Exact Mass: 195.01024700000002
Exact Mass Matches: 195.01024700000002
Found 500 metabolites which its exact mass value is equals to given mass value 195.01024700000002,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Salicyluric acid
Salicyluric acid is an aryl glycine conjugate formed by the body to eliminate excess salicylates, including aspirin. Aspirin is rapidly hydrolysed to salicylic acid which is further metabolized to various compounds, including salicyluric acid (SU) as well as various acyl and phenolic glucuronides, and hydroxylated metabolites. SU is the major metabolite of SA excreted in urine and it is present in the urine of people who have not taken salicylate drugs, although it has no anti-inflammatory effects in humans or in animals. More salicyluric acid (SU) is excreted in the urine of vegetarians than in non-vegetarians, primarily because fruits and vegetables are important sources of dietary salicylates. However, significantly less (10-15X) SU is excreted by vegetarians than individuals taking low-dose aspirin (PMID: 12944546). The induction of the salicyluric acid formation is one of the saturable pathways of salicylate elimination. The formation of the methyl ester of salicyluric acid is observed during the quantitation of salicyluric acid and other salicylate metabolites in urine by high-pressure liquid chromatography. This methyl ester formation causes artificially low values for salicyluric acid and high values for salicylic acid. (PMID: 6101164, 6857178). Salicyluric acid has been found to be a microbial metabolite. Constituent of milk KEIO_ID H028 Salicyluric acid is an endogenous metabolite.
Dopaquinone
Dopaquinone, also known as o-dopaquinone or L-dopaquinone, is a member of the class of compounds known as L-alpha-amino acids. L-alpha-amino acids are alpha-amino acids which have the L-configuration of the alpha-carbon atom. Dopaquinone is slightly soluble (in water) and a moderately acidic compound (based on its pKa). L-Dopaquinone is a metabolite of L-DOPA and a precursor of melanin. Melanin is synthesized from tyrosine by hydroxylation to dihydroxyphenylalanine (DOPA) and subsequent oxidation to dopaquinone. Both reactions are catalyzed by the enzyme tyrosinase, which is the rate-limiting step. Dopaquinone has an ortho-quinone ring, which is known to be neurotoxic and highly reactive with many other compounds (PMID: 413870). Dopaquinone typically combines with cysteine to form pheomelanin (a pigment-polymer). Alternatively, dopaquinone can be converted to leucodopachrome and eventually to eumelanin (also a pigment-polymer). Dopaquinone can be found in skin and feces. Within the cell, dopaquinone is primarily located in the cytoplasm. Dopaquinone is involved in several metabolic disorders, some of which include transient tyrosinemia, hawkinsinuria, tyrosinemia type I, and alkaptonuria. Chronically high levels of dopaquinone are associated with Parkinsons disease (PD). Many Parkinsons patients are treated with L-DOPA. However, long-term treatment with L-DOPA may actually worsen symptoms or result in neurotic and psychotic symptoms. These may be due to dopachrome and dopaquinone accumulating in the brain of L-DOPA treated patients (PMID: 19131041, PMID: 12373519). Dopaquinone is a substrate of enzyme monophenol monooxygenase [EC 1.14.18.1] in tyrosine metabolism pathway (KEGG). [HMDB]
1,2-Epoxy-3-(p-nitrophenoxy)propane
D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors
Leucodopachrome
Leucodopachrome is an indolic intermediate in the melanogenesis pathway, the non-enzymatically product of dopaquinone through cyclization in a reaction whose operation is determined by a pH greater than 4 (melanin synthesis in human pigment cell lysates is maximal at pH 6.8). Leucodopachrome participates in redox exchange with dopaquinone to give the eumelanin precursor dopachrome plus dopa. Dopaquinone (the quinone intermediate resulting from tyrosinase-mediated oxidation of tyrosine, monophenol dihydroxyphenylalanine:oxygen oxidoreductase, EC 1.14.18.1) could be a toxic metabolite in melanin biosynthesis. (PMID: 6807981, 1445949, 413870, 11461115, 11171088, 12755639) [HMDB]. Leucodopachrome is found in many foods, some of which are chives, saffron, leek, and red beetroot. Leucodopachrome is an indolic intermediate in the melanogenesis pathway, the non-enzymatic product of dopaquinone through cyclization in a reaction whose operation is determined by a pH greater than 4 (melanin synthesis in human pigment cell lysates is maximal at pH 6.8). Leucodopachrome participates in redox exchange with dopaquinone to give the eumelanin precursor dopachrome plus DOPA. Dopaquinone (the quinone intermediate resulting from tyrosinase-mediated oxidation of tyrosine, monophenol dihydroxyphenylalanine:oxygen oxidoreductase, EC 1.14.18.1) could be a toxic metabolite in melanin biosynthesis (PMID: 6807981, 1445949, 413870, 11461115, 11171088, 12755639).
