Tetrahydrofuran
![Medchemexpress LLC Spiro[1H,3H-naphtho[1,8-cd]pyran-1,9'-[9H]xanthen]-3-one, 3',6'-dihydroxy- | 41307-63-5 | 99.9% | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000231270.png-250.jpg)
Medchemexpress LLC Spiro[1H,3H-naphtho[1,8-cd]pyran-1,9'-[9H]xanthen]-3-one, 3',6'-dihydroxy- | 41307-63-5 | 99.9% | 25 MG
Resorcinolnaphthalein is a small-molecule research reagent (C24H14O5) used as an ACE2 enhancer in biochemical assays. It is supplied as a high-purity solid suitable for in vitro research.
- Functions as an ACE2 enhancer with reported EC50 of 19.5 μM.
- High purity as measured by LCMS (99.9%).
- Provided as a light yellow to orange solid; available in solid quantities and as a 10 mM solution in DMSO.
- Molecular weight 382.4 g/mol; formula C24H14O5.
- Intended for research use only and not for human use.
![Medchemexpress LLC Methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate | 173436-66-3 | ≥95.0% | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000234826.png-250.jpg)
Medchemexpress LLC Methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate | 173436-66-3 | ≥95.0% | 10MG
Methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate | 173436-66-3 | ≥95.0% | 10MG
![Medchemexpress LLC 2-((4-(Benzo[d]thiazol-5-ylamino)-6-(tert-butylsulfonyl)quinazolin-7-yl)oxy)ethyl Dihydrogen Phosphate | 99.5% | 612.63 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000439242-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC 2-((4-(Benzo[d]thiazol-5-ylamino)-6-(tert-butylsulfonyl)quinazolin-7-yl)oxy)ethyl Dihydrogen Phosphate | 99.5% | 612.63 | 50 MG
GSK2983559 is an orally active and potent receptor interacting protein 2 (RIP2) kinase inhibitor. It blocks many proinflammatory cytokine responses in vivo and in human inflammatory bowel disease explant samples.
- Blocks MDP-induced IL-8 in THP-1 cells.
- Inhibits MDP-induced IL-6 in mouse.
Medchemexpress LLC CUR61414 | 334998-36-6 | 99.04% | 550.69 | 100 MG
CUR61414 is a novel, potent, and cell-permeable Hedgehog signaling pathway inhibitor. It is a small-molecule aminoproline compound that selectively binds to smoothened (Smo). This compound can induce apoptosis in cancer cells without affecting neighboring non-tumor cells.
- Potent and cell-permeable Hedgehog signaling pathway inhibitor.
- Selectively binds to smoothened (Smo).
- Induces apoptosis in cancer cells.
- Spares neighboring non-tumor cells.
- Exhibits an IC50 of 100-200 nM.
Medchemexpress LLC Sar-Arg-Val-Tyr-Val-His-NH2 | 2410957-04-7 | 96.6% | 742.87 | 5 MG
Sar-Arg-Val-Tyr-Val-His-NH2 is a Gq-biased agonist. It exhibits 10-fold larger molecular efficacies at the AT1R-Gq fusion protein compared with the AT1R-βarr2 fusion protein.
- Gq-biased agonist
- High purity of 96.6%
- Molecular weight of 742.87
- Stable under recommended storage conditions
- Useful for research on Angiotensin Receptors and GPCR/G Protein pathways
Medchemexpress LLC Cur61414 | 334998-36-6 | 99.0% | 550.69 | 50 MG
CUR61414 is a novel, potent, and cell-permeable Hedgehog signaling pathway inhibitor with an IC50 of 100-200 nM. It is a small-molecule aminoproline class compound that selectively binds to smoothened (Smo) with a Ki value of 44 nM. CUR-61414 can induce apoptosis in cancer cells without affecting neighboring non-tumor cells.
- Novel, potent, and cell-permeable Hedgehog signaling pathway inhibitor.
