Exact Mass: 347.016741

Exact Mass Matches: 347.016741

Found 117 metabolites which its exact mass value is equals to given mass value 347.016741, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Adenosine monophosphate

{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

C10H14N5O7P (347.0631)


Adenosine monophosphate, also known as adenylic acid or amp, is a member of the class of compounds known as purine ribonucleoside monophosphates. Purine ribonucleoside monophosphates are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached. Adenosine monophosphate is slightly soluble (in water) and a moderately acidic compound (based on its pKa). Adenosine monophosphate can be found in a number of food items such as kiwi, taro, alaska wild rhubarb, and skunk currant, which makes adenosine monophosphate a potential biomarker for the consumption of these food products. Adenosine monophosphate can be found primarily in most biofluids, including blood, feces, cerebrospinal fluid (CSF), and urine, as well as throughout all human tissues. Adenosine monophosphate exists in all living species, ranging from bacteria to humans. In humans, adenosine monophosphate is involved in several metabolic pathways, some of which include josamycin action pathway, methacycline action pathway, nevirapine action pathway, and aspartate metabolism. Adenosine monophosphate is also involved in several metabolic disorders, some of which include hyperornithinemia-hyperammonemia-homocitrullinuria [hhh-syndrome], molybdenum cofactor deficiency, xanthinuria type I, and mitochondrial DNA depletion syndrome. Adenosine monophosphate is a drug which is used for nutritional supplementation, also for treating dietary shortage or imbalanc. Adenosine monophosphate, also known as 5-adenylic acid and abbreviated AMP, is a nucleotide that is found in RNA. It is an ester of phosphoric acid with the nucleoside adenosine. AMP consists of the phosphate group, the pentose sugar ribose, and the nucleobase adenine. AMP can be produced during ATP synthesis by the enzyme adenylate kinase. AMP has recently been approved as a Bitter Blocker additive to foodstuffs. When AMP is added to bitter foods or foods with a bitter aftertaste it makes them seem sweeter. This potentially makes lower calorie food products more palatable. [Spectral] AMP (exact mass = 347.06308) and Guanine (exact mass = 151.04941) and 3,4-Dihydroxy-L-phenylalanine (exact mass = 197.06881) and Glutathione disulfide (exact mass = 612.15196) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] AMP (exact mass = 347.06308) and Glutathione disulfide (exact mass = 612.15196) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions. [Spectral] AMP (exact mass = 347.06308) and Adenine (exact mass = 135.0545) 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. Adenosine monophosphate. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=67583-85-1 (retrieved 2024-07-01) (CAS RN: 61-19-8). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction.

   

2'-Deoxyguanosine 5'-monophosphate

{[(2R,3S,5R)-5-(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}phosphonic acid

C10H14N5O7P (347.0631)


2-Deoxyguanosine 5-monophosphate, also known as deoxyguanylic acid or 2-deoxy-GMP, belongs to the class of organic compounds known as purine 2-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2. 2-Deoxyguanosine 5-monophosphate is a purine 2-deoxyribonucleoside 5-monophosphate having guanine as the nucleobase. It exists in all living species, ranging from bacteria to humans. Within humans, 2-deoxyguanosine 5-monophosphate participates in a number of enzymatic reactions. In particular, 2-deoxyguanosine 5-monophosphate can be converted into dGDP which is mediated by the enzyme guanylate kinase. In addition, 2-deoxyguanosine 5-monophosphate can be converted into deoxyguanosine through its interaction with the enzyme cytosolic purine 5-nucleotidase. In humans, 2-deoxyguanosine 5-monophosphate is involved in the metabolic disorder called the gout or kelley-seegmiller syndrome pathway. 2-Deoxyguanosine 5-monophosphate is a derivative of the common nucleic acid GTP, or guanosine triphosphate, in which the -OH (hydroxyl) group on the 2 carbon on the nucleotides pentose has been removed (hence the deoxy- part of the name). Additionally, the diphosphate of the name indicates that two of the phosphoryl groups of GTP have been removed, most likely by hydrolysis . [HMDB] Acquisition and generation of the data is financially supported in part by CREST/JST. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

