Exact Mass: 242.0839

Exact Mass Matches: 242.0839

Found 210 metabolites which its exact mass value is equals to given mass value 242.0839, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Thymidine

1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione

C10H14N2O5 (242.0903)


Deoxythymidine, also known as 2-deoxy-5-methyluridine or 5-methyl-2-deoxyuridine, is a member of the class of 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. Deoxythymidine is soluble (in water) and a very weakly acidic compound (based on its pKa). Deoxythymidine can be synthesized from thymine. Deoxythymidine is also a parent compound for other transformation products, including but not limited to, tritiated thymidine, alpha-tritiated thymidine, and 5,6-dihydrothymidine. Deoxythymidine can be found in a number of food items such as butternut squash, mammee apple, catjang pea, and climbing bean, which makes deoxythymidine a potential biomarker for the consumption of these food products. Deoxythymidine can be found primarily in most biofluids, including blood, amniotic fluid, cerebrospinal fluid (CSF), and urine, as well as throughout most human tissues. Deoxythymidine exists in all living species, ranging from bacteria to humans. In humans, deoxythymidine is involved in the pyrimidine metabolism. Deoxythymidine is also involved in few metabolic disorders, which include beta ureidopropionase deficiency, dihydropyrimidinase deficiency, MNGIE (mitochondrial neurogastrointestinal encephalopathy), and UMP synthase deficiency (orotic aciduria). Moreover, deoxythymidine is found to be associated with canavan disease and degenerative disc disease. Thymidine (deoxythymidine; other names deoxyribosylthymine, thymine deoxyriboside) is a pyrimidine deoxynucleoside. Deoxythymidine is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA. In cell biology it is used to synchronize the cells in G1/early S phase . Thymidine, also known as deoxythymidine or deoxyribosylthymine or thymine deoxyriboside, is a pyrimidine deoxynucleoside. It consists of the nucleobase thymine attached to deoxyribose through a beta N- glycosidic bond. Thymidine also 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. Deoxythymidine (or thymidine) is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA. Therefore, thymidine is essential to all life. Indeed, thymidine exists in all living species, ranging from bacteria to plants to humans. Within humans, thymidine participates in a number of enzymatic reactions. In particular, thymidine can be biosynthesized from 5-thymidylic acid through its interaction with the enzyme cytosolic purine 5-nucleotidase. In addition, thymidine can be converted into 5-thymidylic acid; which is catalyzed by the enzyme thymidine kinase. Deoxythymidine can be phosphorylated with one, two or three phosphoric acid groups, creating dTMP (deoxythymidine monophosphate), dTDP, or dTTP (for the di- and tri- phosphates, respectively). dTMP can be incorporated into DNA via DNA polymerases. In cell biology, thymidine can be used to synchronize the cells in S phase. Derivatives of thymidine are used in a number of drugs, including Azidothymidine (AZT), which is used in the treatment of HIV infection. AZT inhibits the process of reverse transcription in the human immunodeficiency virus. Thymidine is a pyrimidine 2-deoxyribonucleoside having thymine as the nucleobase. It has a role as a metabolite, a human metabolite, an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a thymine. It is an enantiomer of a telbivudine. Thymidine is a pyrimidine deoxynucleoside. Thymidine is the DNA nucleoside T, which pairs with deoxyadenosine (A) in double-stranded DNA. In cell biology it is used to synchronize the cells in S phase. Thymidine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Thymidine is a natural product found in Fritillaria thunbergii, Saussurea medusa, and other organisms with data available. Thymidine is a pyrimidine nucleoside that is composed of the pyrimidine base thymine attached to the sugar deoxyribose. As a constituent of DNA, thymidine pairs with adenine in the DNA double helix. (NCI04) Thymidine is a metabolite found in or produced by Saccharomyces cerevisiae. A nucleoside in which THYMINE is linked to DEOXYRIBOSE. A pyrimidine 2-deoxyribonucleoside having thymine as the nucleobase. KEIO_ID T014; [MS2] KO009272 KEIO_ID T014 Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[1][2][3]. Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[1][2][3].

   

Lumichrome

7,8-dimethyl-1H,2H,3H,4H-benzo[g]pteridine-2,4-dione

C12H10N4O2 (242.0804)


Lumichrome, also known as light folinic acid or 7,8-dimethyl-10-ribitylisoalloxazine, is a derivative of riboflavin (vitamin B2). The chemical structure of lumichrome consists of a heterocyclic isoalloxazine ring, which is a fused pyridine and pyrazine ring system. The isoalloxazine ring contains a methyl group at the 7 and 8 positions and is substituted at the 10 position with a ribityl group, which is a 5-carbon chain derived from ribose with a methyl group at the 2’ position. Photocatalytic Activity: Lumichrome exhibits photocatalytic activity and can act as a photosensitizer. It can absorb light energy and transfer it to other molecules, potentially triggering photochemical reactions. Fluorescence: Lumichrome is known for its fluorescence properties. This characteristic makes it useful in various applications, including fluorescence microscopy and as a labeling agent in biological assays. Antioxidant Properties: Lumichrome has been found to have antioxidant properties. It can scavenge free radicals, which may help in protecting cells from oxidative stress. Metabolic Intermediate: In the body, lumichrome can be formed from riboflavin through photochemical or enzymatic degradation. It may play a role in the metabolism of flavins and could be involved in the recycling of flavin cofactors. Potential Biomarker: Due to its presence in biological tissues and its fluorescence properties, lumichrome has been proposed as a potential biomarker for certain diseases and conditions. Plant Pigment: In plants, lumichrome can be involved in light capture and energy transfer processes, although it is not a chlorophyll pigment. It may contribute to the overall light-harvesting capabilities of plant tissues. While lumichrome has several interesting chemical and biological properties, it is not considered an essential nutrient like its parent compound, riboflavin. Its exact role in biological systems is still an area of ongoing research. Lumichrome, a photodegradation product of Riboflavin, is an endogenous compound in humans. Lumichrome inhibits human lung cancer cell growth and induces apoptosis via a p53-dependent mechanism[1][2].

