BIOPEP-UWM: Peptide Data
ID
Name
Sequence
ILPWKWPWWPWRR~
Chemical Mass
Number of residues
Monoisotopic Mass
EC50
IC50
µM
Additional Information
BIOPEP-UWM database of bioactive peptides SMILES: [H][C@@](CCCNC(N)=N)(NC(=O)[C@]([H])(CCCNC(N)=N)NC(=O)[C@]([H])(CC1=CNC2=C1C=CC=C2)NC(=O)[C@]1([H])CCCN1C(=O)[C@]([H])(CC1=CNC2=C1C=CC=C2)NC(=O)[C@]([H])(CC1=CNC2=C1C=CC=C2)NC(=O)[C@]1([H])CCCN1C(=O)[C@]([H])(CC1=CNC2=C1C=CC=C2)NC(=O)[C@]([H])(CCCCN)NC(=O)[C@]([H])(CC1=CNC2=C1C=CC=C2)NC(=O)[C@]1([H])CCCN1C(=O)[C@]([H])(CC(C)C)NC(=O)[C@@]([H])(N)[C@@H](C)CC)C(N)=O InChI=1S/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 InChIKey=USSYUMHVHQSYNA-SLDJZXPVSA-N The active form of this peptide is C-terminal amide. Indolicidin is active against G(-) bacteria. BBA, 1197, 109-131 (1994). Antiviral peptide according to the BindingDB database; DBAASP database; the EROP-Moscow database Hemolytic peptide according to the Hemolytik database Anticancer peptide according to the CancerPPD database
activity
references
function information
database references
screen and print peptide data
list of peptides