3'-AMP

{[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy}phosphonic acid

C10H14N5O7P (347.0631)


Adenylic acid. Adenine nucleotide containing one phosphate group esterified to the sugar moiety in the 2-, 3-, or 5-position. 3-AMP has been identified in the human placenta (PMID: 32033212). Adenylic acid. Adenine nucleotide containing one phosphate group esterified to the sugar moiety in the 2-, 3-, or 5-position. [HMDB] Acquisition and generation of the data is financially supported in part by CREST/JST. CONFIDENCE standard compound; ML_ID 11

   

Adenosine 2'-phosphate

{[(3R,4R,5R)-2-(6-amino-9H-purin-9-yl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl]oxy}phosphonic acid

C10H14N5O7P (347.0631)


Adenosine 2-phosphate is converted enzymatically from adenosine 2,3-cyclic phosphate via the enzyme 2,3-cyclic-nucleotide 3-phosphodiesterase (EC 3.1.4.37). In the brain, this enzyme acts on 2,3-cyclic AMP more rapidly than on the UMP or CMP derivatives. In the liver, this enzyme acts on 2,3-cyclic CMP more rapidly than on the purine derivatives; it also hydrolyses the corresponding 3,5-cyclic phosphates, more slowly. This latter enzyme has been called cyclic-CMP phosphodiesterase. (KEGG). This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric diester bonds. The systematic name of this enzyme class is nucleoside-2,3-cyclic-phosphate 2-nucleotidohydrolase. (Wikipedia). Adenosine 2-phosphate is converted enzymatically from adenosine 2,3-cyclic phosphate via the enzyme 2,3-cyclic-nucleotide 3-phosphodiesterase (EC 3.1.4.37). In the brain, this enzyme acts on 2,3-cyclic AMP more rapidly than on the UMP or CMP derivatives. In the liver, this enzyme acts on 2,3-cyclic CMP more rapidly than on the purine derivatives; it also hydrolyses the corresponding 3,5-cyclic phosphates, more slowly. This latter enzyme has been called cyclic-CMP phosphodiesterase. (KEGG) Adenosine-2'-monophosphate (2'-AMP) is converted by extracellular 2’,3'-CAMP. Adenosine-2'-monophosphate is further metabolized to extracellular adenosine (a mechanism called the extracellular 2’,3’-cAMP-adenosine pathway). Adenosine-2'-monophosphate inhibits LPS-induced TNF-α and CXCL10 production via A2A receptor activation[1][2]. Adenosine-2'-monophosphate (2'-AMP) is converted by extracellular 2’,3'-CAMP. Adenosine-2'-monophosphate is further metabolized to extracellular adenosine (a mechanism called the extracellular 2’,3’-cAMP-adenosine pathway). Adenosine-2'-monophosphate inhibits LPS-induced TNF-α and CXCL10 production via A2A receptor activation[1][2]. Adenosine-2'-monophosphate (2'-AMP) is converted by extracellular 2’,3'-CAMP. Adenosine-2'-monophosphate is further metabolized to extracellular adenosine (a mechanism called the extracellular 2’,3’-cAMP-adenosine pathway). Adenosine-2'-monophosphate inhibits LPS-induced TNF-α and CXCL10 production via A2A receptor activation[1][2].

   

7-alpha-D-Ribosyladenine 5-phosphate

7-(5-phospho-alpha-D-ribosyl)adenine

C10H14N5O7P (347.0631)


   

Glucolepidiin

{[(1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulphanyl}propylidene)amino]oxy}sulphonic acid

C9H17NO9S2 (347.0345)


Glucolepidiin, also known as ethyl glucosinolate, is a member of the class of compounds known as alkylglucosinolates. Alkylglucosinolates are organic compounds containing a glucosinolate moiety that carries an alkyl chain. Glucolepidiin is soluble (in water) and an extremely strong acidic compound (based on its pKa). Glucolepidiin can be found in garden cress, horseradish, and radish, which makes glucolepidiin a potential biomarker for the consumption of these food products.

