Exact Mass: 495.2264
Exact Mass Matches: 495.2264
Found 500 metabolites which its exact mass value is equals to given mass value 495.2264
,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
GW 1929
GW 1929 is an orally active peroxisome proliferator-activated receptor-γ (PPARγ) agonist with a pKi of 8.84 for human PPAR-γ, and pEC50s of 8.56 and 8.27 for human PPAR-γ and murine PPAR-γ, respectively. GW 1929 (hydrochloride) has antidiabetic efficacy and neuroprotective potential[1][2].
19-Benzyl-7-hydroxy-7,9,16,17-tetramethyl-2,4,15-trioxa-20-azatetracyclo[11.8.0.01,18.014,16]henicosa-5,11-diene-3,8,21-trione
2-(2-Benzoylanilino)-3-[4-[2-[methyl(2-pyridinyl)amino]ethoxy]phenyl]propanoic acid
Silodosin
aeruginosin DA495A|D-Hpla-D-Phe-L-6-epi-Choi-amide
Lys Tyr Ala Asp
WYE-354
WYE-354 is an ATP-competitive mTOR inhibitor with an IC50 of 5 nM. WYE-354 also inhibits PI3Kα and PI3Kγ with IC50s of 1.89 μM and 7.37 μM, respectively. WYE-354 inhibits both mTORC1 and mTORC2. WYE-354 induces autophagy activation in vitro[3]. WYE-354 is an ATP-competitive mTOR inhibitor with an IC50 of 5 nM. WYE-354 also inhibits PI3Kα and PI3Kγ with IC50s of 1.89 μM and 7.37 μM, respectively. WYE-354 inhibits both mTORC1 and mTORC2. WYE-354 induces autophagy activation in vitro[3].
Tyr Ala Asp Lys
Silodosin
G - Genito urinary system and sex hormones > G04 - Urologicals > G04C - Drugs used in benign prostatic hypertrophy > G04CA - Alpha-adrenoreceptor antagonists C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C72900 - Adrenergic Antagonist D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists D000089162 - Genitourinary Agents > D064804 - Urological Agents Silodosin (KAD 3213; KMD 3213) is a potent, selective and orally active α1A-adrenergic receptor (α1A-AR) blocker. Silodosin exhibits high affinity for α1A-AR (Ki=0.036 nM), over 162-fold and 50-fold than for α1B-AR and α1D-AR with Ki values of 21 nM and 2.0 nM, respectively. Silodosin is an effective and well-tolerated agent, it can be used for the investigation of LUTS/BPH[1][3].
Cytochalasin E
D006133 - Growth Substances > D043924 - Angiogenesis Modulating Agents D000970 - Antineoplastic Agents > D020533 - Angiogenesis Inhibitors D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins D006133 - Growth Substances > D006131 - Growth Inhibitors A natural product found in Arthrinium sacchari.
Ala Cys Phe Arg
Ala Cys Arg Phe
Ala Asp Lys Tyr
Ala Asp Tyr Lys
Ala Phe Cys Arg
Ala Phe Met Gln
Ala Phe Gln Met
Ala Phe Arg Cys
Ala Lys Asp Tyr
Ala Lys Tyr Asp
Ala Met Phe Gln
Ala Met Gln Phe
Ala Gln Phe Met
Ala Gln Met Phe
Ala Arg Cys Phe
Ala Arg Phe Cys
Ala Tyr Asp Lys
Ala Tyr Lys Asp
Cys Ala Phe Arg
Cys Ala Arg Phe
Cys Phe Ala Arg
Cys Phe Ile Asn
Cys Phe Leu Asn
Cys Phe Asn Ile
Cys Phe Asn Leu
Cys Phe Gln Val
Cys Phe Arg Ala
Cys Phe Val Gln
Cys Ile Phe Asn
Cys Ile Asn Phe
Cys Leu Phe Asn
Cys Leu Asn Phe
Cys Asn Phe Ile
Cys Asn Phe Leu
