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Cat No. | Product Name | Synonyms | Targets |
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T22767 | ER 50891 | Retinoid Receptor | |
ER-50891 is a potent retinoic acid receptor alpha (RARα) antagonist. er-50891 reduces the inhibitory effect of allosteric retinoic acid and restores osteoblast differentiation induced by bone morphogenetic protein 2. | |||
T38894 | IHVR-17028 | Influenza Virus , Glucosidase | |
IHVR-17028 is a potent broad-spectrum ERα-glucosidase I (α-glucosidase? I) inhibitor with IC50 of 0.24 μM and antiviral activity. IHVR-17028 inhibited BVDV, TCRV and DENV, and EC50 values were 0.4 μM, 0.26 μM and 0.3 μM,... | |||
T70031 | ER-38925 | ||
ER-38925 is a retinoic acid receptor (rar) subtype α-selective agonist | |||
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. | |||
T15554 | IHVR-19029 | Others | |
IHVR-19029 is an effective endoplasmic reticulum (ER) α-glucosidases I and II inhibitor (IC50: 0.48 μM for ER a-glucosidase I). IHVR-19029 efficiently blocks the replication of several hemorrhagic fever viruses, such as ... | |||
T40166 | Bexirestrant | ||
Bexirestrant is an orally active ER-α degrader commonly employed in the research of antiestrogen and antineoplastic therapies. | |||
T27590 | IHVR-11029 | IHVR 11029 | |
IHVR-11029 is a potent inhibitor of ER α-glucosidase. IHVR-11029 is active against multiple hemorrhagic fever viruses and efficiently disrupts the morphogenesis of a broad spectrum of enveloped viruses. | |||
T78102 | ER 50891 quarterhydrate | ||
ER 50891 quarterhydrate is a potent RARα (retinoic acid receptor α) antagonist that markedly diminishes the inhibitory effects of ATRA (all-trans retinoic acid) on osteoblastogenesis induced by BMP 2 (bone morphogenetic ... | |||
T79382 | ER degrader 6 | Estrogen Receptor/ERR | |
ER degrader 6 (compound 35s) is a potent selective estrogen receptor modulator (SERM) with the capacity to degrade Estrogen Receptor (ER)α. It disrupts the microtubule network, inhibiting tubulin polymerization, and effe... | |||
T62793 | EB-0150 | ||
EB-0150 is a potent inhibitor of ER α-glucosidase (α-Glu) I (IC50s: 0.73 μM) and (α-Glu) II (IC50s: 0.0337 μM). EB-0150 is an N-substituted valerian derivative with broad-spectrum antiviral effects. EB-0150 has potential... | |||
T18697 | SNIPER(ER)-87 | Others | |
SNIPER(ER)-87 is a chemical compound composed of a derivative of the inhibitor of apoptosis protein (IAP) ligand LCL161 conjugated to the estrogen receptor α (ERα) ligand 4-hydroxytamoxifen using a PEG linker. It effecti... | |||
T63303 | EB-0176 | ||
EB-0176 is an N-substituted valerian derivative that exhibits broad-spectrum antiviral activity and is a potent ER α-glucosidase (α-Glu) I and II inhibitor with IC50s of 0.6439 and 0.0011 μM, respectively.EB-0176 exhibit... | |||
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... | |||
T27050 | CM-10-18 | CM-1018 | |
CM-10-18 is a potent inhibitor of ER α-glucosidase. CM-10-18 demonstrated superior in vitro antiviral activity against representative viruses from four viral families causing hemorrhagic fever. CM-10-18 efficiently prote... | |||
T62818 | LSD1/ER-IN-1 | ||
LSD1/ER-IN-1 (compound 11g) is a potent inhibitor of ER and LSD1 that acts on LSD1 (IC50: 1.55 μM). LSD1/ER-IN-1 showed good anti-proliferative effect on MCF-7 breast cancer cells (IC50: 8.79 μM). | |||
T63170 | EB-0156 | ||
EB-0156 is a potent inhibitor of ER α-glucosidase (α-Glu) I and II with IC50 values of 0.0479 and <0.001 μM, respectively. EB-0156 is an N-substituted valerian derivative with broad-spectrum antiviral activity. EB-0156 h... | |||
