Loading...
Chemical structure of (Pen⁵)-Urotensin II (4-11) (human)

GA20269

(Pen⁵)-Urotensin II (4-11) (human)

Also known as (2S)-2-[[(4R,7S,10S,13S,16S,19R)-10-(4-aminobutyl)-19-[[(2S)-2-amino-3-carboxypropanoyl]amino]-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

(Pen?)-Urotensin II (4-11) (human) (P5U) is the most potent urotensin-II receptor agonist reported to date· It has been shown to exhibit a 3-fold higher affinity for the receptor (measured in competition experiments) than urotensin-II (human) (H-4768)· P5U might represent a useful tool for the study of the human urotensin-II/orphan G-protein-coupled receptor GPR14 system

ChemicalCAS473902-31-7MW1089.3FormulaC52H68N10O12S2
CAS number
473902-31-7
Molecular weight
1089.3
Formula
C52H68N10O12S2
Solubility
Soluble in DMSO
InChIKey
IWPZSQYTMKMNRX-FLECMKQLSA-N
Catalogue number
GA20269
Brand
GLPBIO
Computed properties PubChem CID 10931175 · XLogP -2.3 · TPSA 417 Ų · H-bond donors 13
XLogP
-2.3
TPSA
417 Ų
H-bond donors
13
H-bond acceptors
16
Rotatable bonds
18
Heavy atoms
76

SMILES CC(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)CCCCN)CC3=CNC4=CC=CC=C43)CC5=CC=CC=C5)NC(=O)[C@H](CC(=O)O)N)(C)C

Computed descriptors from PubChem (CID 10931175), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

Ordering in Israel

Lead time
Ships from the manufacturer to your lab in 8–14 business days; customs and cold chain handled by LABO Scientific.
Pricing
Quoted in ILS, excl. VAT. Add the item to your quote and we confirm the final price, usually the same business day.
Documents
Lot certificate of analysis and manufacturer SDS are emailed with your order confirmation.
Who we serve
Universities, hospitals and biotech companies across Israel. Research use only — not for diagnostic or therapeutic use.