   

HC Yellow No. 4

2-[[2-(2-Hydroxyethoxy)-4-nitrophenyl]amino]-ethanol

C10H14N2O5 (242.0903)


   

gamma-L-Glutamyl-L-propargylglycine

gamma-L-Glutamyl-L-propargylglycine

C10H14N2O5 (242.0903)


   

Elenaic acid

2-[3-formyl-5-(methoxycarbonyl)-2-methyl-3,4-dihydro-2H-pyran-4-yl]acetic acid

C11H14O6 (242.079)


Isolated from olives (Olea europaea) leaves and fruits. Elenaic acid is found in many foods, some of which are herbs and spices, olive, fats and oils, and fruits. Elenaic acid is found in fats and oils. Elenaic acid is isolated from olives (Olea europaea) leaves and fruits.

   

Genipinic acid

2-{3-hydroxy-1H,3H,4H,5H,6H-cyclopenta[c]furan-4-yl}-3-methoxy-3-oxopropanoic acid

C11H14O6 (242.079)


Genipinic acid is found in beverages. Genipinic acid is isolated from the jagua fruit Genipa americana. Isolated from the jagua fruit Genipa americana. Genipinic acid is found in beverages and fruits.

   

Telbivudine

1-[(2S,4R,5S)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

C10H14N2O5 (242.0903)


Telbivudine is only found in individuals that have used or taken this drug. It is a synthetic thymidine nucleoside analog with specific activity against the hepatitis B virus. Telbivudine is orally administered, with good tolerance, lack of toxicity and no dose-limiting side effects.Telbivudine 5–triphosphate inhibits HBV DNA polymerase (reverse transcriptase) by competing with the natural substrate, thymidine 5–triphosphate. This leads to the chain termination of DNA synthesis, thereby inhibiting viral replication. Incorporation of telbivudine 5–triphosphate into viral DNA also causes DNA chain termination, resulting in inhibition of HBV replication. Telbivudine inhibits anticompliment or second-strand DNA. J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals > J05AF - Nucleoside and nucleotide reverse transcriptase inhibitors C471 - Enzyme Inhibitor > C1589 - Reverse Transcriptase Inhibitor > C97452 - Nucleoside Reverse Transcriptase Inhibitor D004791 - Enzyme Inhibitors > D019384 - Nucleic Acid Synthesis Inhibitors D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C254 - Anti-Infective Agent > C281 - Antiviral Agent Telbivudine (Epavudine), an orally active thymidine nucleoside analog, is a potent antiviral inhibitor of hepatitis B virus (HBV) replication[1].

   

1-Pyrenyldiazomethane

1-(diazomethyl)pyrene

C17H10N2 (242.0844)


   

L-Thymidine

4-hydroxy-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-1,2-dihydropyrimidin-2-one

C10H14N2O5 (242.0903)


Isolated from seedlings of Phaseolus vulgaris (kidney bean)

   

alpha-Gardiol

(+)-alpha-Gardiol

C11H14O6 (242.079)


   

(+)-Butalactin

(+)-Butalactin

C11H14O6 (242.079)


   

Tetillapyrone

Tetillapyrone

C11H14O6 (242.079)


   

1,3-Dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-one

1,3-Dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-one

C11H14O6 (242.079)


   

2,3,4-Trihydroxy-3,5-dimethoxypropiophene

2,3-Dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone;

C11H14O6 (242.079)


   
   

Methyl syramuraldehydate

Methyl syramuraldehydate

C11H14O6 (242.079)


   

2-(2-Cyanoacetyl)-N-(tetrahydrofuran-2-ylmethyl)hydrazine-1-carbothioamide

2-(2-Cyanoacetyl)-N-(tetrahydrofuran-2-ylmethyl)hydrazine-1-carbothioamide

C9H14N4O2S (242.0837)


   

5-Methyl-3-deoxyuridine

5-Methyl-3-deoxyuridine

C10H14N2O5 (242.0903)


   

Gardenogenin A

Gardenogenin A

C11H14O6 (242.079)


   

(2S,3S,4S,7S,E)-3,4,7-trihydroxy-7-methyl-2-(prop-1-enyl)-3,4-dihydro-2H-furo[3,4-b]pyran-5(7H)-one|massarilactone D

(2S,3S,4S,7S,E)-3,4,7-trihydroxy-7-methyl-2-(prop-1-enyl)-3,4-dihydro-2H-furo[3,4-b]pyran-5(7H)-one|massarilactone D

C11H14O6 (242.079)


   

Pedatisectine A

Pedatisectine A

C11H10N6O (242.0916)


   

Gloiosiphone A

Gloiosiphone A

C11H14O6 (242.079)


   

Aglucone-Kingiside

Aglucone-Kingiside

C11H14O6 (242.079)


   

Lamiophlomiol B

Lamiophlomiol B

C11H14O6 (242.079)


   

8-hydroxy-3-methyl-2-oxo-2,3,4a,5,8,8a-hexahydro-benzo[1,4]dioxine-6-carboxylic acid methyl ester

8-hydroxy-3-methyl-2-oxo-2,3,4a,5,8,8a-hexahydro-benzo[1,4]dioxine-6-carboxylic acid methyl ester

C11H14O6 (242.079)


   

2,3-Dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one

2,3-Dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one

C11H14O6 (242.079)


   
   

dihydro-4-[4,5-epoxy-1-oxohex-2-enyloxymethyl]-3-hydroxy-2(3H)-furanone

dihydro-4-[4,5-epoxy-1-oxohex-2-enyloxymethyl]-3-hydroxy-2(3H)-furanone

C11H14O6 (242.079)


   

1-o-(2,4-dihydroxy-6-methylbenzoyl)-glycerol

1-o-(2,4-dihydroxy-6-methylbenzoyl)-glycerol

C11H14O6 (242.079)


   

lucknolide B

lucknolide B

C11H14O6 (242.079)


   

2,3,4,5-Tetramethoxybenzoic acid

2,3,4,5-Tetramethoxybenzoic acid

C11H14O6 (242.079)


   

9-hydroxygenipin|genipaol

9-hydroxygenipin|genipaol

C11H14O6 (242.079)


   

1,3-Dimethoxy-7-methyl-1,3-dihydroisobenzofuran-4,5,6-triol

1,3-Dimethoxy-7-methyl-1,3-dihydroisobenzofuran-4,5,6-triol

C11H14O6 (242.079)


   

1-O-(2,4-dihydroxy)phenylacetyl glycerol

1-O-(2,4-dihydroxy)phenylacetyl glycerol

C11H14O6 (242.079)


   

2,4-dioxo-cyclopentane-1,3-dicarboxylic acid diethyl ester

2,4-dioxo-cyclopentane-1,3-dicarboxylic acid diethyl ester

C11H14O6 (242.079)


   

Zhijiangjunsu

Zhijiangjunsu

C11H14O6 (242.079)


   

Thymidine

Thymidine

C10H14N2O5 (242.0903)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.220 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.211 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.213 Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[1][2][3]. Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication[1][2][3].