Cys Asn Ile Phe
Cys Asn Leu Phe
Cys Gln Phe Val
Cys Gln Val Phe
Cys Arg Ala Phe
Cys Arg Phe Ala
Cys Val Phe Gln
Cys Val Gln Phe
Asp Ala Lys Tyr
Asp Ala Tyr Lys
Asp Phe Lys Ser
Asp Phe Ser Lys
Asp Lys Ala Tyr
Asp Lys Phe Ser
Asp Lys Ser Phe
Asp Lys Tyr Ala
Asp Ser Phe Lys
Asp Ser Lys Phe
Asp Tyr Ala Lys
Asp Tyr Lys Ala
Glu Gly Lys Tyr
Glu Gly Tyr Lys
Glu Lys Gly Tyr
Glu Lys Tyr Gly
Glu Tyr Gly Lys
Glu Tyr Lys Gly
Phe Ala Cys Arg
Phe Ala Met Gln
Phe Ala Gln Met
Phe Ala Arg Cys
Phe Cys Ala Arg
Phe Cys Ile Asn
Phe Cys Leu Asn
Phe Cys Asn Ile
Phe Cys Asn Leu
Phe Cys Gln Val
Phe Cys Arg Ala
Phe Cys Val Gln
Phe Asp Lys Ser
Phe Asp Ser Lys
Phe Ile Cys Asn
Phe Ile Asn Cys
Phe Lys Asp Ser
Phe Lys Ser Asp
Phe Leu Cys Asn
Phe Leu Asn Cys
Phe Met Ala Gln
Phe Met Gln Ala
Phe Asn Cys Ile
Phe Asn Cys Leu
Phe Asn Ile Cys
Phe Asn Leu Cys
Phe Gln Ala Met
Phe Gln Cys Val
Phe Gln Met Ala
Phe Gln Thr Thr
Phe Gln Val Cys
Phe Arg Ala Cys
Phe Arg Cys Ala
Phe Ser Asp Lys
Phe Ser Lys Asp
Phe Thr Gln Thr
Phe Thr Thr Gln
Phe Val Cys Gln
Phe Val Gln Cys
Gly Glu Lys Tyr
Gly Glu Tyr Lys
Gly His Pro Trp
Gly His Trp Pro
Gly Lys Glu Tyr
Gly Lys Tyr Glu
Gly Pro His Trp
Gly Pro Trp His
Gly Trp His Pro
Gly Trp Pro His
Gly Tyr Glu Lys
Gly Tyr Lys Glu
His Gly Pro Trp
His Gly Trp Pro
His Pro Gly Trp
His Pro Trp Gly
His Trp Gly Pro
His Trp Pro Gly
Ile Cys Phe Asn
Ile Cys Asn Phe
Ile Phe Cys Asn
Ile Phe Asn Cys
Ile Asn Cys Phe
Ile Asn Phe Cys
Ile Asn Ser Tyr
Ile Asn Tyr Ser
Ile Ser Asn Tyr
Ile Ser Tyr Asn
Ile Tyr Asn Ser
Ile Tyr Ser Asn
Lys Ala Asp Tyr
Lys Ala Tyr Asp
Lys Asp Ala Tyr
Lys Asp Phe Ser
Lys Asp Ser Phe
Lys Asp Tyr Ala
Lys Glu Gly Tyr
Lys Glu Tyr Gly
Lys Phe Asp Ser
Lys Phe Ser Asp
Lys Gly Glu Tyr
Lys Gly Tyr Glu
Lys Met Met Ser
Lys Met Ser Met
Lys Ser Asp Phe
Lys Ser Phe Asp
Lys Ser Met Met
Lys Tyr Asp Ala
Lys Tyr Glu Gly
Lys Tyr Gly Glu
Leu Cys Phe Asn
Leu Cys Asn Phe
Leu Phe Cys Asn
Leu Phe Asn Cys
Leu Asn Cys Phe
Leu Asn Phe Cys
Leu Asn Ser Tyr
Leu Asn Tyr Ser
Leu Ser Asn Tyr
Leu Ser Tyr Asn
Leu Tyr Asn Ser
Leu Tyr Ser Asn
Met Ala Phe Gln
Met Ala Gln Phe
Met Phe Ala Gln
Met Phe Gln Ala
Met Lys Met Ser
Met Lys Ser Met
Met Met Lys Ser
Met Met Ser Lys
Met Gln Ala Phe
Met Gln Phe Ala
Met Ser Lys Met
Met Ser Met Lys
Asn Cys Phe Ile
Asn Cys Phe Leu
Asn Cys Ile Phe
Asn Cys Leu Phe
Asn Phe Cys Ile
Asn Phe Cys Leu
Asn Phe Ile Cys
Asn Phe Leu Cys
Asn Ile Cys Phe
Asn Ile Phe Cys
Asn Ile Ser Tyr
Asn Ile Tyr Ser
Asn Leu Cys Phe
Asn Leu Phe Cys
Asn Leu Ser Tyr
Asn Leu Tyr Ser
Asn Ser Ile Tyr
Asn Ser Leu Tyr
Asn Ser Tyr Ile
Asn Ser Tyr Leu
Asn Thr Val Tyr
Asn Thr Tyr Val
Asn Val Thr Tyr
Asn Val Tyr Thr
Asn Tyr Ile Ser
Asn Tyr Leu Ser
Asn Tyr Ser Ile
Asn Tyr Ser Leu
Asn Tyr Thr Val
Asn Tyr Val Thr
Pro Gly His Trp
Pro Gly Trp His
Pro His Gly Trp
Pro His Trp Gly
Pro Trp Gly His
Pro Trp His Gly
Gln Ala Phe Met
Gln Ala Met Phe
Gln Cys Phe Val
Gln Cys Val Phe
Gln Phe Ala Met
Gln Phe Cys Val
Gln Phe Met Ala
