Exact Mass: 152.0238

Exact Mass Matches: 152.0238

Found 198 metabolites which its exact mass value is equals to given mass value 152.0238, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Xanthine

2,3,6,7-tetrahydro-1H-purine-2,6-dione

C5H4N4O2 (152.0334)


Xanthine, also known as 2,6-dioxopurine, belongs to the class of organic compounds known as xanthines. These are purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety. Xanthine is also classified as an oxopurine. An oxopurine in which the purine ring is substituted by oxo groups at positions 2 and 6 and N-9 is protonated. Xanthine exists in all living species, ranging from bacteria to plants to humans. In plants, several stimulants can be derived from xanthine, including caffeine, theophylline, and theobromine. Derivatives of xanthine (known collectively as xanthines) are a group of alkaloids commonly used for their effects as mild stimulants and as bronchodilators, notably in the treatment of asthma or influenza symptoms. Within humans, xanthine participates in a number of enzymatic reactions. In particular, xanthine can be biosynthesized from guanine; which is mediated by the enzyme guanine deaminase. In addition, xanthine and ribose 1-phosphate can be biosynthesized from xanthosine through the action of the enzyme purine nucleoside phosphorylase. In humans and other primates, xanthine can be converted to uric acid by the action of the xanthine oxidase enzyme. People with rare genetic disorders, specifically xanthinuria and Lesch–Nyhan syndrome, lack sufficient xanthine oxidase and cannot convert xanthine to uric acid. Individuals with xanthinuria have unusually high concentrations of xanthine in their blood and urine, which can lead to health problems such as renal failure and xanthine kidney stones. Individuals with Lesch-Nyhan syndrome have a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT). The HGPRT deficiency causes a build-up of uric acid in all body fluids. This results in both high levels of uric acid in the blood and urine, associated with severe gout and kidney problems. Neurological signs include poor muscle control and moderate intellectual disability. 9H-xanthine is an oxopurine in which the purine ring is substituted by oxo groups at positions 2 and 6 and N-9 is protonated. It has a role as a Saccharomyces cerevisiae metabolite. It is a tautomer of a 7H-xanthine. A purine base found in most body tissues and fluids, certain plants, and some urinary calculi. It is an intermediate in the degradation of adenosine monophosphate to uric acid, being formed by oxidation of hypoxanthine. The methylated xanthine compounds caffeine, theobromine, and theophylline and their derivatives are used in medicine for their bronchodilator effects. (Dorland, 28th ed) Xanthine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Xanthine is a natural product found in Beta vulgaris, Camellia sinensis var. assamica, and other organisms with data available. Xanthine is a purine base found in most body tissues and fluids, certain plants, and some urinary calculi. It is an intermediate in the degradation of adenosine monophosphate to uric acid, being formed by oxidation of hypoxanthine. The methylated xanthine compounds caffeine, theobromine, and theophylline and their derivatives are used in medicine for their bronchodilator effects. (Dorland, 28th ed.). Xanthine is a metabolite found in or produced by Saccharomyces cerevisiae. A purine base found in most body tissues and fluids, certain plants, and some urinary calculi. It is an intermediate in the degradation of adenosine monophosphate to uric acid, being formed by oxidation of hypoxanthine. The methylated xanthine compounds caffeine, theobromine, and theophylline and their derivatives are used in medicine for their bronchodilator effects. (Dorland, 28th ed) An oxopurine in which the purine ring is substituted by oxo groups at positions 2 and 6 and N-9 is protonated. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3].

   

Oxypurinol

1H,2H,4H,5H,6H-pyrazolo[3,4-d]pyrimidine-4,6-dione

C5H4N4O2 (152.0334)


Oxipurinol is a xanthine oxidase inhibitor. Oxipurinol is potentially used for treatment of congestive heart failure. PMID: 15139781. Oxipurinol is a xanthine oxidase inhibitor. Oxipurinol is potentially used for treatment of congestive heart failure. C471 - Enzyme Inhibitor > C1637 - Xanthine Oxidase Inhibitor D004791 - Enzyme Inhibitors CONFIDENCE standard compound; INTERNAL_ID 864; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 855; ORIGINAL_PRECURSOR_SCAN_NO 853 CONFIDENCE standard compound; INTERNAL_ID 864; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 883; ORIGINAL_PRECURSOR_SCAN_NO 881 CONFIDENCE standard compound; INTERNAL_ID 864; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 893; ORIGINAL_PRECURSOR_SCAN_NO 892 CONFIDENCE standard compound; INTERNAL_ID 864; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 861; ORIGINAL_PRECURSOR_SCAN_NO 860 CONFIDENCE standard compound; INTERNAL_ID 864; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 894; ORIGINAL_PRECURSOR_SCAN_NO 892 Acquisition and generation of the data is financially supported in part by CREST/JST. Oxipurinol (Oxipurinol), the major active metabolite of Allopurinol, is an inhibitor of xanthine oxidase. Oxipurinol can be used to regulate blood urate levels and treat gout[1].