   

C11H14O6_3,4,7-Trihydroxy-7-methyl-2-[(1E)-1-propen-1-yl]-2,3,4,7-tetrahydro-5H-furo[3,4-b]pyran-5-one

NCGC00380928-01_C11H14O6_3,4,7-Trihydroxy-7-methyl-2-[(1E)-1-propen-1-yl]-2,3,4,7-tetrahydro-5H-furo[3,4-b]pyran-5-one

C11H14O6 (242.079)


   

7,8-dimethylalloxazine (lumichrome)

7,8-dimethylalloxazine (lumichrome)

C12H10N4O2 (242.0804)


   

Lumichrome

Lumichrome

C12H10N4O2 (242.0804)


A compound showing blue fluorescence, formed by a photolysis of riboflavin in acid or neutral solution. Lumichrome, a photodegradation product of Riboflavin, is an endogenous compound in humans. Lumichrome inhibits human lung cancer cell growth and induces apoptosis via a p53-dependent mechanism[1][2].

   

Thymidine; LC-tDDA; CE10

Thymidine; LC-tDDA; CE10

C10H14N2O5 (242.0903)


   

Thymidine; LC-tDDA; CE40

Thymidine; LC-tDDA; CE40

C10H14N2O5 (242.0903)


   

Thymidine; LC-tDDA; CE20

Thymidine; LC-tDDA; CE20

C10H14N2O5 (242.0903)


   

Thymidine; AIF; CE0; MS2Dec

Thymidine; AIF; CE0; MS2Dec

C10H14N2O5 (242.0903)


   

Thymidine; AIF; CE10; MS2Dec

Thymidine; AIF; CE10; MS2Dec

C10H14N2O5 (242.0903)


   

Thymidine; AIF; CE30; MS2Dec

Thymidine; AIF; CE30; MS2Dec

C10H14N2O5 (242.0903)


   

Thymidine; LC-tDDA; CE30

Thymidine; LC-tDDA; CE30

C10H14N2O5 (242.0903)


   

Epavudine

1-[(2S,4R,5S)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

C10H14N2O5 (242.0903)


J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals > J05AF - Nucleoside and nucleotide reverse transcriptase inhibitors C471 - Enzyme Inhibitor > C1589 - Reverse Transcriptase Inhibitor > C97452 - Nucleoside Reverse Transcriptase Inhibitor D004791 - Enzyme Inhibitors > D019384 - Nucleic Acid Synthesis Inhibitors D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C254 - Anti-Infective Agent > C281 - Antiviral Agent Telbivudine (Epavudine), an orally active thymidine nucleoside analog, is a potent antiviral inhibitor of hepatitis B virus (HBV) replication[1].

   

Genipinic acid

2-{3-hydroxy-1H,3H,4H,5H,6H-cyclopenta[c]furan-4-yl}-3-methoxy-3-oxopropanoic acid

C11H14O6 (242.079)


   

ELENAIC ACID

2-[3-formyl-5-(methoxycarbonyl)-2-methyl-3,4-dihydro-2H-pyran-4-yl]acetic acid

C11H14O6 (242.079)


   

4-(difluoromethoxy)-3-(cyclopropylmethoxy)-benzaldethyde

4-(difluoromethoxy)-3-(cyclopropylmethoxy)-benzaldethyde

C12H12F2O3 (242.0754)


   

allyldiphenylphosphine oxide

allyldiphenylphosphine oxide

C15H15OP (242.086)


   

2-(dimethylamino)ethyl 3-amino-4-chlorobenzoate

2-(dimethylamino)ethyl 3-amino-4-chlorobenzoate

C11H15ClN2O2 (242.0822)


   

3,4,5-TRIMETHOXYPHENYLGLYOXAL HYDRATE

3,4,5-TRIMETHOXYPHENYLGLYOXAL HYDRATE

C11H14O6 (242.079)


   

(1-Fluorovinyl)(methyl)diphenylsilane

(1-Fluorovinyl)(methyl)diphenylsilane

C15H15FSi (242.0927)


   

disperse orange 3

disperse orange 3

C12H10N4O2 (242.0804)


D004396 - Coloring Agents

   

TERT-BUTYL (4-(CHLOROMETHYL)PYRIDIN-2-YL)CARBAMATE

TERT-BUTYL (4-(CHLOROMETHYL)PYRIDIN-2-YL)CARBAMATE

C11H15ClN2O2 (242.0822)


   

(6-CHLOROMETHYL-PYRIDIN-3-YL)-CARBAMIC ACID TERT-BUTYL ESTER

(6-CHLOROMETHYL-PYRIDIN-3-YL)-CARBAMIC ACID TERT-BUTYL ESTER

C11H15ClN2O2 (242.0822)


   

2-Amino-4-(4-ethylphenyl)-5-methylthiophene-3-carbonitrile

2-Amino-4-(4-ethylphenyl)-5-methylthiophene-3-carbonitrile

C14H14N2S (242.0878)


   

2-Amino-4-(3,4-dimethylphenyl)-5-methylthiophene-3-carbonitrile

2-Amino-4-(3,4-dimethylphenyl)-5-methylthiophene-3-carbonitrile

C14H14N2S (242.0878)


   

tert-butyl N-(3-amino-4-chlorophenyl)carbamate

tert-butyl N-(3-amino-4-chlorophenyl)carbamate

C11H15ClN2O2 (242.0822)


   

tert-Butyl 2-chloro-5-methylpyridin-3-ylcarbamate

tert-Butyl 2-chloro-5-methylpyridin-3-ylcarbamate

C11H15ClN2O2 (242.0822)


   

