Exact Mass: 244.0298972

Exact Mass Matches: 244.0298972

Found 129 metabolites which its exact mass value is equals to given mass value 244.0298972, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

2-Deoxyglucose 6-phosphate

2-Deoxy-D-glucopyranose 6-phosphate

C6H13O8P (244.0348028)


KEIO_ID D101

   

Fucose 1-phosphate

{[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phosphonic acid

C6H13O8P (244.0348028)


Fucose 1-phosphate (CAS: 16562-58-6) belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphate group linked to the carbohydrate unit. Fucose 1-phosphate is an intermediate in the reversible synthesis of GDP-L-fucose catalyzed by the enzyme guanosine triphosphate fucose pyrophosphorylase (GFPP, EC 2.7.7.30). The reversible reaction is magnesium-dependent, although the enzyme is partially active when cobalt or manganese is substituted. The reaction is unusual in that, of the four canonical nucleoside triphosphates, only guanosine can be utilized efficiently to form a nucleotide-sugar. Free cytosolic fucose is phosphorylated by L-fucokinase (EC 2.7.1.52) to form fucose-1-phosphate in the salvage pathway of GDP-L-fucose (PMID: 16185085, 14686921). Fucose-1-phosphate is an intermediate in the reversible synthesis of GDP-L-fucose, in a reaction catalyzed by the enzyme guanosine triphosphate fucose pyrophosphorylase (GFPP, E.C. 2.7.7.30) . The reversible reaction is magnesium-dependent, although the enzyme is partially active when cobalt or manganese is substituted. The reaction is unusual in that, of the four canonical nucleoside triphosphates, only guanosine can be utilized efficiently to form a nucleotide-sugar. Free cytosolic fucose is phosphorylated by L-fucokinase (EC 2.7.1.52) to form fucose-1-phosphate in the salvage pathway of GDP-L-fucose. (PMID: 16185085, 14686921) [HMDB]

   

L-Fuculose 1-phosphate

L-Fuculose 1-phosphate

C6H13O8P (244.0348028)


   

Apraclonidine

2,6-dichloro-N1-(4,5-dihydro-1H-imidazol-2-yl)benzene-1,4-diamine

C9H10Cl2N4 (244.02824800000002)


Apraclonidine is only found in individuals that have used or taken this drug.Apraclonidine, also known as iopidine, is a sympathomimetic used in glaucoma therapy.Apraclonidine is a relatively selective alpha2 adrenergic receptor agonist that stimulates alpha1 receptors to a lesser extent. It has a peak ocular hypotensive effect occurring at two hours post-dosing. The exact mechanism of action is unknown, but fluorophotometric studies in animals and humans suggest that Apraclonidine has a dual mechanism of action by reducing aqueous humor production through the constriction of afferent ciliary process vessels, and increasing uveoscleral outflow. S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics > S01EA - Sympathomimetics in glaucoma therapy C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists

   

Gentisein

1,3,7-Trihydroxy-9H-xanthen-9-one, 9CI

C13H8O5 (244.0371718)


Gentisein is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 7. It has a role as a plant metabolite. It is a member of xanthones and a polyphenol. Gentisein is a natural product found in Hypericum scabrum, Cratoxylum formosum, and other organisms with data available. A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 7. Gentisein is found in alcoholic beverages. Gentisein is isolated from Gentiana lutea (yellow gentian Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].

   

Mesuaxanthone B

1,5,6-Trihydroxyxanthone

C13H8O5 (244.0371718)


A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 5 and 6.

   

1,3,5-Trihydroxyxanthone

1,3,5-Trihydroxyxanthone

C13H8O5 (244.0371718)


A member of the class of xanthones that is xanthone substituted by hydroxy groups at positions 1, 3 and 5. It has been isolated from Anaxagorea luzonensis.

