116 Results for "

joint

" in MedChemExpress (MCE) Product Catalog:
Products (116)

116 Results for "joint" in MCE Product Catalog:

Cat. No.: HY-P4096C
Target:  

Inhibitory Antibodies

Research Areas:  

Inflammation/Immunology

Cys-scHAP-1 is an N-terminal cysteine-labeled disordered peptide of HAP-1. Cys-scHAP-1 can be used to construct scHAP-1-targeted liposomes, which bind to human and rabbit fibroblast-like synoviocytes and localize to inflamed joints in vivo in a rat adjuvant-induced arthritis model. Cys-scHAP-1 is applicable to arthritis research .
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Cat. No.: HY-FL0006
Target:  

Others

Research Areas:  

Inflammation/Immunology

BDDE-crosslinked sodium hyaluronate solution is mainly composed of BDDE (1,4‑butanediol diglycidyl ether). Its molecular weight and viscoelasticity are similar to those of normal joint synovial fluid. It can be used as a temporary substitute and supplement for joint fluid, alleviating pain in patients with knee osteoarthritis and improving the function of the knee joint.
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Cat. No.: HY-114848
CAS No.: 60414-06-4
Synonyms: SM1213 hydrochloride; Therafectin hydrochloride
Target:  

Others

Research Areas:  

Others

Amiprilose (SM1213) hydrochloride is a novel synthetic carbohydrate with anti-inflammatory and immunomodulatory properties, which can restore the number of painful and swollen joints, joint pain and swelling index, and grip strength to baseline levels.
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Cat. No.: HY-P4096A
Target:  

Inhibitory Antibodies

Research Areas:  

Inflammation/Immunology

Cys-HAP-1 is a synovium-homing peptide that specifically binds to human and rabbit fibroblast-like synoviocytes, and does not bind to human umbilical vein endothelial cells regardless of TNF-α treatment. Cys-HAP-1 enables targeted drug delivery to inflamed joints after conjugation with liposomes loaded with anti-arthritic agents. Cys-HAP-1 can be used in studies related to adjuvant arthritis .
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Cat. No.: HY-N20132
Category:  

Extract

Target:  

Others

Vitex negundo seed extract is an extract of Vitex negundo used in research on rheumatism and joint inflammation.
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Cat. No.: HY-N20206
Category:  

Extract

Target:  

Others

Rhizoma anemones raddeanae extract is an extract of Anemone raddeana Regel, used in research on joint pain and ulcer pain.
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Cat. No.: HY-N19856
CAS No.: 1032964-19-4
Millettiaspecoside A is a phenolic glycoside found in the caulis of Millettia speciosa. Millettiaspecoside A can be used in research related to joint pain .
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Cat. No.: HY-10794R
CAS No.: 915191-42-3
MF498 (Standard) is the analytical standard of MF498 (HY-10794). This product is intended for research and analytical applications. MF498 is a selective and orally active E prostanoid Receptor 4 (EP4) antagonist with a Ki value of 0.7 nM. MF498 can be used in the research of inflammation, such as rheumatoid and osteoarthritis .
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Cat. No.: HY-N18668
CAS No.: 84775-52-0
Category:  

Extract

Target:  

Bacterial

Curcuma longa extract is derived from the rhizome of the turmeric plant (Curcuma longa), and its active ingredient is curcumin. Curcuma longa extract can be used in research on diseases such as arthritis, joint pain, and muscle soreness.
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Cat. No.: HY-L210
2,023 compounds

Rheumatoid Arthritis (RA) is a autoimmune disease characterized by persistent joint inflammation. The pathology of RA includes immune cell infiltration, synovial lining proliferation, pannus formation, and the destruction of joint cartilage and bone, which is highly disabling. Due to long-term chronic inflammation, RA not only severely affects the quality of life of patients but can also damage multiple organs, leading to lung diseases, cardiovascular diseases, and malignant tumors. The pathogenesis of RA is complex, involving genetic, environmental, and immune factors. With the advancement of high-throughput screening technology, screening for compounds targeting JAK, CCR, MEK, MMP targets may contribute to the development of more effective drugs against Rheumatoid Arthritis (RA).

MCE has collected 2,023 small molecule compounds with definite or potential anti-rheumatoid arthritis activity. This library is of significant value for researching the anti-RA drugs.

Cat. No.: HY-111970
CAS No.: 869796-50-9
SAR113945 is a highly selective IKK-β inhibitor with an IC50 value of 0.4 nM. SAR113945 blocks the canonical NFκB signaling pathway. SAR113945 alleviates hyperalgesia to heat and mechanical stimuli, and exerts effects in a zymosan-induced knee joint inflammation model. SAR113945 is applicable to research related to symptomatic knee osteoarthritis .
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Cat. No.: HY-208740
CAS No.: 2488951-93-3
Target:  

PKC

Research Areas:  

