Exact Mass: 146.0202

Exact Mass Matches: 146.0202

Found 131 metabolites which its exact mass value is equals to given mass value 146.0202, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Di-2-propenyl disulfide, 9CI

Allyl disulfide, United States Pharmacopeia (USP) Reference Standard

C6H10S2 (146.0224)


Di-2-propenyl disulfide, also known as allyl disulfide or 3,3-disulfanediylbis(prop-1-ene), belongs to the class of organic compounds known as allyl sulfur compounds. Allyl sulfur compounds are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS. Di-2-propenyl disulfide is possibly neutral. An organic disulfide where the organic group specified is allyl. Di-2-propenyl disulfide has been detected, but not quantified, in soft-necked garlics. This could make di-2-propenyl disulfide a potential biomarker for the consumption of these foods. 1,2-(2-propenyl)-disulfane, also known as allyl disulfide or 3,3-disulfanediylbis(prop-1-ene), is a member of the class of compounds known as allyl sulfur compounds. Allyl sulfur compounds are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS. 1,2-(2-propenyl)-disulfane can be found in soft-necked garlic, which makes 1,2-(2-propenyl)-disulfane a potential biomarker for the consumption of this food product. Diallyl disulfide is an organic disulfide where the organic group specified is allyl. It has been isolated from garlic and other species of the genus Allium. It has a role as an antineoplastic agent, an antifungal agent and a plant metabolite. Diallyl disulfide is a natural product found in Allium vineale, Allium chinense, and other organisms with data available. An organic disulfide where the organic group specified is allyl. It has been isolated from garlic and other species of the genus Allium. D009676 - Noxae > D000988 - Antispermatogenic Agents > D013089 - Spermatocidal Agents D012102 - Reproductive Control Agents > D003270 - Contraceptive Agents D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D020011 - Protective Agents > D016587 - Antimutagenic Agents D000970 - Antineoplastic Agents Diallyl disulfide inhibits human squalene monooxygenase with an IC50 of 400 μM for squalene epoxidation[1]. Diallyl disulfide inhibits human squalene monooxygenase with an IC50 of 400 μM for squalene epoxidation[1].

   

Oxoglutaric acid

2-oxopentanedioic acid

C5H6O5 (146.0215)


Oxoglutaric acid, also known as alpha-ketoglutarate, alpha-ketoglutaric acid, AKG, or 2-oxoglutaric acid, is classified as a gamma-keto acid or a gamma-keto acid derivative. gamma-Keto acids are organic compounds containing an aldehyde substituted with a keto group on the C4 carbon atom. alpha-Ketoglutarate is considered to be soluble (in water) and acidic. alpha-Ketoglutarate is a key molecule in the TCA cycle, playing a fundamental role in determining the overall rate of this important metabolic process (PMID: 26759695). In the TCA cycle, AKG is decarboxylated to succinyl-CoA and carbon dioxide by AKG dehydrogenase, which functions as a key control point of the TCA cycle. Additionally, AKG can be generated from isocitrate by oxidative decarboxylation catalyzed by the enzyme known as isocitrate dehydrogenase (IDH). In addition to these routes of production, AKG can be produced from glutamate by oxidative deamination via glutamate dehydrogenase, and as a product of pyridoxal phosphate-dependent transamination reactions (mediated by branched-chain amino acid transaminases) in which glutamate is a common amino donor. AKG is a nitrogen scavenger and a source of glutamate and glutamine that stimulates protein synthesis and inhibits protein degradation in muscles. In particular, AKG can decrease protein catabolism and increase protein synthesis to enhance bone tissue formation in skeletal muscles (PMID: 26759695). Interestingly, enteric feeding of AKG supplements can significantly increase circulating plasma levels of hormones such as insulin, growth hormone, and insulin-like growth factor-1 (PMID: 26759695). It has recently been shown that AKG can extend the lifespan of adult C. elegans by inhibiting ATP synthase and TOR (PMID: 24828042). In combination with molecular oxygen, alpha-ketoglutarate is required for the hydroxylation of proline to hydroxyproline in the production of type I collagen. A recent study has shown that alpha-ketoglutarate promotes TH1 differentiation along with the depletion of glutamine thereby favouring Treg (regulatory T-cell) differentiation (PMID: 26420908). alpha-Ketoglutarate has been found to be associated with fumarase deficiency, 2-ketoglutarate dehydrogenase complex deficiency, and D-2-hydroxyglutaric aciduria, which are all inborn errors of metabolism (PMID: 8338207). Oxoglutaric acid has been found to be a metabolite produced by Corynebacterium and yeast (PMID: 27872963) (YMDB). [Spectral] 2-Oxoglutarate (exact mass = 146.02152) and S-Adenosyl-L-homocysteine (exact mass = 384.12159) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] 2-Oxoglutarate (exact mass = 146.02152) and (S)-Malate (exact mass = 134.02152) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. Flavouring ingredient