   

Mercaptopurine

GlaxoSmithKline brand OF 6 mercaptopurine

C5H4N4S (152.0157)


Mercaptopurine is only found in individuals that have used or taken this drug. It is an antimetabolite antineoplastic agent with immunosuppressant properties. It interferes with nucleic acid synthesis by inhibiting purine metabolism and is used, usually in combination with other drugs, in the treatment of or in remission maintenance programs for leukemia. [PubChem]Mercaptopurine competes with hypoxanthine and guanine for the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) and is itself converted to thioinosinic acid (TIMP). This intracellular nucleotide inhibits several reactions involving inosinic acid (IMP), including the conversion of IMP to xanthylic acid (XMP) and the conversion of IMP to adenylic acid (AMP) via adenylosuccinate (SAMP). In addition, 6-methylthioinosinate (MTIMP) is formed by the methylation of TIMP. Both TIMP and MTIMP have been reported to inhibit glutamine-5-phosphoribosylpyrophosphate amidotransferase, the first enzyme unique to the de novo pathway for purine ribonucleotide synthesis. Experiments indicate that radiolabeled mercaptopurine may be recovered from the DNA in the form of deoxythioguanosine. Some mercaptopurine is converted to nucleotide derivatives of 6-thioguanine (6-TG) by the sequential actions of inosinate (IMP) dehydrogenase and xanthylate (XMP) aminase, converting TIMP to thioguanylic acid (TGMP). L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01B - Antimetabolites > L01BB - Purine analogues C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D004791 - Enzyme Inhibitors > D019384 - Nucleic Acid Synthesis Inhibitors D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents C308 - Immunotherapeutic Agent > C574 - Immunosuppressant D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents

   

6,8-Dihydroxypurine

6,7,8,9-tetrahydro-3H-purine-6,8-dione

C5H4N4O2 (152.0334)


6,8-Dihydroxypurine is an endogenous nucleoside found in human fluids. Purine bases are present in higher amounts in tumor-bearing patients compared to healthy controls. DNA hypermethylation is a common finding in malignant cells and has been explored as a therapeutic target for hypomethylating agents. When chemical bonds to DNA, the DNA becomes damaged and proper and complete replication cannot occur to make the normal intended cell. A DNA adduct is an abnormal piece of DNA covalently-bonded to a cancer-causing chemical. This has shown to be the start of a cancerous cell, or carcinogenesis. DNA adducts in scientific experiments are used as bio-markers and as such are themselves measured to reflect quantitatively, for comparison, the amount of cancer in the subject. (PMID: 3506820, 17044778, 17264127, 16799933).

   

S-Methyl benzenecarbothioate

Benzenecarbothioic acid, S-methyl ester

C8H8OS (152.0296)


S-Methyl benzenecarbothioate is a flavouring agent for food Flavouring agent for foods

   

S-Phenyl thioacetate

1-(Phenylsulphanyl)ethan-1-one

C8H8OS (152.0296)


   

9-Sulfanylpurine

9-Sulphanylpurine

C5H4N4S (152.0157)


   

Xanthine

Xanthine

C5H4N4O2 (152.0334)


COVID info from COVID-19 Disease Map, PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3].

   

Phenyl vinyl sulfoxide

Phenyl vinyl sulfoxide

C8H8OS (152.0296)


   

Butyl(methylthio) sulfoxide

Butyl(methylthio) sulfoxide

C5H12OS2 (152.033)


   

(4-chloro-phenyl)-carbamonitrile|(4-chlorophenyl)cyanamide|4-chlorophenyl cyanamide|4-chlorophenylcyanamide|4-Cl-pcyd-H|4-ClpcydH|N-(4-chlorophenyl)cyanamide

(4-chloro-phenyl)-carbamonitrile|(4-chlorophenyl)cyanamide|4-chlorophenyl cyanamide|4-chlorophenylcyanamide|4-Cl-pcyd-H|4-ClpcydH|N-(4-chlorophenyl)cyanamide

C7H5ClN2 (152.0141)


   

4-methoxybenzenecarbothialdehyde

4-methoxybenzenecarbothialdehyde

C8H8OS (152.0296)


   

1-methylsulfinylsulfanylbutane

1-methylsulfinylsulfanylbutane

C5H12OS2 (152.033)


   

mercaptopurine

6-Mercaptopurine

C5H4N4S (152.0157)


L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01B - Antimetabolites > L01BB - Purine analogues C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D004791 - Enzyme Inhibitors > D019384 - Nucleic Acid Synthesis Inhibitors D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents C308 - Immunotherapeutic Agent > C574 - Immunosuppressant D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents CONFIDENCE standard compound; INTERNAL_ID 2786 KEIO_ID M054

   

Xanthine

Xanthine

C5H4N4O2 (152.0334)


COVID info from COVID-19 Disease Map, 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; LRFVTYWOQMYALW_STSL_0180_Xanthine_0500fmol_180506_S2_LC02_MS02_265; 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. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3].