Inflammation/Immunology

PKCζ-IN-2 is an orally active, selective PKCζ inhibitor with an IC50 of 0.1 nM. As an anti-inflammatory agent, PKCζ-IN-2 reduces joint swelling and ameliorates disease progression in a mouse collagen-induced arthritis model. PKCζ-IN-2 can be used for the research of rheumatoid arthritis .
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Cat. No.: HY-111970B
CAS No.: 899418-65-6
SAR113945 monopotassium is a highly selective IKK-β inhibitor with an IC50 value of 0.4 nM. SAR113945 monopotassium blocks the canonical NFκB signaling pathway. SAR113945 monopotassium alleviates hyperalgesia to heat and mechanical stimuli, and exerts effects in a zymosan-induced knee joint inflammation model. SAR113945 monopotassium is applicable to research related to symptomatic knee osteoarthritis .
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Cat. No.: HY-D3200
CAS No.: 3112200-59-3
Dns-LLC is a cell-permeable Cu +-selective fluorescent probe that forms a 1:1 complex with Cu +. The thiol group of Dns-LLC plays a key binding role, while the sulfonamide and amide groups jointly contribute to the stabilization of the complex. Upon binding to Cu + in aqueous buffer solutions, Dns-LLC generates a turn-on fluorescence response, which can be used for the detection of Cu + in the Golgi apparatus .
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Cat. No.: HY-P11626
CAS No.: 67943-21-9
Target:  

Collagen

Research Areas:  

Metabolic Disease

Cyclo(Ala-Hyp) is an orally effective collagen-derived hydroxyproline-containing cyclic dipeptide that can be isolated from the culture supernatant of Lactobacillus plantarum. Cyclo(Ala-Hyp) has an AUC0-6h of 2.350 μg/mL·h, significantly higher than traditional collagen oligopeptides. Cyclo(Ala-Hyp) can be used in research related to liver and kidney function protection, skin care, and joint health.
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Cat. No.: HY-P992358

Target:  

ADAMTS

Research Areas:  

Cardiovascular Disease

GSK2394002 is an antibody inhibitor targeting ADAMTS-4 and ADAMTS-5, with cartilage-penetrating ability following systemic administration. GSK2394002 inhibits the release of aggrecan-derived neoepitopes and reduces cartilage degradation, exhibiting the potential to relieve pain, alleviate hyperalgesia and inhibit the progression of joint damage. GSK2394002 also induces potentially irreversible cardiovascular effects such as increased mean arterial pressure and myocardial ischemia in cynomolgus monkeys .
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Cat. No.: HY-182359
CAS No.: 2763672-36-0
Target:  

JAK STAT

Research Areas:  

Inflammation/Immunology

YYSW001 is a selective and orally acrive JAK1 inhibitor with an IC50 of 6 nM and a Kd of 32.32 μM. YYSW001 blocks JAK1-dependent phosphorylation of STAT6, as well as IL-6-induced phosphorylation of STAT3. YYSW001 suppresses pro-inflammatory cytokine levels, reduces paw swelling, lowers clinical arthritis scores, alleviates joint damage and decreases bone loss. YYSW001 is applicable for the research of rheumatoid arthritis .
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Cat. No.: HY-165564
CAS No.: 113759-19-6
Target:  

Drug Derivative

Research Areas:  

Inflammation/Immunology

SM-8849 is a thiazole derivative with anti-arthritis activity. SM-8849 specifically targets and inactivates T cells involved in delayed-type hypersensitivity (DTH) reactions, thereby inhibiting the core immunopathological process of arthritis, but has little effect on the humoral immune process such as antibody production. In a mouse arthritis model induced by Type II Collagen (HY-NP003), SM-8849 significantly alleviated clinical symptoms, reduced bone destruction and joint damage. SM-8849 can be used for the study of autoimmune diseases such as rheumatoid arthritis .
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Cat. No.: HY-178230
CAS No.: 951015-69-3
Target:  

P2X Receptor Apoptosis

Research Areas:  

Inflammation/Immunology

EVT-401 is an orally active, potent and highly selective human P2X7R antagonist, with an IC50 of 10 nM and a Ki of 7.6 nM for human P2X7R, and an IC50 of 220 nM for mouse P2X7R. EVT-401 promotes apoptosis and induces cell cycle arrest in human rheumatoid arthritis synovial fibroblasts (RA SF), reduces the production of proinflammatory and joint-destructive mediators, and mitigates aggressive phenotypes. EVT-401 exhibits favorable oral bioavailability and a good safety profile, making it suitable for research into rheumatoid arthritis .
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Cat. No.: HY-180782
Triphenyltin(IV) diisopropyl dithiocarbamate (Compound OC2) is an anti-leukemia agent. Triphenyltin(IV) diisopropyl dithiocarbamate exhibits extremely strong cytotoxicity towards Jurkat cells, with an IC₅₀ value of 0.1 μM. Triphenyltin(IV) diisopropyl dithiocarbamate causes DNA damage, which subsequently leads to mitochondrial dysfunction, a large amount of ROS production, and ultimately results in the activation of the mitochondrial apoptosis pathway (involving the activation of Caspase-9/-3) and the G0/G1 phase cell cycle arrest, all of which jointly lead to the death of leukemia cells .
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