HomeProductsBuilding BlocksFunctional GroupsAminesLeucinamide
Chemical structure of CAS 687-51-4

Leucinamide

In Stock•Starting at $9 for 250 mg•Purity ≥ 97%
CAS No.687-51-4
MDL No.MFCD00238027
MFC6H14N2O
MW130.19
InChI KeyFORGMRSGVSYZQR-YFKPBYRVSA-N

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
250 mg97%$9In Stock
1 g97%$16In Stock
5 g97%$43In Stock
10 g97%$75In Stock
25 g97%$147In Stock
100 g97%$515In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

L-leucinamide is an amino acid amide formed by replacing the carboxy OH group of L-leucine with NH2. It is a derivative of L-leucine.

CAS No.687-51-4
Product NameLeucinamide
Heavy Atom Count9Rotatable Bond Count3
Atom Stereo Count1Bond Stereo Count0
HBA2HBD2
TPSA69.110 ŲCharge0
Exact Mass130.11061Complexity101.23
pKa7.130XLogP-0.155

Related Articles

Studies related to this compound and its mechanism of action

L: -Stereoselective amino acid amidase with broad substrate specificity from Brevundimonas diminuta: characterization of a new member of the leucine aminopeptidase family.

Applied microbiology and biotechnology • Vol. 70, Issue 4 • 2006
PMID: 16001251DOI: 10.1007/s00253-005-0068-9

Application of Fourier transform infrared spectroscopy for monitoring hydrolysis and synthesis reactions catalyzed by a recombinant amidase.

Analytical biochemistry • Vol. 346, Issue 1 • 2005
PMID: 16185648DOI: 10.1016/j.ab.2005.07.027

Kinetics and mechanism of a reaction catalyzed by PST-01 protease from Pseudomonas aeruginosa PST-01.

Biotechnology and bioengineering • Vol. 86, Issue 3 • 2004
PMID: 15083515DOI: 10.1002/bit.20052

Rational design of potent and selective NH-linked aryl/heteroaryl cathepsin K inhibitors.

Bioorganic & medicinal chemistry letters • Vol. 14, Issue 16 • 2004
PMID: 15261289DOI: 10.1016/j.bmcl.2004.05.087

Documentation

Similar Products