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Filtered Search Results
Medchemexpress LLC STING agonist-7 | 2767442-46-4 | 97.22% | C17H12N4O4 | 50 MG
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STING agonist-7 is a non-nucleotide STING agonist. It selectively binds to mouse STING but not human STING and penetrates cell membranes poorly. In vitro, STING agonist-7 (compound 11) is active in biochemical assays but inactive in cellular reporter assays.
- Non-nucleotide STING agonist
- Selectively binds to mouse STING
- Poor cell membrane penetration
- Active in biochemical assays
- Inactive in cellular reporter assays
- Solid appearance
- Color is light brown to brown
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![Medchemexpress LLC Acetamide, N-[2-(methylthio)phenyl]- | 6310-41-4 | 99.0% | 181.25 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000387808-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Acetamide, N-[2-(methylthio)phenyl]- | 6310-41-4 | 99.0% | 181.25 | 50 MG
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NSC-41589 is N-[2-(methylsulfanyl)phenyl]acetamide, intended for research use only. This product has not been fully validated for medical applications. It is a solid, white to off-white compound with high purity, offering reliable performance for various laboratory experiments.
- High purity of 99.0%
- Molecular weight of 181.25
- Solid appearance, white to off-white
- Soluble in DMSO up to 100 mg/mL
- Stable for extended periods when stored properly as powder or in solvent
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Sigma Aldrich Fine Chemicals Biosciences Clindamycin 2-phosphate aminoglycoside antibiotic | 24729-96-2 | MFCD07793328 | 50MG
Clindamycin 2-phosphate aminoglycoside antibiotic | Mol Wt: 504.96 | 24729-96-2 | MFCD07793328 | 50MG
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eMolecules 1775-86-6 | 2,3,4,4a,9,9a-Hexahydro-1H-carbazole | MFCD00227735 | 1g
ChemScene | 5-Chloro-2-fluorobenzamide | 5g | 686091316 | CS-0212071 | 261762-57-6 | MFCD01631435 | 173.570 | C7H5ClFNO
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Apexbio Technology LLC Irsogladine 57381-26-7 50mg
Irsogladine (CAS 57381-26-7) is a small molecule inhibitor of phosphodiesterase 4 (PDE4) and exhibits binding affinity for muscarinic acetylcholine receptors In preclinical studies irsogladine administration at 300 and 500 mg/kg/day produced a dose-dependent suppression of angiogenesis in wild-type mice reducing neovascularization by 21% and 45 3% respectively with statistical significance (P 0 02 P 0 001) These properties support its utility in investigating the modulation of cyclic AMP signaling cholinergic pathways and angiogenesis in biomedical research contexts
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![eMolecules 1883441-92-6 | Ambeed | 22-((2Z2Z)-((4499-Tetrahexyl-49-dihydro-s-indaceno[12-b56-b]dithiophene-27-diyl)bis(methanylylidene))bis(3-oxo-23-dihydro-1H-indene-21-diylidene))dimalononitrile | 100mg | 650569949 | A1156310 | 1011.4 | C66H66N4O2S2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502444197.PNG-250.jpg)
eMolecules 1883441-92-6 | Ambeed | 22-((2Z2Z)-((4499-Tetrahexyl-49-dihydro-s-indaceno[12-b56-b]dithiophene-27-diyl)bis(methanylylidene))bis(3-oxo-23-dihydro-1H-indene-21-diylidene))dimalononitrile | 100mg | 650569949 | A1156310 | 1011.4 | C66H66N4O2S2
ChemScene | 37-Dihydrobenzo[12-b45-b]difuran-26-dione | 100mg | 632316986 | CS-0089367 | 30272-74-3 | 190.154 | C10H6O4
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eMolecules 784210-87-3 | Medchem Express | RGB-286638 | 5mg | 415687542 | HY-15504 | MFCD28168009 | 618.56 | C29H37Cl2N7O4
Medchem Express | RGB-286638 | 5mg | 415687542 | HY-15504 | 784210-87-3 | MFCD28168009 | 618.560 | C29H37Cl2N7O4
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Cayman Chemical Tetrazolyl GlycIn 25mg
An NMDA receptor agonist (IC50 = 98 and 36 nM for [3H]CGS19755 and [3H]glutamate, respectively, in radioligand binding assays); It induces degeneration of GABAergic and cholinergic neurons in the striatum of adult rats and the formation of excitotoxic lesions and seizures in neonatal rats (ED50 = 0.071 mg/kg); increases COX-2 expression in striatal neurons and the vasculature near the striatal injection site in a mouse model of excitotoxicity-induced neuronal injury when administered via intrastriatal injection at 5 µM
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Cayman Chemical DIrIthromycIn 250mg
A macrolide antibiotic and prodrug of erythromycylamine that has outstanding activity against Campylobacter
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![Medchemexpress LLC 1-[3-[3-(4-chlorophenyl)propoxy]propyl]piperidine | 362665-56-3 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000230535.png-250.jpg)
Medchemexpress LLC 1-[3-[3-(4-chlorophenyl)propoxy]propyl]piperidine | 362665-56-3 | 100 MG
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Pitolisant is a selective histamine H3 receptor inverse agonist supplied as a research standard for receptor pharmacology and analytical applications. It is intended for use in binding assays, pharmacology studies, and analytical method development.
