- XCT790
-
- $59.00 / 5mg
-
2024-11-19
- CAS:725247-18-7
- Min. Order:
- Purity: 99.74%
- Supply Ability: 10g
- XCT790
-
- $59.00 / 5mg
-
2024-11-19
- CAS:725247-18-7
- Min. Order:
- Purity: 99.74%
- Supply Ability: 10g
- XCT 790
-
- $1.00 / 1KG
-
2020-02-05
- CAS:725247-18-7
- Min. Order: 1KG
- Purity: 98%HPLC
- Supply Ability: 100KG
|
| | XCT 790 Basic information |
| Product Name: | XCT 790 | | Synonyms: | 3-[4-(2,4-bis-trifluoromethylbenzyloxy)-3-methoxyphenyl]-2-cyano-n-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)acrylamide;3-[4-[[2,4-Bis(trifluoromethyl)benzyl]oxy]-3-methoxyphenyl]-2-cyano-N-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)acrylamide XCT 790;XCT 790 3-[4-[[2,4-Bis(trifluoromethyl)benzyl]oxy]-3-methoxyphenyl]-2-cyano-N-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yl)acrylamide;(E)-3-[4-[[2,4-bis(trifluoromethyl)phenyl]methoxy]-3-methoxyphenyl]-2-cyano-N-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]prop-2-enamide;XCT 790; XCT-790;CS-1881;2-Propenamide, 3-[4-[[2,4-bis(trifluoromethyl)phenyl]methoxy]-3-methoxyphenyl]-2-cyano-N-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]-;XCT 790,Inhibitor,Estrogen Receptor/ERR,Autophagy,XCT790,inhibit,XCT-790 | | CAS: | 725247-18-7 | | MF: | C23H13F9N4O3S | | MW: | 596.42 | | EINECS: | | | Product Categories: | | | Mol File: | 725247-18-7.mol |  |
| | XCT 790 Chemical Properties |
| storage temp. | 2-8°C | | solubility | DMSO: ≥10mg/mL | | form | solid | | color | yellow |
| | XCT 790 Usage And Synthesis |
| Description | XCT790 is an inverse agonist of estrogen-related receptor α (ERRα; IC50 = ~300-500 nM). It demonstrates 90-100% inhibition of ERRα constitutive activity and has no significant activity at related nuclear receptors at 10 μM. XCT790 associates with the ligand-binding domain of ERRα and blocks ERRα/PGC-1α-dependent signaling, suppressing the expression of monoamine oxidases A and B. XCT790 induces proteasomal degradation of ERRα and potentiates the degradation of the estrogen receptor ERα by fulvestrant . | | Uses | XCT790 is a potent inverse agonist of ERRα. | | Definition | ChEBI: XCT 790 is a member of cinnamamides. | | Biochem/physiol Actions | XCT 790 is a 5′adenosine monophosphate-activated protein kinase (AMPK) activator. It also acts as a proton ionophore and an uncoupler of oxidative phosphorylation in mitochondria. XCT790 impairs vascular endothelial growth factor (VEGF) and angiopoietin 2 (Ang-2) expression and exhibits suppression of endometrial tumor via estrogen-related receptor (ERRα) inhibition. XCT790 mediates cell cycle arrest and favors apoptosis in triple-negative breast cancer (TNBC). | | storage | Store at +4°C | | references | [1] lu x, peng l, lv m, ding k. recent advance in the design of small molecular modulators of estrogen-related receptors. curr pharm des. 2012;18(23):3421-31.
[2] wu f, wang j, wang y, kwok tt, kong sk, wong c. estrogen-related receptor alpha (erralpha) inverse agonist xct-790 induces cell death in chemotherapeutic resistant cancer cells. chem biol interact. 2009 oct 7;181(2):236-42. |
| | XCT 790 Preparation Products And Raw materials |
|