MedKoo Cat#: 530803 | Name: Lytixar HCl

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Lytixar, also known as LTX-109, is a Synthetic Antimicrobial Peptide, showing activity against Methicillin-Resistant, Vancomycin-Intermediate, Vancomycin-Resistant, Daptomycin-Nonsusceptible, and Linezolid-Nonsusceptible Staphylococcus aureus. LTX-109 demonstrated a MIC range of 2 to 4 μg/ml and dose-dependent rapid bactericidal activity against S. aureus. This activity was not influenced by resistance to other antistaphylococcal agents.

Chemical Structure

Lytixar HCl
Lytixar HCl
CAS#Lytixar HCl

Theoretical Analysis

MedKoo Cat#: 530803

Name: Lytixar HCl

CAS#: Lytixar HCl

Chemical Formula: C43H69N11O3

Exact Mass: 787.5585

Molecular Weight: 788.10

Elemental Analysis: C, 65.53; H, 8.83; N, 19.55; O, 6.09

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Synonym
Lytixar; LTX-109; LTX 109; LTX109; LTX-109 HCl; Lytixar HCl; Lytixar hydrochloride; Lytixar; Voxvoganan;
IUPAC/Chemical Name
L-Argininamide, L-arginyl-2,5,7-tris(1,1-dimethylethyl)-L-tryptophyl-N-(2-phenylethyl)- tetrahydrochloride
InChi Key
LLPGVFVCDNUOCS-VXEPYQPUSA-N
InChi Code
InChI=1S/C43H69N11O3.4ClH/c1-41(2,3)27-23-28-29(35(43(7,8)9)53-34(28)30(24-27)42(4,5)6)25-32(52-37(56)31(44)17-13-20-50-39(46)47)38(57)54(22-19-26-15-11-10-12-16-26)33(36(45)55)18-14-21-51-40(48)49;;;;/h10-12,15-16,23-24,31-33,53H,13-14,17-22,25,44H2,1-9H3,(H2,45,55)(H,52,56)(H4,46,47,50)(H4,48,49,51);4*1H/t31-,32-,33-;;;;/m0..../s1
SMILES Code
[H]Cl.[H]Cl.[H]Cl.[H]Cl.N=C(N)NCCC[C@@H](C(N)=O)N(C([C@H](CC1=C(C(C)(C)C)NC2=C1C=C(C(C)(C)C)C=C2C(C)(C)C)NC([C@@H](N)CCCNC(N)=N)=O)=O)CCC3=CC=CC=C3
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 788.10 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Saravolatz LD, Pawlak J, Martin H, Saravolatz S, Johnson L, Wold H, Husbyn M, Olsen WM. Postantibiotic effect and postantibiotic sub-MIC effect of LTX-109 and mupirocin on Staphylococcus aureus blood isolates. Lett Appl Microbiol. 2017 Nov;65(5):410-413. doi: 10.1111/lam.12792. Epub 2017 Sep 19. PubMed PMID: 28802058. 2: Scott RW, Tew GN. Mimics of Host Defense Proteins; Strategies for Translation to Therapeutic Applications. Curr Top Med Chem. 2017;17(5):576-589. Review. PubMed PMID: 27411325. 3: Nilsson AC, Janson H, Wold H, Fugelli A, Andersson K, Håkangård C, Olsson P, Olsen WM. LTX-109 is a novel agent for nasal decolonization of methicillin-resistant and -sensitive Staphylococcus aureus. Antimicrob Agents Chemother. 2015 Jan;59(1):145-51. doi: 10.1128/AAC.03513-14. Epub 2014 Oct 20. PubMed PMID: 25331699; PubMed Central PMCID: PMC4291342. 4: Bojsen R, Torbensen R, Larsen CE, Folkesson A, Regenberg B. The synthetic amphipathic peptidomimetic LTX109 is a potent fungicide that disturbs plasma membrane integrity in a sphingolipid dependent manner. PLoS One. 2013 Jul 12;8(7):e69483. doi: 10.1371/journal.pone.0069483. Print 2013. PubMed PMID: 23874964; PubMed Central PMCID: PMC3709891. 5: Saravolatz LD, Pawlak J, Johnson L, Bonilla H, Saravolatz LD 2nd, Fakih MG, Fugelli A, Olsen WM. In vitro activities of LTX-109, a synthetic antimicrobial peptide, against methicillin-resistant, vancomycin-intermediate, vancomycin-resistant, daptomycin-nonsusceptible, and linezolid-nonsusceptible Staphylococcus aureus. Antimicrob Agents Chemother. 2012 Aug;56(8):4478-82. doi: 10.1128/AAC.00194-12. Epub 2012 May 14. PubMed PMID: 22585222; PubMed Central PMCID: PMC3421571. 6: Isaksson J, Brandsdal BO, Engqvist M, Flaten GE, Svendsen JS, Stensen W. A synthetic antimicrobial peptidomimetic (LTX 109): stereochemical impact on membrane disruption. J Med Chem. 2011 Aug 25;54(16):5786-95. doi: 10.1021/jm200450h. Epub 2011 Jul 26. PubMed PMID: 21732630.