   

MCPA-thioethyl

2-(4-chloro-2-methylphenoxy)-1-(ethylsulfanyl)ethan-1-one

C11H13ClO2S (244.03247480000002)


   

6-Sulfoquinovose

Sulfoquinovose; 6-Deoxy-6-sulfo-D-glucopyranose; 6-Deoxy-6-sulfo-D-glucose

C6H12O8S (244.0252872)


   

6-Deoxy-6-sulfo-D-fructose

6-deoxy-6-sulfo-D-fructofuranose

C6H12O8S (244.0252872)


   

L-Rhamnulose 1-phosphate

L-Rhamnulose 1-phosphate

C6H13O8P (244.0348028)


A deoxyketohexose phosphate consisting of L-rhamnulose having a monophosphate group at the 1-position.

   

6-Sulfo-alpha-quinovose

6-Sulfo-alpha-quinovose

C6H12O8S (244.0252872)


   

6-deoxy-6-sulfo-beta-D-glucopyranose

6-deoxy-6-sulfo-beta-D-glucopyranose

C6H12O8S (244.0252872)


   

Urolithin C

3,8,9-trihydroxy-6H-benzo[c]chromen-6-one

C13H8O5 (244.0371718)


Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].

   

urolithin M7

Urolithin M-7

C13H8O5 (244.0371718)


   

Urolithin C

3,8,9-trihydroxy-6H-benzo[c]chromen-6-one

C13H8O5 (244.0371718)


A polyphenol metabolite detected in biological fluids [PhenolExplorer] Urolithin C is a biomarker of nut consumption in urine. Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].

   

2-Deoxy-D-glucopyranose 6-phosphate

(3,4,6-Trihydroxyoxan-2-yl)methyl dihydrogen phosphate

C6H13O8P (244.0348028)


   

2-Deoxy-D-arabino-hexose 6-(dihydrogen phosphate)

2-Deoxy-D-arabino-hexose 6-(dihydrogen phosphoric acid)

C6H13O8P (244.0348028)


   

7-Methoxy-4-(trifluoromethyl)coumarin

7-methoxy-4-(trifluoromethyl)-2H-chromen-2-one

C11H7F3O3 (244.03472680000002)


   

1,2,8-Trihydroxyxanthone

1,2,8-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,2,5-Trihydroxyxanthone

1,2,5-Trihydroxyxanthone

C13H8O5 (244.0371718)


A member of the class of xanthones that is 9H-xanthen-9-one substituted bybhydroxy groups at positions 1, 2 and 5. It is isolated from Garcinia subelliptica.

   

1,3,8-Trihydroxyxanthone

1,3,8-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,4,5-Trihydroxyxanthone

1,4,5-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,6,7-Trihydroxyxanthone

1,6,7-Trihydroxy-9H-xanthen-9-one

C13H8O5 (244.0371718)


   

2,4,7-Trihydroxyxanthone

2,4,7-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,3,6-Trihydroxyxanthone

1,3,6-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

Subelliptenone G

Subelliptenone G

C13H8O5 (244.0371718)


   

2,3,4-Trihydroxyxanthone

2,3,4-Trihydroxyxanthone

C13H8O5 (244.0371718)


   
   

7,8-Dihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione

7,8-Dihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione

C13H8O5 (244.0371718)


   
   

2,4,7-Trihydroxy-9H-xanthene-9-one

2,4,7-Trihydroxy-9H-xanthene-9-one

C13H8O5 (244.0371718)


   

3,4,5-Trihydroxy-9H-xanthen-9-one

3,4,5-Trihydroxy-9H-xanthen-9-one

C13H8O5 (244.0371718)


   
   

5-Hydroxy-7-methoxynaphtho[2,3-b]furan-4,9-dione

5-Hydroxy-7-methoxynaphtho[2,3-b]furan-4,9-dione

C13H8O5 (244.0371718)


   

1,4,8-trihydroxyxanthone

1,4,8-trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,4,7-trihydroxyxanthone

1,4,7-trihydroxyxanthone

C13H8O5 (244.0371718)


   

8-Hydroxy-6-methoxynaphtho[2,3-b]furan-4,9-dione

8-Hydroxy-6-methoxynaphtho[2,3-b]furan-4,9-dione

C13H8O5 (244.0371718)