   

Oxaloacetate 4-methyl ester

4-methoxy-2,4-dioxobutanoic acid

C5H6O5 (146.0215)


   

5-Hydroxy-2,4-dioxopentanoate

5-hydroxy-2,4-dioxopentanoic acid

C5H6O5 (146.0215)


   

Methyloxaloacetate

2-methyl-3-oxosuccinic acid

C5H6O5 (146.0215)


   

ACMC-20my24

2(5H)-Furanone,3,4-dihydroxy-5-(hydroxymethyl)-,(5R)-

C5H6O5 (146.0215)


   

3-chlorocyclohexa-3,5-diene-1,2-diol

3-Chloro-cis-1,2-dihydroxycyclohexa-3,5-diene

C6H7ClO2 (146.0135)


   

(Z)-2-CHLORO-2-BUTENE

(Z)-3-((Aminoiminomethyl)thio)-2-propenoic acid

C4H6N2O2S (146.015)


An imidothiocarbamic ester that is (2Z)-prop-2-enoic acid with a carbamimidoylsulfanyl group at position 3.

   

2-Hydroxyparaconate

2-Hydroxyparaconate

C5H6O5 (146.0215)


   

(E,E)-Di-1-propenyl disulfide

(1Z)-1-[(1Z)-Prop-1-en-1-yldisulphanyl]prop-1-ene

C6H10S2 (146.0224)


(Z,Z)-Di-1-propenyl disulfide is found in onion-family vegetables. (Z,Z)-Di-1-propenyl disulfide is a constituent of Allium species. Constituent of the essential oil of Allium subspecies (E,E)-Di-1-propenyl disulfide is found in onion-family vegetables.

   

(E)-1-Propenyl 2-propenyl disulfide

3-[(1Z)-Prop-1-en-1-yldisulphanyl]prop-1-ene

C6H10S2 (146.0224)


(e)-1-propenyl 2-propenyl disulfide is a member of the class of compounds known as allyl sulfur compounds. Allyl sulfur compounds are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS (e)-1-propenyl 2-propenyl disulfide can be found in soft-necked garlic, which makes (e)-1-propenyl 2-propenyl disulfide a potential biomarker for the consumption of this food product. (Z)-1-Propenyl 2-propenyl disulfide is found in onion-family vegetables. (Z)-1-Propenyl 2-propenyl disulfide is a constituent of garlic (Allium sativum).

   

3-Oxoglutaric acid

acetonedicarboxylic acid

C5H6O5 (146.0215)


3-oxoglutaric acid or acetonedicarboxylic acid is a simple carboxylic acid, which may be used as a building block in organic chemistry. It has been found to be a microbial metabolite.