   

2-hydroxy-dAMP

{[(2R,3S,5R)-5-(6-amino-2-hydroxy-9H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}phosphonic acid

C10H14N5O7P (347.0631)


2-hydroxy-damp is a substrate for: 7,8-dihydro-8-oxoguanine triphosphatase.

   

5'-Hydroxypiroxicam

4-Hydroxy-N-(5-hydroxypyridin-2-yl)-2-methyl-1,1-dioxo-2H-1λ⁶,2-benzothiazine-3-carboximidate

C15H13N3O5S (347.0576)


5-Hydroxypiroxicam is only found in individuals that have used or taken Piroxicam. 5-Hydroxypiroxicam is a metabolite of Piroxicam. 5-hydroxypiroxicam belongs to the family of Benzothiazines. These are organic compounds containing a benzene fused to a thiazine ring (a six-member ring with four carbon atoms, one nitrogen atom and one sulfur atom).

   

Vidarabine phosphate

{[5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

C10H14N5O7P (347.0631)


Adenosine monophosphate, also known as 5-adenylic acid and abbreviated AMP, is a nucleotide that is found in RNA. It is an ester of phosphoric acid with the nucleoside adenosine. AMP consists of the phosphate group, the pentose sugar ribose, and the nucleobase adenine. AMP can be produced during ATP synthesis by the enzyme adenylate kinase. AMP has recently been approved as a Bitter Blocker additive to foodstuffs. When AMP is added to bitter foods or foods with a bitter aftertaste it makes them seem sweeter. This potentially makes lower calorie food products more palatable [HMDB] Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction.

   

3-Phosphoadenosine

{9-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-imino-6,9-dihydro-3H-purin-3-yl}phosphonic acid

C10H14N5O7P (347.0631)


   

8,14-Dihydroxyefavirenz

6-chloro-4-[2-(1-hydroxycyclopropyl)ethynyl]-4-(trifluoromethyl)-4H-3,1-benzoxazine-2,8-diol

C14H9ClF3NO4 (347.0172)


   

Zidovudine monophosphate

{[3-azido-5-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methoxy}phosphonic acid

C10H14N5O7P (347.0631)


   

6-(4-(Trifluoromethoxy)phenyl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridine

6-[4-(trifluoromethoxy)phenyl]-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridine

C14H7F6N3O (347.0493)


   

[(2R,5R)-5-(6-Aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate

[(2R,5R)-5-(6-Aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate

C10H14N5O7P (347.0631)


   

Vitacoxib

2-[4-Chloro-5-(4-methylphenyl)-1H-imidazol-1-yl]-5-methanesulphonylpyridine

C16H14ClN3O2S (347.0495)


   
   
   

5-Hydroxypiroxicam

5-Hydroxypiroxicam

C15H13N3O5S (347.0576)


   

2-Deoxyguanosine 3-monophosphate

2-Deoxyguanosine 3-monophosphate

C10H14N5O7P (347.0631)


   
   

SE 175

2-[[4-[(nitrooxy)methyl]benzoyl]thio]-benzoic acid, methyl ester

C16H13NO6S (347.0464)


   

2-Deoxy-5-Guanylic Acid

[(2R,5R)-5-(2-Amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl dihydrogen phosphate

C10H14N5O7P (347.0631)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS relative retention time with respect to 9-anthracene Carboxylic Acid is 0.057 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.055

   

3-Adenylic acid

Adenosine 3-monophosphate From Yeast

C10H14N5O7P (347.0631)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.055 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.056

   

Adenosine 5-monophosphate

Adenosine-5-monophosphate sodium salt

C10H14N5O7P (347.0631)


Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction.

   

2-Deoxyguanosine 5-monophosphate

2-Deoxyguanosine 5-monophosphate

C10H14N5O7P (347.0631)


A purine 2-deoxyribonucleoside 5-monophosphate having guanine as the nucleobase.

