Exact Mass: 153.0426

3-Hydroxyanthranilic acid, also known as 2-amino-3-hydroxy-benzoate or 3-ohaa, belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups. 3-Hydroxyanthranilic acid is a drug. 3-Hydroxyanthranilic acid exists in all living species, ranging from bacteria to humans. Within humans, 3-hydroxyanthranilic acid participates in a number of enzymatic reactions. In particular, 3-hydroxyanthranilic acid and L-alanine can be biosynthesized from L-3-hydroxykynurenine through the action of the enzyme kynureninase. In addition, 3-hydroxyanthranilic acid can be converted into cinnavalininate through the action of the enzyme catalase. 3-Hydroxyanthranilic acid is an intermediate in the metabolism of tryptophan. In humans, 3-hydroxyanthranilic acid is involved in tryptophan metabolism. Outside of the human body, 3-hydroxyanthranilic acid has been detected, but not quantified in brassicas. This could make 3-hydroxyanthranilic acid a potential biomarker for the consumption of these foods. It is new antioxidant isolated from methanol extract of tempeh. It is effective in preventing autoxidation of soybean oil and powder, while antioxidant 6,7,4-trihydroxyisoflavone is not. D000975 - Antioxidants > D016166 - Free Radical Scavengers [Raw Data] CBA14_3-OH-anthranili_pos_30eV_1-6_01_808.txt [Raw Data] CBA14_3-OH-anthranili_neg_40eV_1-6_01_832.txt [Raw Data] CBA14_3-OH-anthranili_pos_40eV_1-6_01_809.txt [Raw Data] CBA14_3-OH-anthranili_neg_20eV_1-6_01_830.txt [Raw Data] CBA14_3-OH-anthranili_neg_10eV_1-6_01_829.txt [Raw Data] CBA14_3-OH-anthranili_pos_10eV_1-6_01_806.txt [Raw Data] CBA14_3-OH-anthranili_pos_20eV_1-6_01_807.txt [Raw Data] CBA14_3-OH-anthranili_neg_30eV_1-6_01_831.txt D020011 - Protective Agents > D000975 - Antioxidants Isolated from Brassica oleracea (cauliflower) 3-Hydroxyanthranilic acid is a tryptophan metabolite in the kynurenine pathway.

Mesalazine

Procter and gamble brand OF mesalamine

Mesalazine is only found in individuals that have used or taken this drug. It is an anti-inflammatory agent, structurally related to the salicylates, which is active in inflammatory bowel disease. It is considered to be the active moiety of sulphasalazine. (From Martindale, The Extra Pharmacopoeia, 30th ed)Although the mechanism of action of mesalazine is not fully understood, it appears to be topical rather than systemic. Mucosal production of arachidonic acid metabolites, both through the cyclooxygenase pathways, i.e., prostanoids, and through the lipoxygenase pathways, i.e., leukotrienes and hydroxyeicosatetraenoic acids, is increased in patients with chronic inflammatory bowel disease, and it is possible that mesalazine diminishes inflammation by blocking cyclooxygenase and inhibiting prostaglandin production in the colon. A - Alimentary tract and metabolism > A07 - Antidiarrheals, intestinal antiinflammatory/antiinfective agents > A07E - Intestinal antiinflammatory agents > A07EC - Aminosalicylic acid and similar agents D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D018501 - Antirheumatic Agents

Aminosalicylic Acid

p-Aminosalicylic acid, monosodium salt, dihydrate

Aminosalicylic Acid is only found in individuals that have used or taken this drug. It is an antitubercular agent often administered in association with isoniazid. The sodium salt of the drug is better tolerated than the free acid. [PubChem]There are two mechanisms responsible for aminosalicylic acids bacteriostatic action against Mycobacterium tuberculosis. Firstly, aminosalicylic acid inhibits folic acid synthesis (without potentiation with antifolic compounds). The binding of para-aminobenzoic acid to pteridine synthetase acts as the first step in folic acid synthesis. Aminosalicylic acid binds pteridine synthetase with greater affinity than para-aminobenzoic acid, effectively inhibiting the synthesis of folic acid. As bacteria are unable to use external sources of folic acid, cell growth and multiplication slows. Secondly, aminosalicylic acid may inhibit the synthesis of the cell wall component, mycobactin, thus reducing iron uptake by M. tuberculosis. J - Antiinfectives for systemic use > J04 - Antimycobacterials > J04A - Drugs for treatment of tuberculosis > J04AA - Aminosalicylic acid and derivatives D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D000995 - Antitubercular Agents C254 - Anti-Infective Agent > C52588 - Antibacterial Agent > C280 - Antitubercular Agent COVID info from PDB, Protein Data Bank KEIO_ID A129 Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