1-(BENZO[D][1,3]DIOXOL-4-YL)PIPERAZINE HYDROCHLORIDE

1-(BENZO[D][1,3]DIOXOL-4-YL)PIPERAZINE HYDROCHLORIDE

C11H15ClN2O2 (242.0822)


   

6-(3,5-difluorophenyl)-6-oxohexanoic acid

6-(3,5-difluorophenyl)-6-oxohexanoic acid

C12H12F2O3 (242.0754)


   

N-butyl-2-chloro-N-methyl-4-nitroaniline

N-butyl-2-chloro-N-methyl-4-nitroaniline

C11H15ClN2O2 (242.0822)


   

5-(3-methoxyphenyl)-1H-[1,2,4]triazolo[1,5-a]pyrimidin-7-one

5-(3-methoxyphenyl)-1H-[1,2,4]triazolo[1,5-a]pyrimidin-7-one

C12H10N4O2 (242.0804)


   

Phosphonic acid,(chloromethyl)-, dibutyl ester (6CI,7CI,8CI,9CI)

Phosphonic acid,(chloromethyl)-, dibutyl ester (6CI,7CI,8CI,9CI)

C9H20ClO3P (242.0839)


   

1-(4-FLUORO-PHENYL)-2-METHYL-PROPAN-2-OL

1-(4-FLUORO-PHENYL)-2-METHYL-PROPAN-2-OL

C15H11FO2 (242.0743)


   

2-[bis(2-hydroxyethyl)amino]-5-nitrophenol

2-[bis(2-hydroxyethyl)amino]-5-nitrophenol

C10H14N2O5 (242.0903)


   

3-BENZYL-1H-PURINE-2,6(3H,7H)-DIONE

3-BENZYL-1H-PURINE-2,6(3H,7H)-DIONE

C12H10N4O2 (242.0804)


   

Di-tert-butyl chloromethylphosphonate

Di-tert-butyl chloromethylphosphonate

C9H20ClO3P (242.0839)


   

4,4,4-TRIFLUORO-2-(2-METHOXYETHYL)-3-OXOBUTYRIC ACID ETHYL ESTER

4,4,4-TRIFLUORO-2-(2-METHOXYETHYL)-3-OXOBUTYRIC ACID ETHYL ESTER

C9H13F3O4 (242.0766)


   

1,1-BIS-(4-FLUOROPHENYL)-BUTA-1,3-DIENE

1,1-BIS-(4-FLUOROPHENYL)-BUTA-1,3-DIENE

C16H12F2 (242.0907)


   

4-(4-Nitrophenyl)piperidine hydrochloride (1:1)

4-(4-Nitrophenyl)piperidine hydrochloride (1:1)

C11H15ClN2O2 (242.0822)


   

1,3-Cyclopentanedicarboxylicacid, 4,5-dioxo-, 1,3-diethyl ester

1,3-Cyclopentanedicarboxylicacid, 4,5-dioxo-, 1,3-diethyl ester

C11H14O6 (242.079)


   

3-benzyl-4-fluoro-1,2-dihydroindazol-6-one

3-benzyl-4-fluoro-1,2-dihydroindazol-6-one

C14H11FN2O (242.0855)


   

4-(Benzyloxy)-6-fluoro-1H-indazole

4-(Benzyloxy)-6-fluoro-1H-indazole

C14H11FN2O (242.0855)


   

methyl 2-fluoro-9H-fluorene-9-carboxylate

methyl 2-fluoro-9H-fluorene-9-carboxylate

C15H11FO2 (242.0743)


   

HC YELLOW NO. 11

HC YELLOW NO. 11

C10H14N2O5 (242.0903)


   

BOC-Oxyma Ethyl 2-(tert-Butoxycarbonyloxyimino)-2-cyanoacetate

BOC-Oxyma Ethyl 2-(tert-Butoxycarbonyloxyimino)-2-cyanoacetate

C10H14N2O5 (242.0903)


   

4-(Pyridin-2-yl)Aminocarbonylphenylboronic Acid

4-(Pyridin-2-yl)Aminocarbonylphenylboronic Acid

C12H11BN2O3 (242.0863)


   

H-Lys(Tfa)-OH

N6-(Trifluoroacetyl)-L-lysine

C8H13F3N2O3 (242.0878)


   

3-Allyl-6-bromo-2-chloropyridine

3-Allyl-6-bromo-2-chloropyridine

C11H15ClN2O2 (242.0822)


   

ethyl 4-tert-butyl-2-chloropyrimidine-5-carboxylate

ethyl 4-tert-butyl-2-chloropyrimidine-5-carboxylate

C11H15ClN2O2 (242.0822)


   

3-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-one

3-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-one

C14H11FN2O (242.0855)


   

4-nitro-N-(pyridin-2-ylmethylideneamino)aniline

4-nitro-N-(pyridin-2-ylmethylideneamino)aniline

C12H10N4O2 (242.0804)


   

1,1-diethylferrocene

1,1-diethylferrocene

C14H18Fe (242.0758)


   

(5ALPHA,6ALPHA)-7,8-DIDEHYDRO-4,5-EPOXY-17-METHYLMORPHINAN-3,6-DIYLBISPYRIDINE-3-CARBOXYLATEHYDROCHLORIDE

(5ALPHA,6ALPHA)-7,8-DIDEHYDRO-4,5-EPOXY-17-METHYLMORPHINAN-3,6-DIYLBISPYRIDINE-3-CARBOXYLATEHYDROCHLORIDE

C11H15ClN2O2 (242.0822)


   

3-Amino-2-phenyl-2H-pyrazolo[4,3-c]pyridine-4,6-diol

4H-Pyrazolo[4,3-c]pyridin-4-one,3-amino-2,5-dihydro-6-hydroxy-2-phenyl-

C12H10N4O2 (242.0804)


   

(4-(ISOBUTYLSULFONYL)PHENYL)BORONIC ACID

(4-(ISOBUTYLSULFONYL)PHENYL)BORONIC ACID

C10H15BO4S (242.0784)


   

(4-(BUTYLSULFONYL)PHENYL)BORONIC ACID

(4-(BUTYLSULFONYL)PHENYL)BORONIC ACID

C10H15BO4S (242.0784)


   

2-(Cyclopentyloxy)-2-phenylacetic acid, sodium salt

2-(Cyclopentyloxy)-2-phenylacetic acid, sodium salt

C13H15NaO3 (242.0919)


