Exact Mass: 270.122

Exact Mass Matches: 270.122

Found 34 metabolites which its exact mass value is equals to given mass value 270.122, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

Hypoglycin B

2-Amino-4-{[1-carboxy-2-(2-methylidenecyclopropyl)ethyl]-C-hydroxycarbonimidoyl}butanoate

C12H18N2O5 (270.1216)


Hypoglycin B is found in fruits. Hypoglycin B is a biologically active component of Blighia sapida (akee apple) Hypoglycin B is a naturally occurring organic compound in the species Blighia sapida. It is particularly concentrated in the fruit of the plant especially in the seeds. Hypoglycin B is toxic if ingested and is a causative agent of Jamaican Vomiting Sickness. It is an amino acid and chemically related to lysine Biologically active component of Blighia sapida (akee apple)

   

Tetaine

Bacilysin

C12H18N2O5 (270.1216)


A non-ribosomally synthesised dipeptide that consists of L-alanyl and anticapsin units linked by a peptide bond.

   

voxtalisib

2-amino-8-ethyl-4-methyl-6-(1H-pyrazol-5-yl)-7H,8H-pyrido[2,3-d]pyrimidin-7-one

C13H14N6O (270.1229)


C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C2152 - Phosphatidylinositide 3-Kinase Inhibitor C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor C274 - Antineoplastic Agent > C1742 - Angiogenesis Inhibitor C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor Voxtalisib (XL765) is a potent PI3K inhibitor, which has a similar activity toward class I PI3K (IC50s=39, 113, 9 and 43?nM for p110α, p110β, p110γ and p110δ, respectively), also inhibits DNA-PK (IC50=150?nM) and mTOR (IC50=157?nM). Voxtalisib (XL765) inhibits mTORC1 and mTORC2 with IC50s of 160 and 910 nM, respectively. Voxtalisib (XL765) is a potent PI3K inhibitor, which has a similar activity toward class I PI3K (IC50s=39, 113, 9 and 43?nM for p110α, p110β, p110γ and p110δ, respectively), also inhibits DNA-PK (IC50=150?nM) and mTOR (IC50=157?nM). Voxtalisib (XL765) inhibits mTORC1 and mTORC2 with IC50s of 160 and 910 nM, respectively.

   

6-(phenylhydrazinylidene)hexane-1,2,3,4,5-pentol

6-(phenylhydrazinylidene)hexane-1,2,3,4,5-pentol

C12H18N2O5 (270.1216)


   

2-(3,4-dihydroxy-1-butylenyl)-5-(2,3,4-trihydroxybutyl)-pyrazine|tatarinine A

2-(3,4-dihydroxy-1-butylenyl)-5-(2,3,4-trihydroxybutyl)-pyrazine|tatarinine A

C12H18N2O5 (270.1216)


   

2-Deoxy-D-araabino-hexonic acid,9CI,8CI-Phenylhydrazide

2-Deoxy-D-araabino-hexonic acid,9CI,8CI-Phenylhydrazide

C12H18N2O5 (270.1216)


   

8-2,6-Dimethylaniline-guanine

8-2,6-Dimethylaniline-guanine

C13H14N6O1 (270.1229)


   

8-2,4-Dimethylaniline-guanine

8-2,4-Dimethylaniline-guanine

C13H14N6O1 (270.1229)


   

O6-Dimethylaniline-guanine

O6-Dimethylaniline-guanine

C13H14N6O1 (270.1229)


   

O4-Ethyl-thymidine

O4-Ethyl-thymidine

C12H18N2O5 (270.1216)


   

O2-Ethyl-thymidine

O2-Ethyl-thymidine

C12H18N2O5 (270.1216)


   

3-Ethyl-thymidine

3-Ethyl-thymidine

C12H18N2O5 (270.1216)


   

bis(o-trimethylsilyl)thymine

bis(o-trimethylsilyl)thymine

C11H22N2O2Si2 (270.122)


   

6-((4-(Aminomethyl)benzyl)oxy)-7H-purin-2-amine

6-((4-(Aminomethyl)benzyl)oxy)-7H-purin-2-amine

C13H14N6O (270.1229)


   

5-(TERT-BUTOXYCARBONYLAMINO-METHYL)-ISOXAZOLE-3-CARBOXYLIC ACID ETHYL ESTER

5-(TERT-BUTOXYCARBONYLAMINO-METHYL)-ISOXAZOLE-3-CARBOXYLIC ACID ETHYL ESTER

C12H18N2O5 (270.1216)


   

epervudine

epervudine

C12H18N2O5 (270.1216)


C254 - Anti-Infective Agent > C281 - Antiviral Agent

   

7-(Tert-Butoxycarbonyl)-1-Oxa-2,7-Diazaspiro[4.4]Non-2-Ene-3-Carboxylic Acid

7-(Tert-Butoxycarbonyl)-1-Oxa-2,7-Diazaspiro[4.4]Non-2-Ene-3-Carboxylic Acid

C12H18N2O5 (270.1216)


   

Voxtalisib

Voxtalisib

C13H14N6O (270.1229)


C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C2152 - Phosphatidylinositide 3-Kinase Inhibitor C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor C274 - Antineoplastic Agent > C1742 - Angiogenesis Inhibitor C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor Voxtalisib (XL765) is a potent PI3K inhibitor, which has a similar activity toward class I PI3K (IC50s=39, 113, 9 and 43?nM for p110α, p110β, p110γ and p110δ, respectively), also inhibits DNA-PK (IC50=150?nM) and mTOR (IC50=157?nM). Voxtalisib (XL765) inhibits mTORC1 and mTORC2 with IC50s of 160 and 910 nM, respectively. Voxtalisib (XL765) is a potent PI3K inhibitor, which has a similar activity toward class I PI3K (IC50s=39, 113, 9 and 43?nM for p110α, p110β, p110γ and p110δ, respectively), also inhibits DNA-PK (IC50=150?nM) and mTOR (IC50=157?nM). Voxtalisib (XL765) inhibits mTORC1 and mTORC2 with IC50s of 160 and 910 nM, respectively.

