconic acid semialdehyde

Aminocarboxymuconic acid semialdehyde

C7H7NO5 (185.0324)


   

(1s,5s,6s)-4-amino-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic acid

(1s,5s,6s)-4-amino-5-hydroxy-2-oxo-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylic acid

C7H7NO5 (185.0324)