592 Results for "

RA

" in MedChemExpress (MCE) Product Catalog:
Products (592)

592 Results for "RA" in MCE Product Catalog:

29
29 Publications Verification
Cat. No.: HY-N0142
CAS No.: 60-82-2
Synonyms: NSC 407292; RJC 02792
Phloretin (NSC 407292; RJC 02792) is a flavonoid extracted from Malus pumila Mill.,has anti-inflammatory activities. Phloridzin is a specific,competitive and orally active inhibitor of sodium/glucose cotransporters in the intestine (SGLT1) and kidney (SGLT2). Phloretin inhibits Yeast-made GLUT1 as well as Human erythrocyte GLUT1 with IC50values of 49 μM and 61 μM,respectively .Phloretin has the potential for the treatment of rheumatoid arthritis (RA) and allergic airway inflammation .
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29
29 Publications Verification
Cat. No.: HY-N0142R
CAS No.: 60-82-2
Synonyms: NSC 407292 (Standard); RJC 02792 (Standard)
Phloretin (Standard) is the analytical standard of Phloretin. This product is intended for research and analytical applications. Phloretin (NSC 407292; RJC 02792) is a flavonoid extracted from Malus pumila Mill., has anti-inflammatory activities. Phloridzin is a specific, competitive and orally active inhibitor of sodium/glucose cotransporters in the intestine (SGLT1) and kidney (SGLT2). Phloretin inhibits Yeast-made GLUT1 as well as Human erythrocyte GLUT1 with IC50values of 49 μM and 61 μM, respectively .Phloretin has the potential for the treatment of rheumatoid arthritis (RA) and allergic airway inflammation .
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22
22 Cited Publications
Cat. No.: HY-14531
CAS No.: 201410-53-9
Purity:  99.61%
Synonyms: R115866
Research Areas:  

Inflammation/Immunology

Talarozole (R115866) is an oral systemic all-trans retinoic acid metabolism blocking agent (RAMBA) which increases intracellular levels of endogenous all-trans retinoic acid (RA). Talarozole inhibits both CYP26A1 and CYP26B1 with IC50s of 5.4 and 0.46 nM, respectively.
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9
9 Cited Publications
Cat. No.: HY-P72566
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: IL-1RN; IL-1RA; IRAP; Interleukin-1 Receptor Antagonist Protein
Species:  
Source:  
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8
8 Cited Publications
Cat. No.: HY-15771
CAS No.: 1351636-18-4
Purity:  99.71%
Synonyms: ONO-4059; GS-4059
Target:  

Btk Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Tirabrutinib (ONO-4059) is an orally active Bruton’s Tyrosine Kinase (BTK) inhibitor (can cross the blood-brain barrier (BBB)), with an IC50 of 6.8 nM. Tirabrutinib irreversibly and covalently binds to BTK and inhibits aberrant B cell receptor signaling. Tirabrutinib can be used in studies of autoimmune diseases and hematological malignancies .
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8
8 Cited Publications
Cat. No.: HY-15771A
CAS No.: 1439901-97-9
Purity:  99.66%
Synonyms: ONO-4059 hydrochloride; GS-4059 hydrochloride
Target:  

Btk Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

Tirabrutinib (ONO-4059) hydrochloride is an orally active Bruton’s Tyrosine Kinase (BTK) inhibitor (can cross the blood-brain barrier (BBB)), with an IC50 of 6.8 nM. Tirabrutinib hydrochloride irreversibly and covalently binds to BTK and inhibits aberrant B cell receptor signaling. Tirabrutinib hydrochloride can be used in studies of autoimmune diseases and hematological malignancies .
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7
7 Cited Publications
Cat. No.: HY-15898
CAS No.: 288250-47-5
Purity:  99.03%
Y-320 is a potent, orally active phenylpyrazoleanilide immunomodulator. Y-320 inhibits IL-17 production by CD4 T cells stimulated with IL-15 with IC50 values of 20 to 60 nM. Y-320 enhances TP53, DMD, and COL17A1 PTC readthrough by G418 and increases cellular protein levels and protein synthesis. Y-320 concomitants use of with a low dose of Paclitaxel (HY-B0015) significantly sensitized multidrug resistance (MDR) tumors by inducing G2/M phase arrest and apoptosis. Y-320 can be used for research of rheumatoid arthritis (RA) and cancer .
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5
5 Cited Publications
Cat. No.: HY-P7029
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuIL-1RA; IL-1RN; IRAP
Species:  
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4
4 Cited Publications
Cat. No.: HY-100739
CAS No.: 1617495-03-0
Purity:  99.04%
Target:  

Proteasome

Research Areas:  