   

2-Amino-2-thiazoline-4-carboxylic acid

2-Amino-delta(2)-thiazoline-4-carboxylic acid, hydrobromide

C4H6N2O2S (146.015)


   

alpha-Ketoglutarate cyanohydrin

alpha-Ketoglutaric acid cyanohydrin

C5H6O5 (146.0215)


   

(E)-2-Propenyl-1-propenyl disulfide

3-[(1E)-prop-1-en-1-yldisulfanyl]prop-1-ene

C6H10S2 (146.0224)


(e)-2-propenyl-1-propenyl disulfide is a member of the class of compounds known as allyl sulfur compounds. Allyl sulfur compounds are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS (e)-2-propenyl-1-propenyl disulfide can be found in soft-necked garlic, which makes (e)-2-propenyl-1-propenyl disulfide a potential biomarker for the consumption of this food product.

   

Methoxymalic acid

(2E)-2-methoxybut-2-enedioic acid

C5H6O5 (146.0215)


Methoxymalic acid, also known as methoxymalate, belongs to dicarboxylic acids and derivatives class of compounds. Those are organic compounds containing exactly two carboxylic acid groups. Methoxymalic acid is soluble (in water) and an extremely strong acidic compound (based on its pKa). Methoxymalic acid can be found in oat, which makes methoxymalic acid a potential biomarker for the consumption of this food product.

   

2,3-Dimethyl-5,6-dithia-bicyclo[2.1.1]-hexane-5-oxide

2,3-Dimethyl-5,6-dithia-bicyclo[2.1.1]-hexane-5-oxide

C6H10S2 (146.0224)


2,3-dimethyl-5,6-dithia-bicyclo[2.1.1]-hexane-5-oxide is a member of the class of compounds known as thiolanes. Thiolanes are organic compounds containing thiolane, a five-member saturated ring containing four carbon atoms and a sulfur atom. 2,3-dimethyl-5,6-dithia-bicyclo[2.1.1]-hexane-5-oxide can be found in garden onion, which makes 2,3-dimethyl-5,6-dithia-bicyclo[2.1.1]-hexane-5-oxide a potential biomarker for the consumption of this food product.

   

Dimethyl 2-oxomalonate

Dimethyl 2-oxomalonate

C5H6O5 (146.0215)


   

3-Ethyl-1,2-dithi-4-ene

3-Ethyl-1,2-dithi-4-ene

C6H10S2 (146.0224)


   

3,4-dihydro-3,4-dihydroxychlorobenzene

3,4-dihydro-3,4-dihydroxychlorobenzene

C6H7ClO2 (146.0135)


   

3-Ethyl-1,2-dithi-5-ene

3-Ethyl-1,2-dithi-5-ene

C6H10S2 (146.0224)


   

Oxoglutaric acid

2-ketoglutaric acid

C5H6O5 (146.0215)


   

Dipropenyl disulfide

Dipropenyl disulfide

C6H10S2 (146.0224)


Annotation level-3

   

alpha-Ketoglutaric acid

alpha-Ketoglutaric acid

C5H6O5 (146.0215)


   

Oxoglutaric acid; LC-tDDA; CE10

Oxoglutaric acid; LC-tDDA; CE10

C5H6O5 (146.0215)


   

Oxoglutaric acid; LC-tDDA; CE20

Oxoglutaric acid; LC-tDDA; CE20

C5H6O5 (146.0215)


   

Oxoglutarate

Oxoglutarate

C5H6O5 (146.0215)


   

3-Oxoglutaric acid

3-oxopentanedioic acid

C5H6O5 (146.0215)


   

(E,E)-Di-1-propenyl disulfide

(1Z)-1-[(1Z)-prop-1-en-1-yldisulfanyl]prop-1-ene

C6H10S2 (146.0224)


   

(E)-1-Propenyl 2-propenyl disulfide

3-[(1Z)-prop-1-en-1-yldisulfanyl]prop-1-ene

C6H10S2 (146.0224)


   

2-Hydroxy-5-aminopyridine hydrochloride

2-Hydroxy-5-aminopyridine hydrochloride

C5H7ClN2O (146.0247)


   

4-Methylpyrimidin-2-olhydrochlorid

4-Methylpyrimidin-2-olhydrochlorid

C5H7ClN2O (146.0247)


   

2(1H)-Pyridinone,4-amino-3,5-difluoro-(9CI)