Gln Phe Thr Thr
Gln Phe Val Cys
Gln Met Ala Phe
Gln Met Phe Ala
Gln Ser Val Tyr
Gln Ser Tyr Val
Gln Thr Phe Thr
Gln Thr Thr Phe
Gln Val Cys Phe
Gln Val Phe Cys
Gln Val Ser Tyr
Gln Val Tyr Ser
Gln Tyr Ser Val
Gln Tyr Val Ser
Arg Ala Cys Phe
Arg Ala Phe Cys
Arg Cys Ala Phe
Arg Cys Phe Ala
Arg Phe Ala Cys
Arg Phe Cys Ala
Ser Asp Phe Lys
Ser Asp Lys Phe
Ser Phe Asp Lys
Ser Phe Lys Asp
Ser Gly Trp Phe
Ser Ile Asn Tyr
Ser Ile Tyr Asn
Ser Lys Asp Phe
Ser Lys Phe Asp
Ser Lys Met Met
Ser Leu Asn Tyr
Ser Leu Tyr Asn
Ser Met Lys Met
Ser Met Met Lys
Ser Asn Ile Tyr
Ser Asn Leu Tyr
Ser Asn Tyr Ile
Ser Asn Tyr Leu
Ser Gln Val Tyr
Ser Gln Tyr Val
Ser Val Gln Tyr
Ser Val Tyr Gln
Ser Trp Phe Gly
Ser Trp Gly Phe
Ser Tyr Ile Asn
Ser Tyr Leu Asn
Ser Tyr Asn Ile
Ser Tyr Asn Leu
Ser Tyr Gln Val
Ser Tyr Val Gln
Thr Phe Gln Thr
Thr Phe Thr Gln
Thr Asn Val Tyr
Thr Asn Tyr Val
Thr Gln Phe Thr
Thr Gln Thr Phe
Thr Thr Phe Gln
Thr Thr Gln Phe
Thr Val Asn Tyr
Thr Val Tyr Asn
Thr Tyr Asn Val
Thr Tyr Val Asn
Val Cys Phe Gln
Val Cys Gln Phe
Val Phe Cys Gln
Val Phe Gln Cys
Val Asn Thr Tyr
Val Asn Tyr Thr
Val Gln Cys Phe
Val Gln Phe Cys
Val Gln Ser Tyr
Val Gln Tyr Ser
Val Ser Gln Tyr
Val Ser Tyr Gln
Val Thr Asn Tyr
Val Thr Tyr Asn
Val Tyr Asn Thr
Val Tyr Gln Ser
Val Tyr Ser Gln
Val Tyr Thr Asn
Trp Ala Tyr Gly
Trp Phe Gly Ser
Trp Phe Ser Gly
Trp Gly Ala Tyr
Trp Gly Phe Ser
Trp Gly His Pro
Trp Gly Pro His
Trp Gly Ser Phe
Trp Gly Tyr Ala
Trp His Gly Pro
Trp His Pro Gly
Trp Pro Gly His
Trp Pro His Gly
Trp Ser Phe Gly
Trp Ser Gly Phe
Trp Tyr Ala Gly
Trp Tyr Gly Ala
Tyr Ala Gly Trp
Tyr Ala Lys Asp
Tyr Ala Trp Gly
Tyr Asp Ala Lys
Tyr Asp Lys Ala
Tyr Glu Gly Lys
Tyr Glu Lys Gly
Tyr Gly Ala Trp
Tyr Gly Glu Lys
Tyr Gly Lys Glu
Tyr Ile Asn Ser
Tyr Ile Ser Asn
Tyr Lys Ala Asp
Tyr Lys Asp Ala
Tyr Lys Glu Gly
Tyr Lys Gly Glu
Tyr Leu Asn Ser
Tyr Leu Ser Asn
Tyr Asn Ile Ser
Tyr Asn Leu Ser
Tyr Asn Ser Ile
Tyr Asn Ser Leu
Tyr Asn Thr Val
Tyr Asn Val Thr
Tyr Gln Ser Val
Tyr Gln Val Ser
Tyr Ser Ile Asn
Tyr Ser Leu Asn
Tyr Ser Asn Ile
Tyr Ser Asn Leu
Tyr Ser Gln Val
Tyr Ser Val Gln
Tyr Thr Asn Val
Tyr Thr Val Asn
Tyr Val Asn Thr
Tyr Val Gln Ser
Tyr Val Ser Gln
Tyr Val Thr Asn
(alphaS)-4-[(1,1-Dimethylethoxy)carbonyl]-alpha-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-1-piperazinepropanoic acid
Gusperimus trihydrochloride
D020011 - Protective Agents > D011837 - Radiation-Protective Agents D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents C308 - Immunotherapeutic Agent > C574 - Immunosuppressant D000970 - Antineoplastic Agents D007004 - Hypoglycemic Agents
2-N-FMOC-AMINO-3-(2-N-BOC-AMINO-PYRROLIDINYL)PROPIONIC ACID
GW1929
GW 1929 is an orally active peroxisome proliferator-activated receptor-γ (PPARγ) agonist with a pKi of 8.84 for human PPAR-γ, and pEC50s of 8.56 and 8.27 for human PPAR-γ and murine PPAR-γ, respectively. GW 1929 (hydrochloride) has antidiabetic efficacy and neuroprotective potential[1][2].