56 Results for "

GP130

" in MedChemExpress (MCE) Product Catalog:
Products (56)

56 Results for "GP130" in MCE Product Catalog:

17
17 Publications Verification
Art. -Nr.: HY-A0036
CAS. Nr.: 198481-33-3
Synonyms: TSE-424 acetate
Target:  

Estrogen Receptor/ERR

Forschungsgebiete:  

Cancer

Bazedoxifene acetate (TSE-424 acetate) is an oral, nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene acetate can be used for the research of osteoporosis. Bazedoxifene acetate also acts as an inhibitor of IL-6/GP130 protein-protein interactions and can be used for the research of pancreatic cancer .
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17
17 Publications Verification
Art. -Nr.: HY-A0031
CAS. Nr.: 198481-32-2
Synonyms: TSE-424
Target:  

Estrogen Receptor/ERR

Forschungsgebiete:  

Neurological Disease Cancer

Bazedoxifene (TSE-424) is an oral, BBB-penetrant nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene can be used for the research of osteoporosis. Bazedoxifene also acts as an inhibitor of IL-6/GP130 protein-protein interactions and can be used for the research of pancreatic cancer .
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17
17 Publications Verification
Art. -Nr.: HY-102084
CAS. Nr.: 1239600-18-0
Reinheit:  98.93%
Target:  

Interleukin Related

Forschungsgebiete:  

Inflammation/Immunology

LMT-28 is an orally active and the first synthetic IL-6 inhibitor that functions through direct binding to gp130. LMT-28 shows low toxicity and selectively inhibits IL-6-induced phosphorylation of STAT3, JAK2, and gp130 .
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10
10 Cited Publications
Art. -Nr.: HY-15614
CAS. Nr.: 895158-95-9
Reinheit:  99.48%
Forschungsgebiete:  

Cancer

SC144 is a first-in-class, orally active gp130 (IL6-beta) inhibitor. SC144 binds gp130, induces gp130 phosphorylation (S782) and deglycosylation, abrogates Stat3 phosphorylation and nuclear translocation, and further inhibits the expression of downstream target genes. SC144 shows potent inhibition of gp130 ligand-triggered signaling. SC144 induces apoptosis in human ovarian cancer cells .
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10
10 Cited Publications
Art. -Nr.: HY-15614A
CAS. Nr.: 917497-70-2
Reinheit:  98.98%
Forschungsgebiete:  

Cancer

SC144 hydrochloride is a first-in-class, orally active gp130 (IL6-beta) inhibitor. SC144 hydrochloride binds gp130, induces gp130 phosphorylation (S782) and deglycosylation, abrogates Stat3 phosphorylation and nuclear translocation, and further inhibits the expression of downstream target genes. SC144 hydrochloride shows potent inhibition of gp130 ligand-triggered signaling. SC144 hydrochloride induces apoptosis in human ovarian cancer cells .
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2
2 Cited Publications
Art. -Nr.: HY-114775
CAS. Nr.: 108237-91-8
Reinheit:  99.92%
RCGD423 is a gp130 modulator, which prevents articular cartilage degeneration and promotes repair.
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1
1 Cited Publications
Art. -Nr.: HY-P76370
Reinheit:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: IL6ST; Interleukin Receptor Beta Chain; Interleukin 6 Cytokine Family Signal Transducer; Membrane Glycoprotein GP130; Interleukin-6 Receptor Subunit Beta; IL6ST Nirs Variant 5; Membrane Glycoprotein 130; IL6ST Nirs Variant 2; IL-6RB; IL6ST Nirs Variant 3
Species:  
Source:  
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Art. -Nr.: HY-121488
CAS. Nr.: 339303-87-6
Reinheit:  99.95%
Target:  

Interleukin Related

Forschungsgebiete:  

Neurological Disease

GP130 receptor agonist-1 is a potent, brain-penetrant and orally active GP130 receptor agonist. GP130 receptor agonist-1 has a neuroprotective effect on NMDA-induced neurotoxicity .
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Art. -Nr.: HY-176294
CAS. Nr.: 750640-55-2
Target:  

Interleukin Related

Forschungsgebiete:  

Others

GP130 modulator-2 (Compound A5) is a GP130 modulator. GP130 modulator-2 can be used for research of disease associated with gp130 activity .
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Art. -Nr.: HY-159742
CAS. Nr.: 2375779-31-8
GP130 modulator-1 (compound A33) is a gp130 signaling pathway modulator. GP130 modulator-1 can be used in the study of inflammatory and degenerative disorders .
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Art. -Nr.: HY-P990012
CAS. Nr.: 2744320-12-3
Synonyms: EBI-031

Target:  

Interleukin Related

Forschungsgebiete:  

