Exact Mass: 228.0422568
Exact Mass Matches: 228.0422568
Found 500 metabolites which its exact mass value is equals to given mass value 228.0422568,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
2'-deoxyuridine
C9H12N2O5 (228.07461819999997)
Deoxyuridine, also known as dU, belongs to the class of organic compounds known as pyrimidine 2-deoxyribonucleosides. Pyrimidine 2-deoxyribonucleosides are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2. It is similar in chemical structure to uridine, but without the 2-hydroxyl group. Deoxyuridine exists in all living organisms, ranging from bacteria to humans. Within humans, deoxyuridine participates in a number of enzymatic reactions. In particular, deoxyuridine can be biosynthesized from deoxycytidine through its interaction with the enzyme cytidine deaminase. In addition, deoxyuridine can be converted into uracil and deoxyribose 1-phosphate through its interaction with the enzyme thymidine phosphorylase. Deoxyuridine is considered to be an antimetabolite that is converted into deoxyuridine triphosphate during DNA synthesis. Laboratory suppression of deoxyuridine is used to diagnose megaloblastic anemia due to vitamin B12 and folate deficiencies. In humans, deoxyuridine is involved in the metabolic disorder called UMP synthase deficiency (orotic aciduria). Outside of the human body, deoxyuridine has been detected, but not quantified in, several different foods, such as lichee, highbush blueberries, agaves, macadamia nut (M. tetraphylla), and red bell peppers. This could make deoxyuridine a potential biomarker for the consumption of these foods. 2-Deoxyuridine is a naturally occurring nucleoside. It is similar in chemical structure to uridine, but without the 2-hydroxyl group. It is considered to be an antimetabolite that is converted to deoxyuridine triphosphate during DNA synthesis. Laboratory suppression of deoxyuridine is used to diagnose megaloblastic anemia due to vitamin B12 and folate deficiencies. [HMDB]. Deoxyuridine is found in many foods, some of which are garden tomato (variety), hickory nut, banana, and hazelnut. Deoxyuridine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=951-78-0 (retrieved 2024-07-01) (CAS RN: 951-78-0). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.
MCPB
D010575 - Pesticides > D006540 - Herbicides D016573 - Agrochemicals CONFIDENCE standard compound; EAWAG_UCHEM_ID 2710 CONFIDENCE standard compound; INTERNAL_ID 578; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5034; ORIGINAL_PRECURSOR_SCAN_NO 5030 CONFIDENCE standard compound; INTERNAL_ID 578; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4996; ORIGINAL_PRECURSOR_SCAN_NO 4991 CONFIDENCE standard compound; INTERNAL_ID 578; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5038; ORIGINAL_PRECURSOR_SCAN_NO 5036 CONFIDENCE standard compound; INTERNAL_ID 578; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5019; ORIGINAL_PRECURSOR_SCAN_NO 5018 CONFIDENCE standard compound; INTERNAL_ID 578; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5021; ORIGINAL_PRECURSOR_SCAN_NO 5016 CONFIDENCE standard compound; INTERNAL_ID 578; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5033; ORIGINAL_PRECURSOR_SCAN_NO 5031
Dosanex
C10H13ClN2O2 (228.06655080000002)
CONFIDENCE standard compound; EAWAG_UCHEM_ID 3204
Mevalonic acid-5P
Mevalonic acid-5p, also known as (R)-5-phosphomevalonate or mevalonate-5p, is a member of the class of compounds known as monoalkyl phosphates. Monoalkyl phosphates are organic compounds containing a phosphate group that is linked to exactly one alkyl chain. Thus, mevalonic acid-5p is considered to be a fatty acid lipid molecule. Mevalonic acid-5p is soluble (in water) and a moderately acidic compound (based on its pKa). Mevalonic acid-5p can be found in a number of food items such as rowanberry, common oregano, caraway, and cherry tomato, which makes mevalonic acid-5p a potential biomarker for the consumption of these food products. Mevalonic acid-5p can be found primarily throughout most human tissues. Mevalonic acid-5p exists in all eukaryotes, ranging from yeast to humans. In humans, mevalonic acid-5p is involved in several metabolic pathways, some of which include pamidronate action pathway, rosuvastatin action pathway, pravastatin action pathway, and lovastatin action pathway. Mevalonic acid-5p is also involved in several metabolic disorders, some of which include hypercholesterolemia, lysosomal acid lipase deficiency (wolman disease), hyper-igd syndrome, and mevalonic aciduria. Mevalonic acid-5P (CAS: 1189-94-2), also known as 5-phosphomevalonic acid, belongs to the class of organic compounds known as monoalkyl phosphates. These are organic compounds containing a phosphate group that is linked to exactly one alkyl chain. Within humans, mevalonic acid-5P participates in many enzymatic reactions. In particular, mevalonic acid-5P can be biosynthesized from mevalonate; which is mediated by the enzyme mevalonate kinase. In addition, mevalonic acid-5P can be converted into mevalonic acid-5-pyrophosphate through its interaction with the enzyme phosphomevalonate kinase. In humans, mevalonic acid-5P is involved in the mevalonate pathway. Outside of the human body, mevalonic acid-5P has been detected, but not quantified in, several different foods, such as oriental wheat, devilfish, pepper (spice), redcurrants, and star fruits. This could make mevalonic acid-5P a potential biomarker for the consumption of these foods.
