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MYP_146230
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Basic Information
amyloid disrupting peptide
—
Standard
8 amino acids
C36H57N9O12
Standard
Sequence
NFGAILSS
Physicochemical Analysis
807.89 Da
5.53
-0.24
-0.44
-0.0300
0.93
0.31
0.45
27.50
110.00
0.1250
0.00
0.00
The radar chart summarizes major physicochemical dimensions for quick comparison, while exact numerical values remain listed on the left.
Residue Composition
Amino Acid Composition
Chemical Descriptors
350.57
-4.36
12.0
12.0
25.0
57.0
1.0
8.0
Structural Visualization
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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Experimental Records
RECORD: Rec_0002516 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
synthetic linear peptide [Linear]
canonical L-amino-acid peptide [L]
Source entry describes small-molecule/peptide conjugation at one terminus; exact terminus not explicitly assigned in source metadata
Conjugate type: amide; Conjugated small molecule: 1,3,5-Benzenetricarboxylic acid
Bio-Activity Profile
-
PaperPeptide Conjugates of Benzene Carboxylic Acids as Agonists and Antagonists of Amylin Aggregation. Bioconjugate Chemistry. 2017 Evidence URLhttps://doi.org/10.1021/acs.bioconjchem.6b00732
RECORD: Rec_0083541 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
synthetic linear peptide [Linear]
canonical L-amino-acid peptide [L]
Source entry describes small-molecule/peptide conjugation at one terminus; exact terminus not explicitly assigned in source metadata
Conjugate type: amide; Conjugated small molecule: Sulfosalicylic acid
Bio-Activity Profile
-
PaperPeptide Conjugates of Benzene Carboxylic Acids as Agonists and Antagonists of Amylin Aggregation. Bioconjugate Chemistry. 2017 Evidence URLhttps://doi.org/10.1021/acs.bioconjchem.6b00732
RECORD: Rec_0247048 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
synthetic linear peptide [Linear]
canonical L-amino-acid peptide [L]
Source entry describes small-molecule/peptide conjugation at one terminus; exact terminus not explicitly assigned in source metadata
Conjugate type: amide; Conjugated small molecule: Mellitic acid
Bio-Activity Profile
-
PaperPeptide Conjugates of Benzene Carboxylic Acids as Agonists and Antagonists of Amylin Aggregation. Bioconjugate Chemistry. 2017 Evidence URLhttps://doi.org/10.1021/acs.bioconjchem.6b00732
RECORD: Rec_0295666 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
synthetic linear peptide [Linear]
canonical L-amino-acid peptide [L]
Source entry describes small-molecule/peptide conjugation at one terminus; exact terminus not explicitly assigned in source metadata
Conjugate type: amide; Conjugated small molecule: ¦Á-Cyano-4-hydroxycinnamic acid
Bio-Activity Profile
-
PaperPeptide Conjugates of Benzene Carboxylic Acids as Agonists and Antagonists of Amylin Aggregation. Bioconjugate Chemistry. 2017 Evidence URLhttps://doi.org/10.1021/acs.bioconjchem.6b00732
RECORD: Rec_0339426 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
synthetic linear peptide [Linear]
canonical L-amino-acid peptide [L]
Source entry describes small-molecule/peptide conjugation at one terminus; exact terminus not explicitly assigned in source metadata
Conjugate type: amide; Conjugated small molecule: Pyromellitic acid
Bio-Activity Profile
-
PaperPeptide Conjugates of Benzene Carboxylic Acids as Agonists and Antagonists of Amylin Aggregation. Bioconjugate Chemistry. 2017 Evidence URLhttps://doi.org/10.1021/acs.bioconjchem.6b00732
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