T28275 | OUP-186 | OUP186 | |
OUP-186 is a high affinity and human/rat species-selective antagonist of histamine H3 receptor. OUP-186 suppressed the proliferation of breast cancer cells. The IC50 values at 48 hours for OUP-186 was approximately 50 μM... | |||
T61690 | MEH-IN-1 | ||
mEH-IN-1 (Compound 62) is a potent inhibitor of microsomal epoxide hydrolase (mEH), with an IC50 value of 2.2 nM. mEH is an α/β-fold hydrolase enzyme that is widely expressed in various mammalian tissues, responsible for... | |||
T35676 | 17β-hydroxy Exemestane | ||
17β-hydroxy Exemestane is the primary active metabolite of exemestane . It is formed by metabolism of exemestane by the cytochrome P450 (CYP) isoforms CYP1A and CYP4A11. 17β-hydroxy Exemestane is an aromatase inhibitor (... |
Cat No. | Product Name | Synonyms | Targets |
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T2930 | α-Lipoic Acid | Lipoic acid,Alphalipoic acid | NF-κB , HIV Protease , Mitochondrial Metabolism , Endogenous Metabolite |
α-Lipoic Acid (Alphalipoic acid) inhibits NF-κB-dependent HIV-1 LTR activation. α-Lipoic Acid induces endoplasmic reticulum (ER) stress-mediated apoptosis in hepatoma cells.α-Lipoic Acid is an antioxidant, which is an es... | |||
TN3084 | 5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-diprenylflavone | Estrogen Receptor/ERR , Others | |
5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-diprenylflavone showed strong anti-proliferation effect on ER-positive breast cancer MCF-7 cells in vitro, with an IC50 value of 4.41 uM. 5,7,3',4'-Tetrahydroxy-3-methoxy-8,5'-dipren... | |||
T72429 | α-Lipoic Acid sodium | Thioctic acid sodium,DL-α-Lipoic acid sodium,Thioctic acid sodium ; (±)-α-Lipoic acid sodium ; DL-α-Lipoic acid sodium,(±)-α-Lipoic acid sodium | |
α-Lipoic Acid (Thioctic acid) sodium, an essential cofactor for mitochondrial enzyme complexes, serves as an antioxidant. It suppresses NF-κB-dependent activation of HIV-1 LTR [1] [2] [3] and triggers ER (endoplasmic ret... |
Cat No. | Product Name | Species | Expression System |
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TMPJ-00762 | ER alpha Protein, Human, Recombinant (His) | Human | E. coli |
Estrogen Receptor is a major ligand-activated transcription factor belonging to the nuclear hormone receptor superfamily. Estrogen Receptor is composed of several domains important for hormone binding, DNA binding, and a... | |||
TMPJ-01384 | MAN1B1 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
Endoplasmic Reticulum Mannosyl-Oligosaccharide 1,2-α-Mannosidase (MAN1B1) belongs to the glycosyl hydrolase 47 family. MAB1B1 is a single-pass type II membrane protein and widely expressed in many tissues. MAB1B1 is invo... | |||
TMPY-03870 | EDEM2 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
EDEM2, also known as C2orf31, belongs to a family of proteins involved in ER-associated degradation (ERAD) of glycoproteins. In the endoplasmic reticulum (ER), misfolded proteins are retrotranslocated to the cytosol and ... | |||
TMPK-00075 | IFN-alpha 1/IFNA1 Protein, Human, Recombinant (hFc) | Human | HEK293 Cells |
IFN-α, a cytokine expressed in human islets from individuals affected by type 1 diabetes, plays a key role in the pathogenesis of diabetes by upregulating inflammation, endoplasmic reticulum (ER) stress and MHC class I o... | |||
TMPK-00074 | IFN-alpha 1/IFNA1 Protein, Mouse, Recombinant (hFc) | Mouse | HEK293 Cells |
IFN-α, a cytokine expressed in human islets from individuals affected by type 1 diabetes, plays a key role in the pathogenesis of diabetes by upregulating inflammation, endoplasmic reticulum (ER) stress and MHC class I o... |