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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T13272 | UT-155 | Androgen Receptor | |
UT-155 is a selective and potent antagonist of the androgen receptor (AR) (Ki: 267 nM for UT-155 binding to AR-LBD). | |||
T5171 | Treprostinil Sodium | UT-15 | VEGFR , c-RET , Prostaglandin Receptor |
Treprostinil Sodium (UT-15) is a potent DP1, IP and EP2 agonist (EC50: 0.6/1.9/6.2 nM). | |||
T13273 | UT-34 | Androgen Receptor | |
UT-34 is a selective and orally active antagonist of second-generation pan-androgen receptor (AR) and degrader(IC50s of 211.7 nM, 262.4 nM and 215.7 nM for wild-type, F876L and W741L AR, respectively), and has anti-prost... | |||
T23323 | SB 611812 | Neurotensin Receptor | |
SB 611812 is an antagonist of urotensin-II (UT) and can be used in studies about the treatment of cardiovascular disease. | |||
T2058 | Palosuran | ACT-058362 | GPR |
Palosuran (ACT-058362) (ACT-058362) is a new potent and specific antagonist of the human UT receptor. | |||
T5150 | Treprostinil | LRX-15,Orenitram,Remodulin | Prostaglandin Receptor |
Treprostinil (Orenitram) is a potent DP1, IP and EP2 agonist (EC50: 0.6/1.9/6.2 nM). | |||
TP1928L1 | [Orn5]-URP acetate | [Orn5]-URP acetate(782485-03-4 free base) | GPR |
[Orn5]-URP acetate is an effective and selective Urotensin-II receptor (UT) antagonist (pEC50 = 7.24). [Orn5]-URP exhibits no agonist activity. | |||
T22476 | (±)-AC 7954 hydrochloride | Neurotensin Receptor | |
(±)-AC 7954 hydrochloride is a urotensin-II (UT) receptor activator. | |||
TP2104L | UFP 803 acetate | Neurotensin Receptor | |
UFP 803 acetate is a potent ligand of urotensin-II (UT) receptor. UFP-803 displays the activity of a lower residual agonist. | |||
T4689 | Palosuran hydrochloride 540769-28-6(free base) | ACT-058362 hydrochloride | GPR |
Palosuran hydrochloride 540769-28-6(free base)(ACT-058362 hydrochloride) is a new potent and specific antagonist of the human UT receptor with an IC50 of 3.6±0.2 nM. | |||
T12848 | SB-657510 | Others , Neurotensin Receptor | |
SB-657510 is a urotensin II (UII) receptor (UT) antagonist. The Ki values of UT for human, monkey, cat, rat and mouse were 61, 17, 30, 65 and 56 nM, respectively. SB-657510 plays an anti-inflammatory role by inhibiting U... | |||
TP2106L | Urantide acetate(669089-53-6 free base) | Neurotensin Receptor | |
Urantide acetate is a selective and competitive urotensin-II (UT) receptor antagonist (pKB = 8.3). Blocks hU-II induced contractions in thoracic aorta ex vivo. Exhibits no effect on noradrenaline or endothelin 1-induced ... | |||
T37527L | [Orn8]-Urotensin II acetate | GPR | |
[Orn8]-Urotensin II acetate is a Urotensin receptor ligand and a partial agonist at Urotensin receptors. | |||
T13977 | (R)-UT-155 | Epigenetic Reader Domain | |
(R)-UT-155 is a selective androgen receptor degrader (SARD) ligand. | |||
T23326 | SB 706375 | Others | |
urotensin-II (UT) receptor antagonist | |||
T22815 | GSK 1562590 hydrochloride | Others | |
urotensin II (UT) receptor antagonist | |||
T75827 | UFP-803 TFA | ||
UFP-803 TFA, a potent ligand for the urotensin-II receptor (UT), exhibits minimal residual agonist activity, rendering it a valuable asset for exploring the UT system's function in physiology and pathology [1]. | |||
T75828 | [Orn5]-URP TFA | ||
[Orn5]-URP TFA acts as a potent and selective antagonist exclusively targeting the Urotensin-II receptor (UT), devoid of any agonist activity, and demonstrates a significant inhibitory efficiency with a pEC50 value of 7.... | |||
TP2106 | Urantide | ||
Selective and competitive urotensin-II (UT) receptor antagonist (pKB = 8.3). Blocks hU-II induced contractions in thoracic aorta ex vivo. Exhibits no effect on noradrenaline or endothelin 1-induced contraction or on acet... | |||
TP1928 | [Orn5]-URP | ||
Urotensin-II (UT) receptor pure antagonist (pEC50 = 7.24). Displays no agonist activity unlike other U-II/URP analogs. Inhibits the action of U-II in the rat aorta ring assay. |