   

Oxipurinol

1H-Pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dione

C5H4N4O2 (152.0334)


C471 - Enzyme Inhibitor > C1637 - Xanthine Oxidase Inhibitor D004791 - Enzyme Inhibitors Oxipurinol (Oxipurinol), the major active metabolite of Allopurinol, is an inhibitor of xanthine oxidase. Oxipurinol can be used to regulate blood urate levels and treat gout[1].

   

6-Mercaptopurine

6-Mercaptopurine

C5H4N4S (152.0157)


   

2-Mercaptopurine

2H-Purine-2-thione,3,9-dihydro-

C5H4N4S (152.0157)


   

Xanthine (not validated)

Xanthine (not validated)

C5H4N4O2 (152.0334)


Annotation level-2

   

Xanthine; LC-tDDA; CE10

Xanthine; LC-tDDA; CE10

C5H4N4O2 (152.0334)


   

Xanthine; LC-tDDA; CE20

Xanthine; LC-tDDA; CE20

C5H4N4O2 (152.0334)


   

Xanthine; LC-tDDA; CE30

Xanthine; LC-tDDA; CE30

C5H4N4O2 (152.0334)


   

Xanthine; LC-tDDA; CE40

Xanthine; LC-tDDA; CE40

C5H4N4O2 (152.0334)


   

Oxypurinol; LC-tDDA; CE10

Oxypurinol; LC-tDDA; CE10

C5H4N4O2 (152.0334)


   

Oxypurinol; LC-tDDA; CE20

Oxypurinol; LC-tDDA; CE20

C5H4N4O2 (152.0334)


   

Oxypurinol; LC-tDDA; CE30

Oxypurinol; LC-tDDA; CE30

C5H4N4O2 (152.0334)


   

Oxypurinol; LC-tDDA; CE40

Oxypurinol; LC-tDDA; CE40

C5H4N4O2 (152.0334)


   

Oxypurinol; AIF; CE0; MS2Dec

Oxypurinol; AIF; CE0; MS2Dec

C5H4N4O2 (152.0334)


   

Oxypurinol; AIF; CE10; MS2Dec

Oxypurinol; AIF; CE10; MS2Dec

C5H4N4O2 (152.0334)


   

Oxypurinol; AIF; CE30; MS2Dec

Oxypurinol; AIF; CE30; MS2Dec

C5H4N4O2 (152.0334)


   

Oxypurinol; AIF; CE0; CorrDec

Oxypurinol; AIF; CE0; CorrDec

C5H4N4O2 (152.0334)


   

Oxypurinol; AIF; CE10; CorrDec

Oxypurinol; AIF; CE10; CorrDec

C5H4N4O2 (152.0334)


   

Oxypurinol; AIF; CE30; CorrDec

Oxypurinol; AIF; CE30; CorrDec

C5H4N4O2 (152.0334)


   

8-Oxohypoxanthine

1H-Purine-6,8-dione,7,9-dihydro-

C5H4N4O2 (152.0334)


   

Methyl thiobenzoate

Benzenecarbothioic acid, S-methyl ester

C8H8OS (152.0296)


   

Furo[3,2-d]pyrimidine-2,4-diol

Furo[3,2-d]pyrimidine-2,4-diol

C6H4N2O3 (152.0222)


   

Cyclopropyl 2-thienyl ketone

Cyclopropyl 2-thienyl ketone

C8H8OS (152.0296)


   

3-(Trifluoromethyl)-5-pyrazolone

3-(Trifluoromethyl)-5-pyrazolone

C4H3F3N2O (152.0197)


   

Tisopurine

4H-Pyrazolo[3,4-d]pyrimidine-4-thione,1,5-dihydro-

C5H4N4S (152.0157)


M - Musculo-skeletal system > M04 - Antigout preparations > M04A - Antigout preparations > M04AA - Preparations inhibiting uric acid production D018501 - Antirheumatic Agents > D006074 - Gout Suppressants C471 - Enzyme Inhibitor > C1637 - Xanthine Oxidase Inhibitor C26170 - Protective Agent > C921 - Uricosuric Agent

   

1,4-dichlorocyclohexane

1,4-dichlorocyclohexane

C6H10Cl2 (152.016)


   

4-amino-2-mercaptopyrimidine-5-carbonitrile

4-amino-2-mercaptopyrimidine-5-carbonitrile

C5H4N4S (152.0157)


   

4H-1-OXA-3,4-DIAZA-PENTALENE-5-CARBOXYLIC ACID

4H-1-OXA-3,4-DIAZA-PENTALENE-5-CARBOXYLIC ACID

C6H4N2O3 (152.0222)