   

1,7,8-Trihydroxyxanthone

1,7,8-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

Norneolambertellin

Norneolambertellin

C13H8O5 (244.0371718)


   
   

3,9,10-trihydro xydibenzo[b,d]pyran-6-one

3,9,10-trihydro xydibenzo[b,d]pyran-6-one

C13H8O5 (244.0371718)


   
   

5-hydroxy-6-methoxynaphtho<2,3-b>furan-4,9-quinone

5-hydroxy-6-methoxynaphtho<2,3-b>furan-4,9-quinone

C13H8O5 (244.0371718)


   
   

alpha-L-(-)-Fucose 1-phosphate bis(cyclohexylammonium) salt

alpha-L-(-)-Fucose 1-phosphate bis(cyclohexylammonium) salt

C6H13O8P (244.0348028)


   
   

L-Fucose 1-phosphate

L-Fucose 1-phosphate

C6H13O8P (244.0348028)


   

3,5-Bis(trifluoromethyl)anisole

3,5-Bis(trifluoromethyl)anisole

C9H6F6O (244.03228179999996)


   

5-(4-CHLORO-3-FLUOROPHENYL)-5-OXOVALERIC ACID

5-(4-CHLORO-3-FLUOROPHENYL)-5-OXOVALERIC ACID

C11H10ClFO3 (244.0302472)


   

benzyl benzenecarbodithioate

benzyl benzenecarbodithioate

C14H12S2 (244.0380392)


   

5-(3-CHLORO-4-FLUOROPHENYL)-5-OXOVALERIC ACID

5-(3-CHLORO-4-FLUOROPHENYL)-5-OXOVALERIC ACID

C11H10ClFO3 (244.0302472)


   

6-thiophen-2-yl-1h-indazole-3-carboxylic acid

6-thiophen-2-yl-1h-indazole-3-carboxylic acid

C12H8N2O2S (244.0306468)


   

1-(3-Trifluoromethylphenyl)imidazoline-2-thione

1-(3-Trifluoromethylphenyl)imidazoline-2-thione

C10H7F3N2S (244.0282018)


   
   

1,2-BIS(PHENYLTHIO)ETHYLENE (CIS- AND TRANS- MIXTURE)

1,2-BIS(PHENYLTHIO)ETHYLENE (CIS- AND TRANS- MIXTURE)

C14H12S2 (244.0380392)


   

N-((5-bromopyridin-3-yl)methyl)-2-methoxyethanamine

N-((5-bromopyridin-3-yl)methyl)-2-methoxyethanamine

C9H13BrN2O (244.02111879999998)


   

3-AMINO-3-(5-CHLORO-2-NITRO-PHENYL)-PROPIONIC ACID

3-AMINO-3-(5-CHLORO-2-NITRO-PHENYL)-PROPIONIC ACID

C9H9ClN2O4 (244.0250824)


   

METHYL 4-ACETYL-3-METHYL-5-(METHYLTHIO)THIOPHENE-2-CARBOXYLATE

METHYL 4-ACETYL-3-METHYL-5-(METHYLTHIO)THIOPHENE-2-CARBOXYLATE

C10H12O3S2 (244.0227842)


   

Mesulfen

Mesulfen

C14H12S2 (244.0380392)


P - Antiparasitic products, insecticides and repellents > P03 - Ectoparasiticides, incl. scabicides, insecticides and repellents > P03A - Ectoparasiticides, incl. scabicides > P03AA - Sulfur containing products D - Dermatologicals > D10 - Anti-acne preparations > D10A - Anti-acne preparations for topical use > D10AB - Preparations containing sulfur C308 - Immunotherapeutic Agent > C574 - Immunosuppressant

   

1,1-Biphenyl,2,3,4,5,6-pentafluoro-

1,1-Biphenyl,2,3,4,5,6-pentafluoro-

C12H5F5 (244.031139)


   

5-(3-CHLORO-5-FLUOROPHENYL)-5-OXOVALERIC ACID

5-(3-CHLORO-5-FLUOROPHENYL)-5-OXOVALERIC ACID

C11H10ClFO3 (244.0302472)


