PXS-6302

SKU:BHB21901536
Overview
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PXS-6302 (CAS 2584947-54-4) is an inhibitor. Relevant to Neuronal Signaling research. Molecular formula C10H10F3NO2S, molecular weight 265.25 g/mol.
CAS Number 2584947-54-4
Molecular Weight 265.25 g/mol
Storage See Certificate of Analysis
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Catalog no. Size
HY-151499-50MG 50 mg
HY-151499-100MG 100 mg
HY-151499-250MG 250 mg
Available Options

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

  • Options: Size: 50 mg, 100 mg, 250 mg
  • Lead time: confirmed on inquiry for every option.
  • Storage: Please store the product under the recommended conditions in the Certificate of Analysis.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: store as stated on the Certificate of Analysis; contact us if you need the condition before ordering.
Field Specification
CAS no. 2584947-54-4
Applications
  • Functional Assay (In Vitro)
Molecular weight 265.25
Molecular formula C10H10F3NO2S
SMILES NC/C=C(C(F)(S(=O)(C1=CC=CC=C1)=O)F)\F
Storage Refer to Certificate of Analysis (CoA) for storage conditions
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-151499
Main SKU BHB21901536
Inhibitors

Compound Overview

PXS-6302 is an irreversible lysyl oxidase inhibitor, with IC50 values of 3.7 μM against bovine LOX, 3.4 μM against recombinant human LOXL1, 0.4 μM against recombinant human LOXL2, 1.5 μM against recombinant human LOXL3, and 0.3 μM against recombinant human LOXL4. It readily penetrates skin, reduces collagen deposition, and significantly improves scar appearance[1]. Its molecular formula is C10H10F3NO2S, with a molecular weight of 265.25 g/mol.

Physical & Chemical Properties

CAS Number 2584947-54-4
Molecular Formula C10H10F3NO2S
Molecular Weight 265.25 g/mol
SMILES NC/C=C(C(F)(S(=O)(C1=CC=CC=C1)=O)F)\F
Signaling Pathway Neuronal Signaling
Solubility In Vitro: DMSO: 100 mg/mL (377.00 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping Room temperature in continental US; may vary elsewhere.

Biological Activity

Activity & Target

3.7 μM (Bovine LOX), 3.4 μM (rh LOXL1), 0.4 μM (rh LOXL2), 1.5 μM (rh LOXL3), 0.3 μM (rh LOXL4)[1]

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]. Chaudhari N, et al. Topical application of an irreversible small molecule inhibitor of lysyl oxidases ameliorates skin scarring and fibrosis. Nat Commun. 2022 Sep 22;13(1):5555. 

Safety

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

In Vitro

SolventSolubilityNotes
DMSO100 mg/mL (377.00 mM)requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility)

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 + 90% (20% SBE-β-CD in saline)
Result2.5 mg/mL (9.43 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 900 μL 20% SBE-β-CD in saline. 20% SBE-β-CD in saline: dissolve 2 g SBE-β-CD powder in 10 mL saline until clear (4°C, store up to one week).

Protocol 2

Composition10% DMSO + 90% Corn Oil
Result2.5 mg/mL (9.43 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

PXS-6302 shows high permeability across a monolayer of cells, such as Caco-2 or MDCKII cells[1].

In Vivo

In porcine models of excisional and burn injury, PXS-6302 inhibits LOX, reduces crosslinking, and improves scar appearance[1]. Topical PXS-6302 (1.5% oil in water cream) applied externally once daily for 28 days, at 500 mg cream per 16 cm2, reduces collagen deposition and cross-linking in murine models of injury and fibrosis[1]. Topical PXS-6302 (0.5, 1.5, or 3% oil in water cream) applied externally at 400 mg cream per 16 cm2 once daily for 12 weeks also significantly improves scar appearance in porcine injury models, without reducing tissue strength[1].

Animal ModelPorcine excision injury model (female Juvenile pigs, 18-20 kg)[1]
Dosage0.5, 1.5, or 3%, oil in water cream; 400 mg cream applied to 16 cm2
AdministrationExternal application; 1, 2 and 3 weeks post-injury; once dayly, for 12 weeks
ResultShowed significantly higher scores for the 3% treated scars suggesting significant improvement in scar appearance.

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

Q.Why is there no price listed?
A.Every size of this product is quoted 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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