   

Adenosine-3-monophosphate

Adenosine-3-monophosphate

C10H14N5O7P (347.0631)


   

2-Adenylic acid

Adenosine-2-monophosphate

C10H14N5O7P (347.0631)


Adenosine-2'-monophosphate (2'-AMP) is converted by extracellular 2’,3'-CAMP. Adenosine-2'-monophosphate is further metabolized to extracellular adenosine (a mechanism called the extracellular 2’,3’-cAMP-adenosine pathway). Adenosine-2'-monophosphate inhibits LPS-induced TNF-α and CXCL10 production via A2A receptor activation[1][2]. Adenosine-2'-monophosphate (2'-AMP) is converted by extracellular 2’,3'-CAMP. Adenosine-2'-monophosphate is further metabolized to extracellular adenosine (a mechanism called the extracellular 2’,3’-cAMP-adenosine pathway). Adenosine-2'-monophosphate inhibits LPS-induced TNF-α and CXCL10 production via A2A receptor activation[1][2]. Adenosine-2'-monophosphate (2'-AMP) is converted by extracellular 2’,3'-CAMP. Adenosine-2'-monophosphate is further metabolized to extracellular adenosine (a mechanism called the extracellular 2’,3’-cAMP-adenosine pathway). Adenosine-2'-monophosphate inhibits LPS-induced TNF-α and CXCL10 production via A2A receptor activation[1][2].

   

Deoxyguanosine 5-monophosphate

Deoxyguanosine 5-monophosphate

C10H14N5O7P (347.0631)


   

Adenosine monophosphate

Adenosine monophosphate

C10H14N5O7P (347.0631)


   

Deoxyguanylic acid

Deoxyguanylic acid

C10H14N5O7P (347.0631)


   
   

AMP; LC-tDDA; CE10

AMP; LC-tDDA; CE10

C10H14N5O7P (347.0631)


   

AMP; LC-tDDA; CE20

AMP; LC-tDDA; CE20

C10H14N5O7P (347.0631)


   

AMP; LC-tDDA; CE30

AMP; LC-tDDA; CE30

C10H14N5O7P (347.0631)


   

AMP; LC-tDDA; CE40

AMP; LC-tDDA; CE40

C10H14N5O7P (347.0631)


   

DEOXYGUANOSINE-MONOPHOSPHATE

DEOXYGUANOSINE-MONOPHOSPHATE

C10H14N5O7P (347.0631)


   

Adenosine-monophosphate

Adenosine-monophosphate

C10H14N5O7P (347.0631)


   

5-Adenylic acid

[5-(6-Aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate

C10H14N5O7P (347.0631)


D000890 - Anti-Infective Agents > D000998 - Antiviral Agents D009676 - Noxae > D000963 - Antimetabolites

   

p-HydroxyPiroxicam

p-HydroxyPiroxicam

C15H13N3O5S (347.0576)


   

Zidovudine monophosphate

Zidovudine monophosphate

C10H14N5O7P (347.0631)


   

Pamabrom

Pamabrom

C11H18BrN5O3 (347.0593)


C78275 - Agent Affecting Blood or Body Fluid > C448 - Diuretic

   

4-IODO-3,5-DIPHENYLISOXAZOLE

4-IODO-3,5-DIPHENYLISOXAZOLE

C15H10INO (346.9807)


   

Benzyltrimethylammonium dichloroiodate

Benzyltrimethylammonium dichloroiodate

C10H16Cl2IN (346.9705)


   

Samarium, tris(h5-2,4-cyclopentadien-1-yl)-

Samarium, tris(h5-2,4-cyclopentadien-1-yl)-

C15H15Sm (347.0371)


   

1-[(2-bromophenyl)methylamino]cyclohexane-1-carboxylic acid

1-[(2-bromophenyl)methylamino]cyclohexane-1-carboxylic acid

C14H19BrClNO2 (347.0288)


   

5-(3-AMINO-5-OXO-2-PYRAZOLIN-1-YL)-2-PHENOXYBENZENESULFONIC ACID

5-(3-AMINO-5-OXO-2-PYRAZOLIN-1-YL)-2-PHENOXYBENZENESULFONIC ACID

C15H13N3O5S (347.0576)


   

Vidarabine phosphate

Vidarabine phosphate

C10H14N5O7P (347.0631)


D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C471 - Enzyme Inhibitor > C29575 - DNA Polymerase Inhibitor C254 - Anti-Infective Agent > C281 - Antiviral Agent D009676 - Noxae > D000963 - Antimetabolites Vidarabine phosphate (Ara-AMP), an antiviral agent, inhibits chronic HBV infection[1][2]. Vidarabine phosphate also against herpes simplex and varicella zoster viruses[3].