Inflammation/Immunology

Vamikibart (EBI-031) is a humanized IgG2κ monoclonal antibody targeting IL-6, with high binding affinity for IL-6 and the IL-6/IL-6R complex. Vamikibart reduces central retinal thickness, resolves intraretinal and subretinal foveal fluid, and decreases the levels of intraocular inflammatory markers. Vamikibart can be used in studies of uveitic macular edema (UME) secondary to non-infectious uveitis .
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Art. -Nr.: HY-N14323
CAS. Nr.: 184877-64-3
Madindoline A is an orally active gp130 antagonist with a KD of 288 μM. Madindoline A inhibits IL-6- and IL-11-induced osteoclastogenesis, suppresses IL-6-stimulated serum amyloid A protein production, inhibits bone resorption and bone loss, and also inhibits IL-6- and IL-11-dependent cell line growth, as well as IL-6-dependent Stat3 tyrosine phosphorylation. Madindoline A is applicable for the research of hormone-dependent postmenopausal osteoporosis .
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Art. -Nr.: HY-P10641
CAS. Nr.: 876460-72-9
Target:  

Exosomes STAT ERK Akt

Forschungsgebiete:  

Cardiovascular Disease

Heart-homing peptide is a heart-targeting peptide with the sequence CRPPR that mediates cardiac endothelial targeting and accumulates in cardiac tissues. Heart-homing peptide mediates the translocation of liposomal and exosomal cargos across cardiac endothelium into interstitial tissues, enhances the accumulation of exosomes in the heart, and inhibits the GP130-STAT3/ERK1/2/AKT pathway. Heart-homing peptide accumulates at sites of ischemia/reperfusion, myocardial infarction and hypertrophy in mice. Heart-homing peptide can be used for the research of cardiovascular diseases .
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Art. -Nr.: HY-A0031A
CAS. Nr.: 198480-56-7
Synonyms: TSE-424 hydrochloride
Target:  

Estrogen Receptor/ERR

Forschungsgebiete:  

Cancer

Bazedoxifene hydrochloride (TSE-424 hydrochloride) is an oral active, BBB-penetrant nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene hydrochloride can be used for the research of osteoporosis. Bazedoxifene hydrochloride acts as an inhibitor of IL-6/GP130 protein-protein interactions. Bazedoxifene hydrochloride can be used for the research of pancreatic cancer .
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Art. -Nr.: HY-A0036R
CAS. Nr.: 198481-33-3
Synonyms: TSE-424 acetate (Standard)
Forschungsgebiete:  

Cancer

Bazedoxifene (acetate) (Standard) is the analytical standard of Bazedoxifene (acetate). This product is intended for research and analytical applications. Bazedoxifene acetate (TSE-424 acetate) is an oral, nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene acetate can be used for the research of osteoporosis. Bazedoxifene acetate also acts as an inhibitor of IL-6/GP130 protein-protein interactions and can be used for the research of pancreatic cancer .
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Art. -Nr.: HY-134042
CAS. Nr.: 42013-48-9
Target:  

Drug Derivative

Forschungsgebiete:  

Neurological Disease

GP130 (G130) is a psychostimulant agent, exhibiting antagonist activity against central nervous system depressing agents [2.
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Art. -Nr.: HY-168072
CAS. Nr.: 2955243-69-1
Forschungsgebiete:  

Cancer

GP130-IN-1 (compound 49) is a potent GP130 inhibitor with significant in vitro antitumor activity and higher selectivity than Bazedoxifene (HY-A0031). GP130-IN-1 induces ultrastructural changes in cells, causing cell cycle arrest in the G0/G1 phase in a time-dependent manner and triggering apoptosis and autophagy. GP130-IN-1 can be used in the study of triple-negative breast cancer .
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Art. -Nr.: HY-148695B
Target:  

Interleukin Related

Forschungsgebiete:  

Inflammation/Immunology

ADR58 sodium is a highly potent and selective human oncostatin M (OSM) antagonist, which can prevent the binding of OSM to the gp130 receptor and specifically antagonize OSM-mediated signaling. ADR58 sodium can be used in the research of rheumatoid arthritis related diseases .
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Art. -Nr.: HY-P991602
Synonyms: TZLS-501

Target:  

Interleukin Related

Forschungsgebiete:  

Cancer

NI-1201 is a monoclonal antibody that targets, in the human IL-6R sequence, the epitope recognized by 25F10 for mice. NI-1201 inhibits both IL-6 cis- and trans-signaling. NI-1201 targets site IIb of hIL-6R. NI-1201 inhibits gp130 binding to IL-6R .
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Art. -Nr.: HY-RS06778
Forschungsgebiete:  

Others

IL6ST Human Pre-designed siRNA Set A contains three designed siRNAs for IL6ST gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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