Exact Mass: 305.97737399999994
Exact Mass Matches: 305.97737399999994
Found 173 metabolites which its exact mass value is equals to given mass value 305.97737399999994
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Uridine 2',3'-cyclic phosphate
C9H11N2O8P (306.02530160000003)
Uridine 2,3-cyclic phosphate is a cyclic nucleotide. A cyclic nucleotide is any nucleotide in which the phosphate group is bonded to two of the sugars hydroxyl groups, forming a cyclical or ring structure. Cyclic phosphates are commonly found at the 3 end of mRNAs and other small RNAs. Uridine 2,3-cyclic phosphate is a substrate for the enzyme 2,3-cyclic nucleotide-3-phosphodiesterase (CNPase, EC 3.1.4.37) which hydrolyses it to Uridine 2-phosphate. CNPase is a unique RNase in that it only cleaves nucleoside 2,3-cyclic phosphates and not the RNA internucleotide linkage, like other RNases such as RNase A and RNase T1. [HMDB] Uridine 2,3-cyclic phosphate is a cyclic nucleotide. A cyclic nucleotide is any nucleotide in which the phosphate group is bonded to two of the sugars hydroxyl groups, forming a cyclical or ring structure. Cyclic phosphates are commonly found at the 3 end of mRNAs and other small RNAs. Uridine 2,3-cyclic phosphate is a substrate for the enzyme 2,3-cyclic nucleotide-3-phosphodiesterase (CNPase, EC 3.1.4.37) which hydrolyses it to Uridine 2-phosphate. CNPase is a unique RNase in that it only cleaves nucleoside 2,3-cyclic phosphates and not the RNA internucleotide linkage, like other RNases such as RNase A and RNase T1.
2,2-Dichloro-N-[2-hydroxy-1-(hydroxymethyl)-2-(4-nitrosophenyl)ethyl]acetamide
C11H12Cl2N2O4 (306.01740920000003)
(-)-Mintlactone
(-)-mintlactone is a member of the class of compounds known as benzenesulfonyl compounds. Benzenesulfonyl compounds are aromatic compounds containing a benzenesulfonyl group, which consists of a monocyclic benzene moiety that carries a sulfonyl group (-)-mintlactone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). (-)-mintlactone can be found in peppermint, which makes (-)-mintlactone a potential biomarker for the consumption of this food product.
uracil 5-beta-D-ribofuranosyl-2,3-cyclic monophosphate
C9H11N2O8P (306.02530160000003)
ascidiathiazone B
C12H6N2O6S (305.99465760000004)
An organic heterotricyclic compound, that is 5,10-dioxo-5,10-dihydro-1H-[1,4]thiazino[3,2-g]quinoline 4,4-dioxide substituted at position 7 by a carboxy group. It is an anti-inflmmatory alkaloid obtained from Aplidium.
3,5-cUMP|3,5-cyclic UMP|CUMP|cyclic uridine 3,5-monophosphate|Cyclic-3,5-UMP|O3,O5-hydroxyphosphoryl-uridine|uridine 3,5-cyclic monophosphate
C9H11N2O8P (306.02530160000003)
Broxuridine
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.
4-(4-CHLORO-3-NITRO-BENZENESULFONYL)-MORPHOLINE
C10H11ClN2O5S (306.00771860000003)
4,4,5,5-tetramethyl-2-(2,4,6-trichlorophenyl)-1,3,2-dioxaborolane
C12H14BCl3O2 (306.01523840000004)
3,5-Bis(trifluoromethyl)phenyldimethylchlorosilane
C10H9ClF6Si (306.00662159999996)
2-(3,5-DICHLORO-2-HYDROXYPHENYL)-4-QUINAZOLINE
C14H8Cl2N2O2 (305.99628079999997)
4-[3-(2,4-Dichlorophenyl)isoxazol-5-yl]pyrimidin-2-amine
C13H8Cl2N4O (306.00751379999997)
methyl 4-bromo-2-methyl-5-methylsulfonylbenzoate
C10H11BrO4S (305.95613860000003)
Rimoprogin
C254 - Anti-Infective Agent > C514 - Antifungal Agent
benzyl N-(6-bromo-3-pyridyl)carbamate
C13H11BrN2O2 (306.00038459999996)
tert-butyl N-(4-bromo-5-formyl-1,3-thiazol-2-yl)carbamate
1-bromo-4-(diethoxyphosphorylmethyl)benzene
C11H16BrO3P (306.00203760000005)
6-BROMO-1-(TETRAHYDRO-2H-PYRAN-2-YL)NAPHTHALEN-2-OL
3-(4-BROMOPHENYL)-5-(THIOPHEN-2-YL)-1,2,4-OXADIAZOLE
2-(4-CHLOROPHENYL)-4,4-BIS(METHYLTHIO)-1,3-BUTADIEN-1,1-DICARBONITRILE
Benzyl (5-bromopyridin-3-yl)carbamate
C13H11BrN2O2 (306.00038459999996)
3-iodoadamantane-1-carboxylic acid
C11H15IO2 (306.01167599999997)
Ethyl 2-(6-Nitro-2,3-dichlorobenzyl)glycine
C11H12Cl2N2O4 (306.01740920000003)