L-2-Aminoethyl seryl phosphate
L-2-Aminoethyl seryl phosphate is found in animal foods. L-2-Aminoethyl seryl phosphate is isolated from numerous animals including chicken, fish and reptile Isolated from numerous animals including chicken, fish and reptiles. L-2-Aminoethyl seryl phosphate is found in fishes and animal foods.
2-Hydroxy-3-carboxy-6-oxo-7-methylocta-2,4-dienoate
Euxanthone
Occurs in Mammea americana (mamey), Platonia insignis (bakuri) and Mangifera indica (mango). Euxanthone is found in fruits and mammee apple. Euxanthone is found in fruits. Euxanthone occurs in Mammea americana (mamey), Platonia insignis (bakuri) and Mangifera indica (mango
Urolithin A
Urolithin A is a secondary metabolite of ellagic acid which may be glucuronidated by liver enzymes during phase II metabolism. A polyphenol metabolite detected in biological fluids [PhenolExplorer] Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis, suppresses cell cycle progression, and inhibits DNA synthesis[1][2]. Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis, suppresses cell cycle progression, and inhibits DNA synthesis[1][2].
1,5-Dihydroxyxanthone
1,5-Dihydroxyxanthone is found in fruits. 1,5-Dihydroxyxanthone is a constituent of Garcinia species, Mammea americana (mamey) Constituent of Garcinia subspecies, Mammea americana (mamey). 1,5-Dihydroxyxanthone is found in fruits and mammee apple.
2,3,5,6-Tetramethylpyrazine phosphate
1-((2S,4S,5R)-4-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
C9H12N2O5 (228.07461819999997)
1-[(2R,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-2-oxolanyl]-2-pyrimidinone
C9H12N2O5 (228.07461819999997)
Aminoethylcysteine ketimine decarboxylated dimer
C9H12N2OS2 (228.03910219999997)
Dioxolane-THYMINE
C9H12N2O5 (228.07461819999997)
2-thiophen-2-yl-1H-quinazolin-4-one
C12H8N2OS (228.03573179999998)
1-((2R,3R,5S)-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
C9H12N2O5 (228.07461819999997)
4-chloro-6,8-dihydroxy-3-methylisochroman-1-one|4-chloro-6-hydroxymellein
C10H9ClO4 (228.01893439999998)
3, 4-Dihydro-7-Chloro-6, 8-dihydroxy-3-methyl-1H-2-benzopyran-1-one
C10H9ClO4 (228.01893439999998)
2-methylimidazo[1,5-b]isoquinoline-1,3,5(2H)-trione
7-chloro-3,4-dihydro-4,8-dihydroxy-3-methyl-1H-2-benzopyran-1-one|7-chloromellein-5-ol
C10H9ClO4 (228.01893439999998)
(3R)-7-chloro-3,6,8-trihydroxy-3,4-dihydronaphthalen-1(2H)-one|7-chloroscytalone
C10H9ClO4 (228.01893439999998)
2-Methyl-9-Chloro-p-mentha-1,3,5,8-tetraene-2,5,10-triol|Z-3-chloro-2-(2-hydroxy-4-methyl-5-methoxyphenyl)-prop-2-en-1-ol
((2S)-4-butyryl-3,5-dioxo-tetrahydro-[2]furyl)-acetic acid|((2S)-4-Butyryl-3,5-dioxo-tetrahydro-[2]furyl)-essigsaeure
Di-Me ester-3-Hydroxy-4-oxo-4H-pyran-2,6-dicarboxylic acid
Euxanthone
Euxanthone is a member of the class of xanthones that is 9H-xanthene substituted by hydroxy group at positions 1 and 7 and an oxo group at position 9. It has been isolated from Cratoxylum cochinchinense. It has a role as a plant metabolite and a metabolite. It is a member of xanthones and a member of phenols. Euxanthone is a natural product found in Garcinia oblongifolia, Hypericum scabrum, and other organisms with data available. A member of the class of xanthones that is 9H-xanthene substituted by hydroxy group at positions 1 and 7 and an oxo group at position 9. It has been isolated from Cratoxylum cochinchinense. Occurs in Mammea americana (mamey), Platonia insignis (bakuri) and Mangifera indica (mango). Euxanthone is found in fruits and mammee apple. Euxanthone is found in fruits. Euxanthone occurs in Mammea americana (mamey), Platonia insignis (bakuri) and Mangifera indica (mango
Deoxyuridine
C9H12N2O5 (228.07461819999997)
2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.
