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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7904 | SR 19881 | Estrogen/progestogen Receptor | |
SR 19881 is a full agonist of ERRγ(EC50 value of 0.39 μM in a binding assay and an EC50 value of 4.7 μM in a cell-based assay). | |||
T0593 | XCT790 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor , Autophagy | |
XCT790 is a potent, selective and inverse agonist of estrogen-related receptor alpha(ERRα). | |||
T5835 | PROTAC ERRα ligand 2 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor | |
PROTAC ERRα ligand 2 is an estrogen-related receptor α (ERRα) inverse agonist( IC50 : 5.67 nM) | |||
T15191 | PROTAC ERRα ligand 1 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor | |
PROTAC ERRα ligand 1 is an α (ERRα) antagonist of estrogen-related receptor (IC50s of 0.04 and 2.8 μM for ERRα and ERRγ, respectively). | |||
T8370 | GSK5182 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor , Reactive Oxygen Species | |
GSK5182 is a highly selective inverse estrogen-related receptor γ agonist (IC50 : 79 nM) | |||
T7709 | (E/Z)-GSK5182 | GSK5182(Z/E) | Estrogen/progestogen Receptor , ROS |
(E/Z)-GSK5182 (GSK5182(Z/E)) is a racemic mixture comprising (E)-GSK5182 and (Z)-GSK5182 isomers. It acts as a highly selective and orally active inverse agonist for the estrogen-related receptor γ (ERRγ), demonstrating ... | |||
T0760 | Cholesterol | Cholesterin,Cholesteryl alcohol | Estrogen Receptor/ERR , MRP , Endogenous Metabolite , ROR |
Cholesterol (cholesteryl alcohol) is a natural product that is the major sterol in mammals and an agonist of estrogen-related receptor α (ERRα). Cholesterol is widely found in the cell membranes of animals and is also us... | |||
T77577 | SLU-PP-332 | Estrogen/progestogen Receptor | |
SLU-PP-332 is a pan-estrogen receptor-related receptor (ERR) agonist with high affinity for ERRα, ERRβ, and ERRγ with EC50 values of 98, 230, and 430 nM, respectively.SLUPP-332 enhances mitochondrial function and cellula... | |||
T11230 | ERRα antagonist-1 | ERR+/- antagonist-1,ERRa antagonist-1 | Estrogen/progestogen Receptor |
ERRα antagonist-1 (ERR+/- antagonist-1) is a high-affinity, selective antagonist of the estrogen-related receptor α (ERRα). It effectively prevents the interaction of ERRα with both Proliferator-activated Receptor γ Coac... | |||
T18609 | PROTAC ERRα Degrader-2 | Others | |
PROTAC ERRα Degrader-2 is a compound consisting of an MDM2 ligand binding group, a linker, and an estrogen-related receptor alpha (ERRα) binding group. This compound is designed to specifically degrade estrogen-related r... | |||
T13700 | GDC-0927 Racemate | SRN-927 Racemate | Others |
GDC-0927 Racemate is a degrader of estrogen receptor, is used in the research of ER-related diseases, potently inhibits ER-α activity, with an IC50 of 0.2 nM. | |||
T18651 | (rel)-PROTAC ERRα Degrader-1 | Others | |
(rel)-PROTAC ERRα Degrader-1 is a relative configuration of PROTAC ERRα Degrader-1, which is an estrogen-related receptor alpha (ERRa) degrader. PROTAC ERRα Degrader-1 consists of an MDM2 ligand binding moiety, a linker ... | |||
T40349 | DS45500853 | ||
DS45500853, an estrogen-related receptor α (ERRα) agonist, acts as an inhibitor of the binding interaction between receptor-interacting protein 140 (RIP140) corepressor peptide (10 nM) and GST-ERRα ligand-binding domain ... | |||
T60441 | DK3 | ||
DK3 is a potent and selective agonist of estrogen-related receptor alpha (ERRα). ERRα is a potential drug target for cancer and metabolic diseases [1]. | |||
T60674 | DK1 | ||
DK1 is a potent estrogen related receptor modulator. DK1 impacts the activity of ERRα receptor and reduces blood glucose. DK1 shows the potential in the diabetes research [1]. | |||
T39838 | (S,R,S)-AHPC-C7-amine | VH032-C7-amine,(S,R,S)-AHPC-C7-amine | |
(S,R,S)-AHPC-C7-amine, also known as VH032-C7-amine, is a chemically synthesized conjugate that functions as an E3 ligase ligand-linker. This compound combines the VH032-based VHL ligand with a specific linker designed f... | |||
T11231 | ERRγ Inverse Agonist 1 | Estrogen/progestogen Receptor | |
ERRγ Inverse Agonist 1 (Compound 12) is a potent, selective and orally bioavailable Estrogen-related Receptor grammar (ERRγ) inverse agonist (IC 50=40 nM) [1]. | |||
T39651 | (S,R,S)-AHPC-C5-NH2 | (S,R,S)-AHPC-C5-NH2,VH032-C5-NH2 | |
(S,R,S)-AHPC-C5-NH2, also known as VH032-C5-NH2, is a synthetic compound designed as an E3 ligase ligand-linker conjugate. This compound combines the VH032-based von Hippel-Lindau (VHL) ligand with a linker, enabling it ... | |||
TMA0424 | Martynoside | ROS | |
Martynoside is a natural selective estrogen receptor modulator, which has antioxidative, anti-muscle fatigue, anticancer and antimetastatic activities. Martynoside has the potential of antagonizing sports anaemia, the me... | |||
T61923 | ERRα antagonist-2 | ||
ERRα antagonist-2 (Compound 11) is a potential Reverse agonist of ERR α (estrogen receptor related receptor α) (IC50=0.80 μ M). ERRα antagonist-2 can inhibit the migration and invasion of ER-negative MDA-MB-231 cells. ER... |