HRG-β1 inhibitors are a specialized class of compounds that act by modulating the activity of the HRG-β1 protein, which is involved in a variety of cellular signaling processes. These inhibitors typically function by binding to the HRG-β1 protein or its associated receptors, disrupting its interaction with other proteins or ligands necessary for its normal activity. Structurally, HRG-β1 inhibitors can range from small molecules to larger, more complex compounds such as peptides. The design of these inhibitors often incorporates key functional groups that enable strong binding interactions, such as hydrogen bonds, van der Waals forces, and electrostatic interactions with the target protein or receptor. This binding blocks HRG-β1's ability to engage in its usual role in signal transduction, thereby inhibiting downstream biological processes associated with its activity.
From a chemical perspective, HRG-β1 inhibitors are optimized for stability and selectivity. They are often engineered to resist degradation under various conditions, including enzymatic or oxidative breakdown, which ensures that they retain their inhibitory function in different environments. These compounds also exhibit diverse physical properties, such as solubility and permeability, which are important considerations for their effective interaction with the HRG-β1 target in biological systems. Additionally, the kinetics of HRG-β1 inhibitors can vary, with some showing rapid, reversible binding, while others form more prolonged, potentially irreversible interactions with their target. These characteristics are fine-tuned through careful chemical synthesis and structural modification to achieve the desired inhibitory effect, with the ultimate goal of efficiently disrupting HRG-β1 activity at a molecular level.
| Produkt | CAS # | Katalog # | Menge | Preis | Referenzen | Bewertung |
|---|---|---|---|---|---|---|
Aspirin | 50-78-2 | sc-202471 sc-202471A | 5 g 50 g | ¥226.00 ¥474.00 | 4 | |
Hemmt die Cyclooxygenase-Enzyme, was sich auf die Entzündungs- und Gerinnungsprozesse auswirken kann. | ||||||
Warfarin | 81-81-2 | sc-205888 sc-205888A | 1 g 10 g | ¥824.00 ¥2775.00 | 7 | |
Hemmt Vitamin-K-abhängige Gerinnungsfaktoren und verändert möglicherweise die Gerinnungswege. | ||||||
Rivaroxaban | 366789-02-8 | sc-208311 | 2 mg | ¥1783.00 | 18 | |
Hemmt direkt den Faktor Xa und beeinflusst möglicherweise die Gerinnungskaskade im Zusammenhang mit der Funktion von HRG-β1. | ||||||
Apixaban | 503612-47-3 | sc-364406 sc-364406A | 10 mg 50 mg | ¥2708.00 ¥7153.00 | 2 | |
Faktor-Xa-Inhibitor, könnte die Thrombinbildung verändern und damit verbundene Signalwege beeinflussen. | ||||||
Clopidogrel | 113665-84-2 | sc-507403 | 1 g | ¥1376.00 | 1 | |
Hemmt den ADP-Rezeptor P2Y12 auf Thrombozyten, was sich möglicherweise auf die Thrombozytenaggregation und damit verbundene Signalwege auswirkt. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | ¥293.00 ¥1343.00 ¥2403.00 | 27 | |
Tyrosinkinase-Inhibitor, könnte Zellsignalwege beeinflussen, die mit Zellwachstum und Zelladhäsion zusammenhängen. | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | ¥1726.00 ¥10583.00 | 5 | |
Hemmt mehrere Rezeptor-Tyrosinkinasen, was sich möglicherweise auf die Angiogenese und die damit verbundene Signalübertragung auswirkt. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | ¥1027.00 ¥1568.00 ¥4219.00 | 36 | |
Glucocorticoid, das die Entzündung moduliert und möglicherweise die Wege der Immunantwort beeinflusst. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | ¥1061.00 ¥2403.00 | 33 | |
Hemmt die Dihydrofolat-Reduktase, was die Zellproliferation und die Immunfunktionen beeinträchtigen kann. | ||||||
hydroxychloroquine | 118-42-3 | sc-507426 | 5 g | ¥643.00 | 1 | |
Moduliert die Immunaktivität und beeinflusst möglicherweise die mit Entzündungen und Autoimmunität zusammenhängenden Signalwege. | ||||||