Ureidovaline

TargetMol
Product Code: TAR-T20562
Supplier: TargetMol
CodeSizePrice
TAR-T20562-5mg5mg£111.00
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Quantity:
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Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Ureidovaline is an intermediate in the Ritonavir synthesis.
CAS:
154212-61-0
Formula:
C14H23N3O3S
Molecular Weight:
313.41
Purity:
0.98
SMILES:
CC(C)[C@@H](C(O)=O)NC(N(C)CC1=CSC(C(C)C)=N1)=O

References

1. Ramel C, Tobler M, Meyer M, Bigler L, Ebert MO, Schellenberg B, Dudler R. Biosynthesis of the proteasome inhibitor syringolin A: the ureido group joining two amino acids originates from bicarbonate. BMC Biochem. 2009 Oct 28;10:26. doi: 10.1186/1471-2091-10-26. PubMed PMID: 19863801; PubMed Central PMCID: PMC2773804. 2. Chen LL, Whitty A, Lobb RR, Adams SP, Pepinsky RB. Multiple activation states of integrin alpha4beta1 detected through their different affinities for a small molecule ligand. J Biol Chem. 1999 May 7;274(19):13167-75. PubMed PMID: 10224072. 3. Moss N, Beaulieu P, Duceppe JS, Ferland JM, Garneau M, Gauthier J, Ghiro E, Goulet S, Guse I, Jaramillo J, Llinas-Brunet M, Malenfant E, Plante R, Poirier M, Soucy F, Wernic D, Yoakim C, D?ziel R. Peptidomimetic inhibitors of herpes simplex virus ribonucleotide reductase with improved in vivo antiviral activity. J Med Chem. 1996 Oct 11;39(21):4173-80. PubMed PMID: 8863795. 4. Luiking YC, Hallemeesch MM, Lamers WH, Deutz NE. NOS3 is involved in the increased protein and arginine metabolic response in muscle during early endotoxemia in mice. Am J Physiol Endocrinol Metab. 2005 Jun;288(6):E1258-64. Epub 2005 Jan 11. Erratum in: Am J Physiol Endocrinol Metab. 2007 Jan;292(1):E369. PubMed PMID: 15644457.