2(1H)-Pyridinone,4-amino-3,5-difluoro-(9CI)

C5H4F2N2O (146.0292)


   

(S)-5-PYRROLIDIN-2-YLMETHYL-1H-TETRAZOLE

(S)-5-PYRROLIDIN-2-YLMETHYL-1H-TETRAZOLE

C6H7ClO2 (146.0135)


   

UNII:48431VN59G

(4R)-2-amino-4,5-dihydro-1,3-thiazole-4-carboxylic acid

C4H6N2O2S (146.015)


   

6-Amino-3-pyridinol hydrochloride (1:1)

6-Amino-3-pyridinol hydrochloride (1:1)

C5H7ClN2O (146.0247)


   

5-(chloromethyl)-3-ethyl-1,2,4-oxadiazole

5-(chloromethyl)-3-ethyl-1,2,4-oxadiazole

C5H7ClN2O (146.0247)


   

(1S,4S)-2-PHENYL-2,5-DIAZABICYCLO[2.2.1]HEPTANEMALEINATE

(1S,4S)-2-PHENYL-2,5-DIAZABICYCLO[2.2.1]HEPTANEMALEINATE

C6H7ClO2 (146.0135)


   

2-chloro-3-hydroxycyclohex-2-en-1-one

2-chloro-3-hydroxycyclohex-2-en-1-one

C6H7ClO2 (146.0135)


   

n-methanesulfonylimidazole

n-methanesulfonylimidazole

C4H6N2O2S (146.015)


   

2-NITROMETHYLENETHIAZOLIDINE

2-NITROMETHYLENETHIAZOLIDINE

C4H6N2O2S (146.015)


   

2,4-Imidazolidinedione,5-(mercaptomethyl)-, (5R)-

2,4-Imidazolidinedione,5-(mercaptomethyl)-, (5R)-

C4H6N2O2S (146.015)


   

3-aminopyridin-4-ol

3-aminopyridin-4-ol

C5H7ClN2O (146.0247)


   

1-(1H-Imidazol-2-yl)ethanone hydrochloride (1:1)

1-(1H-Imidazol-2-yl)ethanone hydrochloride (1:1)

C5H7ClN2O (146.0247)


   

3,3,4,4,4-Pentafluoro-1-butene

3,3,4,4,4-Pentafluoro-1-butene

C4H3F5 (146.0155)


   

2-amino-4,5-difluoropyridin-3-ol

2-amino-4,5-difluoropyridin-3-ol

C5H4F2N2O (146.0292)


   

4-Fluoroisophthalonitrile

4-Fluoroisophthalonitrile

C8H3FN2 (146.028)


   

[(Trimethylsilyl)Methyl]Magnesium Chloride

[(Trimethylsilyl)Methyl]Magnesium Chloride

C4H11ClMgSi (146.0169)


   

Dicyclopropyl disulfide

Dicyclopropyl disulfide

C6H10S2 (146.0224)


   

4,5-difluorobenzene-1,2-diol

4,5-difluorobenzene-1,2-diol

C6H4F2O2 (146.0179)


   

3,5-dicyanofluorobenzene

3,5-dicyanofluorobenzene

C8H3FN2 (146.028)


   

3-Fluorophthalodinitrile

3-Fluorophthalodinitrile

C8H3FN2 (146.028)


   

2-chloro-n-(2-cyanoethyl)-acetamid

2-chloro-n-(2-cyanoethyl)-acetamid

C5H7ClN2O (146.0247)


   

2-(chloromethyl)-5-ethyl-1,3,4-oxadiazole

2-(chloromethyl)-5-ethyl-1,3,4-oxadiazole

C5H7ClN2O (146.0247)


   

2,4-DIFLUORORESORCINOL

2,4-DIFLUORORESORCINOL

C6H4F2O2 (146.0179)


   

2,3-Difluoro-hydroquinone

2,3-Difluoro-hydroquinone

C6H4F2O2 (146.0179)


   

2-Amino-4-pyridinol hydrochloride (1:1)

