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Filtered Search Results
Medchemexpress LLC 38-azido-3,6,9,12,15,18,21,24,27,30,33,36-dodecaoxaoctatriacontan-1-amine | 2803478-25-1 | 98.0% | 614.73 | C26H54N4O12 | 100 MG
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Azido-PEG12-amine is an azide-terminated polyethylene glycol (PEG12) linker bearing a terminal primary amine used in bioconjugation and click-chemistry applications.
- Azide group enables click chemistry (azide-alkyne cycloaddition).
- Terminal primary amine reacts with carboxylic acids, activated NHS esters, and carbonyls.
- PEG12 spacer increases aqueous solubility and reduces steric hindrance.
- Molecular weight 614.73; formula C26H54N4O12.
- High purity (98.0% by NMR) with 1H NMR and MS consistent with structure.
- Storage: sealed, away from moisture and light; in solvent store at -80°C (6 months) or -20°C (1 month).
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Ambeed AMBEED
5000847127 M-PEG7-AMINE 250MG
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Medchemexpress LLC Amisulpride | 71675-85-9 | MFCD00866691 | 99.8% | C17H27N3O4S | 200 MG
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Amisulpride is a racemic (50:50) mixture of R-Amisulpride and S-Amisulpride. It acts as a dopamine D2/D3 receptor antagonist with Ki values of 2.8 nM for human dopamine D2 and 3.2 nM for human dopamine D3 receptors. Amisulpride also functions as a 5-HT7 receptor antagonist with a Ki of 44 nM, making it suitable for use in psychiatric research.
- Racemic mixture
- Dopamine D2/D3 receptor antagonist
- 5-HT7 receptor antagonist
- Suitable for psychiatric research
- D3 receptor Ki: 3.2 nM
- Human D2 receptor Ki: 2.8 nM
- 5-HT7 receptor Ki: 44 nM
- Inhibits quinpirole-elicited [3H]thymidine incorporation
- Increases dopamine release from rat striatum slices
- Increases dopamine synthesis in rat striatum and limbic system
- Increases extracellular dopamine levels
- Decreases striatal ACh levels
- Increases duration of swimming behavior
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Medchemexpress LLC Trilostane (Win 24540) | 13647-35-3 | 99.9% | C20H27NO3 | 200 MG
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Trilostane (Win 24540) is a competitive and orally active 3-β-hydroxysteroiddehydrogenase (3β-HSD) inhibitor. It is a synthetic nonhormonal steroid that can be used for the research of breast cancer and prostate cancer.
- Competitive and orally active 3-β-hydroxysteroiddehydrogenase (3β-HSD) inhibitor.
- Synthetic nonhormonal steroid.
- Used for the research of breast cancer and prostate cancer.
- Influences pregnenolone metabolism in adrenal cortex.
- Selectively inhibits pregnenolone converting to progesterone in the adrenal gland.
- Effectively controls pituitary-dependent hyperadrenocorticism (PDH) in dogs.
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eMolecules 101-38-2 | Gibbs reagent | TargetMol | MFCD00001611 | 210.440 | C6H2Cl3NO | 0.000 | ClN=C1C=C(Cl)C(=O)C(Cl)=C1 | 200mg | 761052535
Gibbs reagent | TargetMol | 101-38-2 | MFCD00001611 | 210.440 | C6H2Cl3NO | 0.000 | ClN=C1C=C(Cl)C(=O)C(Cl)=C1 | 200mg | 761052535
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Medchemexpress LLC Azido-PEG1-amine | 464190-91-8 | ≥98.0% | C4H10N4O | 100 MG
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Azido-PEG1-amine is a PEG-based PROTAC linker designed for the synthesis of PROTACs. It functions as a click chemistry reagent due to its Azide group, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups. PROTACs utilize two ligands connected by a linker to target an E3 ubiquitin ligase and a protein of interest, facilitating selective degradation via the intracellular ubiquitin-proteasome system.
- PEG-based PROTAC linker
- Functions as a click chemistry reagent
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC)
- Utilized in PROTAC synthesis
- Relevant for cancer targeted therapy
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Medchemexpress LLC Palmitoylethanolamide | 544-31-0 | MFCD00020562 | 99.86% | 299.49 | 200 MG
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Palmitoylethanolamide (Standard) is the analytical standard for Palmitoylethanolamide, an active endogenous compound. It is intended for research and analytical applications, and can be used for preventing virus infection of the respiratory tract.
- Analytical standard for Palmitoylethanolamide.
- Intended for research and analytical applications.
- Can be used for preventing virus infection of the respiratory tract.
