153-94-6 | D-Tryptophan

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$13.00	$9.00
250g	98%	in stock	$112.00	$78.00

Description

• Catalog Number: AB45835
• Chemical Name: D-Tryptophan
• CAS Number: 153-94-6
• Molecular Formula: C11H12N2O2
• Molecular Weight: 204.2252
• MDL Number: MFCD00005647
• SMILES: OC(=O)[C@@H](Cc1c[nH]c2c1cccc2)N
• NSC Number: 97942

Computed Properties

• Complexity: 245
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 3
• XLogP3: -1.1

Literature

• Enantiospecific total synthesis of the important biogenetic intermediates along the ajmaline pathway, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epivellosimine and macusine A.

  The Journal of organic chemistry 20100521

• Carbonic anhydrase activators. The first activation study of a coral secretory isoform with amino acids and amines.

  Bioorganic & medicinal chemistry 20100315

• Carbonic anhydrase activators: Activation of the beta-carbonic anhydrase from the pathogenic yeast Candida glabrata with amines and amino acids.

  Bioorganic & medicinal chemistry letters 20100301

• Carbonic anhydrase activators: activation of the beta-carbonic anhydrases from the pathogenic fungi Candida albicans and Cryptococcus neoformans with amines and amino acids.

  Bioorganic & medicinal chemistry 20100201

• Carbonic anhydrase activators. Activation of the membrane-associated isoform XV with amino acids and amines.

  Bioorganic & medicinal chemistry letters 20090701

• Identification of a chemical probe for NAADP by virtual screening.

  Nature chemical biology 20090401

• Carbonic anhydrase activators: activation of the beta-carbonic anhydrase Nce103 from the yeast Saccharomyces cerevisiae with amines and amino acids.

  Bioorganic & medicinal chemistry letters 20090315

• Aromatic D-amino acids act as chemoattractant factors for human leukocytes through a G protein-coupled receptor, GPR109B.

  Proceedings of the National Academy of Sciences of the United States of America 20090310

• Carbonic anhydrase activators: activation of the archaeal beta-class (Cab) and gamma-class (Cam) carbonic anhydrases with amino acids and amines.

  Bioorganic & medicinal chemistry letters 20081201

• Carbonic anhydrase activators: kinetic and X-ray crystallographic study for the interaction of D- and L-tryptophan with the mammalian isoforms I-XIV.

  Bioorganic & medicinal chemistry 20080915

• Carbonic anhydrase activators: Activation of the human cytosolic isozyme III and membrane-associated isoform IV with amino acids and amines.

  Bioorganic & medicinal chemistry letters 20080801

• Carbonic anhydrase activators: activation of the human tumor-associated isozymes IX and XII with amino acids and amines.

  Bioorganic & medicinal chemistry 20080401

• Carbonic anhydrase activators: the first activation study of the human secretory isoform VI with amino acids and amines.

  Bioorganic & medicinal chemistry 20070801

• Carbonic anhydrase activators: activation of the human isoforms VII (cytosolic) and XIV (transmembrane) with amino acids and amines.

  