   

2-Benzoylbenzoyl chloride

2-Benzoylbenzoyl chloride

C14H9ClO2 (244.0291044)


   

7-Methoxy-2-(trifluoromethyl)-4H-chromen-4-one

7-Methoxy-2-(trifluoromethyl)-4H-chromen-4-one

C11H7F3O3 (244.03472680000002)


   

4,4μ-Dimercaptostilbene

4,4μ-Dimercaptostilbene

C14H12S2 (244.0380392)


   

3-benzoylbenzoyl chloride

3-benzoylbenzoyl chloride

C14H9ClO2 (244.0291044)


   

2,4-bis(trifluoromethyl)benzyl alcohol

2,4-bis(trifluoromethyl)benzyl alcohol

C9H6F6O (244.03228179999996)


   

2-Chloro-N-(2-methoxy-4-nitro-phenyl)-acetamide

2-Chloro-N-(2-methoxy-4-nitro-phenyl)-acetamide

C9H9ClN2O4 (244.0250824)


   

1-(chloromethyl)benzo[f]chromen-3-one

1-(chloromethyl)benzo[f]chromen-3-one

C14H9ClO2 (244.0291044)


   

phenoxathiin-4-boronic acid

phenoxathiin-4-boronic acid

C12H9BO3S (244.0365434)


   

4,4,5,5,6,6,6-Heptafluorohexane-1,2-diol

4,4,5,5,6,6,6-Heptafluorohexane-1,2-diol

C6H7F7O2 (244.03342460000002)


   

1,1,2,3,3,3-Hexafluoropropoxybenzene

1,1,2,3,3,3-Hexafluoropropoxybenzene

C9H6F6O (244.03228179999996)


   

2-thiophen-3-yl-3H-benzimidazole-5-carboxylic acid

2-thiophen-3-yl-3H-benzimidazole-5-carboxylic acid

C12H8N2O2S (244.0306468)


   

2-THIOPHEN-2-YL-3H-BENZOIMIDAZOLE-4-CARBOXYLIC ACID

2-THIOPHEN-2-YL-3H-BENZOIMIDAZOLE-4-CARBOXYLIC ACID

C12H8N2O2S (244.0306468)


   

2-Amino-5-bromo-3-(diethylamino)pyrazine

2-Amino-5-bromo-3-(diethylamino)pyrazine

C8H13BrN4 (244.0323518)


   

2-THIOPHEN-2-YL-1H-BENZOIMIDAZOLE-5-CARBOXYLIC ACID

2-THIOPHEN-2-YL-1H-BENZOIMIDAZOLE-5-CARBOXYLIC ACID

C12H8N2O2S (244.0306468)


   

5-(1H-BENZOIMIDAZOL-2-YLSULFANYL)-FURAN-2-CARBALDEHYDE

5-(1H-BENZOIMIDAZOL-2-YLSULFANYL)-FURAN-2-CARBALDEHYDE

C12H8N2O2S (244.0306468)


   
   

N-(5-bromo-2-pyrimidinyl)-N,N-dimethylethane-1,2-diamine

N-(5-bromo-2-pyrimidinyl)-N,N-dimethylethane-1,2-diamine

C8H13BrN4 (244.0323518)


   

2-Bromo-6-(3-methoxypropylamino)pyridine

2-Bromo-6-(3-methoxypropylamino)pyridine

C9H13BrN2O (244.02111879999998)


   

N-(5-Chloro-4-methoxy-2-nitrophenyl)acetamide

N-(5-Chloro-4-methoxy-2-nitrophenyl)acetamide

C9H9ClN2O4 (244.0250824)


   

Benzenemethanol, alpha,alpha-bis(trifluoromethyl)-

Benzenemethanol, alpha,alpha-bis(trifluoromethyl)-

C9H6F6O (244.03228179999996)


   

2,6-Dichloro-9-isopropyl-8-methyl-9H-purine

2,6-Dichloro-9-isopropyl-8-methyl-9H-purine

C9H10Cl2N4 (244.02824800000002)