- Selectively binds to smoothened (Smo).
- Induces apoptosis in cancer cells without affecting neighboring non-tumor cells.
- Able to arrest proliferation of basal cells within BCC-like lesions and induce apoptosis, leading to complete regression of lesions.
- Causes regression of BCC-like lesions in mice exposed to UV light irradiation, with no overt toxicity observed in surrounding skin.
Medchemexpress LLC Mpt0b392 | 1346169-92-3 | 99.6% | 404.44 g/mol | C19H20N2O6S | 10 MG
MPT0B392 is a research-grade microtubule-depolymerizing agent for preclinical studies of tubulin dynamics and cancer drug resistance. It is an orally active quinoline derivative that inhibits tubulin polymerization, activates c-Jun N-terminal kinase (JNK), induces mitotic arrest, and promotes apoptosis. Supplied as a solid or as a 10 mM solution in DMSO for in vitro and in vivo research use.
- Novel microtubule-depolymerizing mechanism supporting tubulin studies.
- Induces JNK activation and mitotic arrest for apoptosis research.
- Available as solid or 10 mM solution in DMSO for flexible dosing.
- High listed purity (99.63%) suitable for biochemical assays.
- Documented molecular weight and formula to aid experimental planning.
Medchemexpress LLC Benzobicyclon | 156963-66-5 | MFCD09751259 | 98.0% | 446.97 g/mol | C22H19ClO4S2 | 100 MG
Benzobicyclon is a research-grade herbicide compound used as a 4-HPPD inhibitor and supplied as an analytical standard for laboratory and analytical applications. It is documented with CAS and molecular identity and is typically provided in a quantified solid form for testing and reference purposes.
- Acts as a 4-HPPD (4-hydroxyphenylpyruvate dioxygenase) inhibitor.
- Intended for research and analytical applications.
- CAS number 156963-66-5 for unambiguous identification.
- Molecular formula C22H19ClO4S2 and molecular weight 446.97 g/mol.
- Supplied as a solid standard with typical purity of 98%.
Selleck Chemical LLC 2-Methyltetrahydrofuran-3-one
2-Methyltetrahydrofuran-3-one is a volatile constituent of the aroma complex of roasted coffee
eMolecules 96-47-9 | 2-Methyltetrahydrofuran | Oakwood Chemicals | MFCD00005367 | 86.134 | C5H10O | 99.000 | CC1CCCO1 | 500g | 480143994
2-Methyltetrahydrofuran | Oakwood Chemicals | 96-47-9 | MFCD00005367 | 86.134 | C5H10O | 99.000 | CC1CCCO1 | 500g | 480143994
eMolecules 121138-01-0 | 3-IODOTETRAHYDROFURAN | AstaTech | MFCD09878873 | 198.003 | C4H7IO | 95.000 | IC1CCOC1 | 5g | 449745312
3-IODOTETRAHYDROFURAN | AstaTech | 121138-01-0 | MFCD09878873 | 198.003 | C4H7IO | 95.000 | IC1CCOC1 | 5g | 449745312
Medchemexpress LLC Rsm-932a | 850807-63-5 | 98.4% | 877.53 g/mol | C46H38Br2Cl2N4 | 10 MG
RSM-932A is a small-molecule choline kinase α (ChoKα) inhibitor used in oncology research. It has demonstrated in vitro antiproliferative activity across multiple tumor-derived cell lines and shown antitumor effects in preclinical models. Supplied as a purified research compound for laboratory use only (not for human or veterinary use).
- Potent choline kinase α inhibitor with demonstrated antiproliferative activity.
- Effective in both in vitro and in vivo preclinical studies.
- High purity suitable for biochemical and cellular assays.
- Molecular weight 877.53 g/mol supports mass-based dosing and analysis.
- Available in small lab-scale quantities for experimental workflows.
- Intended for research use only; not for human or veterinary applications.