TargetMol

Tryptophanamide

Product Code:
 
TAR-T26297
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1
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CodeSizePrice
TAR-T26297-5mg5mg£850.00
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TAR-T26297-50mg50mg£1,661.00
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Quantity:
TAR-T26297-100mg100mg£2,079.00
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This product comes from: United States.
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  • Further Information
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Further Information

Bioactivity:
Tryptophanamide is a chymotrypsin inhibitor.
CAS:
20696-57-5
Formula:
C11H13N3O
Molecular Weight:
203.245
Purity:
0.98
SMILES:
N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O

References

1. Shou M, Terashima H, Aizawa S, Taga A, Yamamoto A, Kodama S. Simultaneous Enantioseparation of Aldohexoses and Aldopentoses Derivatized With L-Tryptophanamide by Reversed Phase HPLC Using Butylboronic Acid as a Complexation Reagent of Monosaccharides. Chirality. 2015 Jul;27(7):417-21. doi: 10.1002/chir.22456. Epub 2015 May 20. PubMed PMID: 25994510. 2. Kowalska-Baron A, Ga??cki K, Wysocki S. Temperature study of indole, tryptophan and N-acetyl-L-tryptophanamide (NATA) triplet-state quenching by iodide in aqueous solution. Spectrochim Acta A Mol Biomol Spectrosc. 2013 Jul;111:42-8. doi: 10.1016/j.saa.2013.03.086. Epub 2013 Mar 29. PubMed PMID: 23602958. 3. BERNHARD RA, NIEMANN C. A DILATOMETRIC INVESTIGATION OF THE ALPHA-CHYMOTRYPSIN-CATALYZED HYDROLYSIS OF NICOTINYL-L-TRYPTOPHANAMIDE. Arch Biochem Biophys. 1965 Apr;110:195-9. PubMed PMID: 14321852. 4. Andrews D, Trezeguet V, Merle M, Graves PV, Muench KH, Labouesse B. Tryptophanamide formation by Escherichia coli tryptophanyl-tRNA synthetase. Eur J Biochem. 1985 Jan 2;146(1):201-9. PubMed PMID: 3881255.