- Signaling Pathways
- Metabolic Enzyme/Protease
- 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 (335)
Related Products (335)
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Recombinant Proteins (22)
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Antibodies (3)
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Abz-SDK(Dnp)P-OH
0 ImagesAbz-SDK(Dnp)P-OH is a fluorescence peptide. Abz-SDK(Dnp)P-OH is the substrate of angiotensin I-converting enzyme (ACE). Abz-SDK(Dnp)P-OH has fluorescent donor-acceptor pair Abz and Dnp (2,4-dinitrophenyl). -
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N-Acetyl-Ser-dAsp-Lys-Pro
0 ImagesSynonyms: Ac-SdKPN-Acetyl-Ser-dAsp-Lys-Pro, an endogenous tetrapeptide secreted by bone marrow, is a specific substrate for the N-terminal site of ACE. -
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(R)-MLN-4760
0 Images(R)-MLN-4760, the R-enantiomer of MLN-4760, is an ACE2 inhibitor, with an IC50 of 8.4 μM. (R)-MLN-4760 is the less active isomer. -
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H-Ile-Trp-OH
0 ImagesSynonyms: Ile-TrpH-Ile-Trp-OH (Ile-Trp), a dipeptide, is an angiotensin-converting enzyme (ACE) inhibitor with an IC50 of 0.7 μM. H-Ile-Trp-OH inhibits predominantly the C-domain of ACE. -
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Delapril hydrochloride
0 ImagesDelapril hydrochloride is an angiotensin-converting enzyme (ACE) inhibitor for the treatment of cardiovascular diseases. -
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Abz-LFK(Dnp)-OH
0 ImagesAbz-LFK(Dnp)-OH is an angiotensin I-converting enzyme (ACE) peptide substrate. Abz-LFK(Dnp)-OH is selective for the C domain of ACE. Abz-LFK(Dnp)-OH can be used to assess ACE activity. -
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Ramipril-d5
0 ImagesSynonyms: HOE-498-d5Ramipril-d5 is the deuterium labeled Ramipril. Ramipril (HOE-498) is an angiotensin-converting enzyme (ACE) inhibitor with IC50 of 5 nM. -
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2-(Methylamino)ethanol
0 Images2-(Methylamino) ethanol (N-Methylethanolamine) is an orally active Phospholipase D inhibitor and analog of Ethanolamine (HY-Y0524). 2-(Methylamino) ethanol reduces the mRNA levels of ACE, ppET-1 and ECE-1, and inhibits MMP-2 activity. 2-(Methylamino) ethanol inhibits Collagen synthesis. 2-(Methylamino) ethanol attenuates ventricular hypertrophy, prevents increased myocardial stiffness and hemodynamic deterioration. 2-(Methylamino) ethanol can capture industrial acid gases and react with carbon dioxide to form carbamates and bicarbonates. 2-(Methylamino) ethanol can be used in studies related to hypertensive heart failure (diastolic heart failure). -
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(±)8(9)-EpETE
0 ImagesSynonyms: (±)8,9-EEQ; (±)8,9-epoxy Eicosatetraenoic acidEicosapentaenoic acid (EPA) is converted to epoxyeicosatetraenoic acids (EpETEs) by several cytochrome P450 isoforms. The major product of this epoxygenase pathway, (±)17(18)-EpETE, relaxes vascular and airway smooth muscle by activating large conductance Ca2+-activated K+ (BKCa) channels by directly interacting with BKα channel subunits. (±)8(9)-EpETE is an epoxygenase pathway product produced from EPA by CYP450 both in vitro and in vivo. -
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H-Trp-Phe-OH
0 ImagesH-Trp-Phe-OH (Trp-Phe) is an ACE inhibitor and endothelial function regulator, with an ACE IC50 of 0.318 mg/mL. H-Trp-Phe-OH increases nitric oxide concentration, reduces endothelin-1 (ET-1) levels, and reverses norepinephrine-mediated endothelial cell dysfunction. H-Trp-Phe-OH exhibits antihypertensive activity. H-Trp-Phe-OH can be used in studies related to hypertension and atherosclerosis. -