Cancer

RA190, a bis-benzylidine piperidon, inhibits proteasome function by covalently binding to cysteine 88 of ubiquitin receptor RPN13.
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4
4 Cited Publications
Cat. No.: HY-50081
CAS No.: 512177-83-2
Target:  

CCR

CCR2-RA-[R] is an allosteric antagonist of the C-C chemokine receptor type 2 (CCR2) with an IC50 of 103 nM.
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4
4 Cited Publications
Cat. No.: HY-10291
CAS No.: 51543-40-9
Purity:  99.58%
Synonyms: (R)-Flurbiprofen; MPC7869
Tarenflurbil ((R)-Flurbiprofen) is the R-enantiomer of the racemate NSAID Flurbiprofen, Tarenflurbil ((R)-Flurbiprofen) inhibits the binding of [ 3H]9-cis-RA to RXRα LBD with IC50 of 75 μM. Tarenflurbil can be used for Alzheimer's disease research.
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4
4 Cited Publications
Cat. No.: HY-P77699
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: IL-15 R alpha; CD215; IL15RA; IL-15RA; IL-15R-alpha1; Interleukin-15; IL-15; IL15
Species:  
Source:  
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4
4 Cited Publications
Cat. No.: HY-N2435
CAS No.: 36700-45-5
[8]-Shogaol, a kind of stimulating compound in ginger, has antiplatelet (IC50=5 μM), anti-cancer and anti-inflammatory activity. [8]-Shogaol inhibited COX-2 (IC50=17.5 μM), which led to the decline of human leukemia cells. 8-Shogaol Selective direction TAK1 sum TAK1-TAB1 (IC50=5 μM), suppress IKK, Akt sum MAPK signal pathway, and reverse synovitis synovial sum Air dampness (RA).
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3
3 Cited Publications
Cat. No.: HY-18099
CAS No.: 878141-96-9
Synonyms: E-52862
Research Areas:  

Neurological Disease

S1RA (E-52862) is a highly selective σ1 receptor (σ1R) antagonist with Kis of 17 nM and 23.5 nM for human σ1R and guinea pig σ1R, respectively. S1RA has Moderate antagonistic activity for human 5-HT2B receptor (Ki= 328 nM). S1RA has antinociceptive effects in neuropathic pain models. S1RA prevents mechanical and cold hypersensitivity in Oxaliplatin (HY-17371)-treated mice .
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3
3 Cited Publications
Cat. No.: HY-18099A
CAS No.: 1265917-14-3
Synonyms: E-52862 hydrochloride
Research Areas:  

Neurological Disease

S1RA (E-52862) hydrochloride is an orally active and selective sigma-1 receptor (σ1R) antagonist with a Ki value of 17 nM. S1RA hydrochloride shows good selectivity against σ2R (Ki >1000 nM). S1RA hydrochloride is a human 5-HT2B receptor antagonist with an IC50 value of 4.7 μM. S1RA hydrochloride inhibits neuropathic pain and activity-induced spinal sensitization .
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3
3 Cited Publications
Cat. No.: HY-P9924
CAS No.: 1143503-69-8
Synonyms: LY2439821

Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology

Ixekizumab (LY2439821) is a humanized IgG4 monoclonal antibody that selectively binds and neutralizes interleukin IL-17A (KD<3 pM). Ixekizumab directly blocks IL-17A binding to IL-17RA (IL-17A receptor) but does not bind to other IL-17 family members. Ixekizumab is used for the research of moderate-to-severe plaque psoriasis .
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3
3 Cited Publications
Cat. No.: HY-P78558
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: IL-15 R alpha; CD215; IL15RA; IL-15RA; IL-15R-alpha1; Interleukin-15; IL-15; IL15
Species:  
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2
2 Cited Publications
Cat. No.: HY-B0524
CAS No.: 5638-76-6
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology Cancer

Betahistine is an orally active histamine H1 receptor agonist and a H3 receptor antagonist . Betahistine is used for the study of rheumatoid arthritis (RA) .
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2
2 Cited Publications
Cat. No.: HY-B0524A
CAS No.: 5579-84-0
Betahistine dihydrochloride is an orally active histamine H1 receptor agonist and a H3 receptor antagonist . Betahistine dihydrochloride is used for the study of rheumatoid arthritis (RA) .
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2
2 Cited Publications
Cat. No.: HY-P990034
CAS No.: 1202526-59-7
Synonyms: MLTA3698A; RG7415; PRO283698

Target:  

Inhibitory Antibodies

Research Areas:  

Inflammation/Immunology

Pateclizumab (MLTA3698A) is a humanized antibody against lymphotoxin α (LTα), a transiently expressed cytokine on activated B and T cells (Th1, Th17), which are implicated in rheumatoid arthritis (RA) pathogenesis .
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