Alpha-Hydroxyhippuric acid
Alpha-Hydroxyhippuric acid, also known as alpha-hydroxybenzoylglycine or a-hydroxyhippate, belongs to the class of organic compounds known as hippuric acids. Hippuric acids are compounds containing hippuric acid, which consists of a of a benzoyl group linked to the N-terminal of a glycine. Alpha-Hydroxyhippuric acid (or Benzamidohydroxyacetic acid) is a carboxylic acid occasionally present in human biofluids. Alpha-hydroxyhippuric acid should not be confused with 2-hydroxyhippuric acid. It is used in the formulation of some herbicides and inks to enhance their action (Patents US 1996-657134, US 1975-627965). It is a substrate for the enzyme peptidyl-alpha-hydroxyglycine alpha-amidating lyase. Alpha-Hydroxyhippuric acid (or Benzamidohydroxyacetic acid) is a hippuric acid derivative that is occasionally present in human biofluids. Alpha-Hydroxyhippuric acid (or Benzamidohydroxyacetic acid) is a carboxylic acid occasionally present in human biofluids. (PMID 10598689, 6511847, 4077949). It is used in the formulation of some herbicides and inks to enhance their action (Patents US 1996-657134, US 1975-627965) [HMDB]
N-acetyl-5-aminosalicylic acid
N-acetyl-5-aminosalicylic acid is a metabolite of mesalazine. Mesalazine, also known as mesalamine or 5-aminosalicylic acid (5-ASA), is an anti-inflammatory drug used to treat inflammatory bowel disease, such as ulcerative colitis and mild-to-moderate Crohns disease. Mesalazine is a bowel-specific aminosalicylate drug that acts locally in the gut and has its predominant actions there, thereby having few systemic side effects. (Wikipedia) D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates
4-Carboxyphenylglycine
4-Carboxyphenylglycine is a group I metabotropic glutamate receptor (mGlu) antagaonist by blocking the cystine/glutamate exchanger. In addition, it has modulating effect on the central action of NMDA receptor antagonist. It plays a role in synaptic plasticity and excitability, long term potentiation and long term depression. D018377 - Neurotransmitter Agents > D018683 - Excitatory Amino Acid Agents > D018691 - Excitatory Amino Acid Antagonists
4-Hydroxyhippurate
4-Hydroxyhippuric acid is a microbial end-product derived from polyphenol metabolism by the microflora in the intestine (PMID: 22932811). It is derived from 4-hydroxybenzoic acid derivatives which may undergo glycination in the liver and kidney (PMID: 20615997). 4-Hydroxyhippuric acid has been identified in the human placenta (PMID: 32033212). A polyphenol metabolite detected in biological fluids [PhenolExplorer]
2-Hydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one
Constituent of Coix lachryma-jobi (Jobs tears), wheat and sweet corn (Zea mays). (R)-2-Hydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one is found in many foods, some of which are coffee and coffee products, cereals and cereal products, fats and oils, and alcoholic beverages. 2-Hydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one is found in alcoholic beverages. 2-Hydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one is a constituent of Coix lachryma-jobi (Jobs tears), wheat and sweet corn (Zea mays).