2-deoxyuridine
C9H12N2O5 (228.07461819999997)
A pyrimidine 2-deoxyribonucleoside having uracil as the nucleobase. D009676 - Noxae > D000963 - Antimetabolites COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.
urolithin A
Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis, suppresses cell cycle progression, and inhibits DNA synthesis[1][2]. Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis, suppresses cell cycle progression, and inhibits DNA synthesis[1][2].
Zebularine
C9H12N2O5 (228.07461819999997)
C471 - Enzyme Inhibitor > C2083 - DNA Methyltransferase Inhibitor C274 - Antineoplastic Agent > C132686 - Demethylating Agent Zebularine (NSC309132; 4-Deoxyuridine) is a DNA methyltransferase inhibitor. Zebularine also inhibits cytidine deaminase with a Ki of 0.95 μM.
5-Chloro-3-phenyl-1H-pyrrolo[2,3-b]pyridine
C13H9ClN2 (228.04542239999998)
Sulfamide, (1,3-dihydro-3-oxo-1-isobenzofuranyl)- (9CI)
C8H8N2O4S (228.02047679999998)
1-bromo-4-(2-methoxypropan-2-yl)benzene
C10H13BrO (228.01497080000001)
3-(Trifluoromethoxy)phenylhydrazine hydrochloride
C7H8ClF3N2O (228.02772239999996)
2-((tert-Butoxycarbonyl)amino)oxazole-5-carboxylic acid
C9H12N2O5 (228.07461819999997)
4-dimethylamino-1-naphthyl isothiocyanate
C13H12N2S (228.07211519999998)
Butanedioic acid,2-(2-chlorophenyl)-
C10H9ClO4 (228.01893439999998)
Imidazo[2,1-b]thiazole-5-carboxaldehyde, 6-phenyl-
C12H8N2OS (228.03573179999998)
methyl 4-(methylsulfonylmethyl)benzoate
C10H12O4S (228.04562719999998)
4-Chloro-5-nitro-6-(1-pyrrolidinyl)pyrimidine
C8H9ClN4O2 (228.04140040000001)
2-Carbethoxy-3-(2-thienyl)propionic acid
C10H12O4S (228.04562719999998)
Phenol,4-bromo-2-(1,1-dimethylethyl)-
C10H13BrO (228.01497080000001)
1-(4-bromophenyl)-2-methyl-propan-2-ol
C10H13BrO (228.01497080000001)
1-(3-chloro-4-fluorophenyl)pyrazolidine-3,5-dione
C9H6ClFN2O2 (228.01018180000003)
1-(2-bromopropyl)-3-methoxybenzene
C10H13BrO (228.01497080000001)
1-(3-Bromopropyl)-2-methoxybenzene
C10H13BrO (228.01497080000001)
2-Amino-5-methyl-4-(4-methylphenyl)thiophene-3-carbonitrile
C13H12N2S (228.07211519999998)
4-(2-(Methacryloyloxy)ethoxy)-4-oxobut-2-enoic acid
1,4-DICHLORO-5,6,7,8-TETRAHYDRO-5,8-ETHANOPHTHALAZINE
C10H10Cl2N2 (228.02210000000002)
7-NITRO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE HYDROCHLORIDE
C10H13ClN2O2 (228.06655080000002)
tert-Butyl (2-chloropyridin-4-yl)carbamate
C10H13ClN2O2 (228.06655080000002)
Ethyl 4-(methylsulfonyl)benzoate
C10H12O4S (228.04562719999998)
2-(4-CHLORO-2-METHYLPHENOXY)PROPANOHYDRAZIDE
C10H13ClN2O2 (228.06655080000002)
ethyl 2-amino-5-carbamoyl-4-methylthiophene-3-carboxylate
