Exact Mass: 305.9753572

Exact Mass Matches: 305.9753572

Found 31 metabolites which its exact mass value is equals to given mass value 305.9753572, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

2-Anthraquinonesulfonyl chloride

2-Anthracenesulfonylchloride, 9,10-dihydro-9,10-dioxo-

C14H7ClO4S (305.9753572)


   
   

Broxuridine

5-Bromo-2-deoxyuridine

C9H11BrN2O5 (305.9851296)


C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C274 - Antineoplastic Agent > C798 - Radiosensitizing Agent D009676 - Noxae > D000963 - Antimetabolites D011838 - Radiation-Sensitizing Agents D000970 - Antineoplastic Agents relative retention time with respect to 9-anthracene Carboxylic Acid is 0.233 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.226 5-BrdU (BrdU) is a nucleoside analog that competes with thymidine for incorporation into DNA. 5-BrdU is commonly used in the detection of proliferating cells.

   

propan-2-yl 2-hydroxy-5-iodobenzoate

propan-2-yl 2-hydroxy-5-iodobenzoate

C10H11IO3 (305.9752926)


   

propyl 4-hydroxy-3-iodobenzoate

propyl 4-hydroxy-3-iodobenzoate

C10H11IO3 (305.9752926)


   

tert-butyl N-(4-bromo-5-formyl-1,3-thiazol-2-yl)carbamate

tert-butyl N-(4-bromo-5-formyl-1,3-thiazol-2-yl)carbamate

C9H11BrN2O3S (305.9673716)


   
   

(5-BROMO-1H-INDOL-2-YL)METHANOL

(5-BROMO-1H-INDOL-2-YL)METHANOL

C10H12BrClN2O2 (305.9770622)


   

3-IODO-4-ISOPROPOXYBENZOIC ACID

3-IODO-4-ISOPROPOXYBENZOIC ACID

C10H11IO3 (305.9752926)


   

4-((5-Bromopyridin-3-yl)sulfonyl)morpholine

4-((5-Bromopyridin-3-yl)sulfonyl)morpholine

C9H11BrN2O3S (305.9673716)


   

3-BROMOBENZALDOXIME

3-BROMOBENZALDOXIME

C10H11IO3 (305.9752926)


   

(4-HYDROXY-PHENYL)-CARBAMICACIDPROP-2-YNYLESTER

(4-HYDROXY-PHENYL)-CARBAMICACIDPROP-2-YNYLESTER

C10H11IO3 (305.9752926)


   

1-Butyl-3-Methylimidazolium Tetrachloroaluminate

1-Butyl-3-Methylimidazolium Tetrachloroaluminate

C8H15AlCl4N2 (305.98047)


   

N-SUCCINIMIDYL 3-(BROMOACETAMIDO)PROPIONATE

N-SUCCINIMIDYL 3-(BROMOACETAMIDO)PROPIONATE

C9H11BrN2O5 (305.9851296)


   

tert-Butyl (2-bromo-6-chloropyridin-3-yl)carbamate

tert-Butyl (2-bromo-6-chloropyridin-3-yl)carbamate

C10H12BrClN2O2 (305.9770622)


   

Methyl 5-iodo-2-methoxy-4-methylbenzoate

Methyl 5-iodo-2-methoxy-4-methylbenzoate

C10H11IO3 (305.9752926)


   

N-(5-bromo-2-methoxypyridin-3-yl)cyclopropanesulfonamide

N-(5-bromo-2-methoxypyridin-3-yl)cyclopropanesulfonamide

C9H11BrN2O3S (305.9673716)


   

Methyl 2-ethoxy-5-iodobenzoate

Methyl 2-ethoxy-5-iodobenzoate

C10H11IO3 (305.9752926)


   

Propyl 2-hydroxy-5-iodobenzoate

Propyl 2-hydroxy-5-iodobenzoate

C10H11IO3 (305.9752926)


   

Methyl 5-iodo-4-methoxy-2-methylbenzoate

Methyl 5-iodo-4-methoxy-2-methylbenzoate

C10H11IO3 (305.9752926)


   

BENZOIC ACID, 3-IODO-4-METHOXY-, ETHYL ESTER

BENZOIC ACID, 3-IODO-4-METHOXY-, ETHYL ESTER

C10H11IO3 (305.9752926)


   

3-(5,6-dichloro-1-benzofuran-2-yl)benzoic acid

3-(5,6-dichloro-1-benzofuran-2-yl)benzoic acid

C15H8Cl2O3 (305.98504779999996)


   

Cyclohexadienyliumiron(0) tricarbonyl tetrafluoroborate

Cyclohexadienyliumiron(0) tricarbonyl tetrafluoroborate

C9H7BF4FeO3 (305.97737399999994)


   

methyl 2-(trimethylstannyl)thiophene-3-carboxylate

methyl 2-(trimethylstannyl)thiophene-3-carboxylate

C9H14O2SSn (305.9736454)


   

TERT-BUTYL (5-BROMO-2-CHLOROPYRIDIN-3-YL)CARBAMATE

TERT-BUTYL (5-BROMO-2-CHLOROPYRIDIN-3-YL)CARBAMATE

C10H12BrClN2O2 (305.9770622)


   

di-(Thiobenzoyl) disulfide

di-(Thiobenzoyl) disulfide

C14H10S4 (305.966534)


   

3-(2,4-dichlorophenyl)-7-hydroxy-4H-chromen-4-one

3-(2,4-dichlorophenyl)-7-hydroxy-4H-chromen-4-one

C15H8Cl2O3 (305.98504779999996)


   

Uridine, 5-bromo-2-deoxy-

Uridine, 5-bromo-2-deoxy-

C9H11BrN2O5 (305.9851296)


   
   

2′-Bromo-2′-deoxyuridine

2′-Bromo-2′-deoxyuridine

C9H11BrN2O5 (305.9851296)


2′-Bromo-2′-deoxyuridine is a purine nucleoside analog. 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].