Tetrahydrofuran
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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran contains 2200L
Tetrahydrofuran (THf) is a widely used organic solvent. On long term storage it forms organic peroxides. This process can be suppressed by adding butylated hydroxytoluene (BHT) as a stabilizer. BHT removes the free radicals required for the peroxide formation. The effect of THf on the biological systems has been studied.
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Medchemexpress LLC 1-[[4-[4-[[4-(4-chloro-N-methylanilino)quinolin-1-ium-1-yl]methyl]phenyl]phenyl]methyl]-N-(4-chlorop | 850807-63-5 | 98.4% | 877.53 | C46H38Br2Cl2N4 | 50 MG
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Selective choline kinase alpha (ChoKα) inhibitor for biochemical and cell-based cancer research. It demonstrates potent in vitro anti-proliferative activity and in vivo antitumor efficacy in xenograft models. Supplied as a solid for laboratory use in small-scale quantities.
- Selective ChoKα inhibition (IC50 ≈ 1 μM).
- Activity against multiple tumor-derived cell lines (IC50 ~1.3-7.1 μM).
- High purity (98.4%).
- Molecular weight 877.53; CAS 850807-63-5.
- Storage: 4 °C sealed; in solvent -80 °C (6 months), -20 °C (1 month).
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Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran | 109-99-9 | MFCD00005356 | 2l
Tetrahydrofuran | Purity: 99% | Mol Wt: 72.11 | 109-99-9 | MFCD00005356 | 2l
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Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran | 109-99-9 | MFCD00005356 | 100ml
Tetrahydrofuran | Purity: 99% | Mol Wt: 72.11 | 109-99-9 | MFCD00005356 | 100ml
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Medchemexpress LLC Broflanilide | 1207727-04-5 | 99.0% | 663.28 | 100 MG
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Broflanilide is an insecticide that converts into Desmethyl-Broflanilide, a powerful antagonist at the insect RDL GABA Receptor. This mechanism inhibits *S. litura* RDL GABAR with an IC50 of 1.3 nM. Desmethyl-Broflanilide shows limited activity against human GABAA α1β2γ2 receptor, mammalian GABAA α1β3γ2 receptor, and human glycine receptor (GlyR) α1β with IC50s greater than 3 μM, and less potent inhibition of GlyR α1-A288Gβ and GlyR α1-A288G (IC50s, 0.706, 0.149 μM).
- Acts as a potent antagonist at the insect resistant-to-dieldrin (RDL) GABA Receptor.
- Inhibits *S. litura* RDL GABAR.
- Exhibits weak activity against human and mammalian GABAA receptors.
- Less potently inhibits GlyR α1-A288Gβ and GlyR α1-A288G.
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Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran suitable for HPLC, >=99.9%, inhibitor-free | 109-99-9 | MFCD00005356 | 4X4L
Tetrahydrofuran suitable for HPLC, >=99.9%, inhibitor-free | Purity: >=99.9% | Mol Wt: 72.11 | 109-99-9 | MFCD00005356 | 4X4L
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Medchemexpress LLC L-Alanine, N-phosphono-, P→6-ester with 2-C-(4-aminopyrrolo[2,1-f]triazin-7-yl)... | 1911579-04-8 | 97.86% | 442.32 | 1 MG
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GS-704277 is an alanine metabolite of Remdesivir. It is further hydrolyzed to GA-441524, a compound with antiviral activity. Remdesivir, a nucleoside analogue, is effective against SARS-CoV-2 (COVID-19) infection.
- Alanine metabolite of Remdesivir
- Further metabolized to GA-441524, which exhibits antiviral activity
- Related to Remdesivir, a nucleoside analogue effective against SARS-CoV-2 (COVID-19) infection
- Functions as a drug metabolite
- Involves the metabolic enzyme/protease pathway
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Medchemexpress LLC N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide | 2922283-38-1 | 98.0% | C93H177N3O3 | 100 MG
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N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide is an analogue of TT3 (HY-148049). TT3 is an ionizable lipid-like material used for mRNA delivery.
- Analogue of TT3, an ionizable lipid-like material for mRNA delivery.
- Available in various quantities.
- For research use only.