2,2-DIFLUORO-3-OXO-3-PHENYL-PROPIONIC ACID ETHYL ESTER
4-Methyl-2-morpholin-4-yl-thiazole-5-carboxylic acid
N-(2-cyanophenyl)thiophene-2-carboxamide
C12H8N2OS (228.03573179999998)
4-((4-HYDROXY-6-OXO-1,6-DIHYDROPYRIMIDIN-2-YL)AMINO)BENZONITRILE
(2-(4-fluorophenyl)oxazol-4-yl)methanamine HCl
C10H10ClFN2O (228.04656519999997)
1-METHANESULFINYL-4-METHYLSULFANYL-6,7-DIHYDRO-5H-CYCLOPENTA[D]PYRIDAZINE
C9H12N2OS2 (228.03910219999997)
2-(1H-1,2,4-Triazol-1-yl)-5-(trifluoromethyl)aniline
2-(hydroxyimino)-1-((4-methylphenyl)sulfonyl)eth-2-ylamine
METHYL 3-(METHYLSULFONYL)PHENYLACETATE
C10H12O4S (228.04562719999998)
(2-BUTOXY-5-CHLOROPHENYL)BORONIC ACID
C10H14BClO3 (228.07244740000002)
4-Butoxy-3-chlorophenylboronic acid
C10H14BClO3 (228.07244740000002)
2-(2-HYDROXYETHYLAMINO)-N-(2-CHLOROPHENYL)ACETAMIDE
C10H13ClN2O2 (228.06655080000002)
2-(2-FLUORO-PHENYL)-BENZOOXAZOL-5-YLAMINE
C13H9FN2O (228.06988759999996)
Anpirtoline
C78272 - Agent Affecting Nervous System > C47794 - Serotonin Agonist
5-Chloro-2-phenyl-imidazo[1,2-a]pyridine
C13H9ClN2 (228.04542239999998)
(5-(TERT-BUTOXYCARBONYL)THIOPHEN-2-YL)BORONIC ACID
CARBONIC ACID 4-CHLOROMETHYL-3-METHYL-PHENYL ESTER ETHYL ESTER
(4-(Trifluoromethoxy)phenyl)hydrazine hydrochloride
C7H8ClF3N2O (228.02772239999996)
2-phenylthieno[2,3-d]pyrimidin-4-ol
C12H8N2OS (228.03573179999998)
DIMETHYL 2-(THIOPHEN-2-YLMETHYL)MALONATE
C10H12O4S (228.04562719999998)
Dichlorobis(trimethylsilyl)methane
C7H18Cl2Si2 (228.03240480000002)
2-(3,4-dimethoxyphenylthio)acetic acid
C10H12O4S (228.04562719999998)
6-chloro-2-phenylimidazo[1,2-a]pyridine
C13H9ClN2 (228.04542239999998)
2-(4-Chloro-3,5-dimethylphenoxy)acetohydrazide
C10H13ClN2O2 (228.06655080000002)
POTASSIUM ((BENZYLOXY)METHYL)TRIFLUOROBORATE
C8H9BF3KO (228.03355899999997)
3-[4-(METHYLSULFONYL)PHENYL]PROPANOIC ACID
C10H12O4S (228.04562719999998)
5-amino-4-cyano-1-phenyl-1H-pyrazole-3-carboxylic acid
ETHYL 4-METHYL-2-(METHYLTHIO)-6-OXO-1,6-DIHYDROPYRIMIDINE-5-CARBOXYLATE
2-Chloro-4-(ethoxycarbonyl)benzoic acid
C10H9ClO4 (228.01893439999998)
potassium,trifluoro-[2-(2-hydroxyethyl)phenyl]boranuide
C8H9BF3KO (228.03355899999997)
potassium,trifluoro-[4-(2-hydroxyethyl)phenyl]boranuide
C8H9BF3KO (228.03355899999997)
5-Phenylthieno[2,3-d]pyrimidin-4(3H)-one
C12H8N2OS (228.03573179999998)
Chloro(dimethyl)(3-phenoxypropyl)silane
C11H17ClOSi (228.07371419999998)
1,3-Bis(chlorodimethylsilyl)propane
C7H18Cl2Si2 (228.03240480000002)
1-(4-(2,2-DICHLOROCYCLOPROPYL)PHENYL)ETHANONE
C11H10Cl2O (228.01086700000002)
1-(β-D-2-DEOXYRIBOFURANOSYL)-3-NITROPYRROLE
C9H12N2O5 (228.07461819999997)
