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Filtered Search Results
Medchemexpress LLC R -PYRROLIDINE-2-CA 10G | 10G
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R -PYRROLIDINE-2-CA 10G | 10G
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Medchemexpress LLC 3'-Azido-3'-deoxyuridine | 70580-88-0 | C9H11N5O5 | 1 MG
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3'-Azido-3'-deoxyuridine | 70580-88-0 | C9H11N5O5 | 1 MG
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eMolecules (2R,4R)-1-(tert-Butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid | 681128-51-8 | MFCD02684479 | 1g
Ambeed | (2R,4R)-1-(tert-Butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid | 1g | 600835697 | A263644 | | 681128-51-8 | MFCD02684479 | 233.239 | C10H16FNO4
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Medchemexpress LLC Azido-mono-amide-DOTA | 1227407-76-2 | 100.0% | 486.52 g·mol⁻¹ | C19H34N8O7 | 10 MG
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Azido-mono-amide-DOTA is an azide-functional DOTA derivative that acts as a bifunctional chelator for radiolabeling and bioconjugation. It combines a macrocyclic chelator for stable metal coordination with an azide handle for click chemistry, making it suitable for assembling radiopharmaceuticals and imaging probes in research settings.
- Azide functionality enables copper-free or copper-catalyzed click conjugation.
- Macrocyclic DOTA scaffold provides strong chelation of radiometals.
- High reported purity (99.96%) suitable for research applications.
- Compact molecular weight and defined chemical formula aid analytical characterization.
- Commonly supplied in small milligram quantities for synthesis and labeling workflows.
- CAS number 1227407-76-2 for unambiguous substance identification.
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Medchemexpress LLC (Rac)-NSC305787 hydrochloride | 53868-26-1 | MFCD29924224 | 98.2% | 481.89 | C25H31Cl3N2O | 10 MG
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(Rac)-NSC305787 hydrochloride is a small-molecule ezrin inhibitor supplied as a hydrochloride salt for research use. It binds ezrin with micromolar affinity and inhibits ezrin phosphorylation, showing antitumor activity in preclinical studies.
- Inhibits ezrin with Kd 5.85 μM.
- Inhibits ezrin phosphorylation (IC50 8.3 μM).
- High purity (98.18%).
- Molecular weight 481.89 g/mol.
- Solid, hygroscopic; soluble in DMSO (8 mg/mL), insoluble in water.
- Recommended storage: solid at 4°C; solutions -80°C (6 months), -20°C (1 month).
- Available in multiple pack sizes including 10 mg.
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![Medchemexpress LLC 1H-Pyrano[3,4-f]indolizine-3,6,10(4H)-trione, 4-ethyl-7,8-dihydro-4-hydroxy- | 102978-40-5 | 99.97% | 263.25 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000402469-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 1H-Pyrano[3,4-f]indolizine-3,6,10(4H)-trione, 4-ethyl-7,8-dihydro-4-hydroxy- | 102978-40-5 | 99.97% | 263.25 | 25 MG
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(rac)-Exatecan Intermediate 1 is an isomer of Exatecan Intermediate 1 and an intermediate of Exatecan, a camptothecin-based anticancer agent. It inhibits tumor growth by interfering with the proliferation and division of tumor cells by interacting with DNA. This product is primarily used in research into a variety of cancers including ovarian, lung, and breast cancer.
- Appearance: Solid
- Color: White to light yellow
- Shipping: Room temperature in continental US; may vary elsewhere.
- Storage for powder: -20°C for 3 years, 4°C for 2 years.
- Storage in solvent: -80°C for 6 months, -20°C for 1 month.
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Medchemexpress LLC tert-Butoxycarbonyl-D-valine | 22838-58-0 | ≥97.0% | 217.26 | 500 G
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tert-Butoxycarbonyl-D-valine is a valine derivative. Amino acids and amino acid derivatives have been commercially used as ergogenic supplements, influencing the secretion of anabolic hormones, supplying fuel during exercise, improving mental performance during stress-related tasks, and preventing exercise-induced muscle damage. They are recognized as beneficial ergogenic dietary substances.
- Influences the secretion of anabolic hormones.
- Supplies fuel during exercise.
- Improves mental performance during stress-related tasks.
- Prevents exercise-induced muscle damage.
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Medchemexpress LLC Azido-PEG24-acid | 2195075-62-6 | 99.9% | C51H101N3O26 | 10MG
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Azido-PEG24-acid is a polyethylene glycol (PEG)-based linker bearing a terminal azide, supplied as a solid for use in bioconjugation and linker synthesis. It facilitates efficient click chemistry conjugations and requires low-temperature, moisture-free storage to preserve stability.
- PEG-based linker with terminal azide for click reactions.
