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Details

Stereochemistry ABSOLUTE
Molecular Formula C122H210N32O22.C2H4O2
Molecular Weight 2537.226
Optical Activity UNSPECIFIED
Defined Stereocenters 21 / 21
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PEXIGANAN ACETATE

SMILES

CC(O)=O.CC[C@H](C)[C@H](NC(=O)CN)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC2=CC=CC=C2)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC3=CC=CC=C3)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(N)=O

InChI

InChIKey=ZYMCXUWEZQKVIO-IJAHCEAPSA-N
InChI=1S/C122H210N32O22.C2H4O2/c1-13-77(9)102(152-98(155)71-132)120(174)135-73-100(157)139-86(50-26-35-59-125)110(164)150-96(69-82-44-20-16-21-45-82)118(172)148-93(66-74(3)4)116(170)145-90(54-30-39-63-129)113(167)142-87(51-27-36-60-126)109(163)137-79(11)105(159)141-88(52-28-37-61-127)112(166)143-91(55-31-40-64-130)114(168)149-95(68-81-42-18-15-19-43-81)107(161)134-72-99(156)138-85(49-25-34-58-124)108(162)136-80(12)106(160)147-97(70-83-46-22-17-23-47-83)119(173)153-101(76(7)8)121(175)146-92(56-32-41-65-131)115(169)154-103(78(10)14-2)122(176)151-94(67-75(5)6)117(171)144-89(53-29-38-62-128)111(165)140-84(104(133)158)48-24-33-57-123;1-2(3)4/h15-23,42-47,74-80,84-97,101-103H,13-14,24-41,48-73,123-132H2,1-12H3,(H2,133,158)(H,134,161)(H,135,174)(H,136,162)(H,137,163)(H,138,156)(H,139,157)(H,140,165)(H,141,159)(H,142,167)(H,143,166)(H,144,171)(H,145,170)(H,146,175)(H,147,160)(H,148,172)(H,149,168)(H,150,164)(H,151,176)(H,152,155)(H,153,173)(H,154,169);1H3,(H,3,4)/t77-,78-,79-,80-,84-,85-,86-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,101-,102-,103-;/m0./s1

HIDE SMILES / InChI
Pexiganan is a 22-amino-acid synthetic cationic peptide. It is an analog of magainin 2, which is a host defense peptide isolated from frog skin. The drug is thought to act by disturbing the permeability of the cell membrane or cell wall. Pexiganan exhibited in vitro broad-spectrum antibacterial activity when it was tested against 3,109 clinical isolates of gram-positive and gram-negative, anaerobic and aerobic bacteria. It is currently in phase 3 clinical trials as a topical antimicrobial agent for the treatment of mild infections associated with diabetic foot ulcers. In vitro data for pexiganan acetate suggest that the drug does have hemolytic activity at concentrations relevant for antibacterial activity. In association with tigecycline, pexiganan administration could overcome antibiotic resistance and increase the effectiveness of treatment against P. aeruginosa sepsis.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pexiganan acetate.
1998 Dec
In vitro antibacterial properties of pexiganan, an analog of magainin.
1999 Apr
In vitro spectrum of pexiganan activity when tested against pathogens from diabetic foot infections and with selected resistance mechanisms.
2015 Mar
What Is the 'Minimum Inhibitory Concentration' (MIC) of Pexiganan Acting on Escherichia coli?-A Cautionary Case Study.
2016
In vitro spectrum of pexiganan activity; bactericidal action and resistance selection tested against pathogens with elevated MIC values to topical agents.
2016 Sep
In Vitro Activities of Pexiganan and 10 Comparator Antimicrobials against 502 Anaerobic Isolates Recovered from Skin and Skin Structure Infections.
2017 Dec
In Vitro Activity of Pexiganan and 10 Comparator Antimicrobials against 234 Isolates, Including 93 Pasteurella Species and 50 Anaerobic Bacterial Isolates Recovered from Animal Bite Wounds.
2017 Jun
Efficacy of Pexiganan Combination with Tigecycline in a Mouse Model of Pseudomonas aeruginosa Sepsis.
2018
Cost-effective downstream processing of recombinantly produced pexiganan peptide and its antimicrobial activity.
2018 Jan 24

Sample Use Guides

1% cream (frequency of administration not stated)
Route of Administration: Topical
Name Type Language
PEXIGANAN ACETATE
MI   USAN  
USAN  
Official Name English
MSI-78
Code English
LOCILEX
Common Name English
GLYCYL-L-ISOLEUCYLGLYCYL-L-LYSYL-L-PHENYLALANYL-L-LEUCYL-L-LYSYL-L-LYSYL-L-ALANYL-L-LYSYL-L-LYSYL-L-PHENYLALANYLGLYCYL-L-LYSYL-L-ALANYL-L-PHENYLALANYL-L-VALYL-L-LYSYL-L-ISOLEUCYL-L-LEUCYL-L-LYSYL-L-LYSINAMIDE ACETATE
Common Name English
PEXIGANAN ACETATE [MI]
Common Name English
CYTOLEX
Brand Name English
PEXIGANAN ACETATE [USAN]
Common Name English
Code System Code Type Description
PUBCHEM
16137672
Created by admin on Sat Dec 16 00:43:55 GMT 2023 , Edited by admin on Sat Dec 16 00:43:55 GMT 2023
PRIMARY
NCI_THESAURUS
C166896
Created by admin on Sat Dec 16 00:43:55 GMT 2023 , Edited by admin on Sat Dec 16 00:43:55 GMT 2023
PRIMARY
CAS
172820-23-4
Created by admin on Sat Dec 16 00:43:55 GMT 2023 , Edited by admin on Sat Dec 16 00:43:55 GMT 2023
PRIMARY
ChEMBL
CHEMBL2108556
Created by admin on Sat Dec 16 00:43:55 GMT 2023 , Edited by admin on Sat Dec 16 00:43:55 GMT 2023
PRIMARY
MERCK INDEX
m8578
Created by admin on Sat Dec 16 00:43:55 GMT 2023 , Edited by admin on Sat Dec 16 00:43:55 GMT 2023
PRIMARY Merck Index
USAN
II-49
Created by admin on Sat Dec 16 00:43:55 GMT 2023 , Edited by admin on Sat Dec 16 00:43:55 GMT 2023
PRIMARY
FDA UNII
63S35FF5KS
Created by admin on Sat Dec 16 00:43:55 GMT 2023 , Edited by admin on Sat Dec 16 00:43:55 GMT 2023
PRIMARY