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Filtered Search Results
Medchemexpress LLC Racemate of OSMI-1 | 2748153-92-4 | 96.5% | 25MG
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Racemate of OSMI-1 | 2748153-92-4 | 96.5% | 25MG
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eMolecules 3 5 6-TRICHLORO-1 2 4-TRIAZ 1G
5000188857 3 5 6-TRICHLORO-1 2 4-TRIAZ 1G
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Medchemexpress LLC Deltasonamide 2 hydrochloride | 2448341-55-5 | 99.8% | 10MG
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Deltasonamide 2 hydrochloride | 2448341-55-5 | 99.8% | 10MG
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Medchemexpress LLC HY-A0013A 500mg Medchemexpress, Bosentan (hydrate) CAS:157212-55-0 Purity:>98%
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Medchemexpress, HY-A0013A 500mg Bosentan (hydrate) CAS:157212-55-0 Bosentan hydrate is a competitive and dual antagonist of endothelin-1 (ET) for the ETA and ETB receptors with Ki of 4.7 nM and 95 nM in human SMC, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Cayman Chemical Ndesmethyl Sildenafil citrat
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A major metabolite of sildenafil; formed via oxidative metabolism of sildenafil by CYP3A4, CYP3A5, and CYP3A7
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Medchemexpress LLC SB 258719 | 195199-95-2 | 338.51 | 100 MG
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SB 258719 is a selective 5-HT7 receptor antagonist with a high affinity (pKi=7.5) for the receptor. It is used in the research of cancer and neurological diseases. For research use only; not sold to patients.
- Selective 5-HT7 receptor antagonist with high affinity (pKi=7.5)
- Used for research of cancer and neurological disease
- Produces a concentration-related rightward-shift of the 5-CT concentration-response curve
- Significantly attenuates 5-CT-induced hypothermia in mice
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eMolecules 402713-81-9 | Medchem Express | SB-399885 hydrochloride | 5mg | 446257985 | HY-103099 | MFCD09970355 | 482.8 | C18H22Cl3N3O4S
Medchem Express | BPU-11 | 5mg | 784543790 | HY-119102 | 909664-41-1 | 501.634 | C32H31N5O
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Medchemexpress LLC Sulfasalazine | 599-79-1 | 99.6% | 398.39 | 1 ML
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Sulfasalazine is an anti-rheumatic agent used for the research of rheumatoid arthritis and ulcerative colitis. It functions by suppressing NF-κB activity and is recognized as a type 1 ferroptosis inducer.
- Suppresses NF-κB activity
- Induces type 1 ferroptosis
- Inhibits TNFα-, LPS-, or phorbol ester-induced NFκB activation
- Prevents TNFα-induced nuclear translocation of NFκB
- Suppresses glioma growth in vivo
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MEDCHEMEXPRESS LLC LEVOSULPIRIDE 100MG
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501874327 LEVOSULPIRIDE 100MG
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eMolecules 447410-57-3 | Medchem Express | SB756050 | 10mg | 446257568 | HY-102016 | MFCD02585318 | 500.58 | C21H28N2O8S2
Ambeed | 4-Bromo-3-methylbenzene-12-diamine | 100mg | 490537084 | A219961 | 952511-74-9 | MFCD18642364 | 201.067 | C7H9BrN2
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Apexbio Technology LLC YAP-TEAD Inhibitor 1 (Peptide 17) 1mg
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YAP-TEAD Inhibitor 1 Peptide 17 is a cyclic peptide inhibitor targeting the protein-protein interaction between YAP (Yes-associated protein) and TEAD transcription factors It is designed to disrupt the YAP TEAD interaction thereby blocking downstream signaling pathways mediated by the YAP-TEAD complex YAP-TEAD Inhibitor 1 Peptide 17 exerts its biological activity primarily through direct inhibition of the YAP TEAD binding interface The peptide demonstrates inhibitory activity with an IC50 value of 25 nM Based on these pharmacological properties YAP-TEAD Inhibitor 1 Peptide 17 holds research potential in studying cellular mechanisms involving the Hippo pathway and for investigating therapeutic strategies related to YAP-dependent cancers and proliferative disorders
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Accela Chembio Inc 4-(difluoromethoxy)benzenesulfonamide | 1g | 874781-09-6 | MFCD03407973 | 95+% | Shelf Life: 1260 Days | Light Sensitive
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4-(difluoromethoxy)benzenesulfonamide | 1g | 874781-09-6 | MFCD03407973 | 95+% | Shelf Life: 1260 Days | Light Sensitive
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Medchemexpress LLC Pci-27483 | 871266-63-6 | 99.10% | 596.57 | 100 MG
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Pci-27483 | 871266-63-6 | 99.10% | 596.57 | 100 MG
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Accela Chembio Inc 4-fluoro-3-nitrobenzenesulfonamide | 25g | 406233-31-6 | MFCD08703185 | 97+% | Shelf Life: 1260 Days | Regular
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4-fluoro-3-nitrobenzenesulfonamide | 25g | 406233-31-6 | MFCD08703185 | 97+% | Shelf Life: 1260 Days | Regular
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Medchemexpress LLC Sultiame | 61-56-3 | 98.9% | 290.36 g/mol | C10H14N2O4S2 | 100 MG
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Sultiame is a carbonic anhydrase inhibitor widely used as an antiepileptic agent. This product is provided as research-grade analytical material intended for laboratory studies, assay calibration, and pharmacology investigations.
- Provides carbonic anhydrase inhibition for mechanism-of-action studies.
- Used as an antiepileptic agent in pharmacology and toxicology research.
- Analytical standard suitable for assay, calibration, and reference use.
- High purity, approximately 98.9%.
- Molecular weight 290.36 g/mol; formula C10H14N2O4S2.
- CAS number 61-56-3 for unambiguous identification.
- Available as solid and as a 10 mM DMSO solution for ready-to-use preparations.
- Multiple pack sizes available, including 100 MG solid.
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