   

(2S)-2-amino-5-[[(1S)-1-carboxy-2-(2-methylidenecyclopropyl)ethyl]amino]-5-oxopentanoic acid

(2S)-2-amino-5-[[(1S)-1-carboxy-2-(2-methylidenecyclopropyl)ethyl]amino]-5-oxopentanoic acid

C12H18N2O5 (270.1216)


   

Unii-T83F0X4ngn

Unii-T83F0X4ngn

C12H18N2O5 (270.1216)


   

Hypoglycine b

(2S,4S)-hypoglycin B

C12H18N2O5 (270.1216)


An L-glutamyl amino acid that is (2S,4S)-hypoglycin A in which the amino group has been acylated by the gamma-carboxy group of L-glutamic acid.

   

bacilysin zwitterion

bacilysin zwitterion

C12H18N2O5 (270.1216)


A peptide zwitterion obtained by transfer of a proton from the carboxy to the amino group of bacilysin; major species at pH 7.3.

   

Hypoglycin B

Hypoglycin B

C12H18N2O5 (270.1216)


A diastereoisometic mixture containing (2S,4R)- and (2S,4S)-hypoglycin B. A metabolite of hypoglycin A found in unripe ackee fruit.

   

(2S,4R)-hypoglycin B

(2S,4R)-hypoglycin B

C12H18N2O5 (270.1216)


A 5-L-glutamyl amino acid resulting from the formal condensation of the amino group of (2S,4R)-hypoglycin A with the gamma-carboxy group of L-glutamic acid.

   

(2s)-2-amino-4-{[(1s)-1-carboxy-2-[(1s)-2-methylidenecyclopropyl]ethyl]-c-hydroxycarbonimidoyl}butanoic acid

(2s)-2-amino-4-{[(1s)-1-carboxy-2-[(1s)-2-methylidenecyclopropyl]ethyl]-c-hydroxycarbonimidoyl}butanoic acid

C12H18N2O5 (270.1216)


   

4-[5-(3,4-dihydroxybut-1-en-1-yl)pyrazin-2-yl]butane-1,2,3-triol

4-[5-(3,4-dihydroxybut-1-en-1-yl)pyrazin-2-yl]butane-1,2,3-triol

C12H18N2O5 (270.1216)


   

2-[(2-amino-1-hydroxypropylidene)amino]-3-[(1r,2r,6r)-5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl]propanoic acid

2-[(2-amino-1-hydroxypropylidene)amino]-3-[(1r,2r,6r)-5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl]propanoic acid

C12H18N2O5 (270.1216)


   

2-[(2-amino-1-hydroxypropylidene)amino]-3-{5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl}propanoic acid

2-[(2-amino-1-hydroxypropylidene)amino]-3-{5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl}propanoic acid

C12H18N2O5 (270.1216)


   

(2s)-2-aminopropanoyl (2s)-2-amino-3-[(1r,6r)-5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl]propanoate

(2s)-2-aminopropanoyl (2s)-2-amino-3-[(1r,6r)-5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl]propanoate

C12H18N2O5 (270.1216)


   

(2r,3s)-4-{5-[(1e,3s)-3,4-dihydroxybut-1-en-1-yl]pyrazin-2-yl}butane-1,2,3-triol

(2r,3s)-4-{5-[(1e,3s)-3,4-dihydroxybut-1-en-1-yl]pyrazin-2-yl}butane-1,2,3-triol

C12H18N2O5 (270.1216)


   

(2s)-2-amino-4-{[(1s)-1-carboxy-2-(2-methylidenecyclopropyl)ethyl]-c-hydroxycarbonimidoyl}butanoic acid

(2s)-2-amino-4-{[(1s)-1-carboxy-2-(2-methylidenecyclopropyl)ethyl]-c-hydroxycarbonimidoyl}butanoic acid

C12H18N2O5 (270.1216)


   

(2s)-2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-3-[(1r,2s,6r)-5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl]propanoic acid

(2s)-2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-3-[(1r,2s,6r)-5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl]propanoic acid

C12H18N2O5 (270.1216)


   

2-amino-4-{[1-carboxy-2-(2-methylidenecyclopropyl)ethyl]-c-hydroxycarbonimidoyl}butanoic acid

2-amino-4-{[1-carboxy-2-(2-methylidenecyclopropyl)ethyl]-c-hydroxycarbonimidoyl}butanoic acid

C12H18N2O5 (270.1216)


   

(2s)-2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-3-[(1r,2r,6r)-5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl]propanoic acid

(2s)-2-{[(2s)-2-amino-1-hydroxypropylidene]amino}-3-[(1r,2r,6r)-5-oxo-7-oxabicyclo[4.1.0]heptan-2-yl]propanoic acid

C12H18N2O5 (270.1216)