2-Amino-4-pyridinol hydrochloride (1:1)

C5H7ClN2O (146.0247)


   

2-Aminopyridin-3-ol hydrochloride

2-Aminopyridin-3-ol hydrochloride

C5H7ClN2O (146.0247)


   

4-chloro-1,1,1-trifluorobutane

4-chloro-1,1,1-trifluorobutane

C4H6ClF3 (146.011)


   

5-Fluoro-6-hydroxy-2,4(1H,3H)-pyrimidinedione

5-Fluoro-6-hydroxy-2,4(1H,3H)-pyrimidinedione

C4H3FN2O3 (146.0128)


   

3-FURANCARBOXIMIDAMIDE HYDROCHLORIDE

3-FURANCARBOXIMIDAMIDE HYDROCHLORIDE

C5H7ClN2O (146.0247)


   

Sodium 4-methylbenzenethiolate

Sodium 4-methylbenzenethiolate

C7H7NaS (146.0166)


   

4-Fluorophthalonitrile

4-Fluorophthalonitrile

C8H3FN2 (146.028)


   

1-(1H-Imidazol-4-yl)ethanone hydrochloride (1:1)

1-(1H-Imidazol-4-yl)ethanone hydrochloride (1:1)

C5H7ClN2O (146.0247)


   

2-(5-Mercapto-tetrazol-1-yl)-ethano; l

2-(5-Mercapto-tetrazol-1-yl)-ethano; l

C3H6N4OS (146.0262)


   

1-(1H-PYRAZOL-5-YL)ETHAN-1-ONE HYDROCHLORIDE

1-(1H-PYRAZOL-5-YL)ETHAN-1-ONE HYDROCHLORIDE

C5H7ClN2O (146.0247)


   

1,3-Benzenediol,4,6-difluoro-(9CI)

1,3-Benzenediol,4,6-difluoro-(9CI)

C6H4F2O2 (146.0179)


   

Succinic acid, epoxymethyl- (7CI)

Succinic acid, epoxymethyl- (7CI)

C5H6O5 (146.0215)


   

FURAN-2-CARBOXIMIDAMIDE HYDROCHLORIDE

FURAN-2-CARBOXIMIDAMIDE HYDROCHLORIDE

C5H7ClN2O (146.0247)


   

2-Fluoroterephthalonitrile

2-Fluoroterephthalonitrile

C8H3FN2 (146.028)


   

3-(Chloromethyl)-5-ethyl-1,2,4-oxadiazole

3-(Chloromethyl)-5-ethyl-1,2,4-oxadiazole

C5H7ClN2O (146.0247)


   

2-Hydroxypentanedioate

2-Hydroxypentanedioate

C5H6O5-2 (146.0215)


   

Allyl prop-1-enyl disulfide

1-Propenyl 2-propenyl disulfide

C6H10S2 (146.0224)


(e)-1-propenyl 2-propenyl disulfide is a member of the class of compounds known as allyl sulfur compounds. Allyl sulfur compounds are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS (e)-1-propenyl 2-propenyl disulfide can be found in soft-necked garlic, which makes (e)-1-propenyl 2-propenyl disulfide a potential biomarker for the consumption of this food product.

   

2-Methyl-3-oxobutanedioic acid

2-Methyl-3-oxobutanedioic acid

C5H6O5 (146.0215)


   

(4S)-2-amino-4,5-dihydro-1,3-thiazole-4-carboxylic acid

(4S)-2-amino-4,5-dihydro-1,3-thiazole-4-carboxylic acid

C4H6N2O2S (146.015)


   

Disulfide, di-1-propenyl

Disulfide, di-1-propenyl

C6H10S2 (146.0224)


   

NSC-17391

InChI=1\C5H6O5\c6-3(5(9)10)1-2-4(7)8\h1-2H2,(H,7,8)(H,9,10

C5H6O5 (146.0215)


   

AI3-35128

4-01-00-02098 (Beilstein Handbook Reference)

C6H10S2 (146.0224)


D009676 - Noxae > D000988 - Antispermatogenic Agents > D013089 - Spermatocidal Agents D012102 - Reproductive Control Agents > D003270 - Contraceptive Agents D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D020011 - Protective Agents > D016588 - Anticarcinogenic Agents D020011 - Protective Agents > D016587 - Antimutagenic Agents D000970 - Antineoplastic Agents Diallyl disulfide inhibits human squalene monooxygenase with an IC50 of 400 μM for squalene epoxidation[1]. Diallyl disulfide inhibits human squalene monooxygenase with an IC50 of 400 μM for squalene epoxidation[1].

