Exact Mass: 269.08907660000006

Exact Mass Matches: 269.08907660000006

Found 79 metabolites which its exact mass value is equals to given mass value 269.08907660000006, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

5-Deoxy-5-fluoroadenosine

5-Fluoro-5-deoxy-adenosine

C10H12FN5O3 (269.09241340000005)


   

5-(2-Propoxyphenyl)-7H-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

5-(2-Propoxyphenyl)-7H-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

C13H11N5O2 (269.0912706)


   

7-Aminodesmethylflunitrazepam

7-amino-5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2-ol

C15H12FN3O (269.0964354)


   

Lagociclovir

2-amino-9-[4-fluoro-5-(hydroxymethyl)oxolan-2-yl]-6,9-dihydro-1H-purin-6-one

C10H12FN5O3 (269.09241340000005)


   

BE-39907B

BE-39907B

C14H11N3O3 (269.08003759999997)


   

4-Nitrobenzo-12-crown-4

4-Nitrobenzo-12-crown-4

C12H15NO6 (269.089933)


   

1-(4-fluorobenzyl)-1H-indole-3-carboxylic acid

1-(4-fluorobenzyl)-1H-indole-3-carboxylic acid

C16H12FNO2 (269.0852024)


   

C9H12ClN7O

C9H12ClN7O (269.0791812)


   

12-Deoxyascididemin

12-Deoxyascididemin

C18H11N3 (269.0952926)


   

Dichotomide IX

Dichotomide IX

C14H11N3O3 (269.08003759999997)


A natural product found in Stellaria dichotoma var. lanceolata.

   

acortatarin B

acortatarin B

C12H15NO6 (269.089933)


   

Dichotomide VI

Dichotomide VI

C14H11N3O3 (269.08003759999997)


A beta-carboline alkaloid that is 9H-beta-carboline substituted by acetyl group at position 1, a hydroxy group at position 8 and an aminocarbonyl at position 3. It has been isolated from Stellaria dichotoma var. lanceolata.

   

6-(CHLOROMETHYL)-4-(3-METHOXYPROPYL)-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE

6-(CHLOROMETHYL)-4-(3-METHOXYPROPYL)-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE

C13H16ClNO3 (269.0818656)


   

2-[(3,4,5-trimethoxybenzoyl)amino]acetic acid

2-[(3,4,5-trimethoxybenzoyl)amino]acetic acid

C12H15NO6 (269.089933)


   

3-(1H-BENZOIMIDAZOL-2-YL)-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHEN-2-YLAMINE

3-(1H-BENZOIMIDAZOL-2-YL)-4,5,6,7-TETRAHYDRO-BENZO[B]THIOPHEN-2-YLAMINE

C15H15N3S (269.098663)


   

2-Chloro-6-methoxypyridine-4-boronic acid pinacol ester

2-Chloro-6-methoxypyridine-4-boronic acid pinacol ester

C12H17BClNO3 (269.0989952)


   

(4-cyano-3-fluorophenyl) 4-ethylbenzoate

(4-cyano-3-fluorophenyl) 4-ethylbenzoate

C16H12FNO2 (269.0852024)


   

tert-Butyl 4-chloro-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate

tert-Butyl 4-chloro-5,6-dihydropyrido[3,4-d]pyrimidine-7(8H)-carboxylate

C12H16ClN3O2 (269.09309859999996)


   

6-benzamido-2-chloro-hexanoic acid

6-benzamido-2-chloro-hexanoic acid

C13H16ClNO3 (269.0818656)


   

2-(CHLOROACETYL)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE

2-(CHLOROACETYL)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE

C13H16ClNO3 (269.0818656)


   

1-(1H-Benzo[d]imidazol-2-yl)-3-methyl-4-oxo-1,4-dihydropyridine-2-carboxylic acid

1-(1H-Benzo[d]imidazol-2-yl)-3-methyl-4-oxo-1,4-dihydropyridine-2-carboxylic acid

C14H11N3O3 (269.08003759999997)


   

2′-Deoxy-2′-fluoroadenosine

2′-Deoxy-2′-fluoroadenosine

C10H12FN5O3 (269.09241340000005)


2′-Deoxy-2′-fluoroadenosine can be used for the?synthesis?of 2′-Deoxy-2′-fluoro-modified oligonucleotides hybridized with RNA. 2′-Deoxy-2′-fluoroadenosine can be cleaved efficiently by E. coli purine nucleoside phosphorylase (PNP) to the toxic agent 2-fluoroadenine (FAde). 2′-Deoxy-2′-fluoroadenosine shows excellent in vivo activity against tumors expressing E. coli PNP[1].

