CAS 140896-21-5
:indolicidin
Description:
Indolicidin is a peptide composed of 13 amino acids, primarily known for its antimicrobial properties. It is derived from the indole-containing amino acid tryptophan and exhibits a unique structure that contributes to its biological activity. Indolicidin is characterized by its ability to disrupt bacterial membranes, making it effective against a range of Gram-positive and Gram-negative bacteria, as well as some fungi. The peptide's mechanism of action involves binding to the lipid bilayer of microbial cells, leading to membrane destabilization and cell lysis. Additionally, indolicidin has been studied for its potential applications in therapeutic settings, particularly in combating antibiotic-resistant infections. Its stability and efficacy in various environments make it a subject of interest in the field of antimicrobial research. However, further studies are needed to fully understand its pharmacokinetics, toxicity, and potential side effects in clinical applications. Overall, indolicidin represents a promising avenue for the development of new antimicrobial agents.
Formula:C100H132N26O13
InChI:InChI=1/C100H132N26O13/c1-5-57(4)85(102)95(136)123-79(45-56(2)3)96(137)124-42-20-36-82(124)92(133)118-76(46-58-51-110-68-28-11-6-23-63(58)68)89(130)116-74(33-16-17-39-101)88(129)121-80(49-61-54-113-71-31-14-9-26-66(61)71)97(138)125-43-21-38-84(125)94(135)120-78(48-60-53-112-70-30-13-8-25-65(60)70)91(132)122-81(50-62-55-114-72-32-15-10-27-67(62)72)98(139)126-44-22-37-83(126)93(134)119-77(47-59-52-111-69-29-12-7-24-64(59)69)90(131)117-75(35-19-41-109-100(106)107)87(128)115-73(86(103)127)34-18-40-108-99(104)105/h6-15,23-32,51-57,73-85,110-114H,5,16-22,33-50,101-102H2,1-4H3,(H2,103,127)(H,115,128)(H,116,130)(H,117,131)(H,118,133)(H,119,134)(H,120,135)(H,121,129)(H,122,132)(H,123,136)(H4,104,105,108)(H4,106,107,109)/t57-,73-,74-,75-,76-,77-,78-,79-,80-,81-,82-,83-,84-,85-/m0/s1
SMILES:CC[C@H](C)[C@@H](C(=N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=N[C@@H](Cc1c[nH]c2ccccc12)C(=N[C@@H](CCCCN)C(=N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCC[C@H]1C(=N[C@@H](Cc1c[nH]c2ccccc12)C(=N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N1CCC[C@H]1C(=N[C@@H](Cc1c[nH]c2ccccc12)C(=N[C@@H](CCCNC(=N)N)C(=N[C@@H](CCCNC(=N)N)C(=N)O)O)O)O)O)O)O)O)O)O)N
Synonyms:- H-Ile-Leu-Pro-Trp-Lys-Trp-Pro-Trp-Trp-Pro-Trp-Arg-Arg-NH2
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
Indolicidin
CAS:<p>For cellular and molecular biology applications</p>Color and Shape:Lyophilized Powder, WhiteIndolicidin
CAS:This cationic, tryptophan-rich peptide was purified from bovine granulocytes. Indolicidin shows potent antimicrobial activity in vitro against bacteria and fungi. It is also highly cytotoxic to T-line cells.Formula:C100H132N26O13Purity:> 96%Color and Shape:Whitish PowderMolecular weight:1906.32Indolicidin
CAS:Indolicidin: 13-amino acid peptide, highest tryptophan content, carboxamidated C-terminal arginine.Formula:C100H132N26O13Purity:>99.99%Color and Shape:SolidMolecular weight:1906.28Indolicidin TFA Salt
CAS:Controlled Product<p>Applications Indolicidin is an antimicrobial peptide containing multiple tryptophan residues.<br></p>Formula:C100H132N26O13•x(C2HF3O2)Color and Shape:NeatMolecular weight:1906.2811402






