adenoregulin

Modify Date: 2025-08-27 12:52:05

adenoregulin Structure
adenoregulin structure
Common Name adenoregulin
CAS Number 149260-68-4 Molecular Weight N/A
Density N/A Boiling Point N/A
Molecular Formula C142H242N40O42 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of adenoregulin


Adenoregulin (Dermaseptin b2) is an antimicrobial peptide antibiotic. Adenoregulin is active against Gram-negative and Gram-positive bacteria, yeast and fungi. Adenoregulin also enhances the binding of agonists to the A1 adenosine receptor[1].

 Names

Name (4S)-4-[[(2S)-6-amino-2-[[2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S,3S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[(2-aminoacetyl)amino]-4-methyl-pentanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-3-hydroxy-propanoyl]amino]hexanoyl]amino]-3-methyl-pentanoyl]amino]hexanoyl]amino]-4-carboxy-butanoyl]amino]-3-methyl-butanoyl]amino]acetyl]amino]hexanoyl]amino]-5-[[(1S)-2-[[(1S)-2-[[(1S)-5-amino-1-[[(1S)-2-[[(1S)-2-[[(1S)-2-[[(1S)-5-amino-1-[[(1S)-2-[[(1S)-2-[[2-[[(1S)-5-amino-1-[[(1S)-2-[[(1S)-2-[[(1S)-1-[[2-[[(1S)-2-[[(1S)-1-[[(1S)-2-[[(1S)-3-carboxy-1-[[(1S)-2-[[(1S)-1-carboxy-2-methyl-propyl]amino]-1-methyl-2-oxo-ethyl]carbamoyl]propyl]amino]-1-(hydroxymethyl)-2-oxo-ethyl]carbamoyl]-2-methyl-propyl]amino]-1-methyl-2-oxo-ethyl]amino]-2-oxo-ethyl]carbamoyl]-3-methyl-butyl]amino]-1-methyl-2-oxo-ethyl]amino]-1-methyl-2-oxo-ethyl]carbamoyl]pentyl]amino]-2-oxo-ethyl]amino]-1-methyl-2-oxo-ethyl]amino]-1-methyl-2-oxo-ethyl]carbamoyl]pentyl]amino]-1-methyl-2-oxo-ethyl]amino]-1-methyl-2-oxo-ethyl]amino]-1-methyl-2-oxo-ethyl]carbamoyl]pentyl]amino]-1-methyl-2-oxo-ethyl]amino]-1-methyl-2-oxo-ethyl]amino]-5-oxo-pentanoic acid

 adenoregulin Biological Activity

Description Adenoregulin (Dermaseptin b2) is an antimicrobial peptide antibiotic. Adenoregulin is active against Gram-negative and Gram-positive bacteria, yeast and fungi. Adenoregulin also enhances the binding of agonists to the A1 adenosine receptor[1].
Related Catalog
Target

149260-68-4

References

[1]. Mor A, et al. Isolation and structure of novel defensive peptides from frog skin. Eur J Biochem. 1994 Jan 15;219(1-2):145-54.  

[2]. Baek HJ, et al. Ligand binding inhibitors of A1 adenosine receptor from Rana rugosa are phospholipase A2s. Eur J Biochem. 2000 Mar;267(5):1340-6.  

 Chemical & Physical Properties

Molecular Formula C142H242N40O42
InChIKey PYGMIKHWUKCELA-HODHKHPLSA-N
SMILES CCC(C)C(NC(=O)C(CCCCN)NC(=O)C(CO)NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)C(CC(C)C)NC(=O)CN)C(=O)NC(CCCCN)C(=O)NC(CCC(=O)O)C(=O)NC(C(=O)NCC(=O)NC(CCCCN)C(=O)NC(CCC(=O)O)C(=O)NC(C)C(=O)NC(C)C(=O)NC(CCCCN)C(=O)NC(C)C(=O)NC(C)C(=O)NC(C)C(=O)NC(CCCCN)C(=O)NC(C)C(=O)NC(C)C(=O)NCC(=O)NC(CCCCN)C(=O)NC(C)C(=O)NC(C)C(=O)NC(CC(C)C)C(=O)NCC(=O)NC(C)C(=O)NC(C(=O)NC(CO)C(=O)NC(CCC(=O)O)C(=O)NC(C)C(=O)NC(C(=O)O)C(C)C)C(C)C)C(C)C
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