   

H-D-Arg(NO2)-Ome.HCl

H-D-Arg(NO2)-Ome.HCl

C7H16ClN5O4 (269.08907660000006)


   

2-Deoxy-2-fluoroadenosine

Adenosine,2-deoxy-2-fluoro-

C10H12FN5O3 (269.09241340000005)


   

5-Chloro-6-methoxypyridine-3-boronic acid pinacol ester

5-Chloro-6-methoxypyridine-3-boronic acid pinacol ester

C12H17BClNO3 (269.0989952)


   

5-Chloro-2-methoxypyridine-3-boronic acid pinacol ester

5-Chloro-2-methoxypyridine-3-boronic acid pinacol ester

C12H17BClNO3 (269.0989952)


   

ETHYL 4-CHLORO-2-(PIPERIDIN-1-YL)PYRIMIDINE-5-CARBOXYLATE

ETHYL 4-CHLORO-2-(PIPERIDIN-1-YL)PYRIMIDINE-5-CARBOXYLATE

C12H16ClN3O2 (269.09309859999996)


   

(4-Piperidin-1-ylsulfonylphenyl)boronic acid

(4-Piperidin-1-ylsulfonylphenyl)boronic acid

C11H16BNO4S (269.0893046)


   

3-(Piperidin-1-ylsulfonyl)phenylboronic acid

3-(Piperidin-1-ylsulfonyl)phenylboronic acid

C11H16BNO4S (269.0893046)


   

2-methyl-5-(pyrrolidin-1-ylsulfonyl)phenylboronic acid

2-methyl-5-(pyrrolidin-1-ylsulfonyl)phenylboronic acid

C11H16BNO4S (269.0893046)


   

METHYL 4-ISOPROPOXY-5-METHOXY-2-NITROBENZOATE

METHYL 4-ISOPROPOXY-5-METHOXY-2-NITROBENZOATE

C12H15NO6 (269.089933)


   

2-(Piperidin-1-ylsulfonyl)phenylboronic acid

2-(Piperidin-1-ylsulfonyl)phenylboronic acid

C11H16BNO4S (269.0893046)


   

Benaxibine

Benaxibine

C12H15NO6 (269.089933)


   

tert-butyl 3-chloro-7,8-dihydro-5H-pyrido[4,3-c]pyridazine-6-carboxylate

tert-butyl 3-chloro-7,8-dihydro-5H-pyrido[4,3-c]pyridazine-6-carboxylate

C12H16ClN3O2 (269.09309859999996)


   

3-Chloro-2-methoxypyridine-4-boronic acid pinacol ester

3-Chloro-2-methoxypyridine-4-boronic acid pinacol ester

C12H17BClNO3 (269.0989952)


   

METHYL 4-(4-OXO-4,7-DIHYDRO-3H-PYRROLO[2,3-D]PYRIMIDIN-6-YL)BENZOATE

METHYL 4-(4-OXO-4,7-DIHYDRO-3H-PYRROLO[2,3-D]PYRIMIDIN-6-YL)BENZOATE

C14H11N3O3 (269.08003759999997)


   

6-Chloro-2-methoxypyridine-3-boronic acid pinacol ester

6-Chloro-2-methoxypyridine-3-boronic acid pinacol ester

C12H17BClNO3 (269.0989952)


   

tert-Butyl 4-chloro-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate

tert-Butyl 4-chloro-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate

C12H16ClN3O2 (269.09309859999996)


   

Ethyl 5-chloro-6-piperazin-1-ylpyridine-3-carboxylate

Ethyl 5-chloro-6-piperazin-1-ylpyridine-3-carboxylate

C12H16ClN3O2 (269.09309859999996)


   

Adenosine,5-deoxy-2-fluoro-

Adenosine,5-deoxy-2-fluoro-

C10H12FN5O3 (269.09241340000005)