   

ETHYL5-CYANO-1-(PYRIDIN-2-YL)-1H-PYRAZOLE-4-CARBOXYLATE

ETHYL5-CYANO-1-(PYRIDIN-2-YL)-1H-PYRAZOLE-4-CARBOXYLATE

C12H10N4O2 (242.0804)


   

ETHYL5-CYANO-1-(PYRIDIN-4-YL)-1H-PYRAZOLE-4-CARBOXYLATE

ETHYL5-CYANO-1-(PYRIDIN-4-YL)-1H-PYRAZOLE-4-CARBOXYLATE

C12H10N4O2 (242.0804)


   

Thiourea,N-phenyl-N-(phenylmethyl)-

Thiourea,N-phenyl-N-(phenylmethyl)-

C14H14N2S (242.0878)


   

tert-Butylferrocene

tert-Butylferrocene

C14H18Fe (242.0758)


   

N-(PIPERIDIN-3-YL)PYRAZINE-2-CARBOXAMIDE HYDROCHLORIDE

N-(PIPERIDIN-3-YL)PYRAZINE-2-CARBOXAMIDE HYDROCHLORIDE

C10H15ClN4O (242.0934)


   

3-[3-(methylamino)-4-nitrophenoxy]propane-1,2-diol

3-[3-(methylamino)-4-nitrophenoxy]propane-1,2-diol

C10H14N2O5 (242.0903)


   

6-(2,5-Difluorophenyl)-6-oxohexanoic acid

6-(2,5-Difluorophenyl)-6-oxohexanoic acid

C12H12F2O3 (242.0754)


   

Butylferrocene

Butylferrocene

C14H18Fe (242.0758)


   

3-(2-Chloroethyl)-6,7,8,9-tetrahydro-9-hydroxy-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one

3-(2-Chloroethyl)-6,7,8,9-tetrahydro-9-hydroxy-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one

C11H15ClN2O2 (242.0822)


   

tert-Butyl (2-amino-3-chlorophenyl)carbamate

tert-Butyl (2-amino-3-chlorophenyl)carbamate

C11H15ClN2O2 (242.0822)


   

tert-butyl N-[5-(chloromethyl)pyridin-2-yl]carbamate

tert-butyl N-[5-(chloromethyl)pyridin-2-yl]carbamate

C11H15ClN2O2 (242.0822)


   

thymidine, [2-14c]

thymidine, [2-14c]

C10H14N2O5 (242.0903)


   

2-chloro-5-methoxy-N-piperidin-4-ylpyrimidin-4-amine

2-chloro-5-methoxy-N-piperidin-4-ylpyrimidin-4-amine

C10H15ClN4O (242.0934)


   

ETHYL 5,6,7,8-TETRAHYDRO-1,7-NAPHTHYRIDINE-3-CARBOXYLATE HYDROCHLORIDE

ETHYL 5,6,7,8-TETRAHYDRO-1,7-NAPHTHYRIDINE-3-CARBOXYLATE HYDROCHLORIDE

C11H15ClN2O2 (242.0822)


   

2-Methyl-2-propanyl [(2-chloro-4-pyridinyl)methyl]carbamate

2-Methyl-2-propanyl [(2-chloro-4-pyridinyl)methyl]carbamate

C11H15ClN2O2 (242.0822)


   
   

DIPHENYLMETHANETHIOL ACETATE

DIPHENYLMETHANETHIOL ACETATE

C15H14OS (242.0765)


   

3-(1-Methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-5-carboxyl ic acid

3-(1-Methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-5-carboxyl ic acid

C12H10N4O2 (242.0804)


   

(4-fluorophenyl)-(3-phenyloxiran-2-yl)methanone

(4-fluorophenyl)-(3-phenyloxiran-2-yl)methanone

C15H11FO2 (242.0743)


   

iproclozide

iproclozide

C11H15ClN2O2 (242.0822)


N - Nervous system > N06 - Psychoanaleptics > N06A - Antidepressants > N06AF - Monoamine oxidase inhibitors, non-selective C78272 - Agent Affecting Nervous System > C265 - Antidepressant Agent C471 - Enzyme Inhibitor > C667 - Monoamine Oxidase Inhibitor

   

2,2-Biphenyldiyldiboronic acid

2,2-Biphenyldiyldiboronic acid

C12H12B2O4 (242.0922)


   

Carbamic acid, (2-chloro-4-pyridinyl)Methyl-, 1,1-dimethylethyl ester (9CI)

Carbamic acid, (2-chloro-4-pyridinyl)Methyl-, 1,1-dimethylethyl ester (9CI)

C11H15ClN2O2 (242.0822)


   

Isobutyl 3,5-diamino-4-chloro benzoate

Isobutyl 3,5-diamino-4-chloro benzoate

C11H15ClN2O2 (242.0822)


   

Thiourea,N-(diphenylmethyl)-

Thiourea,N-(diphenylmethyl)-

C14H14N2S (242.0878)


   

PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE

PHENYL 2-(TRIMETHYLSILYL)ETHYL SULFONE

C11H18O2SSi (242.0797)


   

1-[4-Hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione

2,4(1H,3H)-Pyrimidinedione,1-(2-deoxy-b-D-threo-pentofuranosyl)-5-methyl-

C10H14N2O5 (242.0903)


1-(2-Deoxy-β-D-threo-pentofuranosyl)thymine is a thymidine analog. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis[1].