   

(E)-2-Propenyl-1-propenyl disulfide

3-[(1E)-prop-1-en-1-yldisulfanyl]prop-1-ene

C6H10S2 (146.0224)


(e)-2-propenyl-1-propenyl disulfide is a member of the class of compounds known as allyl sulfur compounds. Allyl sulfur compounds are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS (e)-2-propenyl-1-propenyl disulfide can be found in soft-necked garlic, which makes (e)-2-propenyl-1-propenyl disulfide a potential biomarker for the consumption of this food product. Constituent of garlic (Allium sativum). (E)-1-Propenyl 2-propenyl disulfide is found in garlic and onion-family vegetables.

   

Diallyl disulfide

Di-2-propenyl disulfide, 9CI

C6H10S2 (146.0224)


Di-2-propenyl disulfide, 9CI or simply allyl disulfide is a principal constituent of garlic (Allium sativum). It is found in in onion (Allium cepa), ramsons (Allium ursinum), chive (Allium schoenoprasum) and Chinese chives (Allium tuberosum). It is also found in raw cabbage and seeds of herb-Sophia (Descurainia sophia). It can be used as a flavouring ingredient. Allyl disulfide is a potential nutriceutical. 1,2-(2-propenyl)-disulfane, also known as allyl disulfide or 3,3-disulfanediylbis(prop-1-ene), is a member of the class of compounds known as allyl sulfur compounds. Allyl sulfur compounds are compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS. 1,2-(2-propenyl)-disulfane can be found in soft-necked garlic, which makes 1,2-(2-propenyl)-disulfane a potential biomarker for the consumption of this food product. Diallyl disulfide inhibits human squalene monooxygenase with an IC50 of 400 μM for squalene epoxidation[1]. Diallyl disulfide inhibits human squalene monooxygenase with an IC50 of 400 μM for squalene epoxidation[1].

   

Garlicin

Diallyl disulfide

C6H10S2 (146.0224)


Isolated from garlic (Allium sativa). Garlicin is found in onion-family vegetables. Diallyl disulfide inhibits human squalene monooxygenase with an IC50 of 400 μM for squalene epoxidation[1]. Diallyl disulfide inhibits human squalene monooxygenase with an IC50 of 400 μM for squalene epoxidation[1].

   

alpha-Ketoglutarate cyanohydrin

alpha-Ketoglutaric acid cyanohydrin

C5H6O5 (146.0215)


   

(2R)-2-hydroxypentanedioate

(2R)-2-hydroxypentanedioate

C5H6O5-2 (146.0215)


   

(2S)-2-hydroxypentanedioate

(2S)-2-hydroxypentanedioate

C5H6O5-2 (146.0215)


   

(2R,3S)-3-Methylmalate

(2R,3S)-3-Methylmalate

C5H6O5-2 (146.0215)


   

Citramalate

Citramalate

C5H6O5-2 (146.0215)


   

(1R,2R)-3-chlorocyclohexa-3,5-diene-1,2-diol

(1R,2R)-3-chlorocyclohexa-3,5-diene-1,2-diol

C6H7ClO2 (146.0135)


   

(S)-2-Methylmalate

(S)-2-Methylmalate

C5H6O5-2 (146.0215)


   

(R)-2-Methylmalate

(R)-2-Methylmalate

C5H6O5-2 (146.0215)


   

N-[(carbamoylamino)carbonyl]carbamate

N-[(carbamoylamino)carbonyl]carbamate

C3H4N3O4- (146.0202)