   

(2R,3R,5S)-2-(6-amino-2-fluoropurin-9-yl)-5-(hydroxymethyl)oxolan-3-ol

(2R,3R,5S)-2-(6-amino-2-fluoropurin-9-yl)-5-(hydroxymethyl)oxolan-3-ol

C10H12FN5O3 (269.09241340000005)


   

DIETHYL-3,4-ETHYLENEDIOXYPYRROLE-2,5-DI&

DIETHYL-3,4-ETHYLENEDIOXYPYRROLE-2,5-DI&

C12H15NO6 (269.089933)


   

Methyl 3-(2-amino-4-pyrimidinyl)-1H-pyrrolo[2,3-b]pyridine-4-carb oxylate

Methyl 3-(2-amino-4-pyrimidinyl)-1H-pyrrolo[2,3-b]pyridine-4-carb oxylate

C13H11N5O2 (269.0912706)


   

tert-butyl 2-chloro-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate

tert-butyl 2-chloro-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate

C12H16ClN3O2 (269.09309859999996)


   

METHYL 5-(ACETYLOXY)-4-(2-METHOXY-2-OXOETHYL)-2-METHYL-1H-PYRROLE-3-CARBOXYLATE

METHYL 5-(ACETYLOXY)-4-(2-METHOXY-2-OXOETHYL)-2-METHYL-1H-PYRROLE-3-CARBOXYLATE

C12H15NO6 (269.089933)


   

Lagociclovir

Lagociclovir

C10H12FN5O3 (269.09241340000005)


   

L-NAME (hydrochloride)

Methyl N5-(imino(nitroamino)methyl)-L-ornithine monohydrochloride

C7H16ClN5O4 (269.08907660000006)


   

(2R,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)- 2,3-Butanediol

(2R,3R)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)- 2,3-Butanediol

C12H13F2N3O2 (269.0975782)


   

2-Aminopurine-9-beta-D-(2-deoxy-2-fluoro)arabino-riboside

2-Aminopurine-9-beta-D-(2-deoxy-2-fluoro)arabino-riboside

C10H12FN5O3 (269.09241340000005)


   

Indolo[3,2,1-de]acridin-8-one

Indolo[3,2,1-de]acridin-8-one

C19H11NO (269.0840596)


   

(4-Methyl-3-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid

(4-Methyl-3-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid

C11H16BNO4S (269.0893046)


   

2-chloro-3-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

2-chloro-3-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

C12H17BClNO3 (269.0989952)


   

ethyl 1-(6-chloropyridazin-3-yl)piperidine-4-carboxylate

ethyl 1-(6-chloropyridazin-3-yl)piperidine-4-carboxylate

C12H16ClN3O2 (269.09309859999996)


   

METHYL 4-AMINO-5-BROMO-2-METHOXYBENZENECARBOXYLATE

METHYL 4-AMINO-5-BROMO-2-METHOXYBENZENECARBOXYLATE

C13H16ClNO3 (269.0818656)


   

(2-Methyl-4-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid

(2-Methyl-4-(pyrrolidin-1-ylsulfonyl)phenyl)boronic acid

C11H16BNO4S (269.0893046)


   

9-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine

9-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine

C10H12FN5O3 (269.09241340000005)


   

ethyl 2-[tert-butoxycarbonylimino]-3,3,3-trifluoro-propionate

ethyl 2-[tert-butoxycarbonylimino]-3,3,3-trifluoro-propionate

C10H14F3NO4 (269.087488)


   

2-AMINO-6-BENZYL-4,5,6,7-TETRAHYDRO-THIENO[2,3-C]PYRIDINE-3-CARBONITRILE

2-AMINO-6-BENZYL-4,5,6,7-TETRAHYDRO-THIENO[2,3-C]PYRIDINE-3-CARBONITRILE

C15H15N3S (269.098663)


   

Pildralazine

Pildralazine

C8H17Cl2N5O (269.0810092)


   

1-(5-CHLORO-2,4-DIMETHOXYPHENYL)-4-PIPERIDONE

1-(5-CHLORO-2,4-DIMETHOXYPHENYL)-4-PIPERIDONE

C13H16ClNO3 (269.0818656)


   

Pardoprunox hydrochloride

Pardoprunox hydrochloride

C12H16ClN3O2 (269.09309859999996)


C78272 - Agent Affecting Nervous System > C66884 - Dopamine Agonist Pardoprunox (SLV-308) hydrochloride is a partial dopamine D2 and D3 receptor partial agonist and a serotonin 5-HT1A receptor agonist, with pEC50s of 8, 9.2, and 6.3, respectively[1].