3-Hydroxyhippuric acid
3-Hydroxyhippuric acid is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction: acyl-CoA + glycine < -- > CoA + N-acylglycine. 3-Hydroxyhippuric acid is an organic acid found in normal human urine. 3-Hydroxyhippuric acid is a metabolite of rutin detected in urine after consumption of tomato juice (a source of rutin). 3-Hydroxyhippuric acid has its origin in dietary procyanidins (a major source of polyphenols consisting of elementary flavan-3-ol (epi)catechin units). 3-Hydroxyhippuric acid is a microbial aromatic acid metabolite derived from dietary polyphenols and flavonoids, found in normal human urine (PMID: 12592675, 2338430, 17015248, 14556848, 12742116). It is a marker of gut Clostridium species. Higher levels are associated with higher levels of Clostridia (PMID: 27123458). 3-Hydroxyhippuric acid is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids. However, the excretion of certain acyl glycines is increased in several inborn errors of metabolism. In certain cases the measurement of these metabolites in body fluids can be used to diagnose disorders associated with mitochondrial fatty acid beta-oxidation. Acyl glycines are produced through the action of glycine N-acyltransferase (EC 2.3.1.13) which is an enzyme that catalyzes the chemical reaction: COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 3-Hydroxyhippuric acid is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids.
2-Hydroxy-6,7-dimethoxybenzoxazole
2-Hydroxy-6,7-dimethoxybenzoxazole is found in cereals and cereal products. 2-Hydroxy-6,7-dimethoxybenzoxazole is a constituent of the dried tissues of Zea mays (sweet corn)
L-Dopaquinone
Implicated in food discolouration (enzymatic browning). Implicated in food discolouration (enzymatic browning)
4-Acetamidosalicylic acid
D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates
2-Amino-6-nitrobenzothiazole
C7H5N3O2S (195.01024700000002)
Benzoic acid, 2-(acetyloxy)-5-amino-
D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates
Acetyl 4-aminosalicylic acid
D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates
Elmustine
C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D009676 - Noxae > D009153 - Mutagens
1-3-(4,5-dihydrofuranone)-5-(hydroxymethyl)-pyrrole-2-carboxyaldehyde
1-3-(4,5-dihydrofuranone)-5-(hydroxymethyl)-pyrrole-2-carboxyaldehyde is a member of the class of compounds known as alpha amino acid esters. Alpha amino acid esters are ester derivatives of alpha amino acids. 1-3-(4,5-dihydrofuranone)-5-(hydroxymethyl)-pyrrole-2-carboxyaldehyde is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 1-3-(4,5-dihydrofuranone)-5-(hydroxymethyl)-pyrrole-2-carboxyaldehyde can be found in common pea, which makes 1-3-(4,5-dihydrofuranone)-5-(hydroxymethyl)-pyrrole-2-carboxyaldehyde a potential biomarker for the consumption of this food product.
3,4-dihydroxyphenylpyruvate
3,4-dihydroxyphenylpyruvate, also known as 3-(3,4-dihydroxyphenyl)-2-oxopropanoate, belongs to phenylpyruvic acid derivatives class of compounds. Those are compounds containing a phenylpyruvic acid moiety, which consists of a phenyl group substituted at the second position by an pyruvic acid. 3,4-dihydroxyphenylpyruvate is slightly soluble (in water) and a moderately acidic compound (based on its pKa). 3,4-dihydroxyphenylpyruvate can be found in a number of food items such as potato, skunk currant, dock, and towel gourd, which makes 3,4-dihydroxyphenylpyruvate a potential biomarker for the consumption of these food products.
o-Hydroxyhippuric acid
MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; ONJSZLXSECQROL-UHFFFAOYSA-N_STSL_0215_o-Hydroxyhippuric acid_8000fmol_190326_S2_LC02MS02_058; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. Salicyluric acid is an endogenous metabolite.
4-Acetamidosalicylic acid
D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates
2-Acetylpyridin-6-monothiocarbonsaeure-S-methylester
4-hydroxyphenylpyruvic acid oxime
A ketoxime obtained by condensation of the keto group of 4-hydroxyphenylpyruvic acid with hydroxylamine.
