| Size | Price | |
|---|---|---|
| 500mg | ||
| 1g | ||
| Other Sizes |
LCL-PEG3-N3 hydrochloride is a research-grade E3 ligase ligand designed for use in targeted protein degradation and chemical biology applications. This compound functions as a decoy oligonucleotide E3 ligase ligand and is commonly utilized in the development of chimeric molecules such as LCL-ER(dec), which are engineered to induce the degradation of estrogen receptors.
Structurally, LCL-PEG3-N3 (HCl) features a PEG3 linker terminated with an azide (N₃) functional group. The polyethylene glycol spacer enhances molecular flexibility and solubility, enabling efficient spatial alignment during conjugation. The azide moiety allows for precise bioorthogonal reactions, making this compound a versatile building block in molecular assembly and protein degradation research.
LCL-PEG3-N3 hydrochloride is widely used in the design and synthesis of bifunctional and chimeric molecules, particularly in studies focused on estrogen receptor modulation and degradation. As an E3 ligase ligand, it supports investigations into ubiquitin–proteasome system targeting and regulated protein turnover.
The compound is highly compatible with click chemistry methodologies. It readily undergoes copper-catalyzed azide–alkyne cycloaddition (CuAAC) with alkyne-bearing molecules, enabling stable and selective conjugation. In addition, strain-promoted alkyne–azide cycloaddition (SPAAC) can occur with strained alkynes such as BCN or DBCO groups, offering copper-free reaction options suitable for sensitive biological systems.
With a purity of ≥98%, LCL-PEG3-N3 (HCl) is supplied with comprehensive documentation, including a certificate of analysis, product data, instructions for use, and a safety data sheet. It can be integrated into a variety of experimental workflows, including ligand conjugation, protein degradation studies, and advanced chemical biology research.
LCL-PEG3-N3 hydrochloride is intended for research use only and is not approved for diagnostic, therapeutic, or clinical applications. It provides researchers with a reliable and flexible tool for exploring estrogen receptor degradation, click chemistry strategies, and targeted protein modulation in preclinical research settings.
Contact InvivoChem to request a quote, review technical documentation, or discuss how LCL-PEG3-N3 hydrochloride can be integrated into your experimental workflows.
| Targets |
DNA-PK
|
|---|---|
| ln Vitro |
In order to confirm the nature of M2 and M3, authentic samples of both NU7199 and NU7200 (Figure 1) were compared to the spectra of the pseudomolecular ions at m/z 300 in plasma and urine. Two peaks were detected at m/z 300 in both plasma and urine and retention times and product ion spectra indicated that M2 corresponds to NU7199 and M3 to NU7200 (data not shown).[1]
|
| References |
[1]. Preclinical pharmacokinetics and metabolism of a novel prototype DNA-PK inhibitor NU7026. Br J Cancer. 2005 Oct 31;93(9):1011-8.
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| Additional Infomation |
This study investigated the in vitro radiosensitizing effect, pharmacokinetics, and time-dependent metabolism of NU7026, a novel DNA-dependent protein kinase (DNA-PK) inhibitor. At a dose of 10 μM (which is itself non-toxic to cells), NU7026 required at least 4 hours of exposure combined with 3 Gy radiation to produce a significant radiosensitizing effect in CH1 human ovarian cancer cells. In mice, intravenous injection of 5 mg/kg NU7026 resulted in rapid plasma clearance (0.108 L/h), primarily due to its extensive metabolism. Bioavailability after intraperitoneal (ip) and oral (po) administration of 20 mg/kg NU7026 was 20% and 15%, respectively. Analysis of the plasma and urinary metabolic profiles of NU7026 revealed that the compound undergoes various hydroxylation reactions. The glucuronide conjugate of the dihydroxylated metabolite was the major urinary excretion product. The fact that the main oxidation site is the C-2 position of the morpholine ring confirms that the plasma clearance rate of NU7107 (an analog of NU7026, in which both the C-2 and C-6 positions of the morpholine ring are methylated) is four times slower than that of NU7026. Pharmacokinetic simulations predict that to achieve the drug exposure required for radiosensitization, NU7026 would need to be administered intraperitoneally four times daily at a dose of 100 mg kg⁻¹. [1]
|
| Molecular Formula |
C17H17NO4
|
|---|---|
| Molecular Weight |
299.32118
|
| Exact Mass |
299.115
|
| Elemental Analysis |
C, 68.21; H, 5.72; N, 4.68; O, 21.38
|
| CAS # |
842122-14-9
|
| PubChem CID |
11415324
|
| Appearance |
Typically exists as solid at room temperature
|
| Density |
1.3±0.1 g/cm3
|
| Boiling Point |
515.4±50.0 °C at 760 mmHg
|
| Flash Point |
265.5±30.1 °C
|
| Vapour Pressure |
0.0±1.4 mmHg at 25°C
|
| Index of Refraction |
1.653
|
| LogP |
1.82
|
| Hydrogen Bond Donor Count |
2
|
| Hydrogen Bond Acceptor Count |
5
|
| Rotatable Bond Count |
6
|
| Heavy Atom Count |
22
|
| Complexity |
423
|
| Defined Atom Stereocenter Count |
0
|
| SMILES |
O=C1C=C(NCCOCCO)OC2=C1C=CC3=CC=CC=C32
|
| InChi Key |
UQJNMNYCRLPGSK-UHFFFAOYSA-N
|
| InChi Code |
InChI=1S/C17H17NO4/c19-8-10-21-9-7-18-16-11-15(20)14-6-5-12-3-1-2-4-13(12)17(14)22-16/h1-6,11,18-19H,7-10H2
|
| Chemical Name |
2-[2-(2-hydroxyethoxy)ethylamino]benzo[h]chromen-4-one
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| Synonyms |
NU7200; NU 7200; CHEMBL179968; 2-((2-(2-Hydroxyethoxy)ethyl)amino)-4H-benzo[h]chromen-4-one; 2-[2-(2-hydroxyethoxy)ethylamino]benzo[h]chromen-4-one; SCHEMBL13346530; BDBM50159618; 2-[2-(2-Hydroxy-ethoxy)-ethylamino]-benzo[h]chromen-4-one; NU-7200
|
| HS Tariff Code |
2934.99.9001
|
| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
|
| Solubility (In Vitro) |
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
|
|---|---|
| Solubility (In Vivo) |
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.
Injection Formulations
Injection Formulation 1: DMSO : Tween 80： Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution → 50 μL Tween 80 → 850 μL Saline)(e.g. IP/IV/IM/SC) *Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution. Injection Formulation 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO → 400 μLPEG300 → 50 μL Tween 80 → 450 μL Saline) Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO → 900 μL Corn oil) Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals). View More
Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO → 900 μL (20% SBE-β-CD in saline)] Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium) Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals). View More
Oral Formulation 3: Dissolved in PEG400 (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 3.3409 mL | 16.7045 mL | 33.4091 mL | |
| 5 mM | 0.6682 mL | 3.3409 mL | 6.6818 mL | |
| 10 mM | 0.3341 mL | 1.6705 mL | 3.3409 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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