   

(Z)-2-hydroxypent-2-enedioic acid

(Z)-2-hydroxypent-2-enedioic acid

C5H6O5 (146.0215)


   

2-Hydroxy-3-methylbutanedioate

2-Hydroxy-3-methylbutanedioate

C5H6O5-2 (146.0215)


   

3-Hydroxypentanedioate

3-Hydroxypentanedioate

C5H6O5-2 (146.0215)


   

2-Amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate

2-Amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate

C4H6N2O2S (146.015)


   

Thiomorpholine-3-carboxylate

Thiomorpholine-3-carboxylate

C5H8NO2S- (146.0276)


   

dehydro-L-arabinono-1,4-lactone

dehydro-L-arabinono-1,4-lactone

C5H6O5 (146.0215)


   

(4R)-2-amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate

(4R)-2-amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate

C4H6N2O2S (146.015)


   

(R)-2-methyl-3-oxosuccinic acid

(R)-2-methyl-3-oxosuccinic acid

C5H6O5 (146.0215)


   

alpha-ketoglutarate-13C4

alpha-ketoglutarate-13C4

C5H6O5 (146.0215)


   

2-Hydroxy-2-pentenedioic acid

2-Hydroxy-2-pentenedioic acid

C5H6O5 (146.0215)


   

(4S)-2-amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate

(4S)-2-amino-4,5-dihydro-1,3-thiazol-3-ium-4-carboxylate

C4H6N2O2S (146.015)


   

2-Oxoglutaric acid

2-Ketoglutaric Acid-13C1

C5H6O5 (146.0215)


An oxo dicarboxylic acid that consists of glutaric acid bearing an oxo substituent at position 2. It is an intermediate metabolite in Krebs cycle.

   

Dehydro-D-arabinono-1,4-lactone

2(5H)-Furanone,3,4-dihydroxy-5-(hydroxymethyl)-,(5R)-

C5H6O5 (146.0215)


A gamma-lactone that is 5-(hydroxymethyl)furan-2(5H)-one substituted at positions 3 and 4 by hydroxy groups (the 5R-stereoisomer).

   

4-methoxy-2,4-dioxobutanoic acid

4-methoxy-2,4-dioxobutanoic acid

C5H6O5 (146.0215)


   

5-hydroxy-2,4-dioxopentanoic acid

5-hydroxy-2,4-dioxopentanoic acid

C5H6O5 (146.0215)


   

3-oxopentanedioic acid

3-oxopentanedioic acid

C5H6O5 (146.0215)


   

citramalate(2-)

citramalate(2-)

C5H6O5 (146.0215)


A dicarboxylic acid dianion that is obtained by removal of a proton from both of the carboxylic acid groups of citramalic acid.

   

3-Chloro-cis-1,2-dihydroxycyclohexa-3,5-diene

3-Chloro-cis-1,2-dihydroxycyclohexa-3,5-diene

C6H7ClO2 (146.0135)


   

L-citramalate(2-)

L-citramalate(2-)

C5H6O5 (146.0215)


A citramalate(2-) that is the conjugate acid of L-citramalic acid.

   

2-hydroxyglutarate(2-)

2-hydroxyglutarate(2-)

C5H6O5 (146.0215)


A dicarboxylic acid dianion resulting from the removal of a proton from both of the carboxylic acid groups of 2-hydroxyglutaric acid.

   

2-Amino-delta(2)-thiazoline-4-carboxylic acid

2-Amino-delta(2)-thiazoline-4-carboxylic acid

C4H6N2O2S (146.015)


A 1,3-thiazole that is 4,5-dihydro-1,3-thiazole which is substituted at positions 2 and 4 by an amino and a carboxy group, respectively.

   

3-hydroxyglutarate(2-)

3-hydroxyglutarate(2-)

C5H6O5 (146.0215)


A dicarboxylic acid dianion resulting from the deprotonation of the two carboxy groups of 3-hydroxyglutaric acid; major species at pH 7.3.