N-Acetyl Mesalazine
D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates CONFIDENCE standard compound; INTERNAL_ID 2725 CONFIDENCE standard compound; INTERNAL_ID 8622
Salicyluric acid
An N-acylglycine in which the acyl group is specified as 2-hydroxybenzoyl. Salicyluric acid is an endogenous metabolite.
alpha-Hydroxyhippuric acid
An N-acyl-amino acid that is N-benzoylglycine substituted by a hydroxy group at C-2. CONFIDENCE standard compound; INTERNAL_ID 159
Benzadox
CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2812; ORIGINAL_PRECURSOR_SCAN_NO 2809 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2809; ORIGINAL_PRECURSOR_SCAN_NO 2807 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2808; ORIGINAL_PRECURSOR_SCAN_NO 2805 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2798; ORIGINAL_PRECURSOR_SCAN_NO 2795 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2886; ORIGINAL_PRECURSOR_SCAN_NO 2885 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2812; ORIGINAL_PRECURSOR_SCAN_NO 2808 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5998; ORIGINAL_PRECURSOR_SCAN_NO 5994 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5992; ORIGINAL_PRECURSOR_SCAN_NO 5987 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6028; ORIGINAL_PRECURSOR_SCAN_NO 6025 CONFIDENCE standard compound; INTERNAL_ID 382; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6027; ORIGINAL_PRECURSOR_SCAN_NO 6023
2-Amino-6-nitrobenzothiazole
C7H5N3O2S (195.01024700000002)
CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3663; ORIGINAL_PRECURSOR_SCAN_NO 3661 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3417; ORIGINAL_PRECURSOR_SCAN_NO 3415 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3434; ORIGINAL_PRECURSOR_SCAN_NO 3432 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3656; ORIGINAL_PRECURSOR_SCAN_NO 3654 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3725; ORIGINAL_PRECURSOR_SCAN_NO 3720 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3660; ORIGINAL_PRECURSOR_SCAN_NO 3656 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7557; ORIGINAL_PRECURSOR_SCAN_NO 7554 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7532; ORIGINAL_PRECURSOR_SCAN_NO 7530 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7592; ORIGINAL_PRECURSOR_SCAN_NO 7589 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7565; ORIGINAL_PRECURSOR_SCAN_NO 7563 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX503; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7584; ORIGINAL_PRECURSOR_SCAN_NO 7582 CONFIDENCE standard compound; INTERNAL_ID 1098; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7618; ORIGINAL_PRECURSOR_SCAN_NO 7616
m-Hydroxyhippuric acid
An N-acylglycine that is hippuric acid (N-benzoylglycine) substituted at position 3 on the phenyl ring by a hydroxy group.
3-Hydroxyhippurate
3-Hydroxyhippuric acid is an acyl glycine. Acyl glycines are normally minor metabolites of fatty acids.
4-carboxyphenylglycine