   

5-Methyl-1-β-L-ribofuranosyl-2,4(1H,3H)-pyrimidinedione

5-Methyl-1-β-L-ribofuranosyl-2,4(1H,3H)-pyrimidinedione

C10H14N2O5 (242.0903)


   

1-(4-Fluorophenyl)-1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinecarbonitrile

1-(4-Fluorophenyl)-1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinecarbonitrile

C14H11FN2O (242.0855)


   

ethyl 2-[(3,4-difluorophenyl)hydrazinylidene]propanoate

ethyl 2-[(3,4-difluorophenyl)hydrazinylidene]propanoate

C11H12F2N2O2 (242.0867)


   

3-Deoxy-3-methyluridine

3-Deoxy-3-methyluridine

C10H14N2O5 (242.0903)


   

3-Cyclobutoxy-4-difluoromethoxy-benzaldehyde

3-Cyclobutoxy-4-difluoromethoxy-benzaldehyde

C12H12F2O3 (242.0754)


   

2-PHENYL-2-TRIFLUOROMETHYLCYCLOHEXANONE

2-PHENYL-2-TRIFLUOROMETHYLCYCLOHEXANONE

C13H13F3O (242.0918)


   

4,4-Biphenyldiboronic acid

4,4′-biphenyldiboronic acid

C12H12B2O4 (242.0922)


   

4-borono-[1,1-biphenyl]-4-carboxylic acid

4-borono-[1,1-biphenyl]-4-carboxylic acid

C13H11BO4 (242.075)


   

Trans-4-(3,4,5-trifluorophenyl)cyclohexanecarbaldehyde

Trans-4-(3,4,5-trifluorophenyl)cyclohexanecarbaldehyde

C13H13F3O (242.0918)


   

6-(Benzyloxy)-4-fluoro-1H-indazole

6-(Benzyloxy)-4-fluoro-1H-indazole

C14H11FN2O (242.0855)


   

2-(1H-INDOL-3-YL)-2-THIEN-2-YLETHANAMINE

2-(1H-INDOL-3-YL)-2-THIEN-2-YLETHANAMINE

C14H14N2S (242.0878)


   

ALPHA-THYMIDINE

ALPHA-THYMIDINE

C10H14N2O5 (242.0903)


   

N,N-dipyridin-2-yloxamide

N,N-dipyridin-2-yloxamide

C12H10N4O2 (242.0804)


   

1-(Pyridin-4-yl)piperidine-4-carboxylic acid hydrochloride

1-(Pyridin-4-yl)piperidine-4-carboxylic acid hydrochloride

C11H15ClN2O2 (242.0822)


   

1-[(3,4-DIFLUOROPHENYL)ETHYNYL]-4-ETHYLBENZENE

1-[(3,4-DIFLUOROPHENYL)ETHYNYL]-4-ETHYLBENZENE

C16H12F2 (242.0907)


   

2-((TERT-BUTOXYCARBONYLAMINO)METHYL)OXAZOLE-4-CARBOXYLIC ACID

2-((TERT-BUTOXYCARBONYLAMINO)METHYL)OXAZOLE-4-CARBOXYLIC ACID

C10H14N2O5 (242.0903)


   

1,2-Diisonicotinoylhydrazine

1,2-Diisonicotinoylhydrazine

C12H10N4O2 (242.0804)


   

1-Triazene,3-(4-nitrophenyl)-1-phenyl-

1-Triazene,3-(4-nitrophenyl)-1-phenyl-

C12H10N4O2 (242.0804)


   

TERT-BUTYL ((6-CHLOROPYRIDIN-3-YL)METHYL)CARBAMATE

TERT-BUTYL ((6-CHLOROPYRIDIN-3-YL)METHYL)CARBAMATE

C11H15ClN2O2 (242.0822)


   

5-Pyrimidinecarboxamide, 4-amino-2-(ethylthio)-N-Methoxy-N-Methyl-

5-Pyrimidinecarboxamide, 4-amino-2-(ethylthio)-N-Methoxy-N-Methyl-

C9H14N4O2S (242.0837)


   

2-(2-Benzoxazolylamino)-6-methylpyrimidin-4(3H)-one

2-(2-Benzoxazolylamino)-6-methylpyrimidin-4(3H)-one

C12H10N4O2 (242.0804)


   

tert-butyl 3,5-difluoro-4-formylbenzoate

tert-butyl 3,5-difluoro-4-formylbenzoate

C12H12F2O3 (242.0754)


   

S-8510 free base

S-8510 free base

C12H10N4O2 (242.0804)


   

3-Deazacytidine

3-Deazacytidine

C10H14N2O5 (242.0903)


   

5-Methyl-2-deoxypseudouridine

5-Methyl-2-deoxypseudouridine

C10H14N2O5 (242.0903)


   
   

1-beta-Ribofuranosyl-1,3-diazepinone

1-beta-Ribofuranosyl-1,3-diazepinone

C10H14N2O5 (242.0903)


   

Telbivudine

Telbivudine

C10H14N2O5 (242.0903)


J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals > J05AF - Nucleoside and nucleotide reverse transcriptase inhibitors C471 - Enzyme Inhibitor > C1589 - Reverse Transcriptase Inhibitor > C97452 - Nucleoside Reverse Transcriptase Inhibitor D004791 - Enzyme Inhibitors > D019384 - Nucleic Acid Synthesis Inhibitors D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C254 - Anti-Infective Agent > C281 - Antiviral Agent Telbivudine (Epavudine), an orally active thymidine nucleoside analog, is a potent antiviral inhibitor of hepatitis B virus (HBV) replication[1].

   

Elenolic acid

Elenolic acid

C11H14O6 (242.079)


   

Thymidine-methyl-T

Thymidine-methyl-T

C10H14N2O5 (242.0903)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

N-(4-fluorobenzylidene)benzohydrazide

N-(4-fluorobenzylidene)benzohydrazide

C14H11FN2O (242.0855)


   

3,4,7-trihydroxy-7-methyl-2-[(E)-prop-1-enyl]-3,4-dihydro-2H-furo[3,4-b]pyran-5-one

3,4,7-trihydroxy-7-methyl-2-[(E)-prop-1-enyl]-3,4-dihydro-2H-furo[3,4-b]pyran-5-one

C11H14O6 (242.079)


   

methyl [(2S)-4-butanoyl-3-hydroxy-5-oxo-2,5-dihydrofuran-2-yl]acetate

methyl [(2S)-4-butanoyl-3-hydroxy-5-oxo-2,5-dihydrofuran-2-yl]acetate

C11H14O6 (242.079)


   

4-Hydroxy-5-(3,4,5-trihydroxyphenyl)pentanoic acid

4-Hydroxy-5-(3,4,5-trihydroxyphenyl)pentanoic acid

C11H14O6 (242.079)


   

2-Hydroxyethyl 4-hydroxy-3,5-dimethoxybenzoate

2-Hydroxyethyl 4-hydroxy-3,5-dimethoxybenzoate

C11H14O6 (242.079)


