1. Anti-infection
  2. Bacterial
  3. Debio 1453

Debio 1453 is a bactericidal FabI inhibitor potent against N. gonorrhoeae (IC50 = 0.6 nM), including drug-resistant strains. Debio 1453 demonstrates a low propensity for resistance selection and is effective in eradicating both planktonic and intracellular bacteria through a mechanism of concurrently inhibiting FabI and engaging the non-mutable NADH cofactor. Debio 1453 clears antibiotic-resistant N. gonorrhoeae infection in a murine vaginal model. Debio 1453 can be used for gonorrhoea research.

For research use only. We do not sell to patients.

Debio 1453

Debio 1453 Chemical Structure

CAS No. : 2422053-29-8

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Description

Debio 1453 is a bactericidal FabI inhibitor potent against N. gonorrhoeae (IC50 = 0.6 nM), including drug-resistant strains. Debio 1453 demonstrates a low propensity for resistance selection and is effective in eradicating both planktonic and intracellular bacteria through a mechanism of concurrently inhibiting FabI and engaging the non-mutable NADH cofactor. Debio 1453 clears antibiotic-resistant N. gonorrhoeae infection in a murine vaginal model. Debio 1453 can be used for gonorrhoea research[1].

In Vitro

Debio 1453 shows activity against 2024 World Health Organisation N. gonorrhoeae reference strains that include strains resistant to Ceftriaxone (HY-B0712), Azithromycin (HY-17506), Spectinomycin (HY-B0438), Tetracycline (HY-A0107) and Ciprofloxacin (HY-B0356), with MIC range 0.03-0.125 μg/mL[1].
Debio 1453 exhibits potent in vitro activity (MIC50/MIC90 = 0.06 μg/mL) against 100 contemporary clinical N. gonorrhoeae isolates, with MICs ranging from 0.008 to 0.125 μg/mL[1].
Debio 1453 (0-16x MIC, 0-24 h) displays rapid bactericidal killing against both antibiotic-susceptible and extensively drug-resistant (XDR) N. gonorrhoeae in a time-dependent manner[1].
Debio 1453 (0-8x MIC, 0-24 h) is effective against both internalised antibiotic-susceptible (ATCC 49226) and XDR N. gonorrhoeae (WHO X), eradicating the bacteria to the limit of detection within 24 h for each isolate tested (≥3.1 log10 CFU/mL and ≥2.8 log10 CFU/mL reductions, respectively)[1].
Debio 1453 (4x-16x MIC) exhibits a low propensity for selecting mutants with reduced susceptibility in N. gonorrhoeae in vitro, thus validating FabI as its target[1].
Debio 1453 (0.3-30 μM, 24 h) exhibits no cytotoxicity or negative impact on cell viability in HepG2 cells, and no clastogenic or aneugenic activity in lymphocytes irrespective of the presence or absence of a rat liver metabolic activation system[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay[1]

Cell Line: human hepatocytes (HepG2)
Concentration: 0.3, 1, 3, 10, and 30 μM
Incubation Time: 24 h
Result: Showed no cytotoxicity or negative impact on cell viability at all concentrations tested, including the highest concentration of 30 μM.
In Vivo

Debio 1453 (10-160 mg/kg (dosed as Debio 1453 P), p.o., twice daily for 2 days) shows potent efficacy in murine models of both N. gonorrhoeae vaginal infection and S. aureus thigh infection[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Ovariectomized BALB/c female mice (5-6 weeks) infected intravaginally with N. gonorrhoeae strains[1]
Dosage: 10, 20, 30, 40, 80, and 160 mg/kg (dosed as Debio 1453 P)
Administration: p.o., twice daily for 2 days
Result: Demonstrated efficacy against all tested strains, producing clear dose-response relationships.
Achieved ~3 log10 CFU/mL reductions as compared to the start of treatment (0 h) and eradicated N. gonorrhoeae to the limit of detection by 48 h at multiple dose levels.
Animal Model: Neutropenic female ICR mice infected intravaginally with S. aureus[1]
Dosage: 10, 20, 30, 40, and 80 mg/kg (dosed as Debio 1453 P)
Administration: p.o., twice daily for 2 days
Result: Achieved >1 log10 CFU/mL reductions in thighs at 24 h and >2 log10 CFU reductions at 48 h, displaying efficacy comparable to a supratherapeutic dose of Linezolid (HY-10394).
Molecular Weight

420.46

Formula

C23H24N4O4

CAS No.
SMILES

CC1=C(OC2=C1C=CC=C2)CN(C(/C=C/C3=CN=C4NC([C@H]([C@H](NC4=C3)C)O)=O)=O)C

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Debio 1453
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