4-thiophen-2-yl-2,3-dihydro-1H-1,5-benzodiazepine
C13H12N2S (228.07211519999998)
Trimethyl[(phenylsulfonyl)methyl]silane
C10H16O2SSi (228.06402359999998)
potassium (4-methoxy-2-methylphenyl)trifluoroborate
C8H9BF3KO (228.03355899999997)
4H-1,3-Benzodioxin-6-carboxylic acid, 8-(chloromethyl)-
C10H9ClO4 (228.01893439999998)
1-methylpiperazin-2-one trifluoroacetate
C7H11F3N2O3 (228.07217319999998)
(3-CHLORO-5-ISOBUTOXYPHENYL)BORONIC ACID
C10H14BClO3 (228.07244740000002)
3-Butoxy-2-chlorophenylboronic acid
C10H14BClO3 (228.07244740000002)
6-(Difluoromethoxy)-1H-indazole-3-carboxylic acid
C9H6F2N2O3 (228.03464699999998)
4-[(Dimethylamino)iminomethyl]benzoic acid monohydrochloride
C10H13ClN2O2 (228.06655080000002)
3-(4-Chlorophenyl)-imidazo[1,2-a]pyridine
C13H9ClN2 (228.04542239999998)
7-chloro-2-phenyl-1H-pyrrolo[3,2-b]pyridine
C13H9ClN2 (228.04542239999998)
6-(aminomethyl)-4-methyl-1,4-benzoxazin-3-one,hydrochloride
C10H13ClN2O2 (228.06655080000002)
3-oxopropyl 4-methylbenzenesulfonate
C10H12O4S (228.04562719999998)
2-HYDROXYMETHYL-1 H-BENZOIMIDAZOLE-5-CARBOXYLIC ACID HYDROCHLORIDE
3,3,3-trifluoro-(2-tetrahydrothienylmethyl)propionic acid
6-AMINO-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID HYDROCHLORIDE
C10H13ClN2O2 (228.06655080000002)
7-Amino-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid hydrochloride
C10H13ClN2O2 (228.06655080000002)
7-METHOXY-1,1-DIOXO-1,4-DIHYDRO-2H-1LAMBDA6-BENZO[1,2,4]THIADIAZIN-3-ONE
C8H8N2O4S (228.02047679999998)
N-(2-HYDROXYETHYL)AMMONIUM BENZO-THIAZOLE-2-THIOLATE
C9H12N2OS2 (228.03910219999997)
7-Difluoromethyl-5-methyl-[1,2,4]triazolo-[1,5-a]pyrimidine-2-carboxylic acid
C8H6F2N4O2 (228.04587999999998)
(2-Isopropylthiazol-4-yl)methanamine dihydrochloride
4-CHLORO-1-ETHYL-6-(METHYLTHIO)-1H-PYRAZOLO[3,4-D]PYRIMIDINE
methyl 3-chlorocarbonyl-4-methoxy-benzoate
C10H9ClO4 (228.01893439999998)
2-(4-bromophenyl)-2-Methylpropan-1-ol
C10H13BrO (228.01497080000001)
5-(Difluoromethoxy)-1H-indazole-3-carboxylic acid
C9H6F2N2O3 (228.03464699999998)
Methyl 3-Methyl-4-(methylsulfonyl)benzoate
C10H12O4S (228.04562719999998)
Carbamic acid, N-(3-chloro-2-pyridinyl)-, 1,1-dimethylethyl ester
C10H13ClN2O2 (228.06655080000002)
2-(3-Bromophenyl)-2-Methylpropan-1-ol
C10H13BrO (228.01497080000001)
4-Nitro-L-phenylalanine monohydrate
C9H12N2O5 (228.07461819999997)
3-(5-oxo-1-prop-2-enyl-2-sulfanylideneimidazolidin-4-yl)propanoic acid
3′-Deoxyuridine
C9H12N2O5 (228.07461819999997)
3′-Deoxyuridine is a potential anticancer and antiviral agent. 3'-deoxyuridine inhibits bovine diarrhoea virus (BVDV) production[1].