   

3-(Methylsulfanyl)benzaldehyde

3-(Methylsulfanyl)benzaldehyde

C8H8OS (152.0296)


   

2-(METHYLTHIO)BENZALDEHYDE

2-(METHYLTHIO)BENZALDEHYDE

C8H8OS (152.0296)


   

S-Phenyl thioacetate

S-Phenyl ethanethioate

C8H8OS (152.0296)


   

3-(Methylsulfonyl)propanoic acid

3-(Methylsulfonyl)propanoic acid

C4H8O4S (152.0143)


   

2-Amino-6-chlorobenzonitrile

2-Amino-6-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

1H-Imidazole-1-acetonitrile,2-nitro-(9CI)

1H-Imidazole-1-acetonitrile,2-nitro-(9CI)

C5H4N4O2 (152.0334)


   

3a,7a-Dihydro-1H-imidazo(4,5-d)pyridazine-4,7-dione

3a,7a-Dihydro-1H-imidazo(4,5-d)pyridazine-4,7-dione

C5H4N4O2 (152.0334)


   

7-Chloro-1H-pyrrolo[3,2-c]pyridine

7-Chloro-1H-pyrrolo[3,2-c]pyridine

C7H5ClN2 (152.0141)


   

7-Chloroimidazo[1,2-a]pyridine

7-Chloroimidazo[1,2-a]pyridine

C7H5ClN2 (152.0141)


   

Benzeneacetaldehyde,4-fluoro-a-oxo-

Benzeneacetaldehyde,4-fluoro-a-oxo-

C8H5FO2 (152.0274)


   

1-chlorobenzimidazole

1-chlorobenzimidazole

C7H5ClN2 (152.0141)


   

3-(Trifluoromethyl)isoxazol-5-amine

3-(Trifluoromethyl)isoxazol-5-amine

C4H3F3N2O (152.0197)


   

5-Chloroimidazo[1,2-a]Pyridine

5-Chloroimidazo[1,2-a]Pyridine

C7H5ClN2 (152.0141)


   

4-Chloro-1H-pyrrolo[2,3-b]pyridine

4-Chloro-1H-pyrrolo[2,3-b]pyridine

C7H5ClN2 (152.0141)


   

2-(Chloromethoxy)ethyl acetate

2-(Chloromethoxy)ethyl acetate

C5H9ClO3 (152.024)


   

6-Chloro-7-azaindole

6-Chloro-7-azaindole

C7H5ClN2 (152.0141)


   

cis-1,2-dichlorocyclohexane

cis-1,2-dichlorocyclohexane

C6H10Cl2 (152.016)


   

5-(3-THIENYL)-2H-1,2,3,4-TETRAZOLE

5-(3-THIENYL)-2H-1,2,3,4-TETRAZOLE

C5H4N4S (152.0157)


   

(6-Chloro-3-pyridinyl)acetonitrile

(6-Chloro-3-pyridinyl)acetonitrile

C7H5ClN2 (152.0141)


   

2-Chloro-pyrazolo[1,5-a]pyridine

2-Chloro-pyrazolo[1,5-a]pyridine

C7H5ClN2 (152.0141)


   

5-Chloro-4-azaindole

5-Chloro-4-azaindole

C7H5ClN2 (152.0141)


   

8-Mercaptopurine

8-Mercaptopurine

C5H4N4S (152.0157)


   

3-Chloro-1H-indazole

3-Chloro-1H-indazole

C7H5ClN2 (152.0141)


   

5-Chloro-1H-benzimidazole

5-Chloro-1H-benzimidazole

C7H5ClN2 (152.0141)


   

3-Chloro-1H-pyrrolo[3,2-c]pyridine

3-Chloro-1H-pyrrolo[3,2-c]pyridine

C7H5ClN2 (152.0141)


   

2-(5-chloropyridin-2-yl)acetonitrile

2-(5-chloropyridin-2-yl)acetonitrile

C7H5ClN2 (152.0141)


   

6,7-Dihydro-1-benzothiophen-4(5H)-one

6,7-Dihydro-1-benzothiophen-4(5H)-one

C8H8OS (152.0296)


   

6-Chloroimidazo[1,2-a]pyridine

6-Chloroimidazo[1,2-a]pyridine

C7H5ClN2 (152.0141)


   

2-Cyanoamino-4,6-dihydroxypyrimidine

2-Cyanoamino-4,6-dihydroxypyrimidine

C5H4N4O2 (152.0334)


   

2-ethylsulfonylacetic acid

2-ethylsulfonylacetic acid

C4H8O4S (152.0143)


   

9H-Purin-6-ol, 1-oxide

9H-Purin-6-ol, 1-oxide

C5H4N4O2 (152.0334)


   