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Benazeprilat
0 ImagesSynonyms: CGS 14831Benazeprilat is an orally active and the active metabolite of benazepril, a carboxyl-containing ACE inhibitor with antihypertensive activity. Benazepril is a well-established antihypertensive agent, both in monoresearch and in combination with other classes of drugs including thiazide diuretics and calcium channel blockers. Benazepril is a first-line research in reducing various pathologies associated with CV risk and secondary end-organ damage. -
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Ramiprilat-d5
0 ImagesRamiprilat-d5 is deuterium labeled Ramiprilat. Ramiprilat (HOE 498 diacid), an active metabolite of Ramipril, is a potent and orally active angiotensin converting enzyme (ACE) inhibitor with a Ki value of 7 pM. Ramiprilat can be used for high blood pressure and heart failure research. -
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H-Pro-Phe-OH
0 ImagesSynonyms: Pro-PheH-Pro-Phe-OH is a dipeptide containing proline and phenylalanine, which can serve as a substrate for prolinase. H-Pro-Phe-OH can also be used for polypeptide synthesis, where phenylalanine is an aromatic amino acid that can inhibit the activity of Angiotensin-converting enzyme (ACE, HY-P2983). -
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Enalaprilat-d5
0 ImagesSynonyms: MK-422 d5Enalaprilat-d5 is the deuterium labeled Enalaprilat(MK-422), which is an angiotensin-converting enzyme (ACE) inhibitor. -
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Trandolaprilate
0 ImagesCat. No.: HY-A0116CAS No.: 87679-71-8Synonyms: Trandolaprilat; RU 44403Trandolaprilate is a potent angiotensin-converting enzyme (ACE) inhibitor. Trandolaprilate partially inhibits angiotensin-I-mediated c-fos induction. Trandolaprilate is main bioactive metabolite of Trandolapril. Trandolaprilate shows high lipophilicity. -
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- DX600 TFA
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Oleacein
0 ImagesCat. No.: HY-N8630CAS No.: 149183-75-5Oleacein (Compound 9) is an ACE inhibitor that can be isolated from J. grandiflorum. Oleacein is orally active and can be used in the study of metabolic and cardiovascular diseases. -
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Sinapinic acid (Standard)
0 ImagesSynonyms: Sinapic acid (Standard)Sinapinic acid (Sinapic acid) is a phenolic compound isolated from Hydnophytum formicarum Jack. Rhizome, acts as an inhibitor of HDAC, with an IC50 of 2.27 mM, and also inhibits ACE-I activity. Sinapinic acid posssess potent anti-tumor activity, induces apoptosis of tumor cells. Sinapinic acid shows antioxidant and antidiabetic activities. Sinapinic acid reduces total cholesterol, triglyceride, and HOMA-IR index, and also normalizes some serum parameters of antioxidative abilities and oxidative damage in ovariectomized rats. -
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Nicotianamine
0 ImagesCat. No.: HY-121858CAS No.: 34441-14-0Nicotianamine can be isolated from the leaves of Nicotiana Tabacum L.. Nicotianamine is a key biosynthetic precursor of phytosiderophores. Nicotianamine is an iron chelating agent and can promote the transport of iron. Nicotianamine is an angiotensin-converting enzyme (ACE) inhibitor with IC50 values of 76 nM and 59 nM for rhACE2 and rhACE, respectively. Nicotianamine is vital in metal nutrition and metal homeostasis of flowering plants. -
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Lyciumin A
0 ImagesLyciumin A, a cyclic octapeptide, exhibits inhibitory activity on proteases, renin and angiotensin-converting enzyme. Lyciumin A can be used for the research of hypertension. -
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