RORγt Inverse agonist 6
CAS No. 1887161-80-9
RORγt Inverse agonist 6( —— )
Catalog No. M26419 CAS No. 1887161-80-9
RORγt Inverse agonist 6 is an agonist of RORγt inverse. RORγt Inverse agonist 6 can be used in research on Th17-driven autoimmune diseases.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 168 | In Stock |
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| 5MG | 136 | In Stock |
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| 10MG | 201 | In Stock |
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| 25MG | 323 | In Stock |
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| 50MG | 429 | In Stock |
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| 100MG | 551 | In Stock |
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| 200MG | 728 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameRORγt Inverse agonist 6
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NoteResearch use only, not for human use.
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Brief DescriptionRORγt Inverse agonist 6 is an agonist of RORγt inverse. RORγt Inverse agonist 6 can be used in research on Th17-driven autoimmune diseases.
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DescriptionRORγt Inverse agonist 6 is an agonist of RORγt inverse. RORγt Inverse agonist 6 can be used in research on Th17-driven autoimmune diseases.(In Vivo):RORγt Inverse agonist 6 (30 mg/kg; p.o.) inhibits the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose. RORγt Inverse agonist 6 suppresses IL-17A gene expression by IL-23 stimulation in a mouse pharmacodynamics model. RORγt Inverse agonist 6 (1 mg/kg; p.o.) exhibits improved drug exposure with AUC of 1289 ng h/mL.
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In Vitro——
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In VivoRORγt Inverse agonist 6 (compound 43) suppresses IL-17A gene expression by IL-23 stimulation in a mouse pharmacodynamics model.RORγt Inverse agonist 6 (compound 43) exhibits improved drug exposure (mouse AUC: 1289 ng?h/mL at 1 mg/kg, po).RORγt Inverse agonist 6 (compound 43, 30 mg/kg, po, b.i.d) inhibits the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose. Animal Model:Mice.Dosage:30 mg/kg.Administration:Orally twice: at 30 min before and 8 h after IL-23 administration.Result:Inhibited the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose.
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Synonyms——
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PathwayNuclear Receptor/Transcription Factor
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TargetROR
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RecptorADC Linker
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Research Area——
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Indication——
Chemical Information
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CAS Number1887161-80-9
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Formula Weight565.03
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Molecular FormulaC28H29ClN6O5
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (88.49 mM)
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SMILESCC(C)n1c2ccc(NC(=O)N3CCO[C@H](C3)C(=O)Nc3ccc(C#N)c(Cl)c3)cc2c(=O)n(CC2CC2)c1=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Bene?ová M, et al. Preclinical Evaluation of a Tailor-Made DOTA-Conjugated PSMA Inhibitor with Optimized Linker Moiety for Imaging and Endoradiotherapy of Prostate Cancer. J Nucl Med. 2015 Jun;56(6):914-20.
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