34 Results for "

urotensin

" in MedChemExpress (MCE) Product Catalog:
Products (34)

34 Results for "urotensin" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-10655
CAS No.: 540769-28-6
Purity:  99.78%
Synonyms: ACT-058362
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

Palosuran (ACT-058362) is a potent, selective, and orally active antagonist of urotensin II receptor, with an IC50 of 3.6 nM for CHO cell membranes expressing human recombinant receptors. Palosuran can improves pancreatic and renal function in diabetic rats .
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4
4 Cited Publications
Cat. No.: HY-10655A
CAS No.: 2469274-58-4
Purity:  98.67%
Synonyms: ACT-058362 hydrochloride
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

Palosuran hydrochloride (ACT-058362 hydrochloride) is a potent, selective, and orally active antagonist of urotensin II receptor, with an IC50 of 3.6 nM for CHO cell membranes expressing human recombinant receptors. Palosuran hydrochloride can improves pancreatic and renal function in diabetic rats .
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Cat. No.: HY-10656
CAS No.: 474960-44-6
Purity:  99.84%
Target:  

Urotensin Receptor

Research Areas:  

Inflammation/Immunology

SB-657510 is a selective urotensin II (UII) receptor (UT) antagonist. The Ki values are 61, 17, 30, 65 and 56 nM for human, monkey, cat, rat and mouse receptors, respectively. SB-657510 exerts anti-inflammatory effects by inhibiting UII-induced upregulation of inflammatory mediators such as adhesion molecules, cytokines, and tissue factor in human vascular endothelial cells .
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Cat. No.: HY-P1164A
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

Urotensin II (114-124), human TFA, an 11-amino acid residue peptide, is a potent vasoconstrictor and agonist for the orphan receptor GPR14.
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Cat. No.: HY-P1165
CAS No.: 342878-90-4
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

Urotensin II-related peptide is a human urotensin II anague. Urotensin II-related peptide has high affinity for the UT receptor .
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Cat. No.: HY-10664
CAS No.: 345892-71-9
Purity:  99.31%
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

SB-611812 is a urotensin II receptor (UTR) antagonist with the potential in the research of cardiovascular disease .
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Cat. No.: HY-10657
CAS No.: 733734-61-7
Purity:  99.08%
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease Others

SB-706375 is an antagonist of the Urotensin II (UII) receptor. By blocking the Urotensin II receptor, SB-706375 reduces the kidney's response to UII and Urotensin-related peptide (URP) and significantly increases the Glomerular Filtration Rate (GFR). SB-706375 can be used in research on kidney diseases and hypertension .
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Cat. No.: HY-P1483A
Urotensin II, mouse TFA is an endogenous ligand for the orphan G-protein-coupled receptor GPR14 or SENR. Urotensin II, mouse TFA is a potent vasoconstrictor. Urotensin II, mouse TFA plays a physiological role in the central nervous system .
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Cat. No.: HY-P3957
CAS No.: 9047-55-6
Target:  

Urotensin Receptor

Research Areas:  

Others

Urotensin II, teleost fish is a cyclic peptide. It can be isolated from the caudal neurosecretory system of teleost fish .
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Cat. No.: HY-108446
CAS No.: 1003878-07-6
Purity:  ≥99.0%
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

GSK 1562590 hydrochloride is a high affinity and selective antagonist of urotensin-II receptor (UT), with pKis of 9.14-9.66 for mammalian recombinant (mouse, rat, cat, monkey, human) and native UT .
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Cat. No.: HY-P1542
CAS No.: 83930-33-0
Synonyms: Catostomus urotensin I
Target:  

CRFR

Urotensin I (Catostomus urotensin I), 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 CRF receptors in CHO cells, and Kis of 0.4, 1.8, and 5.7 nM for hCRF1, rCRF and mCRF receptors, respectively .
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Cat. No.: HY-P1542B
Synonyms: Catostomus urotensin I TFA
Target:  

CRFR

Urotensin I (Catostomus urotensin I) TFA, 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 CRF receptors in CHO cells, and Kis of 0.4, 1.8, and 5.7 nM for hCRF1, rCRF and mCRF receptors, respectively .
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Cat. No.: HY-P1164
CAS No.: 251293-28-4
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

Urotensin II (114-124), human, an 11-amino acid residue peptide, is a potent vasoconstrictor and agonist for the orphan receptor GPR14.
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Cat. No.: HY-P1168
CAS No.: 479065-85-5
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

[Orn8]-Urotensin II (human), a peptide analog of urotensin II, is a UT receptor agonist. [Orn8]-Urotensin II (human) increases intracellular calcium levels in HEK293 .
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Cat. No.: HY-108055
CAS No.: 669089-53-6
Research Areas:  

Cardiovascular Disease

Urantide is a selective and competitive urotensin-II (UT) receptor antagonist peptide (pKB=8.3) that blocks human urotensin-II (hU-II)-induced contractions in rat thoracic aorta ex vivo. Urantide can be used to study the (patho)physiological role of hU-II in the mammalian cardiovascular system .
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Cat. No.: HY-P1166
CAS No.: 879497-82-2
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

UFP-803 is a potent urotensin-II receptor (UT) ligand. UFP-803 has lower residual agonist activity, so it may be an important tool for the investigations on the role played by the UT system in physiology and pathology .
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Cat. No.: HY-P1483B
Urotensin II, mouse acetate is an endogenous ligand for the orphan G-protein-coupled receptor GPR14 or SENR. Urotensin II, mouse acetate is a potent vasoconstrictor. Urotensin II, mouse acetate plays a physiological role in the central nervous system .
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Cat. No.: HY-P1483
CAS No.: 405137-01-1
Urotensin II, mouse is an endogenous ligand for the orphan G-protein-coupled receptor GPR14 or SENR. Urotensin II, mouse is a potent vasoconstrictor. Urotensin II, mouse plays a physiological role in the central nervous system .
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Cat. No.: HY-10672
CAS No.: 1034708-07-0
Urotensin-II receptor antagonist-1 (compound 1) is a low oral bioavailability (F=0-3%, rat) selective human Urotensin II receptor antagonist, Ki=16 nM (test on HEK293 cells expressing recombinant human UT receptor). Urotensin-II receptor antagonist-1 inhibits cytochrome P450 (IC50=0.75 μM, CYP2D6; 1.4 μM, CYP3A4), inhibits κ-opioid receptor (EC50=3.2 μM), targets cardiac sodium channels (Ki=2.5 μM) .
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Cat. No.: HY-10666
CAS No.: 346729-66-6
Target:  

Urotensin Receptor

Research Areas:  

Cardiovascular Disease

SB-436811 is a human urotensin-II receptor antagonist with a pKi value of 6.7 .
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