Methyl 4-chloro-3-hydroxybutanoate

Methyl 4-chloro-3-hydroxybutanoate

C5H9ClO3 (152.024)


   

4-(2-Thienyl)but-3-en-2-one

4-(2-Thienyl)but-3-en-2-one

C8H8OS (152.0296)


   

4-(Trifluoromethyl)-1,3-oxazol-2-amine

4-(Trifluoromethyl)-1,3-oxazol-2-amine

C4H3F3N2O (152.0197)


   

6-Chloro-1H-indazole

6-Chloro-1H-indazole

C7H5ClN2 (152.0141)


   

4-Amino-2-chlorobenzonitrile

4-Amino-2-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

Methyl (2-chloroethoxy)acetate

Methyl (2-chloroethoxy)acetate

C5H9ClO3 (152.024)


   

2-ethoxyethyl carbonochloridate

2-ethoxyethyl carbonochloridate

C5H9ClO3 (152.024)


   

6-FLUOROISOBENZOFURAN-1(3H)-ONE

6-FLUOROISOBENZOFURAN-1(3H)-ONE

C8H5FO2 (152.0274)


   

1H-imidazo[1,5-a][1,3,5]triazine-2,4-dione

1H-imidazo[1,5-a][1,3,5]triazine-2,4-dione

C5H4N4O2 (152.0334)


   

4-Chloro-1H-pyrrolo[3,2-c]pyridine

4-Chloro-1H-pyrrolo[3,2-c]pyridine

C7H5ClN2 (152.0141)


   

7-Fluorobenzofuran-3(2H)-one

7-Fluorobenzofuran-3(2H)-one

C8H5FO2 (152.0274)


   

(methylthio)benzaldehyde

(methylthio)benzaldehyde

C8H8OS (152.0296)


   

THIOETHANOLAMINE

THIOETHANOLAMINE

C5H9ClO3 (152.024)


   

Chloromethyl isopropyl carbonate

Chloromethyl isopropyl carbonate

C5H9ClO3 (152.024)


   

5-Chloro-7-azaindole

5-Chloro-7-azaindole

C7H5ClN2 (152.0141)


   

3-chloro-1H-pyrrolo[3,2-b]pyridine

3-chloro-1H-pyrrolo[3,2-b]pyridine

C7H5ClN2 (152.0141)


   

3-Methylphosphinicopropionic Acid

3-Methylphosphinicopropionic Acid

C4H9O4P (152.0238)


   

5-(trifluoromethyl)-1,3-oxazol-2-amine

5-(trifluoromethyl)-1,3-oxazol-2-amine

C4H3F3N2O (152.0197)


   

Methyl Methanesulfonylacetate

Methyl Methanesulfonylacetate

C4H8O4S (152.0143)


   

5-FLUOROISOPHTHALALDEHYDE

5-FLUOROISOPHTHALALDEHYDE

C8H5FO2 (152.0274)


   

5-Chloroindazole

5-Chloroindazole

C7H5ClN2 (152.0141)


   

3-Chloro-7-azaindole

3-Chloro-7-azaindole

C7H5ClN2 (152.0141)


   

tetramethylene phosphate

tetramethylene phosphate

C4H9O4P (152.0238)


   

2-Chloro-6-methylnicotinonitrile

2-Chloro-6-methylnicotinonitrile

C7H5ClN2 (152.0141)


   

6-(Chloromethyl)nicotinonitrile

6-(Chloromethyl)nicotinonitrile

C7H5ClN2 (152.0141)


   

2-(2-chloropyridin-4-yl)acetonitrile

2-(2-chloropyridin-4-yl)acetonitrile

C7H5ClN2 (152.0141)


   

5-NITRONICOTINALDEHYDE

5-NITRONICOTINALDEHYDE

C6H4N2O3 (152.0222)


   

6-Fluoro-1-benzofuran-3(2H)-one

6-Fluoro-1-benzofuran-3(2H)-one

C8H5FO2 (152.0274)


   

4-fluorophthalaldehyde

4-fluorophthalaldehyde

C8H5FO2 (152.0274)


   

5-FLUORO-7-HYDROXYBENZOFURAN

5-FLUORO-7-HYDROXYBENZOFURAN

C8H5FO2 (152.0274)


   

2H-Tetrazole,5-(2-thienyl)-

2H-Tetrazole,5-(2-thienyl)-

C5H4N4S (152.0157)


   

7-Chloro-4-azaindole

7-Chloro-4-azaindole

C7H5ClN2 (152.0141)


   

5,6-dihydro-1-benzothiophen-7(4H)-one

5,6-dihydro-1-benzothiophen-7(4H)-one

C8H8OS (152.0296)


   

(Vinylsulfinyl)benzene

(Vinylsulfinyl)benzene

C8H8OS (152.0296)


   

