Hemopressin(rat) structure
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Common Name | Hemopressin(rat) | ||
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CAS Number | 568588-77-2 | Molecular Weight | 1088.26000 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C53H77N13O12 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Hemopressin(rat)Hemopressin(rat) is a nonapeptide derived from the α1-chain of hemoglobin, is originally isolated from rat brain homogenates. Hemopressin(rat) is orally active, selective and inverse agonist of CB1 cannabinoid receptors. Hemopressin(rat) exerts antinociceptive action in inflammatory pain models[1][2]. |
Name | pvnfkflsh |
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Synonym | More Synonyms |
Description | Hemopressin(rat) is a nonapeptide derived from the α1-chain of hemoglobin, is originally isolated from rat brain homogenates. Hemopressin(rat) is orally active, selective and inverse agonist of CB1 cannabinoid receptors. Hemopressin(rat) exerts antinociceptive action in inflammatory pain models[1][2]. |
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Related Catalog | |
In Vivo | Hemopressin(rat) causes hypotension in anesthetized rats and is metabolized in vivo and in vitro by endopeptidase 24.15 (EP24.15), neurolysin (EP24.16), and angiotensin-converting enzyme (ACE)[1]. Oral administration of Hemopressin(rat) inhibits mechanical hyperalgesia of CCI-rats up to 6h. Hemopressin(rat) treatment also decreases Egr-1 immunoreactivity (Egr-1Ir) in the superficial layer of the dorsal horn of the spinal cord of CCI rats[2]. |
References |
Molecular Formula | C53H77N13O12 |
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Molecular Weight | 1088.26000 |
Exact Mass | 1087.58000 |
PSA | 400.15000 |
LogP | 2.70800 |
hemopressin |