Carbonic acid ammonium zirconium salt
C3H8N2O9Zr (305.92768780000006)
Sodium 5-oxo-1-(4-sulfophenyl)-4H-pyrazole-3-carboxylate
C10H7N2NaO6S (305.99225220000005)
Glycine,N-[(2,3-dichloro-6-nitrophenyl)methyl]-, ethyl ester, hydrochloride (1:1)
C11H12Cl2N2O4 (306.01740920000003)
3,4,5-Trichlorophenylboronic acid, pinacol ester
C12H14BCl3O2 (306.01523840000004)
2-BROMO-5-(4-(TRIFLUOROMETHYL)PHENYL)THIOPHENE
C11H6BrF3S (305.93256520000006)
2-(2-chloro-6-fluorobenzyl)-4,5-dichloropyridazine-3-(2h)-one
4-(S)-1-Des(methylamine)-1-oxo-2-(R,S)-hydroxy Sertraline
1,4-Diamino-2,3-dichloro-9,10-anthraquinone
C14H8Cl2N2O2 (305.99628079999997)
(5-bromo-2-propanoylphenyl) methanesulfonate
C10H11BrO4S (305.95613860000003)
tert-Butyl (2-bromo-6-chloropyridin-3-yl)carbamate
Thiazolo[5,4-g]quinoline-7-carboxylic acid,5-ethyl-2,3,5,8-tetrahydro-8-oxo-2-thioxo-
3-(2-METHOXY BENZYLOXY)-1-IODO PROPANE
C11H15IO2 (306.01167599999997)
N-(5-bromo-2-methoxypyridin-3-yl)cyclopropanesulfonamide
ACETIC ACID ACETOXY-(4-CHLORO SULFONYL PHENYL)METHYL ESTER
Benzyl (5-bromopyridin-2-yl)carbamate
C13H11BrN2O2 (306.00038459999996)
3-(5,6-dichloro-1-benzofuran-2-yl)benzoic acid
C15H8Cl2O3 (305.98504779999996)
2-amino-3-(2-Methoxybenzoyl)-5-bromopyridine
C13H11BrN2O2 (306.00038459999996)
Cyclohexadienyliumiron(0) tricarbonyl tetrafluoroborate
C9H7BF4FeO3 (305.97737399999994)
methyl 2-(trimethylstannyl)thiophene-3-carboxylate
Phenylphosphinic acid magnesium salt
C12H12MgO4P2 (306.00613119999997)
TERT-BUTYL (5-BROMO-2-CHLOROPYRIDIN-3-YL)CARBAMATE
3-(3-Bromo-4-methoxyphenyl)benzoic acid, 2-Bromo-4-(3-carboxyphenyl)anisole, 3-Bromo-3-carboxy-4-methoxybiphenyl
4-BROMO-3-(4-FLUOROPHENYL)PROPIOPHENONE
C15H12BrFO (306.00554939999995)
5-[2-(METHYLTHIO)PYRIMIDIN-4-YL]THIOPHENE-2-SULFONYL CHLORIDE
(5-BROMO-2-HYDROXY-4-METHOXYPHENYL)(PHENYL)METHANONE
2-(3-Bromophenyl)-5-(thiophen-2-yl)-1,3,4-oxadiazole
3-(2,4-dichlorophenyl)-7-hydroxy-4H-chromen-4-one
C15H8Cl2O3 (305.98504779999996)
2-[(2-bromophenyl)methoxy]benzoic Acid
ML-097 (CID-2160985) is a pan Ras-related GTPases activator that can activate Rac1, cell division cycle 42, Ras, and Rab7[1].
5-chloro-N-(1,3-dioxo-5-isoindolyl)-2-thiophenecarboxamide
Technetium TC-99M medronate
CH6O8P2Tc (305.95379360000004)
V - Various > V09 - Diagnostic radiopharmaceuticals > V09B - Skeleton > V09BA - Technetium (99mtc) compounds D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D019275 - Radiopharmaceuticals D050071 - Bone Density Conservation Agents > D004164 - Diphosphonates
Deoxyuridine-phosphate
C9H11N2O8P-2 (306.02530160000003)
COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
N-(3-chloro-4-fluorophenyl)-5-pyridin-4-yl-1,3,4-thiadiazol-2-amine
3-chloro-4-fluoro-N-(3-pyridinyl)-1-benzothiophene-2-carboxamide
2,3-cyclic ump
C9H11N2O8P (306.02530160000003)
A 2,3-cyclic pyrimidine nucleotide in which uridine is the parent nucleoside.
dUMP(2-)
C9H11N2O8P (306.02530160000003)
A 2-deoxyribonucleoside 5-monophosphate(2-) obtained by deprotonation of the phosphate OH groups of 2-deoxyuridine 5-monophosphate (dUMP); major species at pH 7.3.
3,5-cyclic UMP
C9H11N2O8P (306.02530160000003)
A 3,5-cyclic pyrimidine nucleotide having uridine as the nucleobase.
D-ribulose 1,5-bisphosphate(4-)
Tetraanion of D-ribulose 1,5-bisphosphate arising from deprotonation of all four phosphate OH groups; major species at pH 7.3.
2′-Bromo-2′-deoxyuridine
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].
1-({2,6-dihydroxy-2-oxo-tetrahydro-2λ⁵-furo[3,4-d][1,3,2]dioxaphosphol-4-yl}methyl)-4-hydroxypyrimidin-2-one
C9H11N2O8P (306.02530160000003)
4-(3-bromopropa-1,2-dien-1-yl)-12-ethyl-3,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(8),9,11-triene
1-[(4ar,6r,7r,7as)-2,7-dihydroxy-2-oxo-tetrahydro-4h-2λ⁵-furo[3,2-d][1,3,2]dioxaphosphinin-6-yl]-4-hydroxypyrimidin-2-one
C9H11N2O8P (306.02530160000003)
2,4-dichloro-6-(5-chloro-3-nitro-1h-pyrrol-2-yl)phenol
C10H5Cl3N2O3 (305.93657500000006)