This work is licensed under a Creative Commons Attribution 4.0 International License.
Penicillin G
General Information
DRACP ID DRACP04528
Peptide Name Penicillin G
Sequence Cv
Sequence Length 2
UniProt ID Not available
PubChem CID Not available
Origin Synthetic
Type Native peptide
Classification
Active ACP
Activity Information
Hemolytic Activity Not available
Normal (non-cancerous) Cytotoxicity Not available
Target Not available
Affinity Not available
Mechanism Not available
Nature Anticancer; Antibacterial
Structure Information
Helicity Not available
Linear/Cyclic Linear
Disulfide/Other Bond Not available
N-terminal Modification BZA
C-terminal Modification Free
Other Modification None
Chiral Mix
Physicochemical Information
Formula C3H5NOS
Absent amino acids ADEFGHIKLMNPQRSTVWY
Common amino acids C
Mass 12116
Pl 5.92
Basic residues 0
Acidic residues 0
Hydrophobic residues 0
Net charge 0
Boman Index 128
Hydrophobicity 125
Aliphatic Index 0
Half Life
/
Extinction Coefficient cystines 0
Absorbance 280nm 0
Polar residues 1
Amino acid distribution
Literature Information
Literature 1
Pubmed ID 34180670
Title Novel Broad-Spectrum Antimicrobial Peptide Derived from Anoplin and Its Activity on Bacterial Pneumonia in Mice
Doi Not available
Year 2021
Literature 2
Pubmed ID 31466017
Title Design and synthesis of new N-terminal fatty acid modified-antimicrobial peptide analogues with potent in vitro biological activity
Doi Not available
Year 2019
Literature 3
Pubmed ID 26879856
Title Salicylanilide N-monosubstituted carbamates: Synthesis and in vitro antimicrobial activity
Doi Not available
Year 2016
Literature 4
Pubmed ID 25593095
Title Synthesis and in vitro biological evaluation of 2-(phenylcarbamoyl)phenyl 4-substituted benzoates
Doi Not available
Year 2015
Literature 5
Pubmed ID 29348811
Title Disconnecting the Estrogen Receptor Binding Properties and Antimicrobial Properties of Parabens through 3,5-Substitution
Doi Not available
Year 2017
Literature 6
Pubmed ID 30685534
Title Synthesis, antimicrobial and cytotoxic activities, and molecular docking studies of N-arylsulfonylindoles containing an aminoguanidine, a semicarbazide, and a thiosemicarbazide moiety
Doi Not available
Year 2019
Literature 7
Pubmed ID 20566769
Title Oligochlorophens are potent inhibitors of Bacillus anthracis
Year
Patent
Patent ID Not available
Patent Title Not available
Other Iinformation Not available
Other Published ID Not available
External Code
DBAASP ID 20466
This work is licensed under a Creative Commons Attribution 4.0 International License.