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Filtered Search Results
Medchemexpress LLC Imiquimod maleate | 896106-16-4 | 99.9% | 100 MG
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Imiquimod maleate is an immune response modifier and a selective toll-like receptor 7 (TLR7) agonist. It demonstrates antiviral and antitumor effects in vivo and is used in research for external genital and perianal warts, cancer, and COVID-19. It appears as a white to off-white solid.
- Molecular weight: 356.38
- Formula: C18H20N4O4
- Ships at room temperature in continental US
- Store at 4°C, sealed, away from moisture
- When in solvent, store at -80°C for 6 months or -20°C for 1 month
- Soluble in DMSO (25 mg/mL) and H2O (2 mg/mL)
- Targets TLR7 and HSV-1
- Used to induce psoriasis models
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Medchemexpress LLC Adavosertib 200mg | 10 MG
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Adavosertib 200mg | 10 MG
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Medchemexpress LLC Tamoxifen | 10540-29-1 | 99.96% | 371.51 | 200 MG
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Tamoxifen is an orally active, selective estrogen receptor modulator (SERM) that blocks estrogen action in breast cells and can activate estrogen activity in other cells, such as bone, liver, and uterine cells. It is a potent Hsp90 activator, enhancing the Hsp90 molecular chaperone ATPase activity. It activates autophagy and induces apoptosis. Tamoxifen can also be dissolved in corn oil for use in inducing gene knockout in CreER transgenic mice.
- Orally active, selective estrogen receptor modulator (SERM)
- Blocks estrogen action in breast cells
- Can activate estrogen activity in bone, liver, and uterine cells
- Potent Hsp90 activator
- Enhances Hsp90 molecular chaperone ATPase activity
- Inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 values of 0.1 μM and 1.8 μM
- Activates autophagy and induces apoptosis
- Can be dissolved in corn oil for gene knockout in CreER transgenic mice
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Ambeed 11bR 8 9 10 11 12 13 14 15Oct
(11bR)-8,9,10,11,12,13,14,15-Octahydro-N,Nbis[(1R)-1-phenylethyl]dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine, 1389329-66-1, 98%
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Apexbio Technology LLC [Ser25] Protein Kinase C (19-31) 136795-05-6 25mg
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[Ser25] Protein Kinase C (19-31) (CAS 136795-05-6) is an oligopeptide derived from the pseudosubstrate regulatory domain (amino acids 19-31) of Protein Kinase C alpha (PKC ) modified by substitution of alanine with serine at residue 25 Its sequence is Arg-Phe-Ala-Arg-Lys-Gly-Ser-Leu-Arg-Gln-Lys-Asn-Val with a molecular weight of 1559 82 and molecular formula C67H118N26O17 It acts as a PKC substrate peptide enabling in vitro measurement of kinase enzymatic activity via serine phosphorylation PKC enzymes participate in diverse cellular processes including adhesion transformation cell cycle control and calcium signaling making this peptide an important tool for kinase activity studies and intracellular signaling research
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eMolecules 7-Hydroxyquinoline-8-carboxylic acid | 1146298-53-4 | MFCD11869106 | 100mg
Ambeed | 7-Hydroxyquinoline-8-carboxylic acid | 100mg | 602850335 | A549352 | | 1146298-53-4 | MFCD11869106 | 189.170 | C10H7NO3
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Chem-Impex International, Inc. Levofloxacin | 100986-85-4 | MFCD00865049 | 1G
Levofloxacin, 100986-85-4, MFCD00865049, 1G
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eMolecules EMOLECULES INC
5000490666 4-CHLORO-3-NITROQUINOLINE 5G
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eMolecules EMOLECULES INC
5000490843 3-FLUORO-4-4 4 5 5-TETRAME 5G
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000569580 AFALANINE-200MG
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000569506 APRONAL-200MG
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Medchemexpress LLC Trifluoperazine dihydrochloride | 440-17-5 | 99.9% | 100 MG
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Trifluoperazine dihydrochloride is a potent antipsychotic agent that functions by blocking central dopamine receptors. This compound also acts as a strong α1-adrenergic receptor antagonist and a NUPR1 inhibitor, demonstrating anticancer activity. Additionally, it is a calmodulin inhibitor and can inhibit P-glycoprotein. Trifluoperazine dihydrochloride is suitable for research related to schizophrenia and has been shown to be a reversible inhibitor of influenza virus morphogenesis.
- Potent antipsychotic agent
- Blocks central dopamine receptors
- Strong α1-adrenergic receptor antagonist
- NUPR1 inhibitor with anticancer activity
- Calmodulin inhibitor
- Inhibits P-glycoprotein
- Suitable for schizophrenia research
- Reversible inhibitor of influenza virus morphogenesis
- IC50 of 16 μM for cytotoxicity in HL-60 cells by MTT assay
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Medchemexpress LLC Tetrabenazine | 200MG
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Tetrabenazine | 200MG
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Medchemexpress LLC 3,6,9,12,15,18-Hexaoxanonadecan-1-amine | 184357-46-8 | ≥97.0% | 5 G
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m-PEG6-Amine is a PEG-based PROTAC linker that can be utilized in the synthesis of PROTACs. It also functions as a cleavable ADC linker employed in the synthesis of antibody-drug conjugates (ADCs).
- PEG-based PROTAC linker
- Utilized in the synthesis of PROTACs
- Cleavable ADC linker
- Employed in the synthesis of antibody-drug conjugates (ADCs)
- PROTACs exploit the intracellular ubiquitin-proteasome system for selective protein degradation
- ADCs comprise an antibody attached to a cytotoxin via an ADC linker
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Ambeed Methyl 2 triphenylphosphoranyl
Methyl 2-(triphenylphosphoranylidene)acetate, 2605-67-6, 98%
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