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Acanthopanaxoside B is a triterpenoid saponin isolated from the leaves of Acanthopanax senticosus. This compound is typically used for research purposes.
Isolated from Acanthopanax senticosus
Triterpenoid saponin
Suitable for research applications
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CG347B is a selective small-molecule inhibitor of histone deacetylase 6 (HDAC6) intended for research use. It is applied in studies of oncology, immunology, and neurology and can be used as an intermediate in the synthesis of metalloenzyme inhibitors. The compound is supplied with characterization data to support experimental reproducibility.
Selective inhibition of HDAC6 enabling targeted biological studies.
Small-molecule structure suitable for cellular and biochemical assays.
High purity for reproducible experimental results.
Documented solubility in DMSO for assay preparation.
Applicable to oncology, immunology, and neurology research models.
Suitable as a synthetic intermediate for metalloenzyme inhibitor development.
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L-826266 is a selective and competitive EP3 receptor antagonist that can be used for convulsive disorders research. It also prevents PGE2-induced decrease of Na+,K+-ATPase activity in adult rat hippocampal slices and delays and increases the latency for clonic and generalized tonic-clonic seizures induced by PTZ in animal models.
Selective and competitive EP3 receptor antagonist
Can be used for convulsive disorders research
Prevents PGE2-induced decrease of Na+,K+-ATPase activity in adult rat hippocampal slices
Delays and increases the latency for clonic and generalized tonic-clonic seizures induced by PTZ in animal models
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L-826266 is a selective and competitive EP3 receptor antagonist that can be used for convulsive disorders research. It prevents the PGE2-induced decrease of Na+,K+-ATPase activity in adult rat hippocampal slices. In vivo, it delays seizures and increases the latency for clonic and generalized tonic-clonic seizures induced by PTZ.
Prevents PGE2-induced decrease of Na+,K+-ATPase activity
Delays seizures
Increases latency for clonic and generalized tonic-clonic seizures
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TMP780 is a small-molecule inverse agonist of the retinoic acid receptor-related orphan receptor γt (RORγt), reported with an in vitro IC50 of 13 nM and used as a research tool to modulate RORγt-dependent Th17 pathways and inflammatory responses.
Potent RORγt inverse agonist with reported IC50 = 13 nM.
Useful for cellular and preclinical studies of Th17/immunoregulatory pathways.
Solid research compound, typically dissolved in DMSO for assays.
Provided in small pack sizes suitable for screening and mechanistic work.
CAS 1422053-03-9 enables database cross-referencing for structure and identifiers.
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TMP780 is a small-molecule inverse agonist of the nuclear receptor RORγt used as a research compound for inflammation and immunology studies. It is reported to have potent biochemical activity and is supplied with high purity for preclinical laboratory use.
Inverse agonist of RORγt (IC50 13 nM).
High reported purity (99.51%).
Molecular formula C31H30N2O4; molecular weight 494.58 g/mol.
Typically supplied as a solid powder; soluble in DMSO.
Available in multiple pack sizes, including 100 mg.
Intended for research use only; not for human or veterinary use.
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TMP780 is a small-molecule inverse agonist of RORγt with a reported IC50 of approximately 13 nM. It is used in inflammation and immunology research to probe RORγt-mediated pathways and to support preclinical studies of cutaneous inflammatory disorders.
Inverse agonist of RORγt with reported IC50 ≈ 13 nM.
Suitable for in vitro and preclinical inflammation and immunology research.
High purity material (~99.5%) for biochemical and cellular assays.
Supplied as a 50 mg research pack for laboratory use.
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
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CG347B is a selective histone deacetylase 6 (HDAC6) inhibitor used as a research tool in oncology, immunology, and neurology studies and as an intermediate in the synthesis of metalloenzyme inhibitors. It is supplied as a white to off-white solid (C16H17N3O2, 283.33 g·mol⁻¹) with reported high purity and well-characterized solubility properties for in vitro and in vivo formulations.
Selective HDAC6 inhibition for epigenetics research
High reported purity (~98.1%) for reliable experimental results
Solid, white to off-white form for straightforward handling and storage
High DMSO solubility (250 mg/mL) suitable for in vitro assays
Soluble in in vivo vehicle at ≥6.25 mg/mL for formulation studies
Available in small research quantities for screening and pilot studies
Manufacturer-provided datasheet, SDS, and COA available for quality assurance
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