Fenebrutinib
CAS No. 1434048-34-6
Fenebrutinib( RG-7845 | GDC-0853 )
Catalog No. M11845 CAS No. 1434048-34-6
An orally bioavailable, selective, non-covalent and reversible BTK inhibitor with IC50 of 2-9 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 47 | In Stock |
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| 5MG | 76 | In Stock |
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| 10MG | 138 | In Stock |
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| 25MG | 311 | In Stock |
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| 50MG | 464 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | 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 NameFenebrutinib
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NoteResearch use only, not for human use.
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Brief DescriptionAn orally bioavailable, selective, non-covalent and reversible BTK inhibitor with IC50 of 2-9 nM.
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DescriptionAn orally bioavailable, selective, non-covalent and reversible BTK inhibitor with IC50 of 2-9 nM; has demonstrated efficacy in pre-clinical autoimmune disease models and is being developed for the treatment of rheumatoid arthritis and lupus, with future development for other autoimmune indications.RheumatoId Arthritis Phase 2 Clinical(In Vitro):Fenebrutinib (GDC-0853) inhibits CD69 expression on CD19+ B cells in human whole blood with an IC50 of 8.4±5.6 nM. Fenebrutinib inhibits CD63 expression on basophils with an IC50 of 30.7±4.1 nM.Fenebrutinib suppresses anti-IgM induced Btk Y223 autophosphorylation in human whole blood (IC50=11 nM).(In Vivo):Fenebrutinib (GDC-0853) dose-dependently reduces ankle thickness following once (0.06, 0.25, 1, 4, and 16 mg/kg QD; orally) or twice (0.125, 0.5, and 2 mg/kg BID; orally) daily in female Lewis rats with developing collagen-induced arthritis.Fenebrutinib (0.2 mg/kg IV and 1.0 mg/kg PO; for rats) and (0.2 mg/kg IV and 0.5 mg/kg PO for dogs) demonstrates the half-lives (t1/2s) of 2.2 and 3.8 h In rats, and dogs, respectively.
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In Vitro——
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In VivoAnimal Model:Female Lewis rats with developing collagen-induced arthritis (CIA) Dosage:0.06, 0.25, 1, 4, and 16 mg/kg once daily (QD); 0.125, 0.5, and 2 mg/kg twice daily (BID) Administration:Dosed orally; for 16 days Result:Dose-dependently reduced ankle thickness following QD and BID dosing regimens.
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SynonymsRG-7845 | GDC-0853
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PathwayTyrosine Kinase
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TargetBTK
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RecptorBTK
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Research AreaInflammation/Immunology
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IndicationRheumatoid Arthritis
Chemical Information
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CAS Number1434048-34-6
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Formula Weight664.7964
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Molecular FormulaC37H44N8O4
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 23 mg/mL
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SMILESCC1CN(CCN1C2=CN=C(C=C2)NC3=CC(=CN(C3=O)C)C4=C(C(=NC=C4)N5CCN6C7=C(CC(C7)(C)C)C=C6C5=O)CO)C8COC8
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Chemical Name2H-Cyclopenta[4,5]pyrrolo[1,2-a]pyrazin-1(6H)-one, 2-[1,6-dihydro-3'-(hydroxymethyl)-1-methyl-5-[[5-[(2S)-2-methyl-4-(3-oxetanyl)-1-piperazinyl]-2-pyridinyl]amino]-6-oxo[3,4'-bipyridin]-2'-yl]-3,4,7,8-tetrahydro-7,7-dimethyl-
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. Erickson RI, et al. J Pharmacol Exp Ther. 2017 Jan;360(1):226-238.
2. Katsumoto, T. 2016 ACR/ARHP Annual Meeting (2016).
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