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UFP 803

Urotensin-II (UT) receptor ligand that competitively antagonizes U-II induced contractions in the rat aorta (pIC50 = 7.46) and prevents plasma extravasation elicited by U-II in mice in vivo. Behaves as a silent antagonist in most in vitro assays and in vivo, but does retain small residual agonist activity under certain conditions in some assays.

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CAT No: R1011

CAS No: 879497-82-2

Synonyms/Alias: UFP803;879497-82-2;UFP 803 TFA;AKOS024457148;DA-58866;PD079336;(2S)-2-[[(4R,7S,13R,16S)-19-[[(2S)-2-amino-3-carboxypropanoyl]amino]-10-(2-aminoethyl)-16-benzyl-7-[(4-hydroxyphenyl)methyl]-13-(1H-indol-3-ylmethyl)-20,20-dimethyl-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]amino]-3-methylbutanoic acid;

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Specification Technical Data Publications Customer reviews and Q&A
M.F/FormulaC50H64N10O12S2
M.W/Mr.1061.2
SequenceOne Letter Code:DXFWXYCV
Three Letter Code:H-Asp-DL-Pen(1)-Phe-D-Trp-DL-Dab-Tyr-Cys(1)-Val-OH
Labeling TargetUrotensin-II receptor
AppearanceWhite lyophilised solid
Purity>98%
Long-term Storage ConditionsSoluble in water
InChIInChI=1S/C50H64N10O12S2/c1-26(2)40(49(71)72)59-47(69)38-25-73-74-50(3,4)41(60-42(64)32(52)23-39(62)63)48(70)57-36(20-27-10-6-5-7-11-27)44(66)56-37(22-29-24-53-33-13-9-8-12-31(29)33)46(68)54-34(18-19-51)43(65)55-35(45(67)58-38)21-28-14-16-30(61)17-15-28/h5-17,24,26,32,34-38,40-41,53,61H,18-23,25,51-52H2,1-4H3,(H,54,68)(H,55,65)(H,56,66)(H,57,70)(H,58,67)(H,59,69)(H,60,64)(H,62,63)(H,71,72)/t32-,34?,35-,36-,37+,38-,40-,41?/m0/s1
InChI KeyLRELVPJTCGYTSS-AAEZYUNISA-N
Isomeric SMILESCC(C)[C@@H](C(=O)O)NC(=O)[C@@H]1CSSC([C@@H](C(=O)N[C@H](C(=O)N[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N1)CC2=CC=C(C=C2)O)CCN)CC3=CNC4=CC=CC=C43)CC5=CC=CC=C5)NC(=O)[C@H](CC(=O)O)N)(C)C
BoilingPointN/A
Melting PointN/A

1. Urinary Metabolites Associated with Blood Pressure on a Low-or High-Sodium Die

2. C-Peptide replacement therapy and sensory nerve function in type 1 diabetic neuropathy

3. Implications of ligand-receptor binding kinetics on GLP-1R signalling

4. Autoinhibition and phosphorylation-induced activation of phospholipase C-γ isozymes

5. Cell-based adhesion assays for isolation of snake venom’s integrin antagonists

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