   

D-2-amino-Delta(2)-thiazoline-4-carboxylic acid

D-2-amino-Delta(2)-thiazoline-4-carboxylic acid

C4H6N2O2S (146.015)


A 2-amino-Delta(2)-thiazoline-4-carboxylic acid that has S configuration.

   

D-2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion

D-2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion

C4H6N2O2S (146.015)


A 2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion that has S-configuration. The major species at pH 7.3.

   

(S)-2-hydroxyglutarate(2-)

(S)-2-hydroxyglutarate(2-)

C5H6O5 (146.0215)


A 2-hydroxyglutarate(2-) that has (2S)-configuration.

   

L-2-amino-Delta(2)-thiazoline-4-carboxylic acid

L-2-amino-Delta(2)-thiazoline-4-carboxylic acid

C4H6N2O2S (146.015)


A 2-amino-Delta(2)-thiazoline-4-carboxylic acid that has R configuration.

   

2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion

2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion

C4H6N2O2S (146.015)


An amino acid zwitterion obtained from 2-amino-Delta(2)-thiazoline-4-carboxylic acid by the transfer of a proton from the carboxy group to the thiazoline nitrogen. The major species at pH 7.3.

   

L-2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion

L-2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion

C4H6N2O2S (146.015)


A 2-amino-Delta(2)-thiazoline-4-carboxylic acid zwitterion that has R-configuration. The major species at pH 7.3.

   

D-citramalate(2-)

D-citramalate(2-)

C5H6O5 (146.0215)


A citramalate(2-) that is the conjugate base of D-citramalic acid.

   

3-methylmalate(2-)

3-methylmalate(2-)

C5H6O5 (146.0215)


A dicarboxylic acid dianion obtained by deprotonation of both carboxy groups of 3-methylmalic acid; major microspecies at pH 7.3

   

(R)-2-hydroxyglutarate(2-)

(R)-2-hydroxyglutarate(2-)

C5H6O5 (146.0215)


A 2-hydroxyglutarate(2-) that has (2R)-configuration.

   

D-erythro-3-methylmalate(2-)

D-erythro-3-methylmalate(2-)

C5H6O5 (146.0215)


Dianion of D-erythro-3-methylmalic acid.

   

Aminothiazolinecarboxylic acid

Aminothiazolinecarboxylic acid

C4H6N2O2S (146.015)


   

3,4-dihydroxy-5-(hydroxymethyl)-5h-furan-2-one

3,4-dihydroxy-5-(hydroxymethyl)-5h-furan-2-one

C5H6O5 (146.0215)


   

1-(prop-1-en-1-yldisulfanyl)prop-1-ene

1-(prop-1-en-1-yldisulfanyl)prop-1-ene

C6H10S2 (146.0224)


   

(3r)-3-hydroxy-5-oxooxolane-3-carboxylic acid

(3r)-3-hydroxy-5-oxooxolane-3-carboxylic acid

C5H6O5 (146.0215)


   

(5r)-3,4-dihydroxy-5-(hydroxymethyl)-5h-furan-2-one

(5r)-3,4-dihydroxy-5-(hydroxymethyl)-5h-furan-2-one

C5H6O5 (146.0215)


   

3-(prop-1-en-1-yldisulfanyl)prop-1-ene

3-(prop-1-en-1-yldisulfanyl)prop-1-ene

C6H10S2 (146.0224)


   

(1e)-1-[(1e)-prop-1-en-1-yldisulfanyl]prop-1-ene

(1e)-1-[(1e)-prop-1-en-1-yldisulfanyl]prop-1-ene

C6H10S2 (146.0224)


   

5-(chloromethyl)-3-methyl-5h-furan-2-one

5-(chloromethyl)-3-methyl-5h-furan-2-one

C6H7ClO2 (146.0135)


   

3-hydroxy-5-oxooxolane-3-carboxylic acid

3-hydroxy-5-oxooxolane-3-carboxylic acid

C5H6O5 (146.0215)