- Enables copper-catalyzed azide-alkyne cycloaddition and strain-promoted cycloaddition.
- High purity (≈99.9%) suitable for synthesis and conjugation.
- Molecular weight ≈1,172.35 g/mol for predictable spacer length.
- Solid, white to light yellow appearance for easy handling.
- Store sealed, away from moisture at low temperatures to maintain stability.
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Medchemexpress LLC Rac-BL-918 | 2435589-07-2 | 98.9% | 533.44 | C23H15F8N3OS | 100MG
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(Rac)-BL-918 is the racemic form of BL-918, a small-molecule activator of UNC-51-like kinase 1 (ULK1) that promotes cytoprotective autophagy. It is intended for preclinical and in vitro research applications where modulation of autophagy or ULK1 activity is required; handle and store according to laboratory safety practices.
- Racemic small-molecule activator of ULK1.
- Induces cytoprotective autophagy in cellular models.
- High purity: 98.9%.
- Molecular weight 533.44 g/mol; formula C23H15F8N3OS.
- Appearance: solid powder; typical package size 100 mg.
- Storage: powder -20°C for long-term; follow solvent storage recommendations when prepared in solution.
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Medchemexpress LLC Reparixin | 266359-83-5 | C14H21NO3S | 50 MG
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Reparixin is a non-competitive allosteric inhibitor that targets the chemokine receptors CXCR1 and CXCR2. It is a potent functional inhibitor of CXCL8-induced biological activities and has been shown to attenuate inflammatory responses in various injury models. This compound is for research use only.
- Non-competitive allosteric inhibitor of CXCR1 and CXCR2 activation
- Potent inhibitor of CXCL8-induced biological activities
- Attenuates inflammatory responses
- Demonstrated to decrease systolic blood pressure and increase blood flow in animal models
- Reduces IL-1β levels in the brain in animal models
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![eMolecules Pharmablock / (3R4R)-1-tert-butoxycarbonylpyrrolidine-34-dicarboxylic acid / 25mg / 629469759 / PBB2191 / 0.000 / 1807916-65-9 / [null] / 259.258 / C11H17NO6](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502456249.PNG-250.jpg)
eMolecules Pharmablock / (3R4R)-1-tert-butoxycarbonylpyrrolidine-34-dicarboxylic acid / 25mg / 629469759 / PBB2191 / 0.000 / 1807916-65-9 / [null] / 259.258 / C11H17NO6
Pharmablock / (3R4R)-1-tert-butoxycarbonylpyrrolidine-34-dicarboxylic acid / 25mg / 629469759 / PBB2191 / 0.000 / 1807916-65-9 / [null] / 259.258 / C11H17NO6
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Medchemexpress LLC (Rac)-TTA-P2 | 918430-49-6 | MFCD11977740 | 98.7% | 431.37 | C21H29Cl2FN2O2 | 10 MG
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Racemic TTA-P2 is a research-grade T-type calcium channel inhibitor used in preclinical studies to probe neuronal excitability, pain mechanisms, and epilepsy models. It is supplied as a solid with high purity and documented physicochemical properties for laboratory use.
- Potent inhibitor of T-type calcium channels for electrophysiology studies.
- High purity suitable for research applications.
- Available in small-scale quantities for preclinical experiments.
- Documented molecular weight and chemical formula for assay planning.
- Stable solid form convenient for storage and handling.
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Medchemexpress LLC (rac)-TBAJ-5307 | 2131783-85-0 | 100 MG
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(rac)-TBAJ-5307 | 2131783-85-0 | 100 MG
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Medchemexpress LLC (Rac)-P1D-34 | 2957895-04-2 | 99.45% | 835.45 | 5 MG
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(Rac)-P1D-34 is a PROTAC-based PIN1 degrader. It is composed of a PIN1 ligand, a cereblon ligand, and a linker. This product possesses anti-cancer activity, with IC50 values of 2248 nM in MV-4-11 cells, 3984 nM in MOLM-13 cells, and 3925 nM in HL-60 cells. This product is for research use only.
- PROTAC-based PIN1 degrader
- Composed of a PIN1 ligand, a cereblon ligand, and a linker
- Exhibits anti-cancer activity in various cell lines
- Suitable for research applications
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eMolecules BENZYL 3-((TERT-BUTOXYCARBONYL)AMINO)-5-HYDROXYPIPERIDINE-1-CARBOXYLATE | 1785642-46-7 | MFCD26727374 | 1g
AstaTech | BENZYL 3-((TERT-BUTOXYCARBONYL)AMINO)-5-HYDROXYPIPERIDINE-1-CARBOXYLATE | 1g | 290681372 | P14083 | 95.000 | 1785642-46-7 | MFCD26727374 | 350.415 | C18H26N2O5
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