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Urotensin I acetate (83930-33-0 Free base)

Catalog No. TP1199L

Urotensin I acetate, a CRF-like neuropeptide, acts as an agonist of CRF receptor with pEC50s of 11.46, 9.36 and 9.85 for human CRF1, human CRF2 and rat CRF2α receptors in CHO cells, and Kis of 0.4, 1.8, and 5.7 nM for hCRF1, rCRF2α and mCRF2β receptors, respectively[1][2].

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
Urotensin I acetate (83930-33-0 Free base) Chemical Structure
Urotensin I acetate (83930-33-0 Free base), CAS N/A
Pack Size Availability Price/USD Quantity
1 mg In stock $ 417.00
5 mg In stock $ 988.00
10 mg In stock $ 1,330.00
25 mg In stock $ 1,970.00
50 mg In stock $ 2,660.00
100 mg In stock $ 3,590.00
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Purity: 96.09%
Purity: 95.44%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Urotensin I acetate, a CRF-like neuropeptide, acts as an agonist of CRF receptor with pEC50s of 11.46, 9.36 and 9.85 for human CRF1, human CRF2 and rat CRF2α receptors in CHO cells, and Kis of 0.4, 1.8, and 5.7 nM for hCRF1, rCRF2α and mCRF2β receptors, respectively[1][2].
In vitro Urotensin I acetate is 2-3 times more potent than CRF or sauvagine in stimulating ACTH release from a superfused goldfish anterior pituitary cell column[3]. Rat tail artery strips were incubated in the presence of 4 x 10(-3) M theophylline and Urotensin I acetate. At the concentrations of 1.50, 7.50 mU/ml but not of 0.75 mU/ml Urotensin I acetate, the content of cAMP increased significantly[4].
In vivo Intraperitoneal injections of urotensin I acetate, a CRF-like neuropeptide isolated from the caudal neurosecretory system of the teleost Catostomus commersoni, ovine CRF and sauvagine all produced significant increases in circulating levels of plasma cortisol in goldfish in which endogenous ACTH secretion was suppressed with betamethasone[3]
Molecular Weight N/A

Storage

keep away from moisture

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. Smart D, et al. Characterisation using microphysiometry of CRF receptor pharmacology. Eur J Pharmacol. 1999 Aug 27;379(2-3):229-35. 2. Reul JM, et al. Corticotropin-releasing factor receptors 1 and 2 in anxiety and depression. Curr Opin Pharmacol. 2002 Feb;2(1):23-33. 3. Fryer J, et al. Urotensin I, a CRF-like neuropeptide, stimulates acth release from the teleost pituitary. Endocrinology. 1983;113(6):2308-2310. 4. Gerritsen ME, et al. Urotensin I effects on intracellular content of cyclic AMP in the rat tail artery. Eur J Pharmacol. 1979;60(2-3):211-220.

Related compound libraries

This product is contained In the following compound libraries:
Peptide Compound Library

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Keywords

Urotensin I acetate (83930-33-0 Free base) GPCR/G Protein CRFR Urotensin I acetate (83930330 Free base) Urotensin I acetate (83930 33 0 Free base) 83930-33-0 Free base Urotensin I Acetate 83930-33-0 inhibitor inhibit

 

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