Salicylhydroxamic acid

2-Hydroxybenzohydroxamic acid

D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents D000890 - Anti-Infective Agents > D000935 - Antifungal Agents COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

5-hydroxy-6-methylnicotinic acid

5-hydroxy-6-methyl-nicotinic acid

Carbapenem-3-carboxylic acid

7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid

A carbapenemcarboxylic acid that is the 3-carboxy derivative of 2,3-didehydro-1-carbapenam. D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams

4-Nitroanisole

4-Nitrophenyl methyl ether

3-Amino-5-hydroxybenzoic acid

3-Amino-4-hydroxybenzoic acid

3-Amino-4-hydroxybenzoic acid is an endogenous metabolite.

o-Hydroxylaminobenzoate

2-Hydroxylaminobenzoic acid

An aminobenzoic acid that is benzoic acid substutited by a hydroxyamino group at position 2.

nitroanisole

1-Methoxy-2-nitrobenzene

CONFIDENCE standard compound; INTERNAL_ID 544; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3751; ORIGINAL_PRECURSOR_SCAN_NO 3746 INTERNAL_ID 544; DATASET 20200303_ENTACT_RP_MIX506; CONFIDENCE standard compound; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3764; ORIGINAL_PRECURSOR_SCAN_NO 3760 CONFIDENCE standard compound; INTERNAL_ID 544; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3769; ORIGINAL_PRECURSOR_SCAN_NO 3768 CONFIDENCE standard compound; INTERNAL_ID 544; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3764; ORIGINAL_PRECURSOR_SCAN_NO 3760

3-Aminosalicylic acid

3-Amino-2-hydroxy-(9ci)benzoic acid

3-Aminosalicylic acid is a derivative of salicylic acid, a common anti-inflammatory drug. [HMDB] 3-Aminosalicylic acid is a derivative of salicylic acid, a common anti-inflammatory drug.

2-Nitro-p-cresol

4-Methyl-2-nitrophenol

2-Nitro-p-cresol belongs to the family of Nitrophenols and Derivatives. These are compounds containing a nitrophenol moiety, which consists of a benzene ring bearing both an hydroxyl group and a nitro group on two different ring carbon atoms.

6-Methoxy-pyridine-3-carboxylic acid

6-Methoxy-pyridine-3-carboxylic acid belongs to the family of Pyridinecarboxylic Acids and Derivatives. These are compounds containing a pyridine ring bearing a carboxylic acid group

2-Fluoroadenine

2-Fluoro-7(9)H-purin-6-ylamine

C5H4FN5 (153.0451)

2-Fluoroadenine is a toxic purine bases. 2-Fluoroadenine has toxicity in nonproliferating and proliferating tumor cells. 2-Fluoroadenine can be used for researching anticancer[1].

3-Methyl-4-nitrophenol

4-Nitro-3-cresol, sodium salt

4-Nitrobenzyl alcohol

p-(Hydroxymethyl)nitrobenzene

2,5-Dihydroxybenzamide

benzamide, 2,5-dihydroxy-

2-Aminooxybenzoic acid

2-(aminooxy)benzoic acid

5-Formyl-2H-pyran-6-carboxamide

NMPCA

1,6-Dihydro-1-methyl-6-oxo-3-pyridinecarboxylic acid, 97\\%

1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid is from Cordyceps bassiana, which is one of Cordyceps species with anti-oxidative, anti-cancer, anti-inflammatory, anti-diabetic, anti-obesity, anti-angiogenic, and anti-nociceptive activities. 1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid targets to block AP-1-mediated luciferase activity, implying it has an anti-inflammatory function[1].

