2749-11-3 | L-Alaninol

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$15.00	$10.00
100g	98%	in stock	$33.00	$23.00
500g	98%	in stock	$70.00	$49.00

Description

• Catalog Number: AB46356
• Chemical Name: L-Alaninol
• CAS Number: 2749-11-3
• Molecular Formula: C3H9NO
• Molecular Weight: 75.1097
• MDL Number: MFCD00064412
• SMILES: C[C@@H](CO)N

Computed Properties

• Complexity: 22.9
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: -1

Literature

• Structural determination of glycopeptidolipids of Mycobacterium smegmatis by high-resolution multiple-stage linear ion-trap mass spectrometry with electrospray ionization.

  Journal of mass spectrometry : JMS 20121001

• Retrobiosynthetic approach delineates the biosynthetic pathway and the structure of the acyl chain of mycobacterial glycopeptidolipids.

  The Journal of biological chemistry 20120831

• Identification of a novel tetrapeptide structure of the Mycobacterium avium glycopeptidolipid that functions as a specific target for the host antibody response.

  Biochemical and biophysical research communications 20120323

• Synthesis of 21-nitrogen substituted pregna-5,17(20)-dienes from pregnenolone.

  Steroids 20120101

• Chirality transfer from a single chiral molecule to 2D superstructures in alaninol on the Cu(100) surface.

  Langmuir : the ACS journal of surfaces and colloids 20110621

• Characterization of protein contributions to cobalt-carbon bond cleavage catalysis in adenosylcobalamin-dependent ethanolamine ammonia-lyase by using photolysis in the ternary complex.

  Journal of the American Chemical Society 20110511

• A colorimetric chiral sensor based on chiral crown ether for the recognition of the two enantiomers of primary amino alcohols and amines.

  Chirality 20110401

• How coenzyme B12-dependent ethanolamine ammonia-lyase deals with both enantiomers of 2-amino-1-propanol as substrates: structure-based rationalization.

  Biochemistry 20110201

• Probing enantioselectivity on chirally modified Cu(110), Cu(100), and Cu(111) surfaces.

  Langmuir : the ACS journal of surfaces and colloids 20101102

• Straightforward synthesis of enantiopure (R)- and (S)-trifluoroalaninol.

  Organic & biomolecular chemistry 20101021

• Absolute configurations and CD spectra of axially chiral biphenyls prepared in a facile manner by crystallization-induced configuration transformation.

  Chirality 20100801

• Highly resolutive separations of hardly soluble synthetic polypeptides by capillary electrophoresis.

  Analytical chemistry 20100101

• Synthesis of highly enantioenriched chiral alpha-aminoorganotins via diastereoselective ring opening of chiral N-(arenesulfonyl) 2-tributylstannyloxazolidines.

  The Journal of organic chemistry 20090821

• Conformational effects in photoelectron circular dichroism of alaninol.

  Chemphyschem : a European journal of chemical physics and physical chemistry 20090803

• Progress in the discovery of selective, high affinity A(2B) adenosine receptor antagonists as clinical candidates.

  Purinergic signalling 20090301

• (S)-N-(5-Chlorothiophene-2-sulfonyl)-beta,beta-diethylalaninol a Notch-1-sparing gamma-secretase inhibitor.

  Bioorganic & medicinal chemistry letters 20090201

• An amine: hydroxyacetone aminotransferase from Moraxella lacunata WZ34 for alaninol synthesis.

  Bioprocess and biosystems engineering 20080601

• D-alaninol adsorption on Cu(100): photoelectron spectroscopy and first-principles calculations.

  The journal of physical chemistry. B 20080403

• New insight brought by density functional theory on the chemical state of alaninol on Cu(100): energetics and interpretation of x-ray photoelectron spectroscopy data.

  The Journal of chemical physics 20080321

• 2-amino-1-propanol versus 1-amino-2-propanol: valence band and C 1s core-level photoelectron spectra.

  The Journal of chemical physics 20071014

• Genomics of glycopeptidolipid biosynthesis in Mycobacterium abscessus and M. chelonae.

  BMC genomics 20070101

• Secrets of soil survival revealed by the genome sequence of Arthrobacter aurescens TC1.

  PLoS genetics 20061201

• A cobalt(III)-salen complex with an axial substituent in the diamine backbone: stereoselective recognition of amino alcohols.

  Journal of the American Chemical Society 20051207

• Hyperglycosylation of glycopeptidolipid of Mycobacterium smegmatis under nutrient starvation: structural studies.

  Microbiology (Reading, England) 20050701

• Carbon position-specific isotope analysis of alanine and phenylalanine analogues exhibiting nonideal pyrolytic fragmentation.

  Analytical chemistry 20050315

• Utilization of a ts-sacB selection system for the generation of a Mycobacterium avium serovar-8 specific glycopeptidolipid allelic exchange mutant.

  Annals of clinical microbiology and antimicrobials 20040101

• Surface-exposed glycopeptidolipids of Mycobacterium smegmatis specifically inhibit the phagocytosis of mycobacteria by human macrophages. Identification of a novel family of glycopeptidolipids.

  The Journal of biological chemistry 20031219

• Biosynthetic specificity of the rhamnosyltransferase gene of Mycobacterium avium serovar 2 as determined by allelic exchange mutagenesis.

  Microbiology (Reading, England) 20031101

• Fluorescence sensing of ammonium and organoammonium ions with tripodal oxazoline receptors.

  Organic letters 20030501

• Stereoretentive C-H bond activation in the aqueous phase catalytic hydrogenation of amino acids to amino alcohols.

  Organic letters 20030220

• Analysis of the electron paramagnetic resonance spectrum of a radical intermediate in the coenzyme B(12)-dependent ethanolamine ammonia-lyase catalyzed reaction of S-2-aminopropanol.

  Biochemistry 20020709

• Transformation of isopropylamine to L-alaninol by Pseudomonas sp. strain KIE171 involves N-glutamylated intermediates.

  Applied and environmental microbiology 20020501

• Thermal study of simple amino-alcohol solutions.

  Cryobiology 20020401

• 5'-Deoxyadenosine contacts the substrate radical intermediate in the active site of ethanolamine ammonia-lyase: 2H and 13C electron nuclear double resonance studies.

  Biochemistry 20010109