ROR gamma-t-IN-1
- CAS No.
- 1426802-50-7
- Chemical Name:
- ROR gamma-t-IN-1
- Synonyms
- GSK805;GSK805 ，S6767;ROR gamma-t-IN-1;GSK805 (GSK-805);GSK805, 10 mM in DMSO;RORγt Inverse Agonist II, GSK805;RORγt Inverse Agonist II, GSK805;GSK805,N-(2,6-Dichloro-2'-(trifluoromethoxy)biphenyl-4-yl)-;4-[4-[(dimethylamino)methyl]-3,5-dimethoxyphenyl]-2-methyl-2,7-naphthyridin-1(2H)-one;N-(2,6-dichloro-2'-(trifluoromethoxy)biphenyl-4-yl)-2-(4-(ethylsulfonyl)phenyl)acetamide
- CBNumber:
- CB13048666
- Molecular Formula:
- C23H18Cl2F3NO4S
- Molecular Weight:
- 532.36
- MDL Number:
- MFCD28902182
- MOL File:
- 1426802-50-7.mol
- MSDS File:
- SDS
- TDS File:
- TDS
| Boiling point | 617.1±55.0 °C(Predicted) |
|---|---|
| Density | 1.434±0.06 g/cm3(Predicted) |
| storage temp. | 2-8°C |
| solubility |
DMF:3.0(Max Conc. mg/mL);5.64(Max Conc. mM) DMSO:68.33(Max Conc. mg/mL);128.36(Max Conc. mM) DMSO:PBS (pH 7.2) (1:2):0.3(Max Conc. mg/mL);0.56(Max Conc. mM) Ethanol:50.0(Max Conc. mg/mL);93.92(Max Conc. mM) |
| form | A crystalline solid |
| pka | 12.33±0.70(Predicted) |
| color | White to off-white |
| InChIKey | CEICQMBWAQAIQX-UHFFFAOYSA-N |
| SMILES | C1(CC(NC2=CC(Cl)=C(C3=CC=CC=C3OC(F)(F)F)C(Cl)=C2)=O)=CC=C(S(CC)(=O)=O)C=C1 |
| UNSPSC Code | 12352200 |
| NACRES | NA.77 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H302-H315-H319-H335 | |||||||||
| Precautionary statements | P261-P264-P270-P271-P280-P301+P312-P330-P302+P352-P321-P304+P340-P305+P351+P338-P332+P313-P362+P364-P337+P313-P403+P233-P405-P501 | |||||||||
| WGK Germany | WGK 3 | |||||||||
| Storage Class | 11 - Combustible Solids | |||||||||
| NFPA 704 |
|
ROR gamma-t-IN-1 price More Price(50)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | 5.31369 | RORγt Inverse Agonist II, GSK805 | 1426802-50-7 | 10 mg | $286 | 2026-04-30 | Buy |
| Cayman Chemical | 9002444 | GSK805 ≥98% | 1426802-50-7 | 1mg | $49 | 2026-04-30 | Buy |
| Cayman Chemical | 9002444 | GSK805 ≥98% | 1426802-50-7 | 5mg | $167 | 2026-04-30 | Buy |
| Cayman Chemical | 9002444 | GSK805 ≥98% | 1426802-50-7 | 10mg | $259 | 2026-04-30 | Buy |
| ChemScene | CS-5079 | GSK805 99.83% | 1426802-50-7 | 5mg | $162 | 2026-06-04 | Buy |
ROR gamma-t-IN-1 Chemical Properties, Uses, Production
Description
GSK805 is a potent, orally bioavailable retinoid-related orphan receptor gamma t (RORγt) inverse agonist that interacts with the receptor''s putative ligand binding domain without exerting significant effects on DNA binding. It inhibits the expression of IL-17 (at 0.5 μM) in naïve CD4+ T cells activated under Th17-cell-polarizing conditions and affects the broader RORγt-dependent gene network, inhibiting the development and pathogenic function of Th17 cells. GSK805 significantly reduces the severity of experimental autoimmune encephalomyelitis (EAE), a mouse model of multiple sclerosis, when given orally to the hosts at 10 mg/kg daily beginning at the time of disease induction.
Uses
GSK805 is an orally active and CNS penetrant RORγt inhibitor. GSK805 inhibits RORγ and Th17 cells differentiation with pIC50 values of 8.4 and >8.2. GSK805 inhibits the function of Th17 cells. GSK805 can be used for the research of immunity[1].
in vivo
GSK805 (10 mg/kg; p.o. once per day for 35 days) improves the situation of mice with experimental autoimmune encephalomyelitis (EAE)[2]. GSK805 (30 mg/kg; p.o. once) inhibits Th17 cell responses in EAE mice[2].
| Animal Model: | C57BL/6 mice were immunized with MOG35–55 plus CFA[2] |
| Dosage: | 10 mg/kg |
| Administration: | Oral gavage; 10 mg/kg once per day; for 35 days |
| Result: | Efficiently ameliorated the severity of EAE in mice. |
| Animal Model: | C57BL/6 mice with EAE[2] |
| Dosage: | 30 mg/kg |
| Administration: | Oral gavage; 30 mg/kg once |
| Result: | Reduced both IFN-γ-IL-17+ and IFN-γ+IL-17+ T cells without altered the frequency of TNF-α+ T cells in EAE mice. |
References
[1] Wang Y, et al. Discovery of Biaryl Amides as Potent, Orally Bioavailable, and CNS Penetrant RORγt Inhibitors. ACS Med Chem Lett. 2015 May 26;6(7):787-792. DOI:10.1021/acsmedchemlett.5b00122
[2] Xiao S, et al. Small-molecule RORγt antagonists inhibit T helper 17 cell transcriptional network by divergent mechanisms. Immunity. 2014 Apr 17;40(4):477-89. DOI:10.1016/j.immuni.2014.04.004
ROR gamma-t-IN-1 Preparation Products And Raw materials
Raw materials
Preparation Products
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Chengdu DingDang Pharmaceutical Co., Ltd. | 028-86040038 | market@dingdangchem.com | China | 1853 | 55 |
| Suzhou Chenrui Biotechnology Co. LTD | 17625585511 | 1580084073@qq.com | China | 992 | 58 |
| Haoyuan Chemexpress Co., Ltd. | 021-58950125 | info@chemexpress.com | China | 7545 | 61 |
| Shanghai Lollane Biological Technology Co.,Ltd. | 021-52996696，15000506266 15000506266 | China | 4859 | 55 | |
| Struchem Co., Ltd. | 0512-63009836 18994340901 | helen@struchem.com | China | 3968 | 60 |
| Guangzhou QiYun Biotechnology Co., Ltd. | 020-61288194 61288195 | 505721671@qq.com | China | 3853 | 58 |
| Shanghai YuanYe Biotechnology Co., Ltd. | 15026964105 | 2881489226@qq.com | China | 89667 | 60 |
| Shanghai Chaolan Chemical Technology Center | QQ：65489617 13301690235 | Sales@ATKchemical.com | China | 9729 | 58 |
| Beijing Solarbio Science & Tecnology Co., Ltd. | 17801761073 18101056239 | 3193328036@qq.com | China | 28150 | 68 |
| Amadis Chemical Company Limited | 571-89925085 | sales@amadischem.com | China | 131885 | 58 |
