687-51-4 | H-Leu-NH2

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$28.00	$20.00
5g	95%	in stock	$65.00	$45.00
25g	95%	in stock	$257.00	$180.00
100g	95%	in stock	$937.00	$656.00

Description

• Catalog Number: AD02200
• Chemical Name: H-Leu-NH2
• CAS Number: 687-51-4
• Molecular Formula: C6H14N2O
• Molecular Weight: 130.18815999999998
• MDL Number: MFCD00238027
• SMILES: N[C@H](C(=O)N)CC(C)C

Computed Properties

• Complexity: 101
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 0.1

Literature

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  Peptides 20120901

• Host-defense peptides in skin secretions of African clawed frogs (Xenopodinae, Pipidae).

  General and comparative endocrinology 20120501

• Host-defense peptides from skin secretions of the tetraploid frogs Xenopus petersii and Xenopus pygmaeus, and the octoploid frog Xenopus lenduensis (Pipidae).

  Peptides 20120101

• Rotational spectra and computational analysis of two conformers of leucinamide.

  The journal of physical chemistry. A 20110901

• Genome duplications within the Xenopodinae do not increase the multiplicity of antimicrobial peptides in Silurana paratropicalis and Xenopus andrei skin secretions.

  Comparative biochemistry and physiology. Part D, Genomics & proteomics 20110601

• Antimicrobial peptides with therapeutic potential from skin secretions of the Marsabit clawed frog Xenopus borealis (Pipidae).

  Comparative biochemistry and physiology. Toxicology & pharmacology : CBP 20101101

• Orthologs of magainin, PGLa, procaerulein-derived, and proxenopsin-derived peptides from skin secretions of the octoploid frog Xenopus amieti (Pipidae).

  Peptides 20100601

• Design and synthesis of selective inhibitors of placental alkaline phosphatase.

  Bioorganic & medicinal chemistry 20100115

• Marine drugs from sponge-microbe association--a review.

  Marine drugs 20100101

• L-Leucinamide hydrogensquarate: spectroscopic and structural elucidation.

  Amino acids 20091001

• HPLC Method for Determination of Enantiomeric Purity of a Novel Respiratory Fluoroquinolone: WCK 1152.

  Indian journal of pharmaceutical sciences 20080101

• HTS, chemical hybridization, and drug design identify a chemically unique antituberculosis agent-coupling serendipity and rational approaches to drug discovery.

  ChemMedChem 20070601

• 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 20060401

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

  Analytical biochemistry 20051101

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

  Bioorganic & medicinal chemistry letters 20040816

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

  Biotechnology and bioengineering 20040505

• First total synthesis of leucamide A.

  The Journal of organic chemistry 20030221

• Identification of cytosolic leucyl aminopeptidase (EC 3.4.11.1) as the major cysteinylglycine-hydrolysing activity in rat liver.

  Biological chemistry 20030201

• Leucamide A: a new cytotoxic heptapeptide from the Australian sponge Leucetta microraphis.

  The Journal of organic chemistry 20020712

• Chiral inversion of (R)-(-)-fenoprofen in guinea-pigs pretreated with clofibrate.

  Veterinary research communications 20020601

• [Kinetics and mechanism of peptide synthesis in solution].

  Bioorganicheskaia khimiia 20020101

• Antimicrobial peptides isolated from skin secretions of the diploid frog, Xenopus tropicalis (Pipidae).

  Biochimica et biophysica acta 20011126