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Filtered Search Results
Selleck Chemical LLC XCT790 S0407-5MG
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XCT-790 (Compound 12) is a potent and selective inverse agonist for estrogen-related receptor (ERR ) with IC50 of 0 37 M XCT-790 (Compound 12) is inactive against ERR and the estrogen receptors ER and ER XCT-790 (Compound 12) significantly inhibits in vivo tumor growth and angiogenesis and induces apoptosis
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Cayman Chemical ANTIBODY n-CHMIMO 1mg
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An analytical reference standard categorized as a synthetic cannabinoid; has been detected in human hair samples tested for verification of drug abstinence; intended for research and forensic applications
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Cayman Chemical ANTIBODY Harmol 5mg
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An analytical reference standard categorized as a β-carboline alkaloid; has been found in Psilocybe mushrooms; intended for research and forensic applications
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Medchemexpress LLC HY-12042 10mg , Pimasertib CAS:1236699-92-5 Purity:>98%
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HY-12042 10mg Pimasertib CAS: 1236699-92-5 Pimasertib (AS703026) is a highly selective, ATP non-competitive allosteric orally available MEK1/2 inhibitor. 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 Takeda-103A 5mg
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A GRK2 inhibitor; selectively inhibits phosphorylation of bovine rod outer segments by GRK2 (IC50 = 54 nM) over phosphorylation by GRK1 and GRK5 at concentrations up to 125 µM; inhibits phosphorylation of bovine rod outer segments by GRK2 containing various mutations, including GRK2L271M, GRK2Y206S, GRK2I197L, and GRK2L235G (IC50s = 24, 55, 106, and 180 nM, respectively)
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Medchemexpress LLC 3Bp-4089 Tfa 5Mg | HY-P3441A-5MG
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3Bp-4089 Tfa 5Mg
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Selleck Chemical LLC Uva Ursi Leaf Extract E3782-5MG
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Arctostaphylos Uva Ursi Leaf Extract is drawed from the Arctostaphylos uva-ursi leaf which could represent a natural product to counter the virulence of Cutibacterium acnes representing a new alternative therapeutic option for the treatment of acne vulgaris
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Selleck Chemical LLC Xanthotoxol S9174-1MG
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Xanthotoxol (8-Hydroxypsoralen 8-Hydroxypsoralene 8-Hydroxyfuranocoumarin Psoralen) a biologically active linear furocoumarin found in a large number of plants shows strong pharmacological activities as anti-inflammatory antioxidant 5-HT antagonistic and neuroprotective effects
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AdipoGen 1 3-bisAminooxypropan 2HCl
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Chemical. CAS 104845-82-1. Formula C3H10N2O2 . 2HCl. MW 179.05. Synthetic. Useful reactant for synthesis in the preparation of Oxa-azamacrocycles, adamantylalkoxyurea derivatives, Dinitrobenzamide-TEMPO derivatives, self-healing hydrogels containing reversible oxime crosslinks or fluorescent probes for DNA abasic site detection.
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Selleck Chemical LLC BAY-593 E1976-100MG
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BAY-593 is an in vivo probe and small molecule inhibitor of geranylgeranyltransferase-I (GGTase-I) blocking oncogenic YAP1/TAZ It exhibits potent anti-tumor activity and inhibits cancer cell proliferation in vitro
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Selleck Chemical LLC APX2009 E1987-100MG
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APX2009 is a second-generation redox-specific inhibitor of APE1/Ref-1 an essential enzyme in the base excision repair (BER) pathway APX2009 effectively reduces breast cancer cell proliferation and colony formation
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Medchemexpress LLC Erythrinin C | 63807-85-2 | 1 MG
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Erythrinin C is an isoflavone that can be isolated from *Erythrina suberosa* var. This compound presents as a white to off-white solid.
- Purity of 98%
- Molecular weight of 354.35
- Molecular formula C20H18O6
- CAS number 63807-85-2
- Isolated from plants, specifically Leguminosae, *Erythrina suberosa* Roxb.
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Selleck Chemical LLC Tamarixetin E2502-1MG
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Tamarixetin (4 -O-Methyl Quercetin) is a natural flavonoid derivative of quercetin and has superior anti-inflammatory properties in bacterial sepsis by increasing the population of IL-10-secreting immune cells
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Cayman Chemical ANTIBODY SenxIn A 25mg
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A Cdk8 inhibitor (IC50 = 0.28 µM); inhibits p21WAF1-induced reporter expression in reporter assay using HT-1080 p21-9 cells (IC50 = 0.68 µM); prevents 17β-estradiol-induced increases in expression of mRNA encoding GREB1, CXCL12, and TFF1 in estrogen-deprived MCF-7, BT474, and T47D cancer cells; decreases intracellular and extracellular viral RNA, the number of infectious particles, as well as dengue virus-induced increases in the levels of mRNA encoding LC3-II in dengue virus-infected Huh7 cells at 25 µM; reduces mitochondrial OCR and increases glycolysis in uninfected and dengue virus-infected Huh7 cells at 12.5 µM
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Medchemexpress LLC Sp4206 | 515846-21-6 | 97.0% | 1 MG
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SP4206 is a small-molecule inhibitor of the interleukin-2 (IL-2) / IL-2Rα interaction; it binds IL-2 with high affinity (Kd = 70 nM) and blocks IL-2 binding to IL-2Rα (Kd = 10 nM). It is supplied as a solid for in vitro research applications.
- Binds IL-2 with high affinity (Kd = 70 nM).
- Blocks IL-2 binding to IL-2Rα (Kd = 10 nM).
- Molecular formula C30H37Cl2N7O6 and molecular weight 662.56 g·mol⁻¹.
- Supplied as 1 mg solid suitable for research use.
- Reported purity approximately 97.0% (HPLC).
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