| Field | Specification |
|---|---|
| CAS no. | |
| Applications | |
| Molecular weight | |
| Molecular formula | C24H29Cl2N9O6 |
| Purity | |
| SMILES | |
| Form | Solid |
| Storage | |
| Shipping | |
| Catalog no. (Mfr.) | |
| Main SKU |
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.
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
| Solvent | Solubility | Notes |
|---|---|---|
| DMSO | 62.5 mg/mL (102.38 mM) | requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility) |
| H2O | 33.33 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
| Composition | 10% DMSO + 40% PEG300 + 5% Tween-80 + 45% saline |
|---|---|
| Result | ≥ 2.5 mg/mL (4.10 mM); clear solution |
| How to prepare | Gives 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
| Composition | 10% DMSO + 90% (20% SBE-β-CD in saline) |
|---|---|
| Result | ≥ 2.5 mg/mL (4.10 mM); clear solution |
| How to prepare | Gives 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
| Composition | 10% DMSO + 90% Corn Oil |
|---|---|
| Result | ≥ 2.5 mg/mL (4.10 mM); clear solution |
| How to prepare | Gives 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
| Composition | PBS |
|---|---|
| Result | 2.94 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.
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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.