2-Chloro-5-methylnicotinonitrile

2-Chloro-5-methylnicotinonitrile

C7H5ClN2 (152.0141)


   

Acetic acid, 2-chloro-,2-methoxyethyl ester

Acetic acid, 2-chloro-,2-methoxyethyl ester

C5H9ClO3 (152.024)


   

4-chloro-1H-pyrrolo[2,3-c]pyridine

4-chloro-1H-pyrrolo[2,3-c]pyridine

C7H5ClN2 (152.0141)


   

(2-Chloro-3-pyridinyl)acetonitrile

(2-Chloro-3-pyridinyl)acetonitrile

C7H5ClN2 (152.0141)


   

6-CHLORO-4-METHYLNICOTINONITRILE

6-CHLORO-4-METHYLNICOTINONITRILE

C7H5ClN2 (152.0141)


   

3-Amino-4-chlorobenzonitrile

3-Amino-4-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

3-(chloromethyl)pyridine-2-carbonitrile

3-(chloromethyl)pyridine-2-carbonitrile

C7H5ClN2 (152.0141)


   

5-(Trifluoromethyl)-1,2-oxazol-3-amine

5-(Trifluoromethyl)-1,2-oxazol-3-amine

C4H3F3N2O (152.0197)


   

4-(chloromethyl)pyridine-2-carbonitrile

4-(chloromethyl)pyridine-2-carbonitrile

C7H5ClN2 (152.0141)


   

3-Amino-5-chlorobenzonitrile

3-Amino-5-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

Thiazolo[4,5-d]pyrimidine,2-amino- (5CI)

Thiazolo[4,5-d]pyrimidine,2-amino- (5CI)

C5H4N4S (152.0157)


   

3-CHLOROIMIDAZO[1,2-A]PYRIDINE

3-CHLOROIMIDAZO[1,2-A]PYRIDINE

C7H5ClN2 (152.0141)


   

trans-1,2-Dichlorocyclohexane

trans-1,2-Dichlorocyclohexane

C6H10Cl2 (152.016)


   

6-Chloro-1H-pyrrolo[3,2-b]pyridine

6-Chloro-1H-pyrrolo[3,2-b]pyridine

C7H5ClN2 (152.0141)


   

[1,3]Thiazolo[5,4-d]pyrimidin-2-amine

[1,3]Thiazolo[5,4-d]pyrimidin-2-amine

C5H4N4S (152.0157)


   

2-Chloro-5-cyano-3-picoline

2-Chloro-5-cyano-3-picoline

C7H5ClN2 (152.0141)


   

3-nitropyridine-2-carbaldehyde

3-nitropyridine-2-carbaldehyde

C6H4N2O3 (152.0222)


   

dl-tartaric-2,3-d2 acid

dl-tartaric-2,3-d2 acid

C4H4D2O6 (152.029)


   

1H-[1,2,4]triazolo[1,5-a]pyrimidine-5,7-dione

1H-[1,2,4]triazolo[1,5-a]pyrimidine-5,7-dione

C5H4N4O2 (152.0334)


   

6-chloro-2-methylnicotinonitrile

6-chloro-2-methylnicotinonitrile

C7H5ClN2 (152.0141)


   

Isothiazolo[4,5-b]pyrazin-3-amine

Isothiazolo[4,5-b]pyrazin-3-amine

C5H4N4S (152.0157)


   

7-Chloro-1H-pyrrolo[2,3-c]pyridine

7-Chloro-1H-pyrrolo[2,3-c]pyridine

C7H5ClN2 (152.0141)


   

2-Chloro-4-methylpyridine-3-carbonitrile

2-Chloro-4-methylpyridine-3-carbonitrile

C7H5ClN2 (152.0141)


   

1-Chloropyrrolo[1,2-a]pyrazine

1-Chloropyrrolo[1,2-a]pyrazine

C7H5ClN2 (152.0141)


   

1H-1,2,3-Triazole,4-nitro-1-(2-propynyl)-(9CI)

1H-1,2,3-Triazole,4-nitro-1-(2-propynyl)-(9CI)

C5H4N4O2 (152.0334)


   

4-(chloromethyl)pyridine-3-carbonitrile

4-(chloromethyl)pyridine-3-carbonitrile

C7H5ClN2 (152.0141)


   

7-chloro-1H-indazole

7-chloro-1H-indazole

C7H5ClN2 (152.0141)


   

2-Chlorobenzimidazole

2-Chlorobenzimidazole

C7H5ClN2 (152.0141)


   

5-Chloro-3-ethynylpyridin-2-amine

5-Chloro-3-ethynylpyridin-2-amine

C7H5ClN2 (152.0141)


   

3-(Trifluoromethyl)-1H-1,2,4-triazol-5-amine

3-(Trifluoromethyl)-1H-1,2,4-triazol-5-amine

C3H3F3N4 (152.031)


   

