Exact Mass: 476.01195780000006

Exact Mass Matches: 476.01195780000006

Found 48 metabolites which its exact mass value is equals to given mass value 476.01195780000006, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Cefazolin sodium

Cephazolin sodium

C14H13N8NaO4S3 (476.01195780000006)


D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D002511 - Cephalosporins D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams C254 - Anti-Infective Agent > C258 - Antibiotic > C260 - Beta-Lactam Antibiotic

   

Ebrotidine

4-Bromo-N-(((2-(((-((diaminomethylene)amino)-4-thiazolyl)methyl)thio)ethyl)amino)methylene)benzenesulfonamide

C14H17BrN6O2S3 (475.9758442)


Ebrotidine is an H2 receptor antagonist with gastroprotective activity against ethanol-, aspirin- or stress-induced gastric mucosal damage. The antisecretory properties of ebrotidine are similar to those of ranitidine, and approximately 10-fold greater than those of cimetidine. Ebrotidine has anti-Helicobacter pylori activity via inhibition of the urease enzyme and the proteolytic and mucolytic activities of the bacterium. However, its activity is synergistic with a number of antibacterial agents. Ebrotidine counteracts the inhibitory effects of H. pylori lipo-polysaccharides. C78276 - Agent Affecting Digestive System or Metabolism > C29701 - Anti-ulcer Agent > C29702 - Histamine-2 Receptor Antagonist D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents Ebrotidine(FI 3542) is a competitive H2-receptor antagonist (Ki= 127.5 nM) with a potent antisecretory activity and evidenced gastroprotection. IC50 Value: 127.5 nM (Ki)[1]; 0.21mg/kg (ED50, histamine- stimulated acid secretion) [2] Target: H2 receptor in vitro: Ebrotidine displaced 3H-thiotidine specific binding to histamine H2-receptors (Ki: 127.5 nmol/l), showing a higher affinity (p < 0.05) than ranitidine (Ki: 190.0 nmol/l) and cimetidine (Ki: 246.1 nmol/l) [1]. in vivo: Following intravenous administration to rats, ebrotidine inhibited histamine- and pentagastrin-stimulated acid secretion in a dose-dependent manner, ED50 being 0.21 and 0.44 mg/kg, respectively [2]. The mean number of gastric erosions seen at endoscopy after treatment with ebrotidine plus ASA (2.0 +/- 0.3) was significantly lower than that after placebo plus ASA (3.7 +/- 0.2). This reduction in lesion core by ebrotidine was accompanied by a significant increase in gastric blood flow (by 15\% in corpus and 26\% in antrum), by a rise in transmucosal potential difference (by 12\%), and by a decrease of mucosal microbleeding [3]. Results of macroscopic assessment revealed that ebrotidine at doses of 50mg and higher/kg body weight effectively prevented mucosal injury, and that the maximal protective effect was achieved by 1h. Physicochemical analysis established that ebrotidine evoked 30\% increase in mucus gel dimension, and showed 20\% increase in phospholipids, and the content of sulfo- (18\%) and sialomucins (21\%) [4].

   

Ellagic acid acetyl-xyloside

(3R,4R,5R,6S)-4,5-dihydroxy-6-({7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-6-yl}oxy)oxan-3-yl acetate

C21H16O13 (476.0590886)


Ellagic acid acetyl-xyloside is a member of the class of compounds known as hydrolyzable tannins. Hydrolyzable tannins are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. Ellagic acid acetyl-xyloside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Ellagic acid acetyl-xyloside can be found in red raspberry, which makes ellagic acid acetyl-xyloside a potential biomarker for the consumption of this food product.

   

Ellagic acid acetyl-arabinoside

(3S,4R,5R,6S)-4,5-dihydroxy-6-({7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-6-yl}oxy)oxan-3-yl acetate

C21H16O13 (476.0590886)


Ellagic acid acetyl-arabinoside is a member of the class of compounds known as hydrolyzable tannins. Hydrolyzable tannins are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. Ellagic acid acetyl-arabinoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Ellagic acid acetyl-arabinoside can be found in red raspberry, which makes ellagic acid acetyl-arabinoside a potential biomarker for the consumption of this food product.