D018377 - Neurotransmitter Agents > D018683 - Excitatory Amino Acid Agents > D018691 - Excitatory Amino Acid Antagonists
p-Hydroxyhippuric Acid
An N-acylglycine that is the 4-hydroxy derivative of hippuric acid.
1H-Imidazole-4-sulfonamide,5-chloro-1-methyl-(9CI)
Methyl 5-(aminosulfonyl)-3-chloro-1-methyl-1H-pyrazole-4-carboxylate
2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione
C9H6ClNO2 (195.00870460000002)
7H-Pyrrolo[2,3-d]pyrimidine,4-methoxy-2-(methylthio)-
Benzenethiol,2-amino-4-chloro-, hydrochloride (1:1)
2(3H)-Naphthalenone,4,4a,5,6,7,8-hexahydro-4a-[[(2-methoxyethoxy)methoxy]methyl]-
C7H5N3O2S (195.01024700000002)
6-Chloro-1H-indole-3-carboxylic acid
C9H6ClNO2 (195.00870460000002)
6-ETHYL-2-MERCAPTO-7H-PYRROLO[2,3-D]PYRIMIDIN-4-OL
2-(chloromethyl)-3,1-benzoxazin-4-one
C9H6ClNO2 (195.00870460000002)
5-Chloro-2-oxoindoline-3-carbaldehyde
C9H6ClNO2 (195.00870460000002)
1,2-Benzisothiazol-3-amine,5-nitro-
C7H5N3O2S (195.01024700000002)
(5-Chloro-1H-indol-2-yl)boronic acid
C8H7BClNO2 (195.02583420000002)
4-aminothieno[3,2-d]pyrimidine-7-carboxylic acid
C7H5N3O2S (195.01024700000002)
2-Chloro-1H-indole-3-carboxylic acid
C9H6ClNO2 (195.00870460000002)
3-chloro-1H-indole-2-carboxylic acid
C9H6ClNO2 (195.00870460000002)
3-Chloro-2-fluoro-N-methylaniline hydrochloride
C7H8Cl2FN (195.00177999999997)
4-Chloro-2-Fluorobenzylamine Hydrochloride
C7H8Cl2FN (195.00177999999997)
(2-chloro-4-fluorophenyl)methanamine,hydrochloride
C7H8Cl2FN (195.00177999999997)
6-chloro-1H-Indole-5-carboxylic acid
C9H6ClNO2 (195.00870460000002)
2-[5-Cyano-2,4-dioxo-3,4-dihydro-(2H)pyrimidin-1-yl]acetic acid
8-AMINO-2,3-DIHYDROBENZO[B][1,4]DIOXINE-5-CARBOXYLIC ACID
2-sulfanylidene-3H-1,3-benzoxazole-6-carboxylic acid
METHYL-3-ISOCYANO-4-CHLOROBENZOATE
C9H6ClNO2 (195.00870460000002)
2-Pyrrolidinecarboxaldehyde, 1-(trifluoroacetyl)- (9CI)
3-(4-CHLOROPHENYL)-5(4H)-ISOXAZOLONE
C9H6ClNO2 (195.00870460000002)
3-(2-CHLOROPHENYL)-5(4H)-ISOXAZOLONE
C9H6ClNO2 (195.00870460000002)
5-Nitro-2,1-benzisothiazol-3-amine
C7H5N3O2S (195.01024700000002)
1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBONYL CHLORIDE
METHYL 4-METHYL-4H-THIENO[3,2-B]PYRROLE-5-CARBOXYLATE
5-(6-chloropyridin-3-yl)-3-methyl-1,2,4-oxadiazole
5-Chloro-1H-indole-3-carboxylic acid
C9H6ClNO2 (195.00870460000002)
7-aminothieno[2,3-b]pyrazine-6-carboxylic acid
C7H5N3O2S (195.01024700000002)
4,5,6,7-TETRAHYDRO-1H-PYRAZOLO[3,4-C]PYRIDINE DIHYDROCHLORIDE
5-aminothieno[2,3-d]pyrimidine-6-carboxylicacid
C7H5N3O2S (195.01024700000002)
1-(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethanone
4-Chloro-1H-indole-6-carboxylic acid
C9H6ClNO2 (195.00870460000002)
2-(CHLOROMETHYL)-5-(PYRIDIN-3-YL)-1,3,4-OXADIAZOLE
6-Chloro-5-methyl-1H-indole-2,3-dione
C9H6ClNO2 (195.00870460000002)
1H-Indole-3-carboxylic acid, 4-chloro-
C9H6ClNO2 (195.00870460000002)
5-(2-chloropyridin-4-yl)-3-methyl-1,2,4-oxadiazole
2-ACETONITRILTHIOPHENE-5-CARBOXYLIC ACID ETHYL ESTER
5,6,7,8-Tetrahydroimidazo[1,5-a]pyrazine dihydrochloride
METHYL2,3-DIHYDRO-[1,4]DIOXINO[2,3-C]PYRIDINE-7-CARBOXYLATE