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Medchemexpress LLC Ambroxide | 6790-58-5 | 236.39 | 100 MG
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Ambroxide is a naturally occurring terpenoid, known as a key constituent of ambergris. This compound is widely utilized in the manufacture of high-end perfumes to enhance aroma quality and extend fragrance lasting time.
- Naturally occurring terpenoid
- Key constituent of ambergris
- Utilized in high-end perfumes
- Enhances aroma quality
- Extends fragrance lasting time
- High purity (98.0%)
- Appears as a white to off-white solid
- Molecular formula: C16H28O
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Medchemexpress LLC PF-00446687 free base | 862281-92-3 | 98.0% | 470.59 g/mol | C28H36F2N2O2 | 50 MG
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PF-00446687 free base is a non-peptide, brain-penetrant small-molecule agonist of the melanocortin-4 receptor (MC4R) used in research on melanocortin signaling and central nervous system pharmacology. It is supplied as a powder for in vitro and in vivo studies and demonstrates low-nanomolar potency and selectivity.
- Selective melanocortin-4 receptor agonist with EC50 12 ± 1 nM.
- Binding affinity (Ki) approximately 27 ± 4 nM.
- Brain-penetrant, suitable for central nervous system studies.
- Provided as a powder with solubility in DMSO 62.5 mg/mL (ultrasonic recommended).
- Molecular formula C28H36F2N2O2 and molecular weight 470.59 g/mol.
- High purity by HPLC (≈98.0% per COA).
- Storage: powder -20°C (long-term) or 4°C (short-term).
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Medchemexpress LLC Deacylmetaplexigenin | 3513-04-0 | 1 MG
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Deacylmetaplexigenin is a natural product and steroid, specifically a pregnane glycoside. This compound has been isolated from plants such as Asclepias incarnata, Cynanchum viminale, and Cynanchum rostellatum.
- Molecular weight: 380.5 g/mol
- XLogP3-AA: -0.4
- Hydrogen bond donors: 5
- Hydrogen bond acceptors: 6
- Rotatable bond: 1
- Topological polar surface area: 118 Ų
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Medchemexpress LLC Ecliptasaponin D | 206756-04-9 | 5 MG
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Ecliptasaponin D is a triterpenoid glucoside isolated from Eclipta alba (L.) Hassk, which is the aerial part of Eclipta prostrate. Eclipta prostrate is considered a nourishing herbal medicine with pleiotropic effects, including anti-inflammatory, hepatoprotective, antioxidant, and immunomodulatory properties.
- Triterpenoid glucoside
- Isolated from Eclipta alba (L.) Hassk
- Anti-inflammatory properties
- Hepatoprotective properties
- Antioxidant properties
- Immunomodulatory properties
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Medchemexpress LLC Tienilic acid (Ticrynafen) | 40180-04-9 | 99.7% | 331.18 | 5 MG
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Tienilic acid (Ticrynafen; ANP 3624) acts as a diuretic hypotensive agent, but it induces hepatotoxicity. It is converted into electrophilic metabolites by cytochrome P450 (CYP) in vitro.
- Functions as a diuretic hypotensive agent.
- Known to induce hepatotoxicity.
- Converted into electrophilic metabolites by cytochrome P450 (CYP) in vitro.
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eMolecules 24808-04-6 | Medchem Express | (-)-Epiafzelechin | 5mg | 713705081 | HY-N0943 | MFCD20260428 | 274.272 | C15H14O5
Ambeed | 9-(4-Bromophenyl)-36-di-tert-butyl-9H-carbazole | 1g | 525197143 | A363941 | 601454-33-5 | MFCD11617971 | 434.421 | C26H28BrN
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Medchemexpress LLC (S)-Tetrahydrofuran-3-ol | 86087-23-2 | MFCD00064327 | 99.9% | C4H8O2 | 25 G
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(S)-Tetrahydrofuran-3-ol is the (S)-enantiomer of Tetrahydrofuran-3-ol. This chemical serves as a significant precursor for the creation of HIV protease inhibitors and can be manufactured through chemical synthesis or enzymatic hydrolysis.
- High purity of 99.94%
- Appears as a colorless to light yellow liquid
- Stable in pure form for 3 years at -20°C or 2 years at 4°C
- Stable in solvent for 6 months at -80°C or 1 month at -20°C
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