EB-47 dihydrochloride

SKU:BHB21900196
Research Validated
Overview
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EB-47 dihydrochloride (CAS 1190332-25-2) is an inhibitor supplied as a solid. Relevant to Cell Cycle/DNA Damage and Epigenetics research. Molecular formula C24H29Cl2N9O6, molecular weight 610.45 g/mol.
Purity 99.58%
CAS Number 1190332-25-2
Molecular Weight 610.45 g/mol
Form Solid
Storage 4°C as supplied; in solvent -80°C
Options selector
Catalog no. Size
HY-108631-5MG 5 mg
HY-108631-10MG 10 mg
HY-108631-25MG 25 mg
HY-108631-50MG 50 mg
HY-108631-100MG 100 mg
HY-108631-200MG 200 mg
HY-108631-500MG 500 mg
HY-108631-1MLX10MM 1 mL x 10 mM (in DMSO)
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, 200 mg, 500 mg, 1 mL x 10 mM (in DMSO)
  • Lead time: varies by selected option.
  • Storage: 4°C, sealed storage, away from moisture. In solvent: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture).
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: refrigerate at 4°C as soon as possible.
Field Specification
CAS no. 1190332-25-2
Applications
  • Functional Assay (In Vitro)
Molecular weight 610.45
Molecular formula C24H29Cl2N9O6
Purity 99.58%
SMILES O=C1NCC2=C(C=CC=C21)NC(CN3CCN(CC3)C([C@H]4O[C@H]([C@@H]([C@@H]4O)O)N5C6=C(N=C5)C(N)=NC=N6)=O)=O.[H]Cl.[H]Cl
Form Solid
Storage 4°C, sealed storage, away from moisture. In solvent: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture).
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-108631
Main SKU BHB21900196
Inhibitors

Compound Overview

EB-47 dihydrochloride is a potent, selective PARP-1/ARTD-1 inhibitor with an IC50 of 45 nM, and it shows more modest potency against ARTD5, with an IC50 of 410 nM. It mimics the substrate NAD+ and extends from the nicotinamide subsite to the adenosine subsite[1]. It is supplied as a white to off-white solid (C24H29Cl2N9O6, MW 610.45) at 99.58% purity.

Physical & Chemical Properties

CAS Number 1190332-25-2
Molecular Formula C24H29Cl2N9O6
Molecular Weight 610.45 g/mol
Purity 99.58%
Appearance Solid
Color White to off-white
SMILES O=C1NCC2=C(C=CC=C21)NC(CN3CCN(CC3)C([C@H]4O[C@H]([C@@H]([C@@H]4O)O)N5C6=C(N=C5)C(N)=NC=N6)=O)=O.[H]Cl.[H]Cl
Signaling Pathway Cell Cycle/DNA Damage; Epigenetics
Solubility In Vitro: DMSO: 62.5 mg/mL (102.38 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
H2O: 33.33 mg/mL (54.60 mM; Requires sonication)
Storage 4°C, sealed storage, away from moisture. In solvent: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture).
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]. Haikarainen T, et al. Evaluation and Structural Basis for the Inhibition of Tankyrases by PARP Inhibitors.ACS Med Chem Lett. 2013 Nov 20;5(1):18-22.

[2]. García-Saura AG, et al. Comparative inhibitory profile and distribution of bacterial PARPs, using Clostridioides difficile CD160 PARP as a model. Sci Rep. 2018 May 23;8(1):8056.

[3]. Jagtap PG, et al. The discovery and synthesis of novel adenosine substituted 2,3-dihydro-1H-isoindol-1-ones: potent inhibitors of poly(ADP-ribose) polymerase-1 (PARP-1).Bioorg Med Chem Lett. 2004 Jan 5;14(1):81-5.

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
DMSO62.5 mg/mL (102.38 mM)requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility)
H2O33.33 mg/mL (54.60 mM)requires sonication

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

If water is used as the stock solvent, dilute to the working solution and sterilize it through a 0.22 μm filter before use.

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
Result≥ 2.5 mg/mL (4.10 mM); clear solution
How to prepareGives a clear solution at ≥ 2.5 mg/mL (saturation not determined). 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% (20% SBE-β-CD in saline)
Result≥ 2.5 mg/mL (4.10 mM); clear solution
How to prepareGives a clear solution at ≥ 2.5 mg/mL (saturation not determined). 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 3

Composition10% DMSO + 90% Corn Oil
Result≥ 2.5 mg/mL (4.10 mM); clear solution
How to prepareGives a clear solution at ≥ 2.5 mg/mL (saturation not determined). 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.

Direct preparation of the working solution

These formulations are prepared directly, without a DMSO stock; use them promptly after preparation.

Protocol 4

CompositionPBS
Result2.94 mg/mL (4.82 mM); clear solution; requires sonication and warming and heat to 60°C

Data provided by the manufacturer.

In Vitro

EB-47 dihydrochloride inhibits CdPARP by more than 50%, with IC50 values of 0.86 μM for CdPARP and 1.0 μM for HsPARP[1].

In Vivo

At day 5, EB-47 dihydrochloride (2 μM; 5 days) reduces the number of embryo implantation sites and blastocysts. PARP1 takes part in embryo implantation[3].

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.

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

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SARM1 executes neuronal parthanatos and promotes excitotoxic cell death. Neuron 2026 Apr 16:S0896-6273(26)00218-7. PMID: 41997149

The CSB chromatin remodeler regulates PARP1- and PARP2-mediated single-strand break repair at actively transcribed DNA regions. Nucleic Acids Res 2023 Aug 11;51(14):7342-7356. PMID: 37326017

Role of KLF5 in enhancing ovarian cancer stemness and PARPi resistance: mechanisms and therapeutic targeting. J Transl Med 2025 Apr 30;23(1):492. PMID: 40307891

SARM1 is an essential component of neuronal Parthanatos. bioRxiv 2025 May 15:2025.05.14.654090. PMID: 40463025

University of New Mexico. 2024 Jul 01.

Research Square Preprint. 2022 Feb.

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