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Filtered Search Results
TARGETMOL CHEMICALS INC 2S-Isoxanthohumol 20MG
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Also available in 1 mL and bulk. Please contact Fisher for quotes. 1. (2S)-Isoxanthohumol shows an antiviral activity towards herpes viruses (HSV1 and HSV2) and bovine viral diarrhea virus (BVDV). 2. Isoxanthohumol is a polyphenol with antioxidant, anti-inflammatory, and antiangiogenic properties, seems to regulate in vivo vascular proliferation and stabilization and the EC-VSMC-inflammatory crosstalk. Purity 98.82%
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Medchemexpress LLC Eltanexor Z-isomer | 1642300-78-4 | 96.0% | 428.29 g/mol | C17H10F6N6O | 100 MG
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Eltanexor Z-isomer is the geometric (Z) isomer of eltanexor, a small-molecule exportin-1 (XPO1/CRM1) inhibitor. Supplied for laboratory research use only, the compound is offered as a solid and as DMSO solutions across multiple pack sizes and is intended for in vitro studies and research applications.
- Less active geometric isomer of the parent compound.
- High purity suitable for research applications.
- Available as solid and as DMSO solution for convenience.
- Characterized by molecular formula and molecular weight for traceability.
- Intended for laboratory research use only; not for human or clinical use.
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Medchemexpress LLC E/Z-necrosulfonamide | 432531-71-0 | MFCD02370191 | 98.8% | 461.47 g/mol | C18H15N5O6S2 | 5 MG
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Racemic necrosulfonamide is a research-use small molecule that inhibits MLKL and Gasdermin D, blocking necroptosis and pyroptosis. It is supplied as a solid for biochemical and cell-based studies and should be handled according to the safety data sheet.
- Inhibits MLKL and Gasdermin D, blocking necroptosis and pyroptosis.
- High purity: 98.8%.
- Molecular weight 461.47 g/mol; formula C18H15N5O6S2.
- Appearance: light yellow to yellow solid.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months).
- Intended for research use only; not for human or animal consumption.
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eMolecules 15-AZIDO-4 7 10 13-TETRAOXA 1G
5000216008 15-AZIDO-4 7 10 13-TETRAOXA 1G
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Molecular Dimensions MOLECULAR DIMENSIONS INC
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NC3975907 WIZARD SCREEN 1 2 COMBO
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Medchemexpress LLC Rac-SCH 563705 | 473728-58-4 | 99.8% | 425.48 | C23H27N3O5 | 50 MG
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(Rac)-SCH 563705 is the racemic form of a potent, orally active antagonist of chemokine receptors CXCR2 and CXCR1, supplied as a high-purity research compound for in vitro and in vivo studies. It exhibits low-nanomolar receptor potency and is provided with analytical documentation and handling guidance.
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Medchemexpress LLC (E/Z)-necrosulfonamide | 432531-71-0 | MFCD02370191 | 98.8% | 461.47 | C18H15N5O6S2 | 10 MG
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(E/Z)-Necrosulfonamide is a racemic small-molecule inhibitor used to study programmed cell death pathways, including necroptosis and pyroptosis. The compound has formula C18H15N5O6S2, molecular weight 461.47, and CAS 432531-71-0.
- Racemic small-molecule inhibitor for cell death pathway studies.
- Active against MLKL and gasdermin D.
- Provided in a 10 mg research quantity.
- High purity (~98.8% by HPLC), suitable for biochemical assays.
- Molecular formula C18H15N5O6S2 and molecular weight 461.47.
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Medchemexpress LLC Milademetan tosylate hydrate | 2095625-97-9 | 98.9% | 808.74 g/mol | C37H44Cl2FN5O8S | 10 MG
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Milademetan tosylate hydrate is the tosylate salt form of milademetan, an orally active small-molecule inhibitor of the MDM2-p53 interaction used in preclinical oncology research. Supplied as a research-use reagent, it is characterized by CAS 2095625-97-9, a molecular weight of 808.74 g/mol, and supporting documentation for laboratory use.
- Salt form (tosylate hydrate) for improved handling and stability.
- Orally active MDM2 inhibitor that facilitates p53 pathway reactivation.
- High purity suitable for analytical and preclinical studies (98.9%).
- Available in small pack sizes suitable for lab-scale experiments.
- Includes datasheet, certificate of analysis, and safety information for lab use.
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Medchemexpress LLC (Rac)-CP-601927 hydrochloride | 230615-01-7 | 99.7% | 263.69 | 25 MG
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(Rac)-CP-601927 hydrochloride is the racemate of CP-601927, acting as a selective nAChR agonist. It demonstrates significant antidepressant-like effects in mice by targeting α4β2 and α3β4 nAChRs.
- Selective nAChR agonist
- Induces antidepressant-like effects in mice
- Decreases cholinergic signaling
- Targets α4β2 and α3β4 nAChRs
- For research use only
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000429374 2-ISOPROPOXY-5-METHY 100MG
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Medchemexpress LLC (Rac)-5-Hydroxymethyl Tolterodine | 200801-70-3 | 99.1% | C22H31NO2 | 500 MG
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(Rac)-5-Hydroxymethyl Tolterodine, also known as (Rac)-Desfesoterodine, is an active metabolite of Tolterodine. It acts as a mAChR antagonist, targeting M1-M5 receptors with specific Ki values ranging from 2.3 nM to 2.9 nM. This compound is primarily utilized in research related to overactive bladder. It presents as a solid, white to off-white substance.
- Functions as a mAChR antagonist
- Targets M1, M2, M3, M4, and M5 receptors
- Used for overactive bladder research
- Solid, white to off-white appearance
- Molecular weight of 341.50
- Inhibits carbachol-induced contraction in guinea-pig urinary bladder strips
- Exhibits significant muscarinic receptor binding activity
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eMolecules TERT-BUTYL 3R-3-AMINOPYR 10G
5000159810 TERT-BUTYL 3R-3-AMINOPYR 10G
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eMolecules METHYL 2-CYANO-3-NITROBENZ 25G
5000217320 METHYL 2-CYANO-3-NITROBENZ 25G
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TARGETMOL CHEMICALS INC Bisindolylmaleimide I 10MG
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Also available in 1 mL, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Bisindolylmaleimide I (GF109203X) is a potent and highly selective protein kinase C (PKC) inhibitor, exhibiting a Ki of 14 nM. Purity 99.08%
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Medchemexpress LLC (1R,3S)-RSL3 | 1219810-13-5 | 99.8% | 440.88 g/mol | C23H21ClN2O5 | 100 MG
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(1R,3S)-RSL3 is the less active enantiomer of the ferroptosis activator RSL3 and is supplied for research use. It is a small-molecule modulator that interacts with glutathione peroxidase 4 (GPX4). Analytical documentation including datasheet, certificate of analysis, and safety data sheet is available from the manufacturer. Molecular formula C23H21ClN2O5; molecular weight 440.88 g/mol; CAS 1219810-13-5.
- Less active enantiomer useful as a stereochemical control in experiments.
- Modulates ferroptosis via interaction with GPX4.
- High listed purity suitable for biochemical and cell-based assays.
- Available in multiple small-scale pack sizes for research workflows.
- Includes downloadable analytical documentation for data validation.
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