1-(2-Bromoethoxy)-2,4-dichlorobenzene
C10H13BrO (228.01497080000001)
(2S,6R)-6-Amino-2-(2-thienyl)-1,4-thiazepan-5-one
C9H12N2OS2 (228.03910219999997)
4-AMINO-N-METHOXY-N-METHYL-2-(METHYLTHIO)PYRIMIDINE-5-CARBOXAMIDE
5-(4-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine
[4-(Ethylsulfonyl)phenyl]acetic acid
C10H12O4S (228.04562719999998)
4-oxo-3,5-dihydropyrrolo[2,3-c]quinoline-1-carboxylic acid
3-Oxetanyl 4-methylbenzenesulfonate
C10H12O4S (228.04562719999998)
Acetic acid,2-(4-chloro-2-methylphenoxy)-, ethyl ester
5H-Tetrazole-5-thione,1,2-dihydro-1-(1-naphthalenyl)-
Benzene,1-(3-bromopropoxy)-3-methyl-
C10H13BrO (228.01497080000001)
4-BROMO-5-ISOPROPYL-2-METHYLBENZENOL
C10H13BrO (228.01497080000001)
tert-Butyl (6-chloropyridin-2-yl)carbamate
C10H13ClN2O2 (228.06655080000002)
Cyclohexanebutanoicacid, nickel(2+) salt (2:1)
C10H18NiO2 (228.06601980000002)
3-(TOLUENE-4-SULFONYL)-PROPIONIC ACID
C10H12O4S (228.04562719999998)
2-(Trifluoromethoxy)phenylhydrazine hydrochloride
C7H8ClF3N2O (228.02772239999996)
Methyl 2-Methyl-4-(methylsulfonyl)benzoate
C10H12O4S (228.04562719999998)
Acetoxy(4-chlorophenyl)acetic acid
C10H9ClO4 (228.01893439999998)
3-(3-Furyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid
5-(3-(Trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-amine
2-methoxy-5-[(E)-prop-1-enyl]benzenesulfonic acid
C10H12O4S (228.04562719999998)
N-(5-chloro-pyridin-2-yl)-oxalamic acid ethyl ester
(7-BROMO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)(PHENYL)METHANONE
1-(3-Bromopropoxy)-2-methylbenzene
C10H13BrO (228.01497080000001)
methyl 2-(4-methylphenyl)sulfonylacetate
C10H12O4S (228.04562719999998)
TERT-BUTYL (5-CHLOROPYRIDIN-2-YL)CARBAMATE
C10H13ClN2O2 (228.06655080000002)
TERT-BUTYL (2-CHLOROPYRIDIN-3-YL)CARBAMATE
C10H13ClN2O2 (228.06655080000002)
TERT-BUTYL (4-CHLOROPYRIDIN-3-YL)CARBAMATE
C10H13ClN2O2 (228.06655080000002)
4-(Trifluoromethyl)-1,3-dihydro-2H-1,5-benzodiazepin-2-one
3-(Difluoromethyl)-4-hydroxy-1H-pyrrolo[2,3-b]pyridine-2-carboxyl ic acid
C9H6F2N2O3 (228.03464699999998)
METHYL 2-(4-(METHYLSULFONYL)PHENYL)ACETATE
C10H12O4S (228.04562719999998)
4-(2-Bromoethyl)-1-methoxy-2-methylbenzene
C10H13BrO (228.01497080000001)
CYCLOBUTANECARBONYL CHLORIDE,1-(4-CHLOROPHENYL)-
C11H10Cl2O (228.01086700000002)
2-(4,6-Diamino-pyrimidin-2-ylsulfanyl)-butyric acid
N-amino-N-[4-(methanesulfonamido)phenyl]methanimidamide
TERT-BUTYL (6-CHLOROPYRIDIN-3-YL)CARBAMATE
C10H13ClN2O2 (228.06655080000002)
(3-Butoxy-5-chlorophenyl)boronic acid
C10H14BClO3 (228.07244740000002)
(5-BUTOXY-2-CHLOROPHENYL)BORONIC ACID
C10H14BClO3 (228.07244740000002)
(2-CHLORO-5-ISOBUTOXYPHENYL)BORONIC ACID
C10H14BClO3 (228.07244740000002)
(3-Butoxy-4-chlorophenyl)boronic acid
C10H14BClO3 (228.07244740000002)
(4-CHLORO-3-ISOBUTOXYPHENYL)BORONIC ACID
C10H14BClO3 (228.07244740000002)
(4-CHLORO-2-ISOBUTOXYPHENYL)BORONIC ACID
C10H14BClO3 (228.07244740000002)
(2-Butoxy-4-chlorophenyl)boronic acid
C10H14BClO3 (228.07244740000002)
6-PHENYL-3,4-DIHYDROTHIENO[3,2-D]PYRIMIDIN-4-ONE
C12H8N2OS (228.03573179999998)
2-Isopropyl-4-bromo-5-methylphenol
C10H13BrO (228.01497080000001)
3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride
C6H8ClF3N4 (228.03895539999996)
1-ethyl-2-methyl-5,6-dichlorobenzimidazole
C10H10Cl2N2 (228.02210000000002)
Ethyl2-(2-formamidothiazol-4-yl)-2-oxoacetate
C8H8N2O4S (228.02047679999998)
6-PHENOXY-3-PYRIDINYL ISOTHIOCYANATE
C12H8N2OS (228.03573179999998)
N-(3-Chlorophenyl)-N2-(2-hydroxyethyl)glycinamide
C10H13ClN2O2 (228.06655080000002)
2-(2-HYDROXYETHYLAMINO)-N-(4-CHLOROPHENYL)ACETAMIDE
C10H13ClN2O2 (228.06655080000002)
4,5,5,5-tetrafluoro-4-(trifluoromethyl)pentan-1-ol
1-methyl-5-nitro-1,3-dihydrobenzo[c]isothiazole 2,2-dioxide
C8H8N2O4S (228.02047679999998)
1-beta-D-Ribofuranosyl-4(1H)-pyrimidinone
C9H12N2O5 (228.07461819999997)
4-Methoxy-2-(methylsulphonyl)acetophenone
C10H12O4S (228.04562719999998)
2-(6-CHLORO-2-PYRIDINYL)-2-PHENYLACETONITRILE
C13H9ClN2 (228.04542239999998)
1-(2,2,2-TRIFLUOROETHYL)-3-(TRIFLUOROMETHYL)BENZENE
2-(2-Bromo-ethoxy)-1,3-dimethyl-benzene
C10H13BrO (228.01497080000001)
2-(2-bromoethoxy)-1,4-dimethylbenzene
C10H13BrO (228.01497080000001)
1-(3-Bromopropyl)-4-methoxybenzene
C10H13BrO (228.01497080000001)
2,4-Diamino-6-(hydroxymethyl)pteridine hydrochloride
2-(2-chloro-5-methylphenoxy)propanehydrazide
C10H13ClN2O2 (228.06655080000002)
3-PHENYLMETHANESULFONYL-PROPIONIC ACID
C10H12O4S (228.04562719999998)
N-(2-Chloro-3-hydroxypyridin-4-yl)pivalamide
C10H13ClN2O2 (228.06655080000002)
Methyl 5,6,7,8-tetrahydro-1,7-naphthyridine-3-carboxylate hydrochloride
C10H13ClN2O2 (228.06655080000002)
4-(2-aminophenoxy)-2-fluorobenzonitrile
C13H9FN2O (228.06988759999996)
3-amino-5-methoxy-3,4-dihydro-1H-quinolin-2-one,hydrochloride
C10H13ClN2O2 (228.06655080000002)
5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
C13H9ClN2 (228.04542239999998)
2,3-Dihydro-5-methyl-4-[(2-methyl-3-furanyl)dithio]furan
METHYL 2-[[(2-CHLORO-3-PYRIDYL)CARBONYL]AMINO]ACETATE
Potassium (4-ethoxyphenyl)trifluoroborate
C8H9BF3KO (228.03355899999997)
2-Propanone,3-(1H-benzimidazol-2-yl)-1,1,1-trifluoro-
2-(4-Chlorophenyl)-2-(pyridin-2-yl)acetonitrile
C13H9ClN2 (228.04542239999998)
5-Pyrimidineaceticacid, 3,4-dihydro-2-(methylthio)-4-oxo-, ethyl ester
3-[2,2-DIFLUOROBENZO[1,3]-DIOXOL-5-YL]ACRYLIC ACID
C10H6F2O4 (228.02341399999997)
4-Methoxy-2-morpholin-4-yl-thiazole-5-carbaldehyde
1-[1-(methylsulfonyl)-3-piperidinyl]methanamine(SALTDATA: HCl)
N-PIPERIDIN-4-YLMETHYL-METHANESULFONAMIDE HYDROCHLORIDE
2-(3-nitropyridin-2-yl)sulfanylpropanoic Acid
C8H8N2O4S (228.02047679999998)
tert-butyl4-chloropyridin-2-ylcarbamate
C10H13ClN2O2 (228.06655080000002)
Methyl 5-(3-cyanophenyl)-1,2-oxazole-3-carboxylate
2-PHENYLTHIENO[3,2-D]PYRIMIDIN-4-OL
C12H8N2OS (228.03573179999998)
POTASSIUMTRIFLUORO(4-METHOXYBENZYL)BORATE
C8H9BF3KO (228.03355899999997)
POTASSIUM 3-(2-HYDROXYETHYL)PHENYLTRIFLUOROBORATE
C8H9BF3KO (228.03355899999997)
1-(bromomethyl)-2-propan-2-yloxybenzene
C10H13BrO (228.01497080000001)
2-Phenyl-2-(2-pyridyl)thioacetamide
C13H12N2S (228.07211519999998)
2-(3,5-dimethyl-1H-pyrrol-2-yl)-1,3-benzothiazole
C13H12N2S (228.07211519999998)
Carlosic acid
A tetronic acid derivative that is furan-2(5H)-one which is substituted at positions 3, 4, and 5 by butanoyl, hydroxy, and carboxymethyl groups, respectively (the S enantiomer).