   
   

Rhamnetin 3,3-disulfate

5-Hydroxy-2-[4-hydroxy-3-(sulfooxy)phenyl]-7-methoxy-3-(sulfooxy)-4H-1-benzopyran-4-one

C16H12O13S2 (475.9719342)


   

6-Hydroxyluteolin 3-methyl ether 6,7-disulfate

5,6,7,4-Tetrahydroxy-3-methoxyflavone 6,7-disulfate

C16H12O13S2 (475.9719342)


   

6-Methoxyluteolin 3,4-disulfate

6-Methoxyluteolin 3,4-disulfate

C16H12O13S2 (475.9719342)


   

Isorhamnetin 3,4-di-O-sulfate

3,4,5,7-Tetrahydroxy-3-methoxyflavone 3,4-di-O-sulfate

C16H12O13S2 (475.9719342)


   

2,6-Bis(2,2,2-trifluoroethoxy)-3-{[3-(trifluoromethyl)-2-pyridyl]thio}benzonitrile

2,6-Bis(2,2,2-trifluoroethoxy)-3-{[3-(trifluoromethyl)-2-pyridyl]thio}benzonitrile

C17H9F9N2O2S (476.02410019999996)


   
   
   

(2R,3S,4R,5S,6S,7R)-2,3,5,6,7-pentachloropentadec-14-en-4-yl hydrogen sulfate

(2R,3S,4R,5S,6S,7R)-2,3,5,6,7-pentachloropentadec-14-en-4-yl hydrogen sulfate

C15H25Cl5O4S (475.9916120000001)


   

3,4-dioxoloellagic acid 4-glucoside|3,4-methylene-4-O-beta-D-glucopyranosylellagic acid|3,4-methylenedioxyellagic acid 4-O-beta-D-glucopyranoside|okicamelliaside

3,4-dioxoloellagic acid 4-glucoside|3,4-methylene-4-O-beta-D-glucopyranosylellagic acid|3,4-methylenedioxyellagic acid 4-O-beta-D-glucopyranoside|okicamelliaside

C21H16O13 (476.0590886)


   

Neoirienone|neoirieone

Neoirienone|neoirieone

C20H30Br2O3 (476.056155)


   
   

Isorhamnetin 3,7-di-O-sulfate

Isorhamnetin 3,7-di-O-sulfate

C16H12O13S2 (475.9719342)


   

Ebrotidine

N-[(4-bromobenzene)sulfonyl]-N-(2-{[(2-carbamimidamido-1,3-thiazol-4-yl)methyl]sulfanyl}ethyl)methanimidamide

C14H17BrN6O2S3 (475.9758442)


C78276 - Agent Affecting Digestive System or Metabolism > C29701 - Anti-ulcer Agent > C29702 - Histamine-2 Receptor Antagonist D018377 - Neurotransmitter Agents > D018494 - Histamine Agents > D006633 - Histamine Antagonists D005765 - Gastrointestinal Agents > D000897 - Anti-Ulcer Agents Ebrotidine(FI 3542) is a competitive H2-receptor antagonist (Ki= 127.5 nM) with a potent antisecretory activity and evidenced gastroprotection. IC50 Value: 127.5 nM (Ki)[1]; 0.21mg/kg (ED50, histamine- stimulated acid secretion) [2] Target: H2 receptor in vitro: Ebrotidine displaced 3H-thiotidine specific binding to histamine H2-receptors (Ki: 127.5 nmol/l), showing a higher affinity (p < 0.05) than ranitidine (Ki: 190.0 nmol/l) and cimetidine (Ki: 246.1 nmol/l) [1]. in vivo: Following intravenous administration to rats, ebrotidine inhibited histamine- and pentagastrin-stimulated acid secretion in a dose-dependent manner, ED50 being 0.21 and 0.44 mg/kg, respectively [2]. The mean number of gastric erosions seen at endoscopy after treatment with ebrotidine plus ASA (2.0 +/- 0.3) was significantly lower than that after placebo plus ASA (3.7 +/- 0.2). This reduction in lesion core by ebrotidine was accompanied by a significant increase in gastric blood flow (by 15\% in corpus and 26\% in antrum), by a rise in transmucosal potential difference (by 12\%), and by a decrease of mucosal microbleeding [3]. Results of macroscopic assessment revealed that ebrotidine at doses of 50mg and higher/kg body weight effectively prevented mucosal injury, and that the maximal protective effect was achieved by 1h. Physicochemical analysis established that ebrotidine evoked 30\% increase in mucus gel dimension, and showed 20\% increase in phospholipids, and the content of sulfo- (18\%) and sialomucins (21\%) [4].

