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ACE-2: Small Molecules and Peptides

Angiotensin converting enzyme 2 (ACE-2), also known as ACEH (ACE homolog), is an integral membrane protein and a zinc metalloprotease of the ACE family. The predicted human ACE-2 protein sequence consists of 805 amino acids, including a N-terminal signal peptide, a single catalytic domain, a C-terminal membrane anchor, and a short cytoplasmic tail. ACE-2 cleaves angiotensins I and II as a carboxypeptidase.

ACE-2 also serves as the receptor for the SARS-CoV and SARS-CoV-2 viruses. The binding of the S1 domain of the SARS Coronavirus Spike protein to ACE-2 initiates viral entry into the host cell. Recently, this interaction between SARS-CoV-2 and ACE-2 has become an area of intense therapeutic interest to develop treatments against COVID-19.

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9 results for "ACE-2 Small Molecules and Peptides" in Products

9 results for "ACE-2 Small Molecules and Peptides" in Products

ACE-2: Small Molecules and Peptides

Angiotensin converting enzyme 2 (ACE-2), also known as ACEH (ACE homolog), is an integral membrane protein and a zinc metalloprotease of the ACE family. The predicted human ACE-2 protein sequence consists of 805 amino acids, including a N-terminal signal peptide, a single catalytic domain, a C-terminal membrane anchor, and a short cytoplasmic tail. ACE-2 cleaves angiotensins I and II as a carboxypeptidase.

ACE-2 also serves as the receptor for the SARS-CoV and SARS-CoV-2 viruses. The binding of the S1 domain of the SARS Coronavirus Spike protein to ACE-2 initiates viral entry into the host cell. Recently, this interaction between SARS-CoV-2 and ACE-2 has become an area of intense therapeutic interest to develop treatments against COVID-19.

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Potent vasoconstrictor peptide

HIF-PH inhibitor; erythropoietic

Pan-histone deacetylase inhibitor

Highly potent inhibitor of SARS-CoV Spike (S) protein and ACE2 interaction

Potent and selective angiotensin-converting enzyme 2 (ACE2) inhibitor

Endogenous precursor to angiotensin II (Cat. No. 1158)

Antibiotic; inhibits 50S ribosomal subunit formation and elongation at transpeptidation

Potent TRPV1 antagonist; also antioxidant; activates Nrf2/ARE signaling

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