6-Chloro-3-Methylpicolinonitrile

6-Chloro-3-Methylpicolinonitrile

C7H5ClN2 (152.0141)


   

6-CHLORO-5-METHYLPICOLINONITRILE

6-CHLORO-5-METHYLPICOLINONITRILE

C7H5ClN2 (152.0141)


   

1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE-2-THIOL

1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE-2-THIOL

C5H4N4S (152.0157)


   

3-CHLORO-6-METHYLPICOLINONITRILE

3-CHLORO-6-METHYLPICOLINONITRILE

C7H5ClN2 (152.0141)


   

(3-Chloro-4-pyridinyl)acetonitrile

(3-Chloro-4-pyridinyl)acetonitrile

C7H5ClN2 (152.0141)


   

1H-1,2,3-Triazole-4-carboxylicacid,5-cyano-,methylester(9CI)

1H-1,2,3-Triazole-4-carboxylicacid,5-cyano-,methylester(9CI)

C5H4N4O2 (152.0334)


   

5-Fluorobenzofuran-3(2H)-one

5-Fluorobenzofuran-3(2H)-one

C8H5FO2 (152.0274)


   

4-Amino-3-chlorobenzonitrile

4-Amino-3-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

2-Amino-5-chlorobenzonitrile

2-Amino-5-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

1-Phenyl-2-sulfanylethanone

1-Phenyl-2-sulfanylethanone

C8H8OS (152.0296)


   

6-CHLORO-4-METHYLPICOLINONITRILE

6-CHLORO-4-METHYLPICOLINONITRILE

C7H5ClN2 (152.0141)


   

8-Chloroimidazo[1,2-a]pyridine

8-Chloroimidazo[1,2-a]pyridine

C7H5ClN2 (152.0141)


   

3-Amino-2-chlorobenzonitrile

3-Amino-2-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

1-Chloroethyl ethyl carbonate

1-Chloroethyl ethyl carbonate

C5H9ClO3 (152.024)


   

1H-Imidazole-4-carboxylicacid,2-amino-5-cyano-(9CI)

1H-Imidazole-4-carboxylicacid,2-amino-5-cyano-(9CI)

C5H4N4O2 (152.0334)


   

6-(Chloromethyl)-2-cyanopyridine

6-(Chloromethyl)-2-cyanopyridine

C7H5ClN2 (152.0141)


   

5-Chloro-1H-pyrrolo[2,3-c]pyridine

5-Chloro-1H-pyrrolo[2,3-c]pyridine

C7H5ClN2 (152.0141)


   

6-Chloro-5-Azaindole

6-Chloro-5-Azaindole

C7H5ClN2 (152.0141)


   

3-Nitroisonicotinaldehyde

3-Nitroisonicotinaldehyde

C6H4N2O3 (152.0222)


   

Thiazolo[5,4-d]pyrimidin-7-amine

Thiazolo[5,4-d]pyrimidin-7-amine

C5H4N4S (152.0157)


   

4-Chloro-1H-indazole

4-Chloro-1H-indazole

C7H5ClN2 (152.0141)


   

(R)-4-Chloro-3-hydroxybutyric acid methyl ester

(R)-4-Chloro-3-hydroxybutyric acid methyl ester

C5H9ClO3 (152.024)


   

4-chloro-6-methylnicotinonitrile

4-chloro-6-methylnicotinonitrile

C7H5ClN2 (152.0141)


   

trans-1,4-dichlorocyclohexane

trans-1,4-dichlorocyclohexane

C6H10Cl2 (152.016)


   

2-Amino-4-Chlorobenzonitrile

2-Amino-4-Chlorobenzonitrile

C7H5ClN2 (152.0141)


   

2-Propanol,1,3-bis(methylthio)-

2-Propanol,1,3-bis(methylthio)-

C5H12OS2 (152.033)


   

4-Chloro-2-cyano-6-methylpyrimidine

4-Chloro-2-cyano-6-methylpyrimidine

C7H5ClN2 (152.0141)


   

4-Nitropicolinaldehyde

4-Nitropicolinaldehyde

C6H4N2O3 (152.0222)


   

5-(2-FURYL)-1,3,4-OXADIAZOL-2(3H)-ONE

5-(2-FURYL)-1,3,4-OXADIAZOL-2(3H)-ONE

C6H4N2O3 (152.0222)


   

9H-Purine-2,6-diol

9H-Purine-2,6-diol

C5H4N4O2 (152.0334)


   

1-methyl-2-cyano-5-nitro-imidazole

1-methyl-2-cyano-5-nitro-imidazole

C5H4N4O2 (152.0334)


   

2-(2-METHOXYETHOXY)ACETYL CHLORIDE

2-(2-METHOXYETHOXY)ACETYL CHLORIDE

C5H9ClO3 (152.024)


   

2-(Chloromethyl)nicotinonitrile

2-(Chloromethyl)nicotinonitrile

C7H5ClN2 (152.0141)