2-(butylthio)-4-oxo-1H-pyrimidine-6-carboxylic acid
3-Methanesulfonyl-benzoic acid ethyl ester
C10H12O4S (228.04562719999998)
1,2,3,4,7,7-Hexafluoro-5-vinylbicyclo[2.2.1]hept-2-ene
8-Hydroxy-2-oxa-bicyclo[3.3.1]non-6-ene-3,5-dicarboxylic acid
N-oxo-2-(phenylsulfonylamino)ethanamide
C8H8N2O4S (228.02047679999998)
S-[2-(Aminosulfonyl)ethyl]-D-Cysteine
C5H12N2O4S2 (228.02384719999998)
AIDS-113822
C9H12N2O5 (228.07461819999997)
D009676 - Noxae > D000963 - Antimetabolites COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine.
5-phospho-beta-D-ribosylaminium(1-)
Conjugate base of 5-phospho-beta-D-ribosylamine. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
(2E,4Z,7S)-7-ammonio-5-formyl-2-hydroxyocta-2,4-dienedioate
(E,2S)-2-azaniumyl-7-hydroxy-4-[(E)-2-oxidoethenyl]-6,7-dioxohept-4-enoate
(E)-2-hydroxy-3-[(E)-4-methyl-3-oxopent-1-enyl]but-2-enedioic acid
(2R)-2-amino-3-[2-aminoethoxy(hydroxy)phosphoryl]oxypropanoic acid
(1S,4R)-1-(2-carboxy-2-oxoethyl)-4-hydroxycyclohex-2-ene-1-carboxylic acid
Tricyclo-decan-9-yl-xanthogenate (racemate)
C11H16OS2 (228.06425259999997)
D004791 - Enzyme Inhibitors > D010726 - Phosphodiesterase Inhibitors D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D006133 - Growth Substances > D006131 - Growth Inhibitors D020011 - Protective Agents > D000975 - Antioxidants D000970 - Antineoplastic Agents
6-(2,4-Dichlorophenyl)-1,5-diazabicyclo[3.1.0]hexane
C10H10Cl2N2 (228.02210000000002)
3-(6-methyl-4-oxo-2-sulfanylidene-1H-pyrimidin-5-yl)propanoic acid methyl ester
8-Hydroxy-2-oxabicyclo[3.3.1]non-6-ene-3,5-dicarboxylic acid
(2E,4Z,6S)-6-ammonio-2-hydroxy-4-(2-oxoethylidene)hept-2-enedioate
4-chloro-N-[(Z)-1-hydrazinyl-2-nitroethenyl]aniline
C8H9ClN4O2 (228.04140040000001)
(Z)-3-(dihydroxymethylidene)-7-methyl-2,6-dioxooct-4-enoic acid
2-Oxo-3-(2,3,4,5-tetrahydroxyphenyl)propanoic acid
2-(2,3,5-Trihydroxy-4-methoxyphenyl)propanoic acid
N,N-Dimethyl-N-(2-(methylsulfonyl)pyrimidin-5-YL)formimidamide
(3R)-3-Hydroxy-3-methyl-5-(phosphonooxy)pentanoic acid
(3r)-5-Hydroxy-3-Methyl-3-(Phosphonooxy)pentanoic Acid
Serine phosphoethanolamine
The O-phosphoethanolamine derivative of serine.
2-Ammonio-3-{[(2-ammonioethoxy)phosphinato]oxy}propanoate
L-serine phosphoethanolamine dizwitterion
Zwitterionic form of L-serine phosphoethanolamine having anionic phosphate and carboxy groups and both amino groups protonated; major species at pH 7.3.
(R)-5-Phosphomevalonic acid
A carboxyalkyl phosphate that is mevalonic acid phosphorylated at position 5.
serine phosphoethanolamine dizwitterion
Dizwitterionic form of serine phosphoethanolamine having anionic carboxy and phosphate groups and both amino groups protonated.