   

Piperidine, 1-​[(3-​bromo-​4-​methoxyphenyl)​sulfonyl]​-​4-​methyl-

Piperidine, 1-​[(3-​bromo-​4-​methoxyphenyl)​sulfonyl]​-​4-​methyl-

C13H18BrNO3S (347.0191)


   

5-Bromo-2,3-diphenyl-1H-indole

5-Bromo-2,3-diphenyl-1H-indole

C20H14BrN (347.031)


   

4-(Benzyloxy)-5-bromo-2-(piperidin-1-yl)pyrimidine

4-(Benzyloxy)-5-bromo-2-(piperidin-1-yl)pyrimidine

C16H18BrN3O (347.0633)


   

4-(4-Bromophenyl)-N,N-dimethylpiperazine-1-sulfonamide

4-(4-Bromophenyl)-N,N-dimethylpiperazine-1-sulfonamide

C12H18BrN3O2S (347.0303)


   

[2-(6-aminopurin-9-yl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate

[2-(6-aminopurin-9-yl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate

C10H14N5O7P (347.0631)


   

[4-(Bromoacetyl)phenyl]carbamic acid phenylmethyl ester

[4-(Bromoacetyl)phenyl]carbamic acid phenylmethyl ester

C16H14BrNO3 (347.0157)


   

5-(4-carboxy-2-nitrophenoxy)benzene-1,3-dicarboxylic acid

5-(4-carboxy-2-nitrophenoxy)benzene-1,3-dicarboxylic acid

C15H9NO9 (347.0277)


   

Methyl 4-bromo-2-(trifluoromethyl)quinoline-3-carboxylate

Methyl 4-bromo-2-(trifluoromethyl)quinoline-3-carboxylate

C13H9BrF3NO2 (346.9769)


   

6-CHLORO-2-(4-CHLOROBENZOYL)INDOL-3-ACETIC ACID

6-CHLORO-2-(4-CHLOROBENZOYL)INDOL-3-ACETIC ACID

C17H11Cl2NO3 (347.0116)


   

4-(6-Bromo-4-propoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)-2-pyrimidinamine

4-(6-Bromo-4-propoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)-2-pyrimidinamine

C14H14BrN5O (347.0382)


   

2-BROMO-1-[4-(MORPHOLIN-4-YLSULFONYL)PHENYL]ETHANONE

2-BROMO-1-[4-(MORPHOLIN-4-YLSULFONYL)PHENYL]ETHANONE

C12H14BrNO4S (346.9827)


   

(2-IODO-BENZYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER

(2-IODO-BENZYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER

C13H18INO2 (347.0382)


   

methyl 2-(butanoylamino)-5-iodobenzoate

methyl 2-(butanoylamino)-5-iodobenzoate

C12H14INO3 (347.0018)


   

methyl 5-iodo-2-morpholin-4-ylbenzoate

methyl 5-iodo-2-morpholin-4-ylbenzoate

C12H14INO3 (347.0018)


   

methyl 3-iodo-4-morpholin-4-ylbenzoate

methyl 3-iodo-4-morpholin-4-ylbenzoate

C12H14INO3 (347.0018)


   

Ethyl 4-(diethylamino)-3-iodobenzoate

Ethyl 4-(diethylamino)-3-iodobenzoate

C13H18INO2 (347.0382)


   

Ethyl 4-(butylamino)-3-iodobenzoate

Ethyl 4-(butylamino)-3-iodobenzoate

C13H18INO2 (347.0382)


   

Butyl 4-(dimethylamino)-3-iodobenzoate

Butyl 4-(dimethylamino)-3-iodobenzoate

C13H18INO2 (347.0382)


   

4-(5-Bromo-thiazol-2-yl)-piperazine-1-carboxylic acid tert-butyl ester

4-(5-Bromo-thiazol-2-yl)-piperazine-1-carboxylic acid tert-butyl ester

C12H18BrN3O2S (347.0303)


