Exact Mass: 627.3288298
Exact Mass Matches: 627.3288298
Found 133 metabolites which its exact mass value is equals to given mass value 627.3288298,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Dabigatran etexilate
C34H41N7O5 (627.3169015999999)
Dabigatran etexilate is an oral prodrug that is metabolized by a serum esterase to dabigatran. It is a synthetic, competitive and reversible direct thrombin inhibitor. Inhibition of thrombin disrupts the coagulation cascade and inhibits the formation of clots. Dabigatran etexilate may be used to decrease the risk of venous thromboembolic events in patients who have undergone total hip or knee replacement surgery, or to prevent stroke and systemic embolism in patients with atrial fibrillation, in whom anticoagulation therapy is indicated. B - Blood and blood forming organs > B01 - Antithrombotic agents > B01A - Antithrombotic agents > B01AE - Direct thrombin inhibitors C78275 - Agent Affecting Blood or Body Fluid > C263 - Anticoagulant Agent > C180619 - Direct Oral Anticoagulant C78275 - Agent Affecting Blood or Body Fluid > C263 - Anticoagulant Agent > C173066 - Direct Thrombin Inhibitor D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors > D015842 - Serine Proteinase Inhibitors D006401 - Hematologic Agents > D000925 - Anticoagulants > D000991 - Antithrombins
Boc-val-pro-arg-mca
C31H45N7O7 (627.3380299999999)
Bulleyaconitine A
(Betas)-beta-(((2S)-2-(4,4-Dimethyl-3-((4-((((2-methylphenyl)amino)carbonyl)amino)phenyl)methyl)-2,5-dioxo-1-imidazolidinyl)-4-methyl-1-oxopentyl)amino)benzenepropanoic acid
bulleyaconitine A
Bulleyaconitine a is a diterpene alkaloid. It is functionally related to an aconitane. Bulleyaconitine A is an analgesic and antiinflammatory drug isolated from Aconitum plants; has several potential targets, including voltage-gated Na+ channels.
Bulleyaconi
Bulleyaconitine a is a diterpene alkaloid. It is functionally related to an aconitane. Bulleyaconitine A is an analgesic and antiinflammatory drug isolated from Aconitum plants; has several potential targets, including voltage-gated Na+ channels.
Foresaconitine
Foresaconitine is a diterpene alkaloid with formula C35H49NO9 that is isolated from several Aconitum species. It has a role as a plant metabolite, a human urinary metabolite and a xenobiotic. It is an acetate ester, a bridged compound, a diterpene alkaloid, an organic heteropolycyclic compound, a polyether, a tertiary amino compound, a benzoate ester and an aromatic ether. It derives from a hydride of an aconitane. CID 20055981 is a natural product found in Aconitum hemsleyanum, Aconitum forrestii, and Aconitum carmichaelii with data available. A diterpene alkaloid with formula C35H49NO9 that is isolated from several Aconitum species.
primary fluorescent chlorophyll catabolite
C35H39N4O7- (627.2818603999999)
Phe Ile Trp Tyr
Phe Ile Tyr Trp
Phe Leu Trp Tyr
Phe Leu Tyr Trp
Phe Trp Ile Tyr
Phe Trp Leu Tyr
Phe Trp Tyr Ile
Phe Trp Tyr Leu
Phe Tyr Ile Trp
Phe Tyr Leu Trp
Phe Tyr Trp Ile
Phe Tyr Trp Leu
Ile Phe Trp Tyr
Ile Phe Tyr Trp
Ile Trp Phe Tyr
Ile Trp Tyr Phe
Ile Tyr Phe Trp
Ile Tyr Trp Phe
Leu Phe Trp Tyr
Leu Phe Tyr Trp
Leu Trp Phe Tyr
Leu Trp Tyr Phe
Leu Tyr Phe Trp
Leu Tyr Trp Phe
Trp Phe Ile Tyr
Trp Phe Leu Tyr
Trp Phe Tyr Ile
Trp Phe Tyr Leu
Trp Ile Phe Tyr
Trp Ile Tyr Phe
Trp Leu Phe Tyr
Trp Leu Tyr Phe
Trp Tyr Phe Ile
Trp Tyr Phe Leu
Trp Tyr Ile Phe
Trp Tyr Leu Phe
Tyr Phe Ile Trp
Tyr Phe Leu Trp
Tyr Phe Trp Ile
Tyr Phe Trp Leu
Tyr Ile Phe Trp
Tyr Ile Trp Phe
Tyr Leu Phe Trp
Tyr Leu Trp Phe
Tyr Trp Phe Ile
Tyr Trp Phe Leu
Tyr Trp Ile Phe
Tyr Trp Leu Phe
Dabigatran etexilate
C34H41N7O5 (627.3169015999999)
5-Hydroxy-6-S-glutathionyl-7,9,11-eicosatrienoic acid
C30H49N3O9S (627.3189344000001)
[(2R,3S,4R,5R,6R)-3-hydroxy-5-[[(3R)-3-hydroxydodecanoyl]amino]-2-(hydroxymethyl)-6-phosphonooxyoxan-4-yl] (3R)-3-hydroxydecanoate
ethyl N-[(2-{[(4-{N-[(hexyloxy)carbonyl]carbamimidoyl}phenyl)amino]methyl}-1-methyl-1H-benzimidazol-5-yl)carbonyl]-N-pyridin-2-yl-beta-alaninate
C34H41N7O5 (627.3169015999999)
Primary fluorescent chlorophyll catabolite(1-)
C35H39N4O7- (627.2818603999999)
A monocarboxylic acid anion that is the conjugate base of primary fluorescent chlorophyll catabolite resulting from the deprotonation of the carboxy group. Major microspecies at pH 7.3 (according to Marvin v 6.2.0.).
1-(3,5-dimethyl-4-isoxazolyl)-3-[(2S,3R)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl-[(4-phenoxyphenyl)methyl]amino]methyl]-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-8-yl]urea
2-amino-3-[[3-heptanoyloxy-2-[(3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoyl]oxypropoxy]-hydroxyphosphoryl]oxypropanoic acid
2-amino-3-[hydroxy-[2-[(5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaenoyl]oxy-3-pentanoyloxypropoxy]phosphoryl]oxypropanoic acid
2-amino-3-[[2-[(7Z,10Z,13Z,16Z,19Z)-docosa-7,10,13,16,19-pentaenoyl]oxy-3-propanoyloxypropoxy]-hydroxyphosphoryl]oxypropanoic acid
leukotriene C3
C30H49N3O9S (627.3189344000001)
A leukotriene that is (5S,7E,9E,11Z)-5-hydroxyicosa-7,9,11-trienoic acid in which a glutathionyl group is attached at position 6 via a sulfide linkage.
PS(25:5)
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Gambogic amide
Gambogic amide is a potent and selective agonist of TrkA and also induces its tyrosine phosphorylation and activation of downstream signaling, including Akt and MAPK. Gambogic amide specifically interacts with the cytoplasmic juxtamembrane domain of the TrkA receptor and triggers its dimerization, leading to activation. Gambogic amide has neuroprotective activity preventing glutamate-induced neuronal cell death. Gambogic amide has improved efficacy in a transient middle cerebral artery occlusion model of stroke and could be used to study neurodegenerative diseases and stroke[1].