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Filtered Search Results
![Medchemexpress LLC Trimethyl[2,3-(dioleyloxy)propyl]ammonium chloride | 104162-48-3 | MFCD00145456 | 98.0% | 670.57 g/mol | C42H84ClNO2 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000282662.png-250.jpg)
Medchemexpress LLC Trimethyl[2,3-(dioleyloxy)propyl]ammonium chloride | 104162-48-3 | MFCD00145456 | 98.0% | 670.57 g/mol | C42H84ClNO2 | 50 MG
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Trimethyl[2,3-(dioleyloxy)propyl]ammonium chloride is a quaternary ammonium, lipid-like reagent used in life-science research. It acts as an amphiphilic cationic lipid for formulation and membrane studies, and can be used as a surfactant or helper lipid in experimental delivery systems. The material is supplied with product documentation and handling information and is intended for research use only.
- Quaternary ammonium headgroup provides cationic charge.
- Two dioleoyl chains confer lipid-like amphiphilicity.
- Amphiphilic character supports bilayer and vesicle formulation.
- Soluble in common organic solvents for formulation workflows.
- Provided with documentation and safety data for lab use.
- Store sealed and away from moisture; refrigerate for prolonged stability.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000760001 2 -AMINO-5 -4-CARBO 250MG
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![Medchemexpress LLC Naphtho[1,2-d]thiazol-2-ylamine | 40172-65-4 | MFCD00051329 | 99.7% | 200.27 | C11H8N2S | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000264707.png-250.jpg)
Medchemexpress LLC Naphtho[1,2-d]thiazol-2-ylamine | 40172-65-4 | MFCD00051329 | 99.7% | 200.27 | C11H8N2S | 5 MG
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SKA-31 (Naphtho[1,2-d]thiazol-2-ylamine, CAS 40172-65-4) is a research-grade small-molecule activator of calcium-activated potassium channels (KCa2/KCa3.1), used to probe ion channel function and endothelial or neuronal hyperpolarization in vitro and in vivo studies.
- Potent channel activator with KCa3.1 EC50 ~260 nM and KCa2 subtype EC50s in the low micromolar range.
- High purity for research use (≈99.7%).
- Small molecular weight and defined composition: 200.27 g/mol; formula C11H8N2S.
- Soluble in DMSO (≈125 mg/mL) and formulatable for in vivo dosing.
- Supplied as a solid powder suitable for biochemical and cellular assays.
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Ambeed AMBEED
5000848650 TRIMETHYL 2-TETRAHYDROP 250MG
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![eMolecules 39061-97-7 | 4-Chloro-3-nitroquinoline | Ambeed | MFCD07369246 | 208.600 | C9H5ClN2O2 | 97.000 | [O-][N+](=O)c1cnc2ccccc2c1Cl | 25g | 491642013](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000471435.jpg-250.jpg)
eMolecules 39061-97-7 | 4-Chloro-3-nitroquinoline | Ambeed | MFCD07369246 | 208.600 | C9H5ClN2O2 | 97.000 | [O-][N+](=O)c1cnc2ccccc2c1Cl | 25g | 491642013
4-Chloro-3-nitroquinoline | Ambeed | 39061-97-7 | MFCD07369246 | 208.600 | C9H5ClN2O2 | 97.000 | [O-][N+](=O)c1cnc2ccccc2c1Cl | 25g | 491642013
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Selleck Chemical LLC Bemnifosbuvir Hemisulfate-25MG
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Bemnifosbuvir Hemisulfate (AT-527 RG-6422 RO 7496998) is a hemi-sulfate salt of AT-511 AT-511 is a potent inhibitor of SARS-CoV-2 with an EC90 of 0 47 M
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Apexbio Technology LLC Tetracycline(Synonyms: Achromycin, Sumycin, Tetracyn, Tetrex, Panmycin, Robitet, Polycycline, Cyclopar), 200mg, CAS: 60-54-8.
