CDFI

SKU:BHB21902113
Overview
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CDFI (CAS 1199797-92-6) is an inhibitor supplied as a solid. Relevant to Anti-infection research. Molecular formula C28H28ClFN2, molecular weight 446.99 g/mol.
Purity 99.43%
CAS Number 1199797-92-6
Molecular Weight 446.99 g/mol
Form Solid
Storage Powder -20°C; in solvent -80°C
Options selector
Catalog no. Size
HY-156009-5MG 5 mg
HY-156009-10MG 10 mg
HY-156009-25MG 25 mg
HY-156009-50MG 50 mg
HY-156009-100MG 100 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
  • Lead time: varies by selected option.
  • Storage: Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: transfer to -20°C as soon as possible.
Field Specification
CAS no. 1199797-92-6
Applications
  • Functional Assay (In Vitro)
Molecular weight 446.99
Molecular formula C28H28ClFN2
Purity 99.43%
SMILES FC1=CC2=C(NC(C3=C(Cl)C=CC=C3)=C2C4CCN(CC4)CC5=C(C)C(C)=CC=C5)C=C1
Form Solid
Storage Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-156009
Main SKU BHB21902113
Inhibitors

Compound Overview

CDFI is an antibacterial agent that targets the bacterial cell wall by inhibiting the lipid II flippase MurJ within the peptidoglycan synthesis pathway, and it can be used to study Staphylococcus aureus infections[1][2]. It is supplied as a white to light yellow solid (C28H28ClFN2, MW 446.99) at 99.43% purity.

Physical & Chemical Properties

CAS Number 1199797-92-6
Molecular Formula C28H28ClFN2
Molecular Weight 446.99 g/mol
Purity 99.43%
Appearance Solid
Color White to light yellow
SMILES FC1=CC2=C(NC(C3=C(Cl)C=CC=C3)=C2C4CCN(CC4)CC5=C(C)C(C)=CC=C5)C=C1
Signaling Pathway Anti-infection
Solubility In Vitro: DMSO: 100 mg/mL (223.72 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Storage Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Fernandes PB, et al. Revisiting the Role of VraTSR in Staphylococcus aureus Response to Cell Wall-Targeting Antibiotics. Bacteriology. 2022 Jul 13;204:e00162-22.

[2]. Dhanda G, et al. Antibiotic Adjuvants: A Versatile Approach to Combat Antibiotic Resistance. ACS Omega. 2023 Mar 14;8(12):10757-10783.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

SolventSolubilityNotes
DMSO100 mg/mL (223.72 mM)requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility)

Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); avoid repeated freeze-thaw cycles.

In Vivo

Choose the formulation that suits the animal model and route of administration; percentages are volume ratios of the final working solution. Start from a clear DMSO stock (see In Vitro above), add the co-solvents one at a time in the order listed, mixing after each addition, and prepare the working solution fresh on the day of dosing. If precipitation or phase separation occurs, gentle warming or sonication can help.

Protocol 1

Composition10% DMSO + 40% PEG300 + 5% Tween-80 + 45% saline
Result2.5 mg/mL (5.59 mM); clear solution; requires sonication
How to prepareGives a clear solution at 2.5 mg/mL. For 1 mL of working solution: add 100 μL DMSO stock (25.0 mg/mL) to 400 μL PEG300; then 50 μL Tween-80; then 450 μL saline to bring the volume to 1 mL. Saline: dissolve 0.9 g sodium chloride in ddH2O and make up to 100 mL.

Protocol 2

Composition10% DMSO + 90% Corn Oil
Result2.5 mg/mL (5.59 mM); clear solution; requires sonication
How to prepareGives a clear solution at 2.5 mg/mL. Use with caution if continuous dosing will exceed two weeks. For 1 mL of working solution: add 100 μL DMSO stock (25.0 mg/mL) to 900 μL corn oil.

Data provided by the manufacturer.

In Vitro

CDFI (0.5-1.5 μg/mL; 60 min) induces the VraTSR system in the S. aureus COL strain and the COL Pvra-sGFP strain[1]. CDFI potentiates β-lactam antibiotics against MRSA through targeting the SAV1754 gene, which is involved in peptidoglycan synthesis[2].

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price on some sizes?
A.Availability and lead time for those sizes are confirmed on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
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  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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