Exact Mass: 265.1075932
Exact Mass Matches: 265.1075932
Found 131 metabolites which its exact mass value is equals to given mass value 265.1075932
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
Thiamine
Thiamine, also known as aneurin or vitamin B1, belongs to the class of organic compounds known as thiamines. Thiamines are compounds containing a thiamine moiety, which is structurally characterized by a 3-[(4-Amino-2-methyl-pyrimidin-5-yl)methyl]-4-methyl-thiazol-5-yl backbone. Thiamine exists in all living species, ranging from bacteria to plants to humans. Thiamine biosynthesis occurs in bacteria, some protozoans, plants, and fungi. Thiamine is a vitamin and an essential nutrient meaning the body cannot synthesize it, and it must be obtained from the diet. It is soluble in water and insoluble in alcohol. Thiamine decomposes if heated. Thiamine was first discovered in 1897 by Umetaro Suzuki in Japan when researching how rice bran cured patients of Beriberi. Thiamine was the first B vitamin to be isolated in 1926 and was first made in 1936. Thiamine plays a key role in intracellular glucose metabolism and it is thought that thiamine inhibits the effect of glucose and insulin on arterial smooth muscle cell proliferation. Thiamine plays an important role in helping the body convert carbohydrates and fat into energy. It is essential for normal growth and development and helps to maintain proper functioning of the heart and the nervous and digestive systems. Thiamine cannot be stored in the body; however, once absorbed, the vitamin is concentrated in muscle tissue. Thiamine has antioxidant, erythropoietic, cognition-and mood-modulatory, antiatherosclerotic, putative ergogenic, and detoxification activities. Natural derivatives of thiamine, such as thiamine monophosphate (ThMP), thiamine diphosphate (ThDP), also sometimes called thiamine pyrophosphate (TPP), thiamine triphosphate (ThTP), and adenosine thiamine triphosphate (AThTP), act as coenzymes in addition to performing unique biological functions. Thiamine deficiency can lead to beriberi, Wernicke–Korsakoff syndrome, optic neuropathy, Leighs disease, African seasonal ataxia (or Nigerian seasonal ataxia), and central pontine myelinolysis. In Western countries, thiamine deficiency is seen mainly in chronic alcoholism. Thiamine supplements or thiamine therapy can be used for the treatment of a number of disorders including thiamine and niacin deficiency states, Korsakovs alcoholic psychosis, Wernicke-Korsakov syndrome, delirium, and peripheral neuritis. In humans, thiamine is involved in the metabolic disorder called 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency. Outside of the human body, Thiamine is found in high quantities in whole grains, legumes, pork, fruits, and yeast and fish. Grain processing removes much of the thiamine content in grains, so in many countries cereals and flours are enriched with thiamine. Thiamine is an essential vitamin. It is found in many foods, some of which are atlantic croaker, wonton wrapper, cereals and cereal products, and turmeric. A - Alimentary tract and metabolism > A11 - Vitamins > A11D - Vitamin b1, plain and in combination with vitamin b6 and b12 > A11DA - Vitamin b1, plain Acquisition and generation of the data is financially supported in part by CREST/JST. D018977 - Micronutrients > D014815 - Vitamins KEIO_ID T056; [MS2] KO009294 KEIO_ID T056
N6-Methyl-2-deoxyadenosine
KEIO_ID M110; [MS2] KO009042 KEIO_ID M110 N-6-Methyl-2-deoxyadenosine is an adenine 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].
Anonaine
Alkaloid from Annona muricata (soursop) and Nelumbo nucifera (East India lotus). Anonaine is found in many foods, some of which are sugar apple, sacred lotus, fruits, and custard apple. Anonaine is found in cherimoya. Anonaine is an alkaloid from Annona muricata (soursop) and Nelumbo nucifera (East India lotus
2,3-Di(4-methoxyphenyl)acrylonitrile
Agaritinal
Agaritinal is found in mushrooms. Agaritinal is isolated from Agaricus campestris (field mushroom). Isolated from Agaricus campestris (field mushroom). Agaritinal is found in mushrooms.