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Tetracycline (CAS 60-54-8) is a broad-spectrum polyketide antibiotic originally isolated from Streptomyces species It functions primarily through reversible binding to the bacterial 30S ribosomal subunit disrupting the interaction of aminoacyl-tRNA with the ribosomal acceptor site and thereby inhibiting bacterial protein synthesis Additionally tetracycline interacts partially with the 50S ribosomal subunit and may compromise bacterial membrane integrity causing leakage of intracellular components Tetracycline remains widely employed in microbiological research as an antibiotic selection marker and a tool for investigating ribosomal functions
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Accela Chembio Inc 2-ethoxy-1-ethoxycarbonyl-1 | 2-dihydroquinoline (eedq) | 100g | 16357-59-8 | MFCD00006703 | 97+% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive/+4
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2-ethoxy-1-ethoxycarbonyl-1 | 2-dihydroquinoline (eedq) | 100g | 16357-59-8 | MFCD00006703 | 97+% | Shelf Life: 1260 Days | Light Sensitive/moisture Sensitive/+4
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Medchemexpress LLC Ranolazine | 95635-55-5 | 99.8% | 200 MG
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Ranolazine (CVT 303) is an anti-angina drug that inhibits the late phase of inward sodium current (INa and IKr) and acts as an antianginal agent. It is also a partial fatty acid oxidation (FAO) inhibitor. This product is for research use only and not sold to patients.
- Inhibits late phase of inward sodium current (INa and IKr)
- Acts as an antianginal agent
- Partial fatty acid oxidation (FAO) inhibitor
- Does not affect heart rate or blood pressure
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Medchemexpress LLC Trifluoperazine dihydrochloride | 440-17-5 | 99.9% | 100 MG
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Trifluoperazine dihydrochloride is a potent antipsychotic agent that functions by blocking central dopamine receptors. This compound also acts as a strong α1-adrenergic receptor antagonist and a NUPR1 inhibitor, demonstrating anticancer activity. Additionally, it is a calmodulin inhibitor and can inhibit P-glycoprotein. Trifluoperazine dihydrochloride is suitable for research related to schizophrenia and has been shown to be a reversible inhibitor of influenza virus morphogenesis.
- Potent antipsychotic agent
- Blocks central dopamine receptors
- Strong α1-adrenergic receptor antagonist
- NUPR1 inhibitor with anticancer activity
- Calmodulin inhibitor
- Inhibits P-glycoprotein
- Suitable for schizophrenia research
- Reversible inhibitor of influenza virus morphogenesis
- IC50 of 16 μM for cytotoxicity in HL-60 cells by MTT assay
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000403372 ENDO CNTINH-03 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000771329 4-PIPERIDYL N-2-BIP 10G
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Apexbio Technology LLC RO4929097(Synonyms: RO-4929097, RO 4929097, Gamma-Secretase Inhibitor RO4929097, RO4929097 γ-secretase inhibitor), 200mg, CAS: 847925-91-1.
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RO4929097 (CAS 847925-91-1) is a potent selective small-molecule inhibitor of -secretase an essential protease in the Notch signaling pathway It inhibits -secretase with high specificity (IC50 4 nM EC50 5 nM) showing minimal inhibitory activity against closely related proteases and over 100-fold selectivity versus a broad spectrum of other proteases By preventing Notch receptor cleavage and subsequent signaling activation RO4929097 suppresses proliferation and tumorigenesis across various tumor models including melanoma breast colorectal pancreatic and lung cancers Clinical studies have assessed RO4929097 alone or combined with other anticancer agents for advanced solid tumors
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Apexbio Technology LLC Ganetespib (STA-9090)(Synonyms: STA-9090, Ganetespib, STA9090, STA 9090), 200mg, CAS: 888216-25-9.
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Ganetespib (STA-9090 CAS 888216-25-9) is a small-molecule inhibitor targeting heat shock protein 90 (Hsp90) It binds competitively to the ATP-binding pocket located at the N-terminal region of Hsp90 disrupting its chaperone activity and subsequently causing degradation of client proteins involved in tumor growth and survival Structurally distinct from geldanamycin-derived inhibitors Ganetespib features a triazolone moiety Preclinical studies have demonstrated antitumor activity across various cancer cell types including lung prostate colon breast cancers melanoma and leukemia highlighting its therapeutic potential for cancer research
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Medchemexpress LLC Cinchonine | 118-10-5 | MFCD00064372 | 99.7% | 294.39 | C19H22N2O | 25g
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Cinchonine is a natural compound present in Cinchona bark with antimalarial antitumor anti-inflammatory anti platelet-aggregation and anti-obesity properties Cinchonine inhibits cells proliferation and autophagy and induces apoptosis through activation of Caspase-3 Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells[1]
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