   

(2S)-2-azaniumyl-5-[[(1S)-1-carboxylato-2-cyanoethyl]amino]-5-oxopentanoate

(2S)-2-azaniumyl-5-[[(1S)-1-carboxylato-2-cyanoethyl]amino]-5-oxopentanoate

C9H12N3O5- (242.0777)


   

4-Hydroxy-5-(2,4,5-trihydroxyphenyl)pentanoic acid

4-Hydroxy-5-(2,4,5-trihydroxyphenyl)pentanoic acid

C11H14O6 (242.079)


   

N,O-Di(2-hydroxyethyl)-2-amino-5-nitrophenol

2-((2-(2-Hydroxyethoxy)-4-nitrophenyl)amino)ethanol

C10H14N2O5 (242.0903)


   

7,8-dimethylisoalloxazine

7,8-dimethylisoalloxazine

C12H10N4O2 (242.0804)


A 7,8-dimethylbenzo[g]pteridine-2,4-dione that is isoalloxazine substituted by methyl groups at positions 7 and 8.

   

methyl (1s,4r,7s,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,4r,7s,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

methyl (1r,4r,7s,8s,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1r,4r,7s,8s,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

methyl (1s,4r,7s,8s,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,4r,7s,8s,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

6-hydroxy-5-[(2s,4r,5s)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3-methylpyran-2-one

6-hydroxy-5-[(2s,4r,5s)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3-methylpyran-2-one

C11H14O6 (242.079)


   

(1s,3s,4s,7r,10s,11s)-3-hydroxy-10-(hydroxymethyl)-10-methoxy-2,9-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-en-8-one

(1s,3s,4s,7r,10s,11s)-3-hydroxy-10-(hydroxymethyl)-10-methoxy-2,9-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-en-8-one

C11H14O6 (242.079)


   

methyl (1r,4ar,7ar)-1,7a-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h-cyclopenta[c]pyran-4-carboxylate

methyl (1r,4ar,7ar)-1,7a-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h-cyclopenta[c]pyran-4-carboxylate

C11H14O6 (242.079)


   

[(3s,4s)-4-hydroxy-5-oxooxolan-3-yl]methyl (2e)-3-[(2r,3s)-3-methyloxiran-2-yl]prop-2-enoate

[(3s,4s)-4-hydroxy-5-oxooxolan-3-yl]methyl (2e)-3-[(2r,3s)-3-methyloxiran-2-yl]prop-2-enoate

C11H14O6 (242.079)


   

methyl (1r,4r,7s,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1r,4r,7s,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

methyl (3r,4as,8r,8as)-8-hydroxy-3-methyl-2-oxo-4a,5,8,8a-tetrahydro-3h-1,4-benzodioxine-6-carboxylate

methyl (3r,4as,8r,8as)-8-hydroxy-3-methyl-2-oxo-4a,5,8,8a-tetrahydro-3h-1,4-benzodioxine-6-carboxylate

C11H14O6 (242.079)


   

methyl (3s,4ar,8s,8ar)-8-hydroxy-3-methyl-2-oxo-4a,5,8,8a-tetrahydro-3h-1,4-benzodioxine-6-carboxylate

methyl (3s,4ar,8s,8ar)-8-hydroxy-3-methyl-2-oxo-4a,5,8,8a-tetrahydro-3h-1,4-benzodioxine-6-carboxylate

C11H14O6 (242.079)


   

methyl 1-hydroxy-8-methyl-6-oxo-1h,4ah,5h,8h,8ah-pyrano[3,4-c]pyran-4-carboxylate

methyl 1-hydroxy-8-methyl-6-oxo-1h,4ah,5h,8h,8ah-pyrano[3,4-c]pyran-4-carboxylate

C11H14O6 (242.079)


   

[(3r,4r,5r)-3,4,5-trihydroxy-6-oxocyclohex-1-en-1-yl]methyl (2e)-but-2-enoate

[(3r,4r,5r)-3,4,5-trihydroxy-6-oxocyclohex-1-en-1-yl]methyl (2e)-but-2-enoate

C11H14O6 (242.079)


   

methyl (1s,4as,8s,8as)-1-hydroxy-8-methyl-6-oxo-1h,4ah,5h,8h,8ah-pyrano[3,4-c]pyran-4-carboxylate

methyl (1s,4as,8s,8as)-1-hydroxy-8-methyl-6-oxo-1h,4ah,5h,8h,8ah-pyrano[3,4-c]pyran-4-carboxylate

C11H14O6 (242.079)


   

3-hydroxy-10-(hydroxymethyl)-10-methoxy-2,9-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-en-8-one

3-hydroxy-10-(hydroxymethyl)-10-methoxy-2,9-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-en-8-one

C11H14O6 (242.079)


   

1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3-methylpyrimidine-2,4-dione

1-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3-methylpyrimidine-2,4-dione

C10H14N2O5 (242.0903)


   

3,4,7-trihydroxy-7-methyl-2-(prop-1-en-1-yl)-2h,3h,4h-furo[3,4-b]pyran-5-one

3,4,7-trihydroxy-7-methyl-2-(prop-1-en-1-yl)-2h,3h,4h-furo[3,4-b]pyran-5-one

C11H14O6 (242.079)


   

methyl 4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl 4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

methyl (1s,7s,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,7s,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

(2s)-2,3-dihydroxypropyl 2,4-dihydroxy-6-methylbenzoate

(2s)-2,3-dihydroxypropyl 2,4-dihydroxy-6-methylbenzoate

C11H14O6 (242.079)


   

methyl (1s,4s,7s,8s,9r,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,4s,7s,8s,9r,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

[(3s,4s)-4-hydroxy-5-oxooxolan-3-yl]methyl (2e)-3-[(2s,3r)-3-methyloxiran-2-yl]prop-2-enoate

[(3s,4s)-4-hydroxy-5-oxooxolan-3-yl]methyl (2e)-3-[(2s,3r)-3-methyloxiran-2-yl]prop-2-enoate

C11H14O6 (242.079)


   

(acetyloxy)[(3s,4r)-3-hydroxy-1h,3h,4h,5h,6h-cyclopenta[c]furan-4-yl]acetic acid

(acetyloxy)[(3s,4r)-3-hydroxy-1h,3h,4h,5h,6h-cyclopenta[c]furan-4-yl]acetic acid

C11H14O6 (242.079)