   

5-Nitropicolinaldehyde

5-Nitropicolinaldehyde

C6H4N2O3 (152.0222)


   

5-Amino-2-chlorobenzonitrile

5-Amino-2-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

5-Fluoro-2-benzofuran-1(3H)-one

5-Fluoro-2-benzofuran-1(3H)-one

C8H5FO2 (152.0274)


   

Benzeneacetaldehyde, 2-fluoro-alpha-oxo- (9CI)

Benzeneacetaldehyde, 2-fluoro-alpha-oxo- (9CI)

C8H5FO2 (152.0274)


   

(6-Chloro-2-pyridinyl)acetonitrile

(6-Chloro-2-pyridinyl)acetonitrile

C7H5ClN2 (152.0141)


   

2-Amino-3-chlorobenzonitrile

2-Amino-3-chlorobenzonitrile

C7H5ClN2 (152.0141)


   

4-(Methylthio)benzaldehyde

4-(Methylthio)benzaldehyde

C8H8OS (152.0296)


   

S-Methyl 4-chloro-3-hydroxybutyrate

S-Methyl 4-chloro-3-hydroxybutyrate

C5H9ClO3 (152.024)


   

Pyrazolo[1,5-a]-1,3,5-triazine-2,4(1H,3H)-dione

Pyrazolo[1,5-a]-1,3,5-triazine-2,4(1H,3H)-dione

C5H4N4O2 (152.0334)


   

3-(Trifluoromethyl)-1H-pyrazol-5(4H)-one

3-(Trifluoromethyl)-1H-pyrazol-5(4H)-one

C4H3F3N2O (152.0197)


   

Methyl 4,4-difluoro-3-oxobutanoate

Methyl 4,4-difluoro-3-oxobutanoate

C5H6F2O3 (152.0285)


   

5-chloro-2-ethynylpyridin-3-amine

5-chloro-2-ethynylpyridin-3-amine

C7H5ClN2 (152.0141)


   

Hypoxanthine 3-N-oxide

Hypoxanthine 3-N-oxide

C5H4N4O2 (152.0334)


An oxopurine that is 3,9-dihydro-6H-purine which is substituted by an oxo group at position 6 and in which the hydrogen attached to the nitrogen at position 3 is replaced by a hydroxy group. It is a major component of Schreckstoff, an alarm pheromone found in fish.

   

Trimethylsilyl methanesulfinate

Trimethylsilyl methanesulfinate

C4H12O2SSi (152.0327)


   

Xanthin

1-H-purine-2,6-dione, 3,7-dihydro(9CI)

C5H4N4O2 (152.0334)


COVID info from COVID-19 Disease Map, PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3]. Xanthine, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine also acts as an intermediate product on the pathway of purine degradation[1][2][3].

   

1-Butyl phosphate

1-Butyl phosphate

C4H9O4P-2 (152.0238)


   

Dithiobis(diaminomethylium)

Dithiobis(diaminomethylium)

C2H8N4S2+2 (152.019)


   

S-Methyl benzenecarbothioate

S-Methyl benzenecarbothioate

C8H8OS (152.0296)


   

7,9-Dihydro-1H-purine-6,8-dione

1H-Purine-6,8-dione,7,9-dihydro-

C5H4N4O2 (152.0334)


   

7H-xanthine

7H-xanthine

C5H4N4O2 (152.0334)


An oxopurine in which the purine ring is substituted by oxo groups at positions 2 and 6 and N-7 is protonated.

   

Alloxanthine

Alloxanthine

C5H4N4O2 (152.0334)


A pyrazolopyrimidine that is 4,5,6,7-tetrahydro-H-pyrazolo[3,4-d]pyrimidine substituted by oxo groups at positions 4 and 6.

   

Dihydroxypurine

Dihydroxypurine

C5H4N4O2 (152.0334)


   

1-[(s)-methanesulfinylsulfanyl]butane

1-[(s)-methanesulfinylsulfanyl]butane

C5H12OS2 (152.033)


   

2-hydroxy-2-methyl-1,2λ⁶-oxathiolane-2,5-dione

2-hydroxy-2-methyl-1,2λ⁶-oxathiolane-2,5-dione

C4H8O4S (152.0143)


   

[(butane-1-sulfinyl)sulfanyl]methane

[(butane-1-sulfinyl)sulfanyl]methane

C5H12OS2 (152.033)


   

{[(r)-butane-1-sulfinyl]sulfanyl}methane

{[(r)-butane-1-sulfinyl]sulfanyl}methane

C5H12OS2 (152.033)


   

1-(methanesulfinylsulfanyl)butane

1-(methanesulfinylsulfanyl)butane

C5H12OS2 (152.033)


   

ossipurinolo

ossipurinolo

C5H4N4O2 (152.0334)