Vasopressin structure
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Common Name | Vasopressin | ||
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CAS Number | 11000-17-2 | Molecular Weight | 1050.22000 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C43H67N15O12S2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of VasopressinVasopressin is a cyclic nonapeptide that is synthesized centrally in the hypothalamus. Vasopressin participates in the hypothalamic-pituitary-adrenal axis, and regulates pituitary corticotropin secretion by potentiating the stimulatory effects of corticotropin releasing factor. Vasopressin also can act as a neurotransmitter, exerting its action by binding to specific G protein-coupled receptors[1][2][3]. |
Name | Vasopressin |
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Synonym | More Synonyms |
Description | Vasopressin is a cyclic nonapeptide that is synthesized centrally in the hypothalamus. Vasopressin participates in the hypothalamic-pituitary-adrenal axis, and regulates pituitary corticotropin secretion by potentiating the stimulatory effects of corticotropin releasing factor. Vasopressin also can act as a neurotransmitter, exerting its action by binding to specific G protein-coupled receptors[1][2][3]. |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
In Vitro | AVP (0.01 nM-1 μM) induces Ca2+ increase in Chinese hamster ovary cells expressing rat or human V1b receptors[2]. |
In Vivo | Vasopressin (0.03-0.3 μg/kg; i.p.) potentiates corticotropin release provoked by exogenous corticoliberin and increases corticotropin secretion subsequent to body water loss[2]. Vasopressin (0.001-0.1 mg/kg; i.p.) potently increases adjacent lying, where rats meeting for the first time lie passively next to each other[3]. |
References |
Molecular Formula | C43H67N15O12S2 |
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Molecular Weight | 1050.22000 |
Exact Mass | 1049.45000 |
PSA | 505.74000 |
LogP | 1.50910 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
pituitrin |
EINECS 200-050-5 |
VASOPRESSIN ACETATE |
MFCD03839092 |
vasophysin |
leiormone |
tonephin |
VASOPRASSIN |
adh(hormone) |
pitressin |