2-(3-chloro-4-cyanophenyl)acetic acid
C9H6ClNO2 (195.00870460000002)
3-Amino-5,6-dimethyl-3H-thieno[2,3-d]pyrimidin-4-one
2-Nitrothieno[2,3-b]pyridin-3-amine
C7H5N3O2S (195.01024700000002)
5,6-Dihydro-3-(methylamino)-2H-1,4-thiazin-2-one Oxime Hydrochloride
3-Chloro-4-hydroxy-1H-quinolin-2-one
C9H6ClNO2 (195.00870460000002)
(5-(5-METHYLTHIOPHEN-2-YL)-1,3,4-OXADIAZOL-2-YL)METHANAMINE
7-Chloro-1H-indole-4-carboxylic acid
C9H6ClNO2 (195.00870460000002)
1H-Indole-7-carboxylic acid, 4-chloro-
C9H6ClNO2 (195.00870460000002)
5-Chloro-1H-indole-7-carboxylic acid
C9H6ClNO2 (195.00870460000002)
6-Chloro-7-methyl-1H-indole-2,3-dione
C9H6ClNO2 (195.00870460000002)
4,5,6,7-TETRAHYDRO-1H-PYRAZOLO[4,3-C]PYRIDINEDIHYDROCHLORIDE
(2R,3R)-(+)-2,3-EPOXY-3-(4-NITROPHENYL)-1-PROPANOL
(E)-1-(5-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-N-hydroxymethanimi ne
6-(HYDROXYMETHYL)-2H-BENZO[B][1,4]THIAZIN-3(4H)-ONE
2-methyl-4-(trifluoromethyl)-1,3-thiazole-5-carbaldehyde
C6H4F3NOS (194.99656899999997)
1H-Benzimidazole-4-carboxylicacid,2-amino-5-fluoro-(9CI)
4,5,6,7-TETRAHYDROPYRAZOLO[1,5-A]PYRAZINE DIHYDROCHLORIDE
4-METHYL-5-(2-METHYL-3-FURYL)-4H-1,2,4-TRIAZOLE-3-THIOL
4-chloro-7-methyl-1H-indole-2,3-dione
C9H6ClNO2 (195.00870460000002)
(3-CHLORO-PROPYL)-METHYL-CARBAMICACIDTERT-BUTYLESTER
C6H11Cl2NSi (195.00377860000003)
N-(4-Aminopyridin-2-yl)-N-methylamine dihydrochloride
(5-methylpyrimidin-2-yl)methanamine,dihydrochloride
4(3H)-Pyrimidinone,5-amino-6-hydroxy-2-(trifluoromethyl)-
7-Chloro-1H-indole-2-carboxylic acid
C9H6ClNO2 (195.00870460000002)
2,3-Difluoro-6-Methoxy-phenylamine Hydrochloride
C7H8ClF2NO (195.02624519999998)
7-Hydroxy-thieno[3,2-b]pyridine- 6-carboxylic acid
L-idonate
An optically active form of idonate having L-configuration; major species at pH 7.3.
3,4-dihydroxyphenylpyruvate
A 2-oxo monocarboxylic acid anion that results from the removal of a proton from the carboxylic acid group of 3,4-dihydroxyphenylpyruvic acid.
Phosphonatoguanidiniumylacetate(2-)
C3H6N3O5P-2 (195.00450759999998)
(2R,3S,4S)-2,3,4-Trihydroxy-5-oxo-5-(hydroxyamino)pentanoic acid
(2E,4Z,6E)-5-formyl-2-hydroxy-8-oxoocta-2,4,6-trienoate
2-hydroxy-4-[(1E)-3-oxoprop-1-en-1-yl]-2H-pyran-6-carboxylate
(2E,4Z,5E)-2-hydroxy-7-oxo-(2-oxoethylidene)hepta-2,5-dienoate
2-hydroxy-3-[(1E)-3-oxoprop-1-en-1-yl]-2H-pyran-6-carboxylate
4-[(E)-3-hydroxyprop-1-enyl]-6-oxopyran-2-carboxylate
(2S,3R,4R)-2,3,4,5-tetrahydroxy-2-(hydroxymethyl)pentanoate
Phosphonatoguanidiniumylacetate(2-)
C3H6N3O5P (195.00450759999998)
Dianion of phosphoguanidinoacetic acid having anionic carboxylic acid and phosphoramido groups and a protonated imino group.
leucopterin (keto form)
A member of the class of pterins that is 3,4,5,6,7,8-hexahydropteridine substituted by an amino group at position 2 and oxo groups at positions 4, 6 and 7. It is a pigment found in the wings of butterflies.
leucopterin (enol form)
A member of the class of pteridines that is pteridine substituted by an amino group at position 2 and hydroxy groups at positions 4, 6 and 7.