   

(3,5-Bis(trifluoromethyl)phenyl)methanol

(3,5-Bis(trifluoromethyl)phenyl)methanol

C9H6F6O (244.03228179999996)


   

(Hydrazinocarbonyl)ferrocene

(Hydrazinocarbonyl)ferrocene

C11H12FeN2O (244.0298972)


   

1-(4-trifluoromethylphenyl)imidazoline-2-thione

1-(4-trifluoromethylphenyl)imidazoline-2-thione

C10H7F3N2S (244.0282018)


   

4-chloro-2H-benzo[h]chromene-3-carbaldehyde

4-chloro-2H-benzo[h]chromene-3-carbaldehyde

C14H9ClO2 (244.0291044)


   

1-chloro-3H-benzo[f]chromene-2-carbaldehyde

1-chloro-3H-benzo[f]chromene-2-carbaldehyde

C14H9ClO2 (244.0291044)


   

Imidazo[1,2-a]pyridine-7-carboxylic acid, 2-(2-thienyl)

Imidazo[1,2-a]pyridine-7-carboxylic acid, 2-(2-thienyl)

C12H8N2O2S (244.0306468)


   

1-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)-3,5-DIMETHYL-1H-PYRAZOLE HYDROBROMIDE

1-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)-3,5-DIMETHYL-1H-PYRAZOLE HYDROBROMIDE

C8H13BrN4 (244.0323518)


   
   

poassium 3-methoxyethylether phenyl trifluoroborate

poassium 3-methoxyethylether phenyl trifluoroborate

C8H9BF3KO2 (244.028474)


   

1-Bromo-2-fluoro-4-pentylbenzene

1-Bromo-2-fluoro-4-pentylbenzene

C11H14BrF (244.0262836)


   

(2-Chloro-4-methoxy-5-(methoxycarbonyl)phenyl)boronic acid

(2-Chloro-4-methoxy-5-(methoxycarbonyl)phenyl)boronic acid

C9H10BClO5 (244.030979)


   

2-CHLORO-N-(2-HYDROXY-5-NITROBENZYL)ACETAMIDE

2-CHLORO-N-(2-HYDROXY-5-NITROBENZYL)ACETAMIDE

C9H9ClN2O4 (244.0250824)


   

Benzenemethanol, a,3-bis(trifluoromethyl)-

Benzenemethanol, a,3-bis(trifluoromethyl)-

C9H6F6O (244.03228179999996)


   

2,5-Bis(trifluoromethyl)benzyl alcohol

2,5-Bis(trifluoromethyl)benzyl alcohol

C9H6F6O (244.03228179999996)


   

1-(2-Trifluoromethylphenyl)imidazoline-2-thione

1-(2-Trifluoromethylphenyl)imidazoline-2-thione

C10H7F3N2S (244.0282018)


   

3-AMINO-3-(4-CHLORO-3-NITRO-PHENYL)-PROPIONIC ACID

3-AMINO-3-(4-CHLORO-3-NITRO-PHENYL)-PROPIONIC ACID

C9H9ClN2O4 (244.0250824)


   

Methyl 7-(trifluoromethyl)-1-benzofuran-2-carboxylate

Methyl 7-(trifluoromethyl)-1-benzofuran-2-carboxylate

C11H7F3O3 (244.03472680000002)


   
   

potassium O-(2-ethylhexyl) dithiocarbonate

potassium O-(2-ethylhexyl) dithiocarbonate

C9H17KOS2 (244.03578519999996)


   
   

2-Deoxy-D-arabino-hexose 6-(dihydrogen phosphate)

2-Deoxy-D-arabino-hexose 6-(dihydrogen phosphate)

C6H13O8P (244.0348028)


   

2-{[(2-chloro-6-fluorophenyl)methyl]sulfanyl}-4,5-dihydro-1H-imidazole

2-{[(2-chloro-6-fluorophenyl)methyl]sulfanyl}-4,5-dihydro-1H-imidazole

C10H10ClFN2S (244.02372219999998)


   

[(3S,4R,5S)-3,4,5-trihydroxy-2-keto-hexyl] dihydrogen phosphate

[(3S,4R,5S)-3,4,5-trihydroxy-2-keto-hexyl] dihydrogen phosphate

C6H13O8P (244.0348028)


   

2-deoxy-glucose-6-phosphate

2-deoxy-glucose-6-phosphate

C6H13O8P (244.0348028)


   

Gentisein

9H-Xanthen-9-one, 1,3,7-trihydroxy-

C13H8O5 (244.0371718)


Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].

