PG 106 TFA

Modify Date: 2025-08-21 03:31:44

PG 106 TFA Structure
PG 106 TFA structure
Common Name PG 106 TFA
CAS Number 944111-22-2 Molecular Weight 1008.18000
Density 1.40±0.1 g/cm3 (20 °C, 760 mmHg) Boiling Point N/A
Molecular Formula C51H69N13O9 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of PG 106 TFA


PG106 is a potent and selective human melanocortin 3 (hMC3) receptor antagonist (IC50=210 nM) and has noactivity at hMC4 receptors (EC50=9900 nM) and hMC5 receptor[1].

 Names

Name L-Lysinamide, N-acetyl-L-norleucyl-L-α-aspartyl-β-alanyl-3-(2-naphthalenyl)-D-alanyl-L-arginyl-L-tryptophyl-, (2→7)-lactam
Synonym More Synonyms

 PG 106 TFA Biological Activity

Description PG106 is a potent and selective human melanocortin 3 (hMC3) receptor antagonist (IC50=210 nM) and has noactivity at hMC4 receptors (EC50=9900 nM) and hMC5 receptor[1].
Related Catalog
Target

IC50: 210 nM (hMC3 receptor) EC50: 9900 nM (hMC4 receptor)[1]

References

[1]. Paolo Grieco, et al. Further structure-activity studies of lactam derivatives of MT-II and SHU-9119: their activity and selectivity at human melanocortin receptors 3, 4, and 5. Peptides

 Chemical & Physical Properties

Density 1.40±0.1 g/cm3 (20 °C, 760 mmHg)
Molecular Formula C51H69N13O9
Molecular Weight 1008.18000
Exact Mass 1007.53000
PSA 353.58000
LogP 4.81610
InChIKey ZFZDDBJAFMOQSH-JHMPFZGISA-N
SMILES CCCCC(NC(C)=O)C(=O)NC1CC(=O)NCCCCC(C(N)=O)NC(=O)C(Cc2c[nH]c3ccccc23)NC(=O)C(CCCN=C(N)N)NC(=O)C(Cc2ccc3ccccc3c2)NC(=O)CCNC1=O

 Synonyms

MMPIP hydrochloride
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