- Selective H3 receptor inverse agonist (Ki = 0.16 nM).
- Used as an analytical reference material and in pharmacology studies.
- Chemical formula C17H26ClNO; molecular weight 295.8 g·mol-1.
- CAS number 362665-56-3; MFCD18782650.
- Available as a 100 mg research standard; handle per laboratory safety procedures.
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Medchemexpress LLC Lithospermic acid | 28831-65-4 | 99.4% | 538.46 g·mol⁻¹ | C27H22O12 | 10 MG
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Lithospermic acid is a plant-derived polycyclic phenolic carboxylic acid isolated from Salvia miltiorrhiza, supplied as a research reagent for biochemical and pharmacological studies including antioxidant, hepatoprotective, and enzyme inhibition investigations.
- High purity (99.4%).
- Solid, off-white to light yellow appearance.
- Molecular formula C27H22O12; molecular weight 538.46 g·mol⁻¹.
- Used in antioxidant, hepatoprotective, and enzyme inhibition research.
- Recommended storage -20°C; protect from light; store under nitrogen.
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Medchemexpress LLC Carbetocin | 37025-55-1 | MFCD01076600 | 99.5% | 1048.21 | C47H73N11O14S | 10 MG
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Carbetocin acetate is an oxytocin receptor agonist peptide supplied as a research reagent for preclinical studies, including postpartum hemorrhage and central oxytocin receptor activity. It is reported to cross the blood-brain barrier.
- Research-grade oxytocin receptor agonist.
- High purity (99.5%).
- Molecular weight 1048.21 g/mol.
- Chemical formula C47H73N11O14S.
- White to off-white powder supplied as 10 mg.
- Store sealed, protected from moisture and light; powder: -80°C for long term, -20°C for short term.
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Medchemexpress LLC CRBN modulator-1 | 2407829-65-4 | 98.0% | 324.29 | 100 MG
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CRBN modulator-1 is a Thalidomide analog and a CRBN modulator, extracted from WO2020006262A1, compound 10. It has an IC50 of 3.5 μM and a Ki of 0.98 μM. This product is for research use only and not sold to patients.
- Thalidomide analog and CRBN modulator
- IC50 of 3.5 μM
- Ki of 0.98 μM
- For research use only
- Solid appearance
- Light green to green color
- Purity of 98.0%
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Medchemexpress LLC DUB-IN-3 | 924296-17-3 | 99.0% | C16H9N5O | 100 MG
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DUB-IN-3 (compound 22c) is a potent and selective inhibitor of the deubiquitinating enzyme USP8 with an IC50 value of 0.56 μM. This compound is a solid, light yellow to yellow in appearance, with a purity of 99.0%. It holds promise for research in various fields including cancer, neurodegenerative diseases, inflammation, viral infection, and cardiovascular disease.
- Potent and selective inhibitor of USP8
- Suitable for research into cancer
- Aids research in neurodegenerative diseases
- Useful for inflammation studies
- Applicable for viral infection research
- Supports cardiovascular disease research
- Purity of 99.0%
- Chemical formula: C16H9N5O
- Soluble in DMSO (25 mg/mL)
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Medchemexpress LLC Rosabulin | 501948-05-6 | 98.7% | 400.45 | 100 MG
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Rosabulin (STA 5312) is a potent and orally active microtubule inhibitor that inhibits microtubule assembly. It exhibits broad-spectrum anti-tumor activity.
- Potent and orally active microtubule inhibitor.
- Inhibits microtubule assembly.
- Demonstrates broad-spectrum anti-tumor activity.
- Exhibits substantial anti-proliferative activity against a wide range of cancer cell lines in vitro, including hematologic and solid tumor cell lines (leukemia, lymphoma, breast, colon, uterine) with IC50 values in the nanomolar range.
- Cell lines with multi-drug resistant (MDR) phenotypes are similarly sensitive.
- Has shown in vivo activity in several murine tumors and human tumor xenograft models, including drug-resistant tumors, when dosed orally or intravenously.
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