   

AIDS-011160

1,3,5-trihydroxy-9-xanthenone

C13H8O5 (244.0371718)


   

6-Deoxy-3-O-Sulfo-Alpha-L-Mannopyranose

6-Deoxy-3-O-Sulfo-Alpha-L-Mannopyranose

C6H12O8S (244.0252872)


   

L-rhamnitol 1-phosphate

L-rhamnitol 1-phosphate

C6H13O8P-2 (244.0348028)


   

Fuculose 1-phosphate

Fuculose 1-phosphate

C6H13O8P (244.0348028)


   

alpha-L-fucose 1-phosphate

alpha-L-fucose 1-phosphate

C6H13O8P (244.0348028)


   

[(2S,3S,4S,5S)-3,4,5,6-tetrahydroxyoxan-2-yl]methanesulfonic acid

[(2S,3S,4S,5S)-3,4,5,6-tetrahydroxyoxan-2-yl]methanesulfonic acid

C6H12O8S (244.0252872)


   

[(2S,3S,4S,5S,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methanesulfonic acid

[(2S,3S,4S,5S,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methanesulfonic acid

C6H12O8S (244.0252872)


   

apraclonidine

apraclonidine

C9H10Cl2N4 (244.02824800000002)


S - Sensory organs > S01 - Ophthalmologicals > S01E - Antiglaucoma preparations and miotics > S01EA - Sympathomimetics in glaucoma therapy C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D000322 - Adrenergic Agonists

   

beta-L-Fucose 1-phosphate

beta-L-Fucose 1-phosphate

C6H13O8P (244.0348028)


The beta-anomer of L-fucose 1-phosphate.

   

1,5,6-Trihydroxyxanthone

1,5,6-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

2-Deoxy-D-glucopyranose 6-phosphate

2-Deoxy-D-glucopyranose 6-phosphate

C6H13O8P (244.0348028)


   

6-deoxy-6-sulfo-D-fructofuranose

6-deoxy-6-sulfo-D-fructofuranose

C6H12O8S (244.0252872)


A carbohydrate sulfonate that is D-fructofuranose in which the hydroxy group at at position 6 is replaced by a sulfo group.

   

2-Deoxy-D-glucose 6-phosphate

2-Deoxy-D-glucose 6-phosphate

C6H13O8P (244.0348028)


A deoxyaldohexose phosphate comprising 2-deoxy-D-glucose having the phosphate group at the 6-position.

   

6-sulfo-beta-D-quinovose

6-sulfo-beta-D-quinovose

C6H12O8S (244.0252872)


A 6-sulfo-D-quinovose (6-deoxy-6-sulfo-D-glucopyranose) that has beta configuration at the anomeric centre.

   

6-sulfo-alpha-D-quinovose

6-sulfo-alpha-D-quinovose

C6H12O8S (244.0252872)


A 6-sulfo-D-quinovose that has alpha configuration at the anomeric centre.

   

L-fucopyranose 1-phosphate

L-fucopyranose 1-phosphate

C6H13O8P (244.0348028)


   

6-Sulfo-d-quinovose

6-Sulfo-d-quinovose

C6H12O8S (244.0252872)


A carbohydrate sulfonate that is D-quinovose (6-deoxy-D-glucose) in which one of the methyl hydrogens at position 6 is replaced by a sulfo group.

   
   

Deoxy-glucose phosphate

Deoxy-glucose phosphate

C6H13O8P (244.0348028)