Eduline
Eduline is found in pomes. Eduline is an alkaloid from seeds of Casimiroa edulis (Mexican apple). Alkaloid from seeds of Casimiroa edulis (Mexican apple). Eduline is found in pomes.
Eduleine
Eduleine is found in pomes. Eduleine is an alkaloid from Casimiroa edulis (Mexican apple). Alkaloid from Casimiroa edulis (Mexican apple). Eduleine is found in pomes.
D-1-[(3-Carboxypropyl)amino]-1-deoxyfructose
D-1-[(3-Carboxypropyl)amino]-1-deoxyfructose is found in fruits. D-1-[(3-Carboxypropyl)amino]-1-deoxyfructose is isolated from stored apricots and peaches. Isolated from stored apricots and peaches. D-1-[(3-Carboxypropyl)amino]-1-deoxyfructose is found in fruits.
(3S,4R,5R)-1,3,4,5,6-Pentahydroxy-1-morpholin-4-ylhexan-2-one
3-(6-Aminopurin-9-yl)-5-(hydroxymethyl)cyclopentane-1,2-diol
N-(2-Chlorophenyl)-N-(2-cyanoethyl)-N-isopropylurea
C13H16ClN3O (265.09818359999997)
1-Deoxy-1-(N-gamma-amino-buttersaeure)-D-fructose|1-Deoxy-1--D-fructose
(Z)-2-phenylethenylamide-2,3-Epoxy-6,8-nonadiynoic acid|2,3-Epoxy-6,8-nonadiynoic acid cinnamylamide
anonaine
An aporphine alkaloid that exhibits anti-cancer, trypanocidal and antiplasmodial activites.
THD
Origin: Microbe; Formula(Parent): C12H17N4OS; Bottle Name:Thiamine hydrochloride; PRIME Parent Name:Thiamine; PRIME in-house No.:0350, Pyrimidines
Thiamine
A - Alimentary tract and metabolism > A11 - Vitamins > A11D - Vitamin b1, plain and in combination with vitamin b6 and b12 > A11DA - Vitamin b1, plain D018977 - Micronutrients > D014815 - Vitamins
Aristeromycin
Aristeromycin, an adenosine analog, is an antibiotic and a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor[1][2].
tert-butyl 3-[(methanesulfonyloxy)methyl]azetidine-1-carboxylate
C10H19NO5S (265.09838840000003)
5-(2-ETHYLHEXYL)-4H-THIENO[3,4-C]PYRROLE-4,6(5H)-DIONE
1-propoxyisoquinoline-3-carboximidamide,hydrochloride
C13H16ClN3O (265.09818359999997)
3-hydroxy-1-methyl-2-(4-methylphenyl)quinolin-4-one
1,3-dimethyl-5-[2-(3-methyl-1,3-oxazolidin-2-ylidene)ethylidene]-1,3-diazinane-2,4,6-trione
4-HYDROXY-3-NITROPHENYLBORONIC ACID, PINACOL ESTER
Dipraglurant
C78272 - Agent Affecting Nervous System Dipraglurant (ADX48621) is a potent, selective, orally active and brain penetrant mGluR5 negative allosteric modulator (NAM), with an IC50 of 21 nM. Dipraglurant can reduce Levodopa-induced dyskinesia (LID) in vivo[1][2]. Dipraglurant is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
1-(TERT-BUTOXYCARBONYL)-4,4-DIFLUOROPIPERIDINE-2-CARBOXYLIC ACID
(R)-3-Methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester
C10H19NO5S (265.09838840000003)
6-(Dimethoxymethyl)-2-(trimethylsilyl)furo[3,2-b]pyridine
2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
N-but-3-enyl-4-methyl-N-prop-2-enylbenzenesulfonamide
Lobucavir
