SR 1001 manufacturers
- SR1001
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- $34.00 / 1mg
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2026-01-26
- CAS:1335106-03-0
- Min. Order:
- Purity: 99.04%
- Supply Ability: 10g
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| | SR 1001 Basic information |
| Product Name: | SR 1001 | | Synonyms: | SR 1001;SR1001,N-{4-Methyl-5-[4-(2,2,2-trifluoro-1-hydroxy-1-trifluoroMethyl-ethyl)-phenylsulfaMoyl]-thiazol-2-yl}-acetaMide;N-(5-(N-(4-(1,1,1,3,3,3-Hexafluoro-2-hydroxypropan-2-yl)phenyl)sulphamoyl)-4-methylthiazol-2-yl)acetamide;N-(5-{[4-(1,1,1,3,3,3-Hexafluoro-2-hydroxy-2-propanyl)phenyl]sulfamoyl}-4-methyl-1,3-thiazol-2-yl)acetamide;N-[4-Methyl-5-[[[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl]amino]sulfonyl]-2-thiazolylacetamide;SR-1001;SR 1001;Acetamide, N-[4-methyl-5-[[[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl]amino]sulfonyl]-2-thiazolyl]-;SR1001 >=98% (HPLC) | | CAS: | 1335106-03-0 | | MF: | C15H13F6N3O4S2 | | MW: | 477.4 | | EINECS: | | | Product Categories: | | | Mol File: | 1335106-03-0.mol |  |
| | SR 1001 Chemical Properties |
| density | 1.640±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,2-8°C | | solubility | DMSO: >5mg/mL | | pka | 5.90±0.50(Predicted) | | form | powder | | color | white to beige | | Stability: | Stable for 2 years from date of purchase as supplied. Protect from moisture. Solutions in DMSO may be stored at -20° for up to 3 months. | | InChI | 1S/C15H13F6N3O4S2/c1-7-11(29-12(22-7)23-8(2)25)30(27,28)24-10-5-3-9(4-6-10)13(26,14(16,17)18)15(19,20)21/h3-6,24,26H,1-2H3,(H,22,23,25) | | InChIKey | OZBSSKGBKHOLGA-UHFFFAOYSA-N | | SMILES | CC(=O)Nc1nc(C)c(s1)S(=O)(=O)Nc2ccc(cc2)C(O)(C(F)(F)F)C(F)(F)F |
| Hazard Codes | Xn | | Risk Statements | 22-36 | | Safety Statements | 26 | | WGK Germany | 3 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral
Eye Irrit. 2 |
| | SR 1001 Usage And Synthesis |
| Description | SR1001 (1335106-03-0) is a high affinity synthetic ligand for both RORα and RORγt acting as an inverse agonist. It binds specifically to the ligand-binding domain, inducing a conformational change which leads to diminished affinity for co-activators and increased affinity for co-repressors resulting in suppression of transcriptional activity.1?SR-1001 inhibits the development of murine TH17 cells2 and suppresses the expression of cytokines1. Suppresses insulitis and prevents hyperglycemia in a type 1 diabetes mouse model.3 Protects against pathologic neovascularization in various mouse models of retinopathy.4?Active in vivo | | Uses | SR 1001 is a selective RORc inverse agonist. | | Definition | ChEBI: SR 1001 is a sulfonamide. | | in vivo | SR1001 effectively suppresses the clinical severity of autoimmune disease in mice. Administration of SR1001 to C57BL/6 mice suppresses the expression of hepatic ROR target genes, Cyp7b1, Rev-erbα, and Serpine 1[1]. SR1001 a RORα inverse agonist eliminats the circadian pattern of expression of citrate synthase mRNA in mice[2]. | | References | [1] LAURA A. SOLT. Suppression of TH17 differentiation and autoimmunity by a synthetic ROR ligand[J]. Nature, 2011, 472 7344: 491-494. DOI:10.1038/nature10075
[2] ELÉONORE BEUREL Richard S J Laurie E Harrington. Inflammatory T Helper 17 Cells Promote Depression-like Behavior in Mice[J]. Biological Psychiatry, 2013, 73 7: Pages 622-630. DOI:10.1016/j.biopsych.2012.09.021
[3] LAURA A SOLT. ROR inverse agonist suppresses insulitis and prevents hyperglycemia in a mouse model of type 1 diabetes.[J]. Endocrinology, 2015, 156 3: 869-881. DOI:10.1210/en.2014-1677
[4] YE SUN. Nuclear receptor RORα regulates pathologic retinal angiogenesis by modulating SOCS3-dependent inflammation.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2015, 112 33: 10401-10406. DOI:10.1073/pnas.1504387112 |
| | SR 1001 Preparation Products And Raw materials |
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