Exact Mass: 571.161335
Exact Mass Matches: 571.161335
Found 68 metabolites which its exact mass value is equals to given mass value 571.161335
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Cyclochlorotine
Islanditoxin
Islanditoxin is a mycotoxin produced by the common food storage mould Penicillium islandicu
Cyclochlorotine
Cyclochlorotine is a mycotoxin produced by the common food storage mould Penicillium islandicu
Baloxavir marboxil
C27H23F2N3O7S (571.1224712000001)
Telaglenastat
C471 - Enzyme Inhibitor Telaglenastat (CB-839) is a first-in-class, selective, reversible and orally active glutaminase 1 (GLS1) inhibitor. Telaglenastat selectively inhibits GLS1 splice variants KGA (kidney-type glutaminase) and GAC (glutaminase C) compared to GLS2. The IC50s are 23 nM and 28 nM for endogenous glutaminase in mouse kidney and brain, respectively. Telaglenastat inuduces autophagy and has antitumor activity[1].
(3R,4S)-1-(4-Fluorophenyl)-3-[(3S)-3-(4-fluorophenyl)-3-hydroxypropyl]-4-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]azetidin-2-one
Umbralisib
C31H24F3N5O3 (571.1831149999999)
C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C2152 - Phosphatidylinositide 3-Kinase Inhibitor C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01E - Protein kinase inhibitors C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor C274 - Antineoplastic Agent > C1742 - Angiogenesis Inhibitor C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor
Cys Thr Trp Tyr
C27H33N5O7S (571.2100588000001)
Cys Thr Tyr Trp
C27H33N5O7S (571.2100588000001)
Cys Trp Thr Tyr
C27H33N5O7S (571.2100588000001)
Cys Trp Tyr Thr
C27H33N5O7S (571.2100588000001)
Cys Tyr Thr Trp
C27H33N5O7S (571.2100588000001)
Cys Tyr Trp Thr
C27H33N5O7S (571.2100588000001)
Asp Asp His Trp
Asp Asp Trp His
Asp His Asp Trp
Asp His Trp Asp
Asp Trp Asp His
Asp Trp His Asp
His Asp Asp Trp
His Asp Trp Asp
His Trp Asp Asp
Thr Cys Trp Tyr
C27H33N5O7S (571.2100588000001)
Thr Cys Tyr Trp
C27H33N5O7S (571.2100588000001)
Thr Trp Cys Tyr
C27H33N5O7S (571.2100588000001)
Thr Trp Tyr Cys
C27H33N5O7S (571.2100588000001)
Thr Tyr Cys Trp
C27H33N5O7S (571.2100588000001)
Thr Tyr Trp Cys
C27H33N5O7S (571.2100588000001)
Trp Cys Thr Tyr
C27H33N5O7S (571.2100588000001)
Trp Cys Tyr Thr
C27H33N5O7S (571.2100588000001)
Trp Asp Asp His
Trp Asp His Asp
Trp His Asp Asp
Trp Thr Cys Tyr
C27H33N5O7S (571.2100588000001)
Trp Thr Tyr Cys
C27H33N5O7S (571.2100588000001)
Trp Tyr Cys Thr
C27H33N5O7S (571.2100588000001)
Trp Tyr Thr Cys
C27H33N5O7S (571.2100588000001)
Tyr Cys Thr Trp
C27H33N5O7S (571.2100588000001)
Tyr Cys Trp Thr
C27H33N5O7S (571.2100588000001)
Tyr Thr Cys Trp
C27H33N5O7S (571.2100588000001)
Tyr Thr Trp Cys
C27H33N5O7S (571.2100588000001)
Tyr Trp Cys Thr
C27H33N5O7S (571.2100588000001)
Tyr Trp Thr Cys
C27H33N5O7S (571.2100588000001)
Islanditoxin
Benzamide, N-[1-[(2R)-3,5-di-O-benzoyl-2-deoxy-2-fluoro-2-methyl-α-D-erythro-pentofuranosyl]-1,2-dihydro-2-oxo-4-pyrimidinyl]
baloxavir marboxil
C27H23F2N3O7S (571.1224712000001)
J - Antiinfectives for systemic use > J05 - Antivirals for systemic use > J05A - Direct acting antivirals D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C254 - Anti-Infective Agent > C281 - Antiviral Agent D004791 - Enzyme Inhibitors
(2R)-N-Benzoyl-2-deoxy-2-fluoro-2-methylcytidine 3,5-dibenzoate
Perazine Dimaleate
C28H33N3O8S (571.1988258000001)
D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018492 - Dopamine Antagonists D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants
Imidazol-3-ide;osmium(2+);2-pyridin-2-ylpyridine
C23H19N6Os+ (571.1277144000001)
Umbralisib
C31H24F3N5O3 (571.1831149999999)
C274 - Antineoplastic Agent > C163758 - Targeted Therapy Agent > C2152 - Phosphatidylinositide 3-Kinase Inhibitor C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01E - Protein kinase inhibitors C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor C274 - Antineoplastic Agent > C1742 - Angiogenesis Inhibitor C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor
Telaglenastat
C471 - Enzyme Inhibitor Telaglenastat (CB-839) is a first-in-class, selective, reversible and orally active glutaminase 1 (GLS1) inhibitor. Telaglenastat selectively inhibits GLS1 splice variants KGA (kidney-type glutaminase) and GAC (glutaminase C) compared to GLS2. The IC50s are 23 nM and 28 nM for endogenous glutaminase in mouse kidney and brain, respectively. Telaglenastat inuduces autophagy and has antitumor activity[1].
(3R,4S)-1-(4-Fluorophenyl)-3-[(3S)-3-(4-fluorophenyl)-3-hydroxypropyl]-4-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]azetidin-2-one
N-[(2R,3R)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-2-pyrazinecarboxamide
N-[(2R,3S)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-2-pyrazinecarboxamide
N-[(2S,3R)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-2-pyrazinecarboxamide
N-[(2R,3R)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-2-pyrazinecarboxamide
N-[(2S,3S)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-2-pyrazinecarboxamide
(3S,7R,9S,13S,16R)-17,18-dichloro-13-ethyl-3,9-bis(hydroxymethyl)-7-phenyl-1,4,8,11,14-pentazabicyclo[14.3.0]nonadecane-2,5,10,12,15-pentone
4-O-methylrhodomycin D
An anthracycline that is aklavinone having a 3-amino-2,3,6-trideoxy-alpha-L-lyxo-hexopyranosyl residue and a methyl group attached as positions 4 and 7 respectively.
17,18-Dichloro-9-ethyl-3,6-bis(hydroxymethyl)-13-phenyl-1,4,7,10,14-pentazabicyclo[14.3.0]nonadecane-2,5,8,11,15-pentone
1,5-dimethyl (2s)-2-[(6as)-5-chloro-6a-methyl-9-(2-methylbut-2-enoyl)-3-[(1e,3s)-3-methylpent-1-en-1-yl]-6,8-dioxofuro[2,3-h]isoquinolin-2-yl]pentanedioate
C30H34ClNO8 (571.1972834000001)