   
   
   

(4-Bromobutyl)(triphenyl)phosphonium bromide

(4-Bromobutyl)(triphenyl)phosphonium bromide

C22H23Br2P (475.99040080000003)


   

sodium,formaldehyde,2-hydroxybenzenesulfonate,4-(4-hydroxyphenyl)sulfonylphenol

sodium,formaldehyde,2-hydroxybenzenesulfonate,4-(4-hydroxyphenyl)sulfonylphenol

C19H17NaO9S2 (476.0211672)


   

1-[4-chloro-3-(trifluoromethyl)phenyl]-3-[4-[6-(1,2,4-oxadiazol-3-yl)pyrimidin-4-yl]oxyphenyl]urea

1-[4-chloro-3-(trifluoromethyl)phenyl]-3-[4-[6-(1,2,4-oxadiazol-3-yl)pyrimidin-4-yl]oxyphenyl]urea

C20H12ClF3N6O3 (476.06114679999996)


   
   

PH-797804

3-(3-Bromo-4-((2,4-difluorobenzyl)oxy)-6-methyl-2-oxopyridin-1(2H)-yl)-N,4-dimethylbenzamide

C22H19BrF2N2O3 (476.0547028000001)


   

(R,R)-1,2-Bis(Trifluoromethanesulfonamido)-1,2-Diphenylethane

(R,R)-1,2-Bis(Trifluoromethanesulfonamido)-1,2-Diphenylethane

C16H14F6N2O4S2 (476.02991560000004)


   

6,13-dibromo-9,10-dimethoxy-1a,2,3,4,4a,5-hexahydro-1H-indeno[2,1-d]fluorene

6,13-dibromo-9,10-dimethoxy-1a,2,3,4,4a,5-hexahydro-1H-indeno[2,1-d]fluorene

C22H22Br2O2 (475.99864319999995)


   

Sitaxentan sodium

Sitaxentan sodium

C18H14ClN2NaO6S2 (475.98794940000005)


Sitaxsentan sodium (IPI 1040 sodium; TBC11251 sodium) is an orally active, highly selective antagonist of endothelin A receptors.

   

[[[1-[5-[2-Chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenyl]-2-methoxyethylidene]amino]oxy]acetic acid methyl ester

[[[1-[5-[2-Chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenyl]-2-methoxyethylidene]amino]oxy]acetic acid methyl ester

C19H16ClF3N2O7 (476.0598092)


   

(Trimethylsilylmethyl)triphenylphosphonium iodide

(Trimethylsilylmethyl)triphenylphosphonium iodide

C22H26IPSi (476.0586076)


   

(3-BROMOBUTYL)TRIPHENYLPHONIUM BROMIDE

(3-BROMOBUTYL)TRIPHENYLPHONIUM BROMIDE

C22H23Br2P (475.99040080000003)


   

1H,1H,2H,3H-PERFLUOROUNDEC-2-EN-1-OL

1H,1H,2H,3H-PERFLUOROUNDEC-2-EN-1-OL

C11H5F17O (476.00689239999997)


   

bis(chlorophenyl)phenylsulphonium hexafluorophosphate(1-)

bis(chlorophenyl)phenylsulphonium hexafluorophosphate(1-)

C18H13Cl2F6PS (475.97568000000007)


   

N,N-((1S,2S)-1,2-DIPHENYLETHANE-1,2-DIYL)BIS(1,1,1-TRIFLUOROMETHANESULFONAMIDE)

N,N-((1S,2S)-1,2-DIPHENYLETHANE-1,2-DIYL)BIS(1,1,1-TRIFLUOROMETHANESULFONAMIDE)

C16H14F6N2O4S2 (476.02991560000004)


   