   

ethyl 4-(5,6-dichloro-1-methylindol-2-yl)benzoate

ethyl 4-(5,6-dichloro-1-methylindol-2-yl)benzoate

C18H15Cl2NO2 (347.048)


   

TRICARBONYLTRIS(PROPIONITRILE)MOLYBDENUM (0)

TRICARBONYLTRIS(PROPIONITRILE)MOLYBDENUM (0)

C12H15MoN3O3 (347.0167)


   

tert-butyl N-[3-bromo-1-(3-chlorophenyl)propyl]carbamate

tert-butyl N-[3-bromo-1-(3-chlorophenyl)propyl]carbamate

C14H19BrClNO2 (347.0288)


   

Hexaamminecobalt(III) nitrate

Hexaamminecobalt(III) nitrate

CoH18N9O9 (347.0559)


   

4-(4-bromo-3-((methoxymethoxy) methyl)phenoxy) benzonitrile

4-(4-bromo-3-((methoxymethoxy) methyl)phenoxy) benzonitrile

C16H14BrNO3 (347.0157)


   

2-AMino-3-(4-broMobenzoyl)phenyloxoacetic Acid

2-AMino-3-(4-broMobenzoyl)phenyloxoacetic Acid

C15H10BrNO4 (346.9793)


   

samarium acetate hydrate

samarium acetate hydrate

C6H11O7Sm (346.9702)


   

1,3,6,8-Tetranitro-9H-carbazole

1,3,6,8-Tetranitro-9H-carbazole

C12H5N5O8 (347.0138)


   

5H-Pyrrolo3,2-dpyrimidine, 7-bromo-4-methoxy-5-(phenylmethoxy)methyl-

5H-Pyrrolo3,2-dpyrimidine, 7-bromo-4-methoxy-5-(phenylmethoxy)methyl-

C15H14BrN3O2 (347.0269)


   

3-iodo-1-methyl-2-p-tolyl-1h-indole

3-iodo-1-methyl-2-p-tolyl-1h-indole

C16H14IN (347.0171)


   

3-iodo-4-(morpholin-4-ylmethyl)benzoic acid

3-iodo-4-(morpholin-4-ylmethyl)benzoic acid

C12H14INO3 (347.0018)


   

Formycin-5-monophosphate

Formycin-5-monophosphate

C10H14N5O7P (347.0631)


D000970 - Antineoplastic Agents > D000903 - Antibiotics, Antineoplastic > D005573 - Formycins

   

2-Deoxyguanosine 3-(dihydrogen phosphate)

2-Deoxyguanosine 3-(dihydrogen phosphate)

C10H14N5O7P (347.0631)


   

6-(4-(Trifluoromethoxy)phenyl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridine

6-(4-(Trifluoromethoxy)phenyl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridine

C14H7F6N3O (347.0493)


   

rac 8,14-Dihydroxy Efavirenz

rac 8,14-Dihydroxy Efavirenz

C14H9ClF3NO4 (347.0172)


   

(E)-4-(4-bromophenyl)-2-((E)-(furan-2-ylmethylene)hydrazono)-2,3-dihydrothiazole

(E)-4-(4-bromophenyl)-2-((E)-(furan-2-ylmethylene)hydrazono)-2,3-dihydrothiazole

C14H10BrN3OS (346.9728)


   

5-{[(2,4-dichlorobenzyl)sulfanyl]methyl}-4-isopropyl-4H-1,2,4-triazole-3-thiol

5-{[(2,4-dichlorobenzyl)sulfanyl]methyl}-4-isopropyl-4H-1,2,4-triazole-3-thiol

C13H15Cl2N3S2 (347.0084)


   

alpha-Adenosine monophosphate

alpha-Adenosine monophosphate

C10H14N5O7P (347.0631)


   

7-alpha-D-Ribofuranosyl-2-aminopurine-5-phosphate

7-alpha-D-Ribofuranosyl-2-aminopurine-5-phosphate

C10H14N5O7P (347.0631)


   

8-hydroxy-dAMP

8-hydroxy-dAMP

C10H14N5O7P (347.0631)


A purine 2-deoxyribonucleoside 5-monophosphate that is that is dAMP in which the hydrogen at position 8 of the purine base has been replaced by a hydroxy group.