5-Hydroxyanthranilic acid

2-Amino-5-hydroxybenzoic acid

D000890 - Anti-Infective Agents > D013424 - Sulfanilamides

Oxime-1-(2-Furanyl)-1, 2-propanedione

3,4-Dihydroxybenzaldoxime

2-(Dimethylamino)ethanesulfonic acid

C4H11NO3S (153.046)

methyl 5-formyl-1H-pyrrole-2-carboxylate

4-METHOXYNICOTINIC ACID

3,5-Dihydroxybenzamide

2,3-Dihydroxybenzamide

1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid

3-oxoethylidene-7-oxo-4-oxa-1-azabicyclo [3.2.0] heptane

Methyl 5-hydroxypicolinate

5-hydroxy-pyridine-2-carboxylic acid methyl ester, AldrichCPR

Methyl 5-hydroxypyridine-2-carboxylate is a phenolic acid that can found in the stems of Mahonia fortune. Methyl 5-hydroxypyridine-2-carboxylate exhibits NO inhibitory effects in vitro[1].

3-Hydroxyanthranilate

3-Hydroxyanthranilic acid

3-Hydroxyanthranilic acid is a tryptophan metabolite in the kynurenine pathway.

Mesalamine

5-Aminosalicylic acid

A - Alimentary tract and metabolism > A07 - Antidiarrheals, intestinal antiinflammatory/antiinfective agents > A07E - Intestinal antiinflammatory agents > A07EC - Aminosalicylic acid and similar agents D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D018501 - Antirheumatic Agents CONFIDENCE standard compound; INTERNAL_ID 8621

4-Methyl-2-nitrophenol

CONFIDENCE standard compound; INTERNAL_ID 36

3-Hydroxyanthranilic acid

An aminobenzoic acid that is benzoic acid substituted at C-2 by an amine group and at C-3 by a hydroxy group. It is an intermediate in the metabolism of the amino acid tryptophan. D000975 - Antioxidants > D016166 - Free Radical Scavengers D020011 - Protective Agents > D000975 - Antioxidants MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; WJXSWCUQABXPFS-UHFFFAOYSA-N_STSL_0003_3-hydroxyanthranillic acid_8000fmol_180416_S2_LC02_MS02_37; 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. 3-Hydroxyanthranilic acid is a tryptophan metabolite in the kynurenine pathway.

3-Aminosalicylic acid

5-Aminosalicylic acid

4-Aminosalicylic acid

J - Antiinfectives for systemic use > J04 - Antimycobacterials > J04A - Drugs for treatment of tuberculosis > J04AA - Aminosalicylic acid and derivatives D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D000995 - Antitubercular Agents C254 - Anti-Infective Agent > C52588 - Antibacterial Agent > C280 - Antitubercular Agent COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; WUBBRNOQWQTFEX-UHFFFAOYSA-N_STSL_0188_4-Aminosalicylic Acid_0125fmol_180831_S2_L02M02_81; 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.

3,4-AHBA

3-Amino-4-hydroxybenzoic acid

3-Amino-4-hydroxybenzoic acid is an endogenous metabolite.

AHBA

3-Amino-5-hydroxybenzoic acid

3-Amino-4-hydroxybenzoic acid

3-Amino-4-hydroxybenzoic acid is an endogenous metabolite.

3-Amino-5-hydroxybenzoate

3-Amino-5-hydroxybenzoic acid

3-Amino-4-hydroxybenzoate

3-Amino-4-hydroxybenzoic acid

3-Amino-4-hydroxybenzoic acid is an endogenous metabolite.

Salicylhydroxamic acid

5-Aminosalicylic acid

Paser

3-Amino-2-hydroxy-(9ci)benzoic acid

4-Hydroxy-2-methylnicotinic acid

1-Methyl-6-oxo-1,6-dihydropyridine-2-carboxylic acid

3-Nitrobenzyl alcohol

3-Nitrobenzenemethanol

1H-Pyrrole-2-carboxylic acid, 5-formyl-1-methyl- (9CI)

2-Methyl-6-nitrophenol

4,6-Difluoroindole

N-Allyl-2,2,2-trifluoroacetamide

C5H6F3NO (153.0401)

2-Methyl-5-nitrophenol

1H-Pyrrole-2-carboxylicacid,5-acetyl-

5,7-Difluoroindole

5-Methoxy-2-pyridinecarboxylic acid

METHYL 6-OXO-1,6-DIHYDRO-3-PYRIDINECARBOXYLATE

Benzamide,2,6-dihydroxy-

2-Methoxyisonicotinic acid

2-Amino-4-hydroxybenzoic acid

Benzoicacid,2-amino-4-hydroxy-

2-Chlorobicyclo[2.2.1]hept-5-ene-2-carbonitrile

Phenol, methylnitro-

1,3,5-benzenetricarbonitrile

C9H3N3 (153.0327)

6-(Hydroxymethyl)nicotinic acid

5-methoxy-nicotinic acid

2-Chloro-5-cyclopropylpyridine

3-NITROANISOLE

4-Nitrobenzyl alcohol

(4-Nitrophenyl)methanol

A member of the class of benzyl alcohols that is benzyl alcohol substituted at the para-position by a nitro group.

