| Size | Price | Stock | Qty |
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| 500mg |
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| 1g |
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| Other Sizes |
| Targets |
α-Cyclobutylglycine does not have a defined primary drug target. Its role is as a synthetic intermediate and a glycine derivative. The compound is used to introduce a cyclobutyl-substituted glycine residue into peptides, which can then interact with various biological targets. Glycine derivatives are often used to modulate the activity of peptides and proteins. However, α-Cyclobutylglycine itself is not known to directly bind to or modulate any specific enzyme or receptor. Its utility lies in its ability to alter the properties of peptide-based drug candidates.
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| ln Vitro |
Commercial ergot supplements have been made from amino acids and their derivatives. They affect the release of anabolic hormones, the availability of fuel for activity, the ability to think clearly under pressure, and the prevention of muscular damage brought on by exertion. They are regarded as advantageous synergistic food ingredients [1].
In vitro activity data for α-Cyclobutylglycine is primarily related to its role as a chemical precursor. It does not exhibit intrinsic pharmacological activity in cell-free or cell-based assays. The compound is used in vitro to synthesize peptides that are then evaluated for biological activity. Amino acid derivatives like this one are commercially used as ergogenic supplements, where they may influence the release of anabolic hormones and fuel availability. However, the specific in vitro activity of α-Cyclobutylglycine has not been characterized beyond its utility in peptide synthesis. |
| ln Vivo |
There is no reported in vivo activity for α-Cyclobutylglycine as it is not a drug substance. The compound is used exclusively in research settings for the chemical synthesis of peptides and other molecules. Any in vivo effects would be attributed to the final peptide products synthesized using this building block, rather than the building block itself. As a non-proteinogenic amino acid, it is not administered to animals for pharmacological evaluation. Its role is confined to the laboratory.
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| Enzyme Assay |
In vitro enzyme/receptor binding assays are not applicable to α-Cyclobutylglycine as it is not a biologically active compound. However, a general protocol for assessing the binding affinity of peptides synthesized from this building block could involve radioligand binding assays. In such an assay, increasing concentrations of the test peptide are incubated with a membrane preparation containing the target receptor and a fixed concentration of a radiolabeled ligand. After incubation, the mixture is filtered to separate bound from free ligand, and the radioactivity is measured. This approach is standard for evaluating receptor-ligand interactions.
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| Cell Assay |
α-Cyclobutylglycine is not used in cell-based assays as a test compound. The compound serves as a reagent for peptide synthesis. A typical cell-based assay would involve the final peptide product. For example, a cell viability assay could be performed using cultured cancer cells to evaluate the anti-proliferative effects of a peptide synthesized from this building block. Cells are seeded in 96-well plates and treated with various concentrations of the peptide for 24-72 hours. Cell viability is then assessed using a standard assay such as MTT or CCK-8.
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| Animal Protocol |
In vivo animal experiments are not performed with α-Cyclobutylglycine itself. The compound is a research chemical used exclusively for peptide synthesis. If a peptide drug candidate synthesized from this building block were to be evaluated in vivo, a typical protocol might involve administering the peptide to mice via a suitable route. For example, in a disease model, mice would be treated with the peptide, and relevant biomarkers or disease progression would be monitored to assess efficacy.
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| ADME/Pharmacokinetics |
Pharmacokinetic properties of α-Cyclobutylglycine have not been characterized as it is not a drug candidate. The compound is intended for research use only. As a synthetic intermediate, its absorption, distribution, metabolism, and excretion (ADME) profile is not relevant to its intended use. The compound is typically stored as a powder at room temperature. Any pharmacokinetic studies would be performed on the final peptide products synthesized using this building block.
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| Toxicity/Toxicokinetics |
The toxicity profile of α-Cyclobutylglycine has not been extensively studied, as it is a research chemical and not a pharmaceutical drug. The compound is classified for research use only and is not intended for human or veterinary use. Standard laboratory safety precautions should be followed when handling this compound. General toxicity data for amino acid derivatives suggest low acute toxicity, but specific toxicological information for this compound is not available.
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| References | |
| Additional Infomation |
α-Cyclobutylglycine is a synthetic amino acid derivative used as a building block in peptide and nucleoside analogue synthesis. It is not a drug and has no approved therapeutic indications or clinical trial history. The compound is commercially available from various chemical suppliers for research purposes only. Its primary application is in the field of medicinal chemistry for the preparation of peptides with modified conformational properties. The cyclobutyl group introduces steric hindrance, which can influence the bioactivity of the resulting peptides.
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| Molecular Formula |
C6H11NO2
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|---|---|
| Molecular Weight |
129.16
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| Exact Mass |
129.078
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| CAS # |
28024-69-3
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| PubChem CID |
14352283
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| Appearance |
White to off-white solid powder
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| Density |
1.2±0.1 g/cm3
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| Boiling Point |
260.9±23.0 °C at 760 mmHg
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| Melting Point |
157-161℃
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| Flash Point |
111.6±22.6 °C
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| Vapour Pressure |
0.0±1.1 mmHg at 25°C
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| Index of Refraction |
1.537
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| LogP |
0.25
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| Hydrogen Bond Donor Count |
2
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| Hydrogen Bond Acceptor Count |
3
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| Rotatable Bond Count |
2
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| Heavy Atom Count |
9
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| Complexity |
120
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| Defined Atom Stereocenter Count |
0
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| SMILES |
O([H])C(C([H])(C1([H])C([H])([H])C([H])([H])C1([H])[H])N([H])[H])=O
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| InChi Key |
FZENWFNLDOYYFB-UHFFFAOYSA-N
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| InChi Code |
InChI=1S/C6H11NO2/c7-5(6(8)9)4-2-1-3-4/h4-5H,1-3,7H2,(H,8,9)
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| Chemical Name |
2-amino-2-cyclobutylacetic acid
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| HS Tariff Code |
2934.99.9001
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| 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)
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| 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
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|---|---|
| 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 | 7.7423 mL | 38.7117 mL | 77.4234 mL | |
| 5 mM | 1.5485 mL | 7.7423 mL | 15.4847 mL | |
| 10 mM | 0.7742 mL | 3.8712 mL | 7.7423 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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