(η-cumene)-(η-cyclopentadienyl)iron(II) hexafluoroantimonate

(η-cumene)-(η-cyclopentadienyl)iron(II) hexafluoroantimonate

C14H17F6FeSb (475.9622004)


   

mercuric salicylate

mercuric salicylate

C14H10HgO6 (476.018368)


   

sodium,formaldehyde,4-hydroxybenzenesulfonic acid,4-(4-hydroxyphenyl)sulfonylphenolate

sodium,formaldehyde,4-hydroxybenzenesulfonic acid,4-(4-hydroxyphenyl)sulfonylphenolate

C19H17NaO9S2 (476.0211672)


   
   
   

Benzamide, N-(cyclopropylmethoxy)-3,4,5-trifluoro-2-((4-iodo-2-methylphenyl)amino)-

Benzamide, N-(cyclopropylmethoxy)-3,4,5-trifluoro-2-((4-iodo-2-methylphenyl)amino)-

C18H16F3IN2O2 (476.02085819999996)


   

[10-(4-chlorophenyl)-2,6,8-trioxo-3,4a,5,5a,6,8,8a,9,9a,10-decahydro-5,9-methano[1,3]thiazolo[5,4:5,6]thiopyrano[2,3-f]isoindol-7(2H)-yl]acetic acid

[10-(4-chlorophenyl)-2,6,8-trioxo-3,4a,5,5a,6,8,8a,9,9a,10-decahydro-5,9-methano[1,3]thiazolo[5,4:5,6]thiopyrano[2,3-f]isoindol-7(2H)-yl]acetic acid

C21H17ClN2O5S2 (476.0267382)


   

2-({4-[(5-Chloro-1H-indol-2-YL)sulfonyl]piperazin-1-YL}carbonyl)thieno[3,2-B]pyridine 4-oxide

2-({4-[(5-Chloro-1H-indol-2-YL)sulfonyl]piperazin-1-YL}carbonyl)thieno[3,2-B]pyridine 4-oxide

C20H17ClN4O4S2 (476.0379712)


   

(2S,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-3-oxido-4-oxochromen-2-yl)-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylate

(2S,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-3-oxido-4-oxochromen-2-yl)-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylate

C21H16O13-2 (476.0590886)


   

4-Bromo-3-(carboxymethoxy)-5-[4-[[oxo(3-pyridinyl)methyl]amino]phenyl]-2-thiophenecarboxylic acid

4-Bromo-3-(carboxymethoxy)-5-[4-[[oxo(3-pyridinyl)methyl]amino]phenyl]-2-thiophenecarboxylic acid

C19H13BrN2O6S (475.96776580000005)


   

N-[2-[(5Z)-2,4-dioxo-5-(pyridin-3-ylmethylidene)-1,3-thiazolidin-3-yl]ethyl]-4-methylsulfonyl-3-nitrobenzamide

N-[2-[(5Z)-2,4-dioxo-5-(pyridin-3-ylmethylidene)-1,3-thiazolidin-3-yl]ethyl]-4-methylsulfonyl-3-nitrobenzamide

C19H16N4O7S2 (476.0460386)


   

2-[(2Z)-2-[[4-(4-chlorophenyl)-1,3-thiazol-2-yl]methylidene]-4-oxo-1,3-thiazolidin-3-yl]-N-(2-chloropyridin-3-yl)acetamide

2-[(2Z)-2-[[4-(4-chlorophenyl)-1,3-thiazol-2-yl]methylidene]-4-oxo-1,3-thiazolidin-3-yl]-N-(2-chloropyridin-3-yl)acetamide

C20H14Cl2N4O2S2 (475.99352039999997)


   

(1r,4r,5s,6s,9r)-9-bromo-4-{[(1r,4r)-4-bromo-1-hydroxy-3,3-dimethylcyclohexyl]methyl}-6-methyl-11-oxatricyclo[4.3.2.0¹,⁵]undecan-10-one

(1r,4r,5s,6s,9r)-9-bromo-4-{[(1r,4r)-4-bromo-1-hydroxy-3,3-dimethylcyclohexyl]methyl}-6-methyl-11-oxatricyclo[4.3.2.0¹,⁵]undecan-10-one

C20H30Br2O3 (476.056155)