D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D044966 - Anti-Retroviral Agents D004791 - Enzyme Inhibitors > D019384 - Nucleic Acid Synthesis Inhibitors C254 - Anti-Infective Agent > C281 - Antiviral Agent
5-(Piperidin-3-yl)-3-(pyridin-3-yl)-1,2,4-oxadiazole hydrochloride
C13H16ClN3O (265.09818359999997)
4-(5-phenyl-1,3,4-oxadiazol-2-yl)piperidine hydrochloride
C13H16ClN3O (265.09818359999997)
(R)-5-chloro-2-(5-Methyl-1,4-diazepan-1-yl)benzo[d]oxazole
C13H16ClN3O (265.09818359999997)
3-phenyl-5-piperidin-4-yl-1,2,4-oxadiazole,hydrochloride
C13H16ClN3O (265.09818359999997)
(R)-1-Boc-3-methanesulfonyloxypyrrolidine
C10H19NO5S (265.09838840000003)
5-PHENYL-3-(PIPERIDIN-3-YL)-1,2,4-OXADIAZOLE HYDROCHLORIDE
C13H16ClN3O (265.09818359999997)
4-[(3-ETHOXY-3-OXOPROPYL)CARBAMOYL]BENZENEBORONIC ACID
5-nitro-2-piperazin-1-yl-benzoic acid methyl ester
1-(4-chlorophenyl)- 1,3,8-triazaspiro[4.5]decan-4-one
C13H16ClN3O (265.09818359999997)
1-[(3-amino-2-chloroquinolin-4-yl)amino]-2-methylpropan-2-ol
C13H16ClN3O (265.09818359999997)
5-Chloro-2-(hexahydro-5-methyl-1H-1,4-diazepin-1-yl)benzoxazole
C13H16ClN3O (265.09818359999997)
2-(Pyrimidin-2-ylaminomethylene)-malonic acid diethyl ester
NSC59984
NSC59984 induces mutant p53 protein degradation via MDM2 and the ubiquitin-proteasome pathway[1]. NSC59984 acts by targeting GOF-mutant p53 and stimulates p73 to restore the p53 pathway signaling[2].
(S)-1-Boc-3-methanesulfonyloxy-pyrrolidine
C10H19NO5S (265.09838840000003)
Galidesivir
COVID info from DrugBank, clinicaltrial, clinicaltrials, clinical trial, clinical trials D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C471 - Enzyme Inhibitor > C29575 - DNA Polymerase Inhibitor C254 - Anti-Infective Agent > C281 - Antiviral Agent Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS
N-(2-ACRYLOYLOXYETHYL)-N,N-DIMETHYL-N-(3-SULFOPROPYL)AMMONIUM BETAINE
C10H19NO5S (265.09838840000003)
Methanone,[2-(1-methylethyl)-3-benzofuranyl]-4-pyridinyl-
3-(3-ETHOXY-3-OXOPROPYLCARBAMOYL)PHENYLBORONIC ACID
1-[4-(5-Fluoro-2-hydroxybenzoyl)-1-piperidinyl]-ethanone
3-Fluoro-4-Hydroxybenzaldehyde O-(Cyclohexylcarbonyl)oxime
(3S,4R,5R)-1,3,4,5,6-Pentahydroxy-1-morpholin-4-ylhexan-2-one
2-amino-9-[2,3-bis(hydroxymethyl)cyclobutyl]-3H-purin-6-one
6-[(4-Methylphenyl)sulfonyl]-6-azabicyclo[3.2.1]octane
tert-butyl N-[(E)-(3-nitrophenyl)methylideneamino]carbamate
6-Methoxy-2-pyridin-4-ylmethylene-3,4-dihydro-2H-naphthalen-1-one
2-[3-[(6-Amino-2-methyl-4-pyrimidinyl)methyl]-4-methyl-5-thiazol-3-iumyl]ethanol
4H-Pyrido[1,2-a]pyrimidine-3-carboxylic acid, 6,7,8,9-tetrahydro-9-(hydroxyimino)-6-methyl-4-oxo-, ethyl ester
thiamine(1+)
A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.
N1-Methyl-2'-deoxyadenosine
N1-Methyl-2'-deoxyadenosine, DNA adduct 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].