159237-99-7
159237-99-7
Chemical Structure
Phe-Met-Arg-Phe amide trifluoroacetate
- CAS No.: 159237-99-7
- Formula:C33H44F6N8O8S
- Molecular Weight:826.81
IUPAC Name: (S)-N-((S)-1-amino-1-oxo-3-phenylpropan-2-yl)-2-((S)-2-((S)-2-amino-3-phenylpropanamido)-4-(methylthio)butanamido)-5-guanidinopentanamide bis(2,2,2-trifluoroacetate)
InChIKey: XVODPBULIXCTET-PAHQJZCISA-N
SMILES: N[C@@H](CC1=CC=CC=C1)C(N[C@@H](CCSC)C(N[C@@H](CCCNC(N)=N)C(N[C@H](C(N)=O)CC2=CC=CC=C2)=O)=O)=O.O=C(O)C(F)(F)F.O=C(O)C(F)(F)F
Biological Activity: Phe-Met-Arg-Phe amide trifluoroacetate is an activator of K+ current, with ED50 of 23 nM in the peptidergic caudodorsal neurons.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Phe-Met-Arg-Phe amide trifluoroacetate | 98.85% | Phe-Met-Arg-Phe amide trifluoroacetate is an activator of K+ current, with ED50 of 23 nM in the peptidergic caudodorsal neurons. | ||||||||||||||||||||
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DTP3 TFA | 98.20% | DTP3 TFA is a potent and selective GADD45β/MKK7 (growth arrest and DNA-damage-inducible β/mitogen-activated protein kinase kinase 7) inhibitor. DTP3 TFA targets an essential, cancer-selective cell-survival module downstream of the NF-κB pathway. | ||||||||||||||||||||
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PPACK II diTFA | 95.56% | PPACK II diTFA is an irreversible and specific glandular and plasma kallikreins inhibitor. | ||||||||||||||||||||
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Phe-Met-Arg-Phe, amide | Phe-Met-Arg-Phe, amide dose dependently (ED50=23 nM) activates a K+ current in the peptidergic caudodorsal neurons. | |||||||||||||||||||||
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Phe-Met-Arg-Phe, amide acetate | Phe-Met-Arg-Phe, amide acetate dose dependently (ED50=23 nM) activates a K+ current in the peptidergic caudodorsal neurons. | |||||||||||||||||||||
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FMRF | 99.72% | FMRF is a peptide consisting of 4 amino acid residues. | ||||||||||||||||||||
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LIH383 | LIH383 is an agonist of ACKR3 (CXCR7) (EC50=0.61 nM). LIH383 efficiently induces the recruitment of β-arrestin to ACKR3 but does not trigger typical G protein signaling. | |||||||||||||||||||||
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[Met5]-Enkephalin, amide TFA | 99.37% | [Met5]-Enkephalin, amide TFA is an agonist for δ opioid receptors as well as putative ζ (zeta) opioid receptors. | ||||||||||||||||||||
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Substance P (7-11) | 99.08% | Substance P (7-11) is a C-terminal fragment of Substance P which can cause an increase in the intracellular calcium concentration. | ||||||||||||||||||||
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YMRF-NH2 | YMRF-NH2 is a neuropeptide. YMRF-NH2 binds to FMRFa-R with an EC50 value of 31 nM. | |||||||||||||||||||||
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Substance P (6-11) | Substance P (6-11) is the C-terminal hexapeptideamide of Substance P (HY-P0201). Substance P (6-11) binds to NK-1 tachykinin receptor. Substance P (6-11) shows depolarization of motoneurons and a hypotensive effect. | |||||||||||||||||||||
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