Benzaldehyde,2,4-dihydroxy-, oxime

(S)-2-(+)-AMINO-3,3-DIMETHYL-1,1-DIPHENYLBUTANE

3-Methyl-5-nitrophenol

2,5-Difluoro-4-methylbenzonitrile

3-Ethynylaniline HCl

5-(Hydroxymethyl)picolinic acid

6-fluoro-9H-purin-2-amine

C5H4FN5 (153.0451)

4-Methyl-3-nitrophenol

1-METHYL-2-OXO-1,2-DIHYDROPYRIDINE-4-CARBOXYLIC ACID

2,4-Difluoro-5-methylbenzoni trile

5-CARBOXY-2-METHYLPYRIDINE 1-OXIDE

3,5-Difluoro-4-methylbenzonitrile

2-(HYDROXYMETHYL)NICOTINIC ACID

Methyl isonicotinate 1-oxide

4-Chloroindoline

3-Methoxyisonicotinic acid

Methyl 4-formyl-1H-pyrrole-2-carboxylate

2-Methyl-4-nitrophenol

6-Nitro-m-cresol

Ethanolomine Thioglycholate

Monoethanolamine thioglycolate

C4H11NO3S (153.046)

Monoethanolamine thioglycolate. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=126-97-6 (retrieved 2024-08-05) (CAS RN: 126-97-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

4,7-Difluoro-1H-indole

FMOC-L-INDOLINE-2-CARBOXYLIC ACID

5-METHYL-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBOXYLIC ACID

4-Chloro-2-cyclopropylpyridine

5,6-Difluoroindole

2,6(1H,3H)-Pyridinedione,5-acetyl- (9ci)

2(1H)-Pyridinone,3-(acetyloxy)-

Methyl 3-aminoisonicotinate

5-Cyclopropylisoxazole-3-Carboxylic Acid

2,3-difluoro-4-methylbenzonitrile

2-(Hydroxymethyl)-4-pyridinecarboxylicacid

1,4-THIAZEPANE 1-OXIDE HYDROCHLORIDE

C5H12ClNS (153.0379)

2-HYDROXYETHANESULFONIC ACID DIMETHYLAMIDE

C4H11NO3S (153.046)

2,5-Difluorobenzyl cyanide

2-Chloro-6,7-dihydro-5H-cyclopenta[b]pyridine

4-Chloro-6,7-dihydro-5H-cyclopenta[b]pyridine

1-Pyridin-2-ylthiourea

Methyl 6-oxo-1,6-dihydropyridine-2-carboxylate

7-chloroindoline

Methyl 1,2-dihydro-2-oxopyridine-4-carboxylate

4-Chloroisoindoline

3-Methoxypicolinic acid

Methyl 4-oxo-1,4-dihydro-3-pyridinecarboxylate

6-Amino-3-pyridinecarbothioamide

2-cyclopropyl-1,3-oxazole-4-carboxylic acid

3,5-Difluorobenzyl cyanide

5-HYDROXY-2-METHYLNICOTINIC ACID

6,7-difluoro-1H-indole

2-Amino-6-hydroxybenzoic acid

piperidine-4-thiol,hydrochloride

C5H12ClNS (153.0379)

Methyl 5-hydroxynicotinate

6-Chloro-2,3-dihydro-1H-indole

6-Methyl-4-oxo-1,4-dihydropyridine-3-carboxylic acid

Methyl 3-hydroxyisonicotinate

Isoindoline hydrochloride

4,5-Difluoroindole

1H-Azepine-3-carboxylicacid,2,3-dihydro-2-oxo-(9CI)

Methyl 4-hydroxy-2-pyridinecarboxylate

1H-Pyrrole-2-carboxylic acid, 4-formyl-1-methyl- (9CI)

(3-Pyridinyloxy)acetic acid

2-(2,6-Difluorophenyl)acetonitrile

2-(3,4-Difluorophenyl)acetonitrile

2-(2,4-Difluorophenyl)acetonitrile

2,3-Difluorobenzyl cyanide

(4-NITRO-PHENYL)-ACETYLCHLORIDE

2-chloro-4-prop-2-enylpyridine

2,2-difluoro-2-phenylacetonitrile

2-AMINO-4-HYDROXYPTERIDINE-6-CARBOXYLICACID

3,4-Difluoro-2-methylbenzonitrile

2-Hydroxy-4-methylpridine-3-carboxylic acid

tetrahydro-2H-thiopyran-4-amine hydrochloride

C5H12ClNS (153.0379)

