Tetrahydrofuran
![Medchemexpress LLC N,N'-1,3-phenylenebis[2,3-dihydroxy-benzamide] | 368449-04-1 | 98.6% | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000232665.png-250.jpg)
Medchemexpress LLC N,N'-1,3-phenylenebis[2,3-dihydroxy-benzamide] | 368449-04-1 | 98.6% | 50 MG
MST-312 (Telomerase Inhibitor IX) is a small-molecule telomerase inhibitor derived from epigallocatechin gallate (EGCG). It is supplied as a white to off-white solid for laboratory research in oncology and telomerase studies.
- Telomerase inhibitor for cancer research.
- Chemically modified derivative of epigallocatechin gallate (EGCG).
- Molecular formula C20H16N2O6 and molecular weight 380.35 g·mol⁻1.
- Purity 98.6%.
- Supplied as a solid with common solubility in DMSO for solution preparation.
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 N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide | 2922283-38-1 | 98.0% | C93H177N3O3 | 100 MG
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.
Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran contains 2
The product is tetrahydrofuran (THf) and it contains 250ppm BHT (Butylated hydroxytoluene) as an inhibitor. THf is widely employed as a solvent. It constitutes the key fragment of various natural products (polyether antibiotics). THf forms double hydrate with hydrogen sulfide. Crystal structure of this double hydrate has been investigated by three-dimensional single-crystal studies. Butane-1 4-diol is formed as an intermediate during the synthesis of THf. Hot THf is useful for the disSOLUTIONon of polyvinylidene chloride (PVDV).
Medchemexpress LLC PF-00446687 free base | 862281-92-3 | 98.0% | 470.59 g/mol | C28H36F2N2O2 | 50 MG
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).
Medchemexpress LLC Tienilic acid (Ticrynafen) | 40180-04-9 | 99.7% | 331.18 | 5 MG
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.
Medchemexpress LLC Nelonicline (ABT-126) | 1026134-63-3 | 99.8% | 313.42 | 50 MG
Nelonicline (ABT-126) is an orally active and selective α7 nicotinic receptor agonist with high affinity to α7 nAChRs in human brain. It is used for the research of schizophrenia and Alzheimer's disease.
- Selective α7 nicotinic receptor agonist
- High affinity to α7 nAChRs
- Used for research of schizophrenia and Alzheimer's disease
- Binds to α3β4* nAChRs with lower efficacy
- 5-HT3 receptor antagonist with lower affinity
- Orally active
Medchemexpress LLC Sodium citrate dihydrate | 6132-04-3 | 98.0% | 500 MG
Sodium citrate dihydrate is a natural product with oral activity found in citrus fruits. It can inhibit the proliferation of tumor cells and induce apoptosis. It also exhibits antibacterial, anti-tumor, and antioxidant activities, and can be used as a cosolvent or buffer. This compound meets USP testing specifications and acts as an anticoagulant.
- Inhibits proliferation of tumor cells and induces apoptosis.
- Exhibits antibacterial, anti-tumor, and antioxidant activities.
- Can be used as a cosolvent or buffer.
- Acts as an anticoagulant by chelating calcium ions.
- Utilized for preparing buffers (e.g., DNA extraction, protein crystallization) and pH adjustment.
- Serves as a chelating agent to remove metal ion interference.
eMolecules 1192-30-9 | TETRAHYDROFURFURYL BROMIDE | AstaTech | MFCD00016894 | 165.030 | C5H9BrO | 95.000 | BrCC1CCCO1 | 100g | 449775922
TETRAHYDROFURFURYL BROMIDE | AstaTech | 1192-30-9 | MFCD00016894 | 165.030 | C5H9BrO | 95.000 | BrCC1CCCO1 | 100g | 449775922
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
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
eMolecules 805243-04-3 | Ambeed | 3-(Bis(benzyloxy)phosphoryl)propanoic acid | 1g | 525098833 | A181500 | MFCD08064320 | 334.308 | C17H19O5P
Ambeed | 3-(Bis(benzyloxy)phosphoryl)propanoic acid | 1g | 525098833 | A181500 | 805243-04-3 | MFCD08064320 | 334.308 | C17H19O5P
Medchemexpress LLC PhosTAC7 | 3016307-75-5 | 99.23% | C58H87ClN2O17 | 50 MG
PhosTAC7 is a heterobifunctional molecule, also known as a Phosphorylation Targeting Chimera (PhosTAC). It is designed to dephosphorylate specific proteins by recruiting serine/threonine protein phosphatase 2A (PP2A), making it a valuable tool for various research applications.
- Selectively modulates the phosphorylation state of individual target proteins.
- Dephosphorylates PDCD4, FOXO3a, and tau proteins.
- Useful in research for cancer.
- Applicable in the study of tau protein-related neurodegenerative diseases, such as Alzheimer's.
- For research use only.
Medchemexpress LLC CCT369260 | 2647503-57-7 | 99.7% | 100 MG
CCT369260 is a chemical probe and an orally active B-cell lymphoma 6 (BCL6) inhibitor. It demonstrates anti-tumor activity and exhibits an IC50 of 520 nM.
- Orally active B-cell lymphoma 6 (BCL6) inhibitor
- Exhibits anti-tumor activity
- IC50 of 520 nM against BCL6
- Significantly inhibits BCL6 in OCI-Ly1 DLBCL xenograft model (in vivo study)
Medchemexpress LLC SR8278 | 1254944-66-5 | 99.9% | C18H19NO3S2 | 50 MG
SR8278 is a REV-ERBα antagonist that inhibits the transcriptional repression activity of REV-ERBα with an EC50 of 0.47 μM. It is utilized to regulate metabolism in organisms, study biological rhythms, and research Duchenne muscular dystrophy and Alzheimer's disease.
- Inhibits REV-ERBα transcriptional repression activity (EC50 of 0.47 μM)
- Regulates metabolism and biological rhythm
- Supports research on Duchenne muscular dystrophy
- Supports research on Alzheimer's disease
- Exerts antidepressant and anxiolytic effects
- Restores circadian rhythm of mood-related behaviors
- Alters REV-ERBα and NURR1 binding activities
Medchemexpress LLC 9,19-Cyclolanostan-3-ol, 24-methylene-, 3-(4-hydroxy-3-methoxyphenyl)-2-propenoate, (3β)- | 469-36-3 | 5 MG
24-Methylenecycloartanyl ferulate is a γ-oryzanol compound. It promotes parvin-beta expression in human breast cancer cells and is a potential ATP-competitive Akt1 inhibitor.
- Purity of 98.53%
- White to off-white solid appearance
- Soluble in DMSO at ≥ 12.5 mg/mL
- Classified as a terpenoid and phenol
- Derived from plants