GSK 2981278
CAS No. 1474110-21-8
GSK 2981278( GSK2981278 | GSK-2981278 )
Catalog No. M12032 CAS No. 1474110-21-8
GSK 2981278 (GSK2981278) is a potent, highly selective RORγ/RORγt inhibitor that potently inhibits IL-17A and IL-22 protein secretion in human peripheral T cell with IC50 of 3.2 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 65 | In Stock |
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| 5MG | 64 | In Stock |
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| 10MG | 93 | In Stock |
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| 25MG | 186 | In Stock |
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| 50MG | 277 | In Stock |
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| 100MG | 418 | In Stock |
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| 200MG | 604 | 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 NameGSK 2981278
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NoteResearch use only, not for human use.
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Brief DescriptionGSK 2981278 (GSK2981278) is a potent, highly selective RORγ/RORγt inhibitor that potently inhibits IL-17A and IL-22 protein secretion in human peripheral T cell with IC50 of 3.2 nM.
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DescriptionGSK 2981278 (GSK2981278) is a potent, highly selective RORγ/RORγt inhibitor that potently inhibits IL-17A and IL-22 protein secretion in human peripheral T cell with IC50 of 3.2 nM; shows no effects on RORα-dependent activation; robustly inhibits RORγ-mediated cytokine production at both the mRNA and protein level, inhibits RORγt-mediated transactivation; attenuates inflammation in mouse model of psoriasis.Psoriasis Phase 2 Clinical(In Vitro):GSK2981278 markedly and potently inhibits IL-17A and IL-22 protein secretion in a concentration dependent manner (IC50 = 3.2 nM) during 5 days of culture under Th17 skewing conditions.GSK2981278 (0.3, 1, 3, 10, 30, 100, 300, 1000 pM; 5 day) potently and selectively inhibits IL-17 and IL-22 levels. Culture in the presence of ≥3 nM GSK2981278 led to a near-complete inhibition of IL-17A protein secretion.(In Vivo):GSK2981278 (1% in ointment; topically; for three days) reduces skin redness and scaling, as well as decreased hyperplasia, as evidenced by a 23% reduction in epidermal thickness. GSK2981278 attenuates inflammation in a mouse model of psoriasis.
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In Vitro——
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In VivoAnimal Model:BALB/c JByRj Female Mice (8 week-old at study initiation; imiquimod (IMQ) mouse model) Dosage:1% Administration:In ointment; topically; for three days Result:Reduced skin redness and scaling, as well as decreased hyperplasia, as evidenced by a 23% reduction in epidermal thickness.
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SynonymsGSK2981278 | GSK-2981278
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PathwayNuclear Receptor/Transcription Factor
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TargetROR
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RecptorRORγ
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Research AreaInflammation/Immunology
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IndicationPsoriasis
Chemical Information
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CAS Number1474110-21-8
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Formula Weight461.617
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Molecular FormulaC25H35NO5S
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Purity>98% (HPLC)
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SolubilityDMSO: 10 mM ( < 1 mg/ml refers to the product slightly soluble or insoluble )
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SMILESO=S(C1=CC=C(OCC2CCOCC2)C(CO)=C1)(N(C3=CC=C(CC)C=C3)CC(C)C)=O
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Chemical NameN-(4-Ethylphenyl)-3-(hydroxymethyl)-N-(2-methylpropyl)-4-[(tetrahydro-2H-pyran-4-yl)methoxy]benzenesulfonamide
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. Kang EG, et al. Br J Dermatol. 2017 Nov 18. doi: 10.1111/bjd.16131.
2. Smith SH, et al. PLoS One. 2016 Feb 12;11(2):e0147979.
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