Exact Mass: 652.3036
Exact Mass Matches: 652.3036
Found 63 metabolites which its exact mass value is equals to given mass value 652.3036
,
within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error
0.001 dalton.
1-(3-Methoxy-4-hydroxyphenyl)-1,2,3-tris(2-methoxy-4-allylphenoxy)propane
Glu Arg Trp Tyr
Glu Arg Tyr Trp
Glu Trp Arg Tyr
Glu Trp Tyr Arg
Glu Tyr Arg Trp
Glu Tyr Trp Arg
Arg Glu Trp Tyr
Arg Glu Tyr Trp
Arg Trp Glu Tyr
Arg Trp Tyr Glu
Arg Tyr Glu Trp
Arg Tyr Trp Glu
Val Trp Trp Tyr
Val Trp Tyr Trp
Val Tyr Trp Trp
Trp Glu Arg Tyr
Trp Glu Tyr Arg
Trp Arg Glu Tyr
Trp Arg Tyr Glu
Trp Val Trp Tyr
Trp Val Tyr Trp
Trp Trp Val Tyr
Trp Trp Tyr Val
Trp Tyr Glu Arg
Trp Tyr Arg Glu
Trp Tyr Val Trp
Trp Tyr Trp Val
Tyr Glu Arg Trp
Tyr Glu Trp Arg
Tyr Arg Glu Trp
Tyr Arg Trp Glu
Tyr Val Trp Trp
Tyr Trp Glu Arg
Tyr Trp Arg Glu
Tyr Trp Val Trp
Tyr Trp Trp Val
4,4-methylenebis(aniline), compound with sodium chloride (3:1)
CH 5450
CH 5450 (Z-Ile-Glu-Pro-Phe-Ome) is a selective short peptide human cardiac chymase inhibitor. CH-5450 inhibits the action of rat MAB elastase 2 on substrate Ang I with an IC50 value of 49 μM and N-succinyl-Ala-Ala-Pro-Phe-p-nitroanilide with an IC50 value of 4.8 μM[1].
N-terminally acetylated Endomorphin-1
N-terminally acetylated Endomorphin-1 is a modified Endomorphin-1.
Z-VEID-FMK
Z-VEID-FMK (Z-VE(OMe)ID(OMe)-FMK) is a selective and irreversible caspase-6 peptide inhibitor. Z-VEID-FMK alleviates the S-(+)-ketamine-induced augmentation of caspase-6 activity, DNA fragmentation, and cell apoptosis[1][2].