- High purity of 99.86%.
- Available in multiple quantities for various research needs.
- Suitable for qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
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Medchemexpress LLC Benzyl-PEG4-amine 1g
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Benzyl-PEG4-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]
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Chemscene CHEMSCENE
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5000578908 BENZYL 3-AMINOPROPYL CARBA 10G
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Medchemexpress LLC TCO-SS-amine | >=95.0% | 304.47 | C13H24N2O2S2 | 5 MG
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TCO-SS-amine is a cleavable antibody-drug conjugate (ADC) linker containing a trans-cyclooctene (TCO) group that enables inverse electron demand Diels-Alder (iEDDA) click reactions with tetrazine-functionalized partners. It is used as a disulfide-cleavable linker in ADC synthesis and as a bioorthogonal click chemistry reagent.
- Cleavable disulfide linker for ADC synthesis.
- Contains a TCO group for iEDDA click chemistry with tetrazines.
- Molecular formula: C13H24N2O2S2.
- Molecular weight: 304.47 g/mol.
- Purity: ≥95.0%.
- Storage: -20°C, protect from light; in solvent: -80°C up to 6 months.
- Available in small research pack sizes such as 5 mg.
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Medchemexpress LLC Prostaglandin H2 | 42935-17-1 | MFCD00222079 | ≥95.0% | 352.47 | 50 UG
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Prostaglandin H2 (PGH2) is an endothelium-derived contracting factor that can cause vasoconstriction. It serves as a common precursor for all prostaglandins and is generated by cells expressing cyclooxygenases. PGH2 can activate PGD2 receptors, induce eosinophil migration, inhibit platelet aggregation, and accelerate the formation of amyloid β1-42 oligomers. It is utilized in research concerning inflammation and neurological conditions, such as Alzheimer's disease.
- Induces eosinophil migration.
- Inhibits platelet aggregation.
- Accelerates formation of amyloid β1-42 oligomers.
- Used in inflammation research.
- Used in neurological disease research.
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Medchemexpress LLC Amifostine (trihydrate) | 112901-68-5 | 100.0% | 200 MG
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Amifostine trihydrate is a broad-spectrum cytoprotective agent and radioprotector. It selectively protects normal tissues from damage caused by radiation and chemotherapy. It acts as a potent hypoxia-inducible factor-α1 (HIF-α1) and p53 inducer, protecting cells by scavenging oxygen-derived free radicals. It also reduces renal toxicity and exhibits antiangiogenic action.
- Broad-spectrum cytoprotective agent
- Radioprotector
- Selectively protects normal tissues from radiation and chemotherapy damage
- Potent HIF-α1 and p53 inducer
- Scavenges oxygen-derived free radicals
- Reduces renal toxicity
- Exhibits antiangiogenic action
- Protects against tert-Butyl hydroperoxide (TBHP)-induced cell damage
- Reduces H9c2 cell apoptosis
- Provides protection against myocardial ischemia/reperfusion injury
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Promega Corporation GLOMAX R GALAXY OPERATIONAL Q
PRSA1501 GLOMAX R GALAXY OPERATIONAL Q
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Medchemexpress LLC Amino-PEG8-amine | 82209-36-7 | ≥98.0% | 100 MG
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Amino-PEG8-amine is a PEG-based (8 units) PROTAC linker used in the synthesis of PROTACs. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PROTAC linker
- Used in the synthesis of PROTACs
- Contains two different ligands connected by a linker; one for an E3 ubiquitin ligase and the other for the target protein
- Exploits the intracellular ubiquitin-proteasome system to selectively degrade target proteins
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Medchemexpress LLC Kaempferol | 520-18-3 | MFCD00004543 | 99.9% | C15H10O6 | 200 MG
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Kaempferol is a naturally occurring flavonoid found in various edible plants. This compound functions as an estrogen receptor alpha inhibitor in breast cancer cells and promotes apoptosis in glioblastoma and lung cancer cells through MEK-MAPK activation. It is recognized as a human endogenous metabolite.
- Inhibits estrogen receptor alpha expression in breast cancer cells.
- Induces apoptosis in glioblastoma and lung cancer cells.
- Demonstrates anti-inflammatory activity.
- Exhibits antioxidant activity in human HepG2 cells.
- Shows antiproliferative activity against certain human cancer cell lines.
- Displays antiallergic activity.
- Demonstrates antiviral activity against influenza A virus.
- Inhibits melanogenesis.
- Inhibits procoagulant activity.
- Induces osteoclast apoptosis.
- Exhibits antiaggregatory activity in human platelets.
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