   

cyclo-acetoacetyl-L-tryptophan

cyclo-acetoacetyl-L-tryptophan

C15H13N2O3- (269.0926128)


   

5-(2-Propoxyphenyl)-7H-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

5-(2-Propoxyphenyl)-7H-[1,2,3]triazolo[4,5-d]pyrimidin-7-one

C13H11N5O2 (269.0912706)


   

(2R)-4,4-dihydroxy-5-nitro-2-(phenylmethyl)pentanoic acid

(2R)-4,4-dihydroxy-5-nitro-2-(phenylmethyl)pentanoic acid

C12H15NO6 (269.089933)


   

2-Amino-9-(2,3-dideoxy-3-fluoropentofuranosyl)-3,9-dihydro-6H-purin-6-one

2-Amino-9-(2,3-dideoxy-3-fluoropentofuranosyl)-3,9-dihydro-6H-purin-6-one

C10H12FN5O3 (269.09241340000005)


   

1-Methyl-5-(1-naphthalenyloxy)-4-nitroimidazole

1-Methyl-5-(1-naphthalenyloxy)-4-nitroimidazole

C14H11N3O3 (269.08003759999997)


   

1-(2,3-Dihydroindol-1-yl)-2-(phenylthio)ethanone

1-(2,3-Dihydroindol-1-yl)-2-(phenylthio)ethanone

C16H15NOS (269.08743)


   

5-(2-furanyl)-N-(3-pyridinylmethyl)-3-isoxazolecarboxamide

5-(2-furanyl)-N-(3-pyridinylmethyl)-3-isoxazolecarboxamide

C14H11N3O3 (269.08003759999997)


   

3-(2-nitrophenyl)-N-3-pyridinylacrylamide

3-(2-nitrophenyl)-N-3-pyridinylacrylamide

C14H11N3O3 (269.08003759999997)


   

cAATrp

cAATrp

C15H13N2O3- (269.0926128)


   

2,3,4-Trimethoxyhippuric acid

2,3,4-Trimethoxyhippuric acid

C12H15NO6 (269.089933)


   

2-[(prop-2-enylthio)-(4,5,6,7-tetrahydro-1H-indol-2-yl)methylidene]propanedinitrile

2-[(prop-2-enylthio)-(4,5,6,7-tetrahydro-1H-indol-2-yl)methylidene]propanedinitrile

C15H15N3S (269.098663)


   

5-Isocyano-2-[[2-(methylaminomethyl)phenyl]thio]aniline

5-Isocyano-2-[[2-(methylaminomethyl)phenyl]thio]aniline

C15H15N3S (269.098663)


   

1-[(Z)-[(4-amino-1,2,5-oxadiazol-3-yl)hydrazinylidene]methyl]naphthalen-2-ol

1-[(Z)-[(4-amino-1,2,5-oxadiazol-3-yl)hydrazinylidene]methyl]naphthalen-2-ol

C13H11N5O2 (269.0912706)


   

5-Fluoro-5-deoxyadenosine

5-Fluoro-5-deoxyadenosine

C10H12FN5O3 (269.09241340000005)


   

5'-Deoxy-5'-fluoroadenosine

5'-Deoxy-5'-fluoroadenosine

C10H12FN5O3 (269.09241340000005)


   

Deoxy-fluoroadenosine

Deoxy-fluoroadenosine

C10H12FN5O3 (269.09241340000005)


   

N-Lactoyl DOPA

N-Lactoyl DOPA

C12H15NO6 (269.089933)


   

3'-Deoxy-3'-fluoroadenosine

3'-Deoxy-3'-fluoroadenosine

C10H12FN5O3 (269.09241340000005)


3'-Deoxy-3'-fluoroadenosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].