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Details

Stereochemistry ABSOLUTE
Molecular Formula C90H127N27O12
Molecular Weight 1779.1451
Optical Activity UNSPECIFIED
Defined Stereocenters 13 / 13
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OMIGANAN

SMILES

CC[C@H](C)[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N3CCC[C@H]3C(=O)N[C@@H](CC4=CNC5=C4C=CC=C5)C(=O)N[C@@H](CC6=CNC7=C6C=CC=C7)C(=O)N8CCC[C@H]8C(=O)N[C@@H](CC9=CNC%10=C9C=CC=C%10)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(N)=O

InChI

InChIKey=MVPAMLBUDIFYGK-BHDRXCTLSA-N
InChI=1S/C90H127N27O12/c1-5-51(4)75(92)85(127)113-68(41-50(2)3)80(122)109-67(32-18-38-102-90(98)99)79(121)114-71(44-54-48-105-62-27-12-8-23-58(54)62)86(128)116-39-19-34-74(116)84(126)112-70(43-53-47-104-61-26-11-7-22-57(53)61)82(124)115-72(45-55-49-106-63-28-13-9-24-59(55)63)87(129)117-40-20-33-73(117)83(125)111-69(42-52-46-103-60-25-10-6-21-56(52)60)81(123)110-66(31-17-37-101-89(96)97)78(120)108-65(30-16-36-100-88(94)95)77(119)107-64(76(93)118)29-14-15-35-91/h6-13,21-28,46-51,64-75,103-106H,5,14-20,29-45,91-92H2,1-4H3,(H2,93,118)(H,107,119)(H,108,120)(H,109,122)(H,110,123)(H,111,125)(H,112,126)(H,113,127)(H,114,121)(H,115,124)(H4,94,95,100)(H4,96,97,101)(H4,98,99,102)/t51-,64-,65-,66-,67-,68-,69-,70-,71-,72-,73-,74-,75-/m0/s1

HIDE SMILES / InChI

Molecular Formula C90H127N27O12
Molecular Weight 1779.1451
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 13 / 13
E/Z Centers 2
Optical Activity UNSPECIFIED

Omiganan (previously known as MBI-226), is a synthetic, linear, 12 amino acid, cationic peptide analog of indolicidin, being developed as a topical gel for prevention of catheter-associated infections. In September 2000, a phase III trial of omiganan for the potential prevention of catheter-related bloodstream infections was initiated. In July 2018 was completed phase III clinical trial where was evaluated the long-term safety of once-daily application of omiganan topical gel in subjects with severe papulopustular rosacea. In addition, omiganan successfully completed phase II clinical trials where was determined its safety/tolerability in patients with mild to moderate atopic dermatitis and in human subjects with facial acne vulgaris. Besides, omiganan is ongoing phase II to explore the efficacy and pharmacodynamic effects of its topical gel in facial seborrheic dermatitis.

Approval Year

PubMed

PubMed

TitleDatePubMed
Omiganan pentahydrochloride (MBI 226), a topical 12-amino-acid cationic peptide: spectrum of antimicrobial activity and measurements of bactericidal activity.
2004 Aug
Omiganan interaction with bacterial membranes and cell wall models. Assigning a biological role to saturation.
2007 May
Antimicrobial activity of omiganan pentahydrochloride against contemporary fungal pathogens responsible for catheter-associated infections.
2008 Mar

Sample Use Guides

Omiganan gel applied once daily
Route of Administration: Transdermal
Omiganan, a bactericidal and fungicidal cationic peptide being developed as a topical gel for prevention of catheter-associated infections, inhibited commonly occurring fungal pathogens including Candida spp. (106 isolates) at
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:19:18 UTC 2023
Edited
by admin
on Sat Dec 16 01:19:18 UTC 2023
Record UNII
618SLL9VBS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OMIGANAN
INN   MI  
INN  
Official Name English
L-LYSINAMIDE, L-ISOLEUCYL-L-LEUCYL-L-ARGINYL-L-TRYPTOPHYL-L-PROLYL-L-TRYPTOPHYL-L-TRYPTOPHYL-L-PROLYL-L-TRYPTOPHYL-L-ARGINYL-L-ARGINYL-
Common Name English
OMIGANAN [MI]
Common Name English
omiganan [INN]
Common Name English
Code System Code Type Description
DRUG BANK
DB06610
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
PUBCHEM
16131445
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
INN
8347
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
EPA CompTox
DTXSID40174370
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
SMS_ID
300000036885
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
MERCK INDEX
m8210
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY Merck Index
FDA UNII
618SLL9VBS
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
ChEMBL
CHEMBL1615933
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
CAS
204248-78-2
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
NCI_THESAURUS
C166886
Created by admin on Sat Dec 16 01:19:19 UTC 2023 , Edited by admin on Sat Dec 16 01:19:19 UTC 2023
PRIMARY
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