   

(2s)-2,3-dihydroxypropyl 2-(2,4-dihydroxyphenyl)acetate

(2s)-2,3-dihydroxypropyl 2-(2,4-dihydroxyphenyl)acetate

C11H14O6 (242.079)


   

(3s,4r)-3-hydroxy-4-(hydroxymethyl)-3-[(2e)-3-(3-methyloxiran-2-yl)prop-2-enoyl]oxolan-2-one

(3s,4r)-3-hydroxy-4-(hydroxymethyl)-3-[(2e)-3-(3-methyloxiran-2-yl)prop-2-enoyl]oxolan-2-one

C11H14O6 (242.079)


   

6-hydroxy-5-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3-methylpyran-2-one

6-hydroxy-5-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3-methylpyran-2-one

C11H14O6 (242.079)


   

methyl (4as,8s,8as)-1-hydroxy-8-methyl-6-oxo-1h,4ah,5h,8h,8ah-pyrano[3,4-c]pyran-4-carboxylate

methyl (4as,8s,8as)-1-hydroxy-8-methyl-6-oxo-1h,4ah,5h,8h,8ah-pyrano[3,4-c]pyran-4-carboxylate

C11H14O6 (242.079)


   

methyl (1r,4r,7r,8s,9r,11r)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1r,4r,7r,8s,9r,11r)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

1,3-dihydroxypropan-2-yl 2,4-dihydroxy-6-methylbenzoate

1,3-dihydroxypropan-2-yl 2,4-dihydroxy-6-methylbenzoate

C11H14O6 (242.079)


   

(2s,3r,4s,7s)-3,4,7-trihydroxy-7-methyl-2-[(1e)-prop-1-en-1-yl]-2h,3h,4h-furo[3,4-b]pyran-5-one

(2s,3r,4s,7s)-3,4,7-trihydroxy-7-methyl-2-[(1e)-prop-1-en-1-yl]-2h,3h,4h-furo[3,4-b]pyran-5-one

C11H14O6 (242.079)


   

methyl 1,7a-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h-cyclopenta[c]pyran-4-carboxylate

methyl 1,7a-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h-cyclopenta[c]pyran-4-carboxylate

C11H14O6 (242.079)


   

methyl (1s,2r,4s,5s,6s,10r)-5,10-dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate

methyl (1s,2r,4s,5s,6s,10r)-5,10-dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate

C11H14O6 (242.079)


   

2,3,6-trihydroxy-6-(methoxymethyl)spiro[4.4]non-2-ene-1,7-dione

2,3,6-trihydroxy-6-(methoxymethyl)spiro[4.4]non-2-ene-1,7-dione

C11H14O6 (242.079)


   

methyl (1s,4s,7r,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,4s,7r,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate

methyl (1r,4as,7r,7as)-1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate

C11H14O6 (242.079)


   

methyl (1s,4s,7s,8s,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,4s,7s,8s,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

methyl (1s,4s,7r,8s,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,4s,7r,8s,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

2,3-dihydroxypropyl 2-(2,4-dihydroxyphenyl)acetate

2,3-dihydroxypropyl 2-(2,4-dihydroxyphenyl)acetate

C11H14O6 (242.079)


   

7,8-dimethylbenzo[g]pteridine-2,4-diol

7,8-dimethylbenzo[g]pteridine-2,4-diol

C12H10N4O2 (242.0804)


   

methyl (1s,4s,7s,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,4s,7s,8r,9s,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

(4-hydroxy-5-oxooxolan-3-yl)methyl (2e)-3-(3-methyloxiran-2-yl)prop-2-enoate

(4-hydroxy-5-oxooxolan-3-yl)methyl (2e)-3-(3-methyloxiran-2-yl)prop-2-enoate

C11H14O6 (242.079)


   

methyl 5,10-dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate

methyl 5,10-dihydroxy-2-methyl-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate

C11H14O6 (242.079)


   

methyl 8-hydroxy-3-methyl-2-oxo-4a,5,8,8a-tetrahydro-3h-1,4-benzodioxine-6-carboxylate

methyl 8-hydroxy-3-methyl-2-oxo-4a,5,8,8a-tetrahydro-3h-1,4-benzodioxine-6-carboxylate

C11H14O6 (242.079)


   

(2s)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one

(2s)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one

C11H14O6 (242.079)


   

methyl (1s,4r,7s,8s,9r,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1s,4r,7s,8s,9r,11s)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

methyl (1r,4r,7r,8r,9r,11r)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

methyl (1r,4r,7r,8r,9r,11r)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.0⁴,¹¹]undec-5-ene-8-carboxylate

C11H14O6 (242.079)


   

methyl 1,5-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h,7ah-cyclopenta[c]pyran-4-carboxylate

methyl 1,5-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h,7ah-cyclopenta[c]pyran-4-carboxylate

C11H14O6 (242.079)


   

methyl 1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate

methyl 1,7-dihydroxy-7-(hydroxymethyl)-1h,4ah,7ah-cyclopenta[c]pyran-4-carboxylate

C11H14O6 (242.079)


   

(2r)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one

(2r)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one

C11H14O6 (242.079)


   

1-[(2r,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3-methylpyrimidine-2,4-dione

1-[(2r,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3-methylpyrimidine-2,4-dione

C10H14N2O5 (242.0903)


   

2,3-dihydroxypropyl 2,4-dihydroxy-6-methylbenzoate

2,3-dihydroxypropyl 2,4-dihydroxy-6-methylbenzoate

C11H14O6 (242.079)


   

methyl (1s,4as,5s,7as)-1,5-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h,7ah-cyclopenta[c]pyran-4-carboxylate

methyl (1s,4as,5s,7as)-1,5-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h,7ah-cyclopenta[c]pyran-4-carboxylate

C11H14O6 (242.079)


   

methyl (1r,4as,5r,7as)-1,5-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h,7ah-cyclopenta[c]pyran-4-carboxylate

methyl (1r,4as,5r,7as)-1,5-dihydroxy-7-(hydroxymethyl)-1h,4ah,5h,7ah-cyclopenta[c]pyran-4-carboxylate

C11H14O6 (242.079)