5-Cyclopropyl-isoxazole-4-carboxylic acid

6-Methoxypicolinic acid

5-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid

4-Acetyl-1H-pyrrole-2-carboxylic acid

3-Fluoro-4-piperidinone hydrochloride

C5H9ClFNO (153.0357)

2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-8-ol

(2-FORMYL-1H-PYRROL-1-YL)ACETIC ACID

3-METHYL-5-(METHYLAMINO)ISOTHIAZOLE-4-CARBONITRILE

5-acetylfuran-2-carboxamide

4-methyl-6-oxo-1H-pyridine-3-carboxylic acid

Methyl 2-Hydroxynicotinate

N,4-dihydroxybenzamide

6-Hydroxy-3-methylpicolinic acid

5-Methyl-6-oxo-1,6-dihydropyridine-2-carboxylic acid

2-Nitrobenzyl alcohol

4-pyridylthiourea

Imidazo[2,1-b]thiazol-6-ylmethanamine

2-(1-methyl-1H-pyrrol-2-yl)-2-oxoacetic acid

N-(p-Chlorobenzylidene)methylamine

N-[(4-CHLOROPHENYL)METHYLENE]METHANAMINE

6-HYDROXY-2-METHYLNICOTINIC ACID

5-formyl-4-methyl-1H-pyrrole-3-carboxylic acid

1H-Furo[3,4-c]pyrrole-4-carboxylicacid,3,5-dihydro-(9CI)

4-(hydroxymethyl)pyridine-3-carboxylic acid

2,4-Difluoro-3-methylbenzonitrile

5-Chloroindoline

Methyl nicotinate 1-oxide

6-(Hydroxymethyl)picolinic acid

3-pyridylthiourea

5-cyclopropyl-1,3-oxazole-4-carboxylic acid

3,5-Difluoro-2-methylbenzonitrile

5-Formyl-3-methyl-1H-pyrrole-2-carboxylic acid

2-Hydroxy-6-methylpyridine-3-carboxylic acid

2-(6-oxo-1H-pyridin-2-yl)acetic acid

4-Hydroxy-6-methylnicotinic acid

T6NJ BO1 CVQ [WWN]

1H-Pyrrole-3-carboxylicacid,5-formyl-1-methyl-(9CI)

4-(trifluoromethyl)-2-Pyrrolidinone

C5H6F3NO (153.0401)

2-Cyclopropyl-oxazole-5-carboxylic acid

5-METHOXYNICOTINIC ACID

METHYL 2-FORMYL-1H-PYRROLE-3-CARBOXYLATE

2-Hydroxy-6-methylisonicotinic acid

3-(Difluoromethyl)benzonitrile

2,5-Difluoro-3-methylbenzonitrile

4,5-Difluoro-2-methylbenzonitrile

4-METHYL-2-OXO-2H-PYRAN-6-CARBOXAMIDE

5-ISOTHIOCYANATO-1,3-DIMETHYL-1H-PYRAZOLE

4-Methoxy-2-pyridinecarboxylic acid

1-methyl-2-oxo-pyridine-3-carboxylic acid

Methyl 5-formylpyrrole-2-carboxylate

2,3-Difluoro-5-methylbenzonitrile

2-(Difluoromethyl)benzonitrile

3-Isothiocyanato-1,5-dimethyl-1H-pyrazole

Bis(5-tetrazolyl)amine

C2H3N9 (153.0511)

2(1H)-Pyridinone,3-acetyl-6-hydroxy- (9ci)

WNR BQ F1

2,3-Dihydro-3-oxo-anthranilate

3-oxo-3-(1H-pyrrol-2-yl)propanoic acid

(6S)-6-amino-5-oxocyclohexa-1,3-diene-1-carboxylic acid

2,3-Dihydro-3-oxoanthranilic acid

An oxo carboxylic acid that is the 2,3-dihydro-3-oxo tautomer of 3-hydroxyanthranilic acid.

4-Nitroanisole

HA 01-0196

3-Methyl-4-nitrophenol

3-Ahba

3-Amino-5-hydroxybenzoic acid