- Signaling Pathways
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- Angiotensin-converting Enzyme (ACE)
Angiotensin-converting Enzyme (ACE)
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Angiotensin-converting Enzyme (ACE) Inhibitors
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Angiotensin-converting Enzyme (ACE) Antagonist
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Angiotensin-converting Enzyme (ACE) Activators
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Angiotensin-converting Enzyme (ACE) Modulator
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Angiotensin-converting Enzyme (ACE) Chemical
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Angiotensin-converting Enzyme (ACE) Control
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Angiotensin-converting Enzyme (ACE) Substrates
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ACE/CD143 Proteins
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Angiotensin-Converting Enzyme 2 (ACE2) Proteins
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Angiotensin-converting Enzyme (ACE) Related Products (342)
Related Products (342)
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Recombinant Proteins (22)
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Antibodies (3)
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Imidapril hydrochloride (Standard)
0 ImagesSynonyms: TA-6366 (Standard)Imidapril (hydrochloride) (Standard) is the analytical standard of Imidapril (hydrochloride). This product is intended for research and analytical applications. Imidapril hydrochloride (TA-6366) is an orally active dual inhibitor of angiotensin-converting enzyme (ACE) and MMP-9. Imidapril hydrochloride inhibits lipopolysaccharide-induced phosphorylation of c-Jun, MKK4 and JNK in monocytes, and downregulates the production of specific inflammatory factors such as TNF-α and IP-10, thereby exerting anti-inflammatory activity. Imidapril hydrochloride also effectively ameliorates mesangial expansion and reduces urinary albumin excretion by inhibiting angiotensin AngII production, lowering glomerular pressure and oxidative stress, thus delaying disease progression. Imidapril hydrochloride can also directly bind to the active site of MMP-9 to inhibit gelatinase activity, and suppress the enlargement of cerebral aneurysms without altering systemic blood pressure. Imidapril hydrochloride is widely applicable to related studies on autoimmune glomerulonephritis, diabetic nephropathy, cerebral aneurysms and other conditions. -
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MB-32
0 ImagesCat. No.: HY-184485MB-32 is a potent and selective allosteric inhibitor of human angiotensin-converting enzyme 2 (hACE2) with a Kd value of 7.078 μM. MB-32 binds to a non-catalytic surface pocket on the N-terminal helix of ACE2, disrupts the interaction between ACE2 and the receptor-binding domain of SARS-CoV-2 spike protein through allosteric action, and preserves the enzymatic activity of ACE2 across different species. MB-32 achieves high concentrations in the airway via intranasal administration, with no detected cardiovascular toxicity. MB-32 can be used for research on coronavirus disease 2019. -
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