   

N-iodoacetyl-glucosamine

N-iodoacetyl-glucosamine

C8H14INO6 (346.9866)


   

[5-(7-amino-2H-pyrazolo[4,3-d]pyrimidin-3-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate

[5-(7-amino-2H-pyrazolo[4,3-d]pyrimidin-3-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate

C10H14N5O7P (347.0631)


   

[9-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-iminopurin-3-yl]phosphonic acid

[9-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-iminopurin-3-yl]phosphonic acid

C10H14N5O7P (347.0631)


   

Adenosine 5-Monophosphate

Adenosine 5-Monophosphate

C10H14N5O7P (347.0631)


   

2-[(4-Bromophenyl)methylthio]-5-(3-pyridinyl)-1,3,4-oxadiazole

2-[(4-Bromophenyl)methylthio]-5-(3-pyridinyl)-1,3,4-oxadiazole

C14H10BrN3OS (346.9728)


   

N-[[[(2,4-dichlorophenyl)-oxomethyl]hydrazo]-sulfanylidenemethyl]-2,2-dimethylpropanamide

N-[[[(2,4-dichlorophenyl)-oxomethyl]hydrazo]-sulfanylidenemethyl]-2,2-dimethylpropanamide

C13H15Cl2N3O2S (347.0262)


   

N-[(2-chlorobenzoyl)oxy]-2-methyl-5-(trifluoromethyl)-1,3-oxazole-4-carboximidamide

N-[(2-chlorobenzoyl)oxy]-2-methyl-5-(trifluoromethyl)-1,3-oxazole-4-carboximidamide

C13H9ClF3N3O3 (347.0285)


   

1-[4-(4-Bromophenyl)-2-thiazolyl]-4-piperidinecarbonitrile

1-[4-(4-Bromophenyl)-2-thiazolyl]-4-piperidinecarbonitrile

C15H14BrN3S (347.0092)


   

N-(1,1-dioxo-2,3-dihydrothiophen-3-yl)-N-(2-ethylphenyl)-2-thiophenecarboxamide

N-(1,1-dioxo-2,3-dihydrothiophen-3-yl)-N-(2-ethylphenyl)-2-thiophenecarboxamide

C17H17NO3S2 (347.065)


   

2-Chloro-5-[[2,3-dihydro-1,4-benzodioxin-3-yl(oxo)methyl]amino]benzoic acid methyl ester

2-Chloro-5-[[2,3-dihydro-1,4-benzodioxin-3-yl(oxo)methyl]amino]benzoic acid methyl ester

C17H14ClNO5 (347.056)


   

N-(5-chloro-2-methoxyphenyl)-2-pyridin-4-yl-4,5-dihydrothiazole-4-carboxamide

N-(5-chloro-2-methoxyphenyl)-2-pyridin-4-yl-4,5-dihydrothiazole-4-carboxamide

C16H14ClN3O2S (347.0495)


   

2-amino-9-(2-deoxy-5-O-phosphono-beta-L-erythro-pentofuranosyl)-1,9-dihydro-6H-purin-6-one

2-amino-9-(2-deoxy-5-O-phosphono-beta-L-erythro-pentofuranosyl)-1,9-dihydro-6H-purin-6-one

C10H14N5O7P (347.0631)


   

8-Amino-9-benzoyl-5-oxa-7-thia-cyclohepta[a]naphthalen-6-one

8-Amino-9-benzoyl-5-oxa-7-thia-cyclohepta[a]naphthalen-6-one

C20H13NO3S (347.0616)


   

O-(alpha-D-mannose-1-phosphoryl)-L-serine

O-(alpha-D-mannose-1-phosphoryl)-L-serine

C9H18NO11P (347.0617)


   

3-({[5-(4-Bromophenyl)-1,3-oxazol-2-yl]methylidene}amino)-2,5-dioxoimidazolidin-1-ide

3-({[5-(4-Bromophenyl)-1,3-oxazol-2-yl]methylidene}amino)-2,5-dioxoimidazolidin-1-ide

C13H8BrN4O3- (346.978)


   

6-(3-hydroxy-1,4-dioxobutan-2-yl)-9-methoxy-3,4-dioxo-1,4-dihydro-3H-furo[3,4-C][1]benzopyran-7-olate

6-(3-hydroxy-1,4-dioxobutan-2-yl)-9-methoxy-3,4-dioxo-1,4-dihydro-3H-furo[3,4-C][1]benzopyran-7-olate

C16H11O9- (347.0403)


   

1-S-[(1Z)-N-(sulfooxy)propanimidoyl]-1-thio-beta-D-glucopyranose

1-S-[(1Z)-N-(sulfooxy)propanimidoyl]-1-thio-beta-D-glucopyranose

C9H17NO9S2 (347.0345)


   

(1S)-13-iodo-1-methyl-16-azatetracyclo[7.6.1.02,7.010,15]hexadeca-2,4,6,10(15),11,13-hexaene

(1S)-13-iodo-1-methyl-16-azatetracyclo[7.6.1.02,7.010,15]hexadeca-2,4,6,10(15),11,13-hexaene

C16H14IN (347.0171)


   

(1R,9S)-13-iodo-1-methyl-16-azatetracyclo[7.6.1.02,7.010,15]hexadeca-2,4,6,10(15),11,13-hexaene

(1R,9S)-13-iodo-1-methyl-16-azatetracyclo[7.6.1.02,7.010,15]hexadeca-2,4,6,10(15),11,13-hexaene

C16H14IN (347.0171)


   

[(2S,3R,4R,5S)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate

[(2S,3R,4R,5S)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate

C10H14N5O7P (347.0631)


   

Adenosine phosphate

Adenosine 5-monophosphate

C10H14N5O7P (347.0631)


A purine ribonucleoside 5-monophosphate having adenine as the nucleobase. COVID info from PDB, Protein Data Bank, COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction.

   
   

7-(5-phospho-alpha-D-ribosyl)adenine

7-(5-phospho-alpha-D-ribosyl)adenine

C10H14N5O7P (347.0631)


   

Glucolepidiin

Glucolepidiin

C9H17NO9S2 (347.0345)


An alkylglucosinolic acid that consists of 1-thio-beta-D-glucopyranose attached to an -N-(sulfooxy)propanimidoyl group at the anomeric sulfur. It occurs in Lepidium sativum (garden cress) and Armoracia lapathifolia (horseraddish). A flavour component; the hydrolysis product, ethyl isothiocyanate, is very pungent and garlic-like.

   

8-oxo-dAMP

8-oxo-dAMP

C10H14N5O7P (347.0631)


A purine 2-deoxyribonucleoside 5-diphosphate that is the 8-oxo derivative of dADP.

   

Adenosine 2-phosphate

Adenosine 2-phosphate

C10H14N5O7P (347.0631)


   

3-AMP

3-AMP

C10H14N5O7P (347.0631)


An adenosine 3-phosphate with a monophosphate group at the 3-position.

   

ROCK-IN-5

ROCK-IN-5

C16H11ClFN3OS (347.0295)


ROCK-IN-5 (compound I-B-37) is a potent inhibitor of ROCK, ERK, GSK, and AGC protein kinases. ROCK-IN-5 has the potential for proliferative, cardiac and neurodegenerative diseases research[1].

   

SCH-202676 (hydrobromide)

SCH-202676 (hydrobromide)

C15H14BrN3S (347.0092)


SCH-202676 hydrobromide is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). SCH-202676 hydrobromide has antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 μM[1][2][3][4]. SCH-202676 hydrobromide is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). SCH-202676 hydrobromide has antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 μM[1][2][3][4].

   
   

[3-hydroxy-5-(6-hydroxy-2-imino-3h-purin-9-yl)oxolan-2-yl]methoxyphosphonic acid

[3-hydroxy-5-(6-hydroxy-2-imino-3h-purin-9-yl)oxolan-2-yl]methoxyphosphonic acid

C10H14N5O7P (347.0631)