11000-17-2

11000-17-2 structure

Name: Vasopressin
Chemical Name: Vasopressin
CAS Number: 11000-17-2
Molecular Formula: C₄₃H₆₇N₁₅O₁₂S₂
Molecular Weight: 1050.22000
Catalog: API Hormone and endocrine-regulating drugs Pituitary hormone
Create Date: 2018-09-02 13:36:26
Modify Date: 2024-01-05 17:25:05
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].

Name	Vasopressin
Synonyms	pituitrin EINECS 200-050-5 VASOPRESSIN ACETATE MFCD03839092 vasophysin leiormone tonephin VASOPRASSIN adh(hormone) pitressin

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].
Related Catalog	Research Areas >> Neurological Disease
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	[1]. Baribeau DA, et, al. Oxytocin and vasopressin: linking pituitary neuropeptides and their receptors to social neurocircuits. Front Neurosci. 2015 Sep 24;9:335. [2]. Ramos L, et, al. Acute prosocial effects of oxytocin and vasopressin when given alone or in combination with 3,4-methylenedioxymethamphetamine in rats: involvement of the V1A receptor. Neuropsychopharmacology. 2013 Oct;38(11):2249-59. [3]. Gal CSL, et, al. Characterization of (2S,4R)-1-[5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-methoxy-phenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-N,N-dimethyl-2-pyrrolidine carboxamide (SSR149415), a selective and orally active vasopressin V1b receptor antagonist. J Pharmacol Exp Ther. 2002 Mar;300(3):1122-30.

Molecular Formula	C₄₃H₆₇N₁₅O₁₂S₂
Molecular Weight	1050.22000
Exact Mass	1049.45000
PSA	505.74000
LogP	1.50910

CHEMICAL IDENTIFICATION

RTECS NUMBER :: YW8200000

CHEMICAL NAME :: Vasopressin

CAS REGISTRY NUMBER :: 11000-17-2

LAST UPDATED :: 199504

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 220 iu/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 13,415,1963 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X4661 No. of Facilities: 114 (estimated) No. of Industries: 1 No. of Occupations: 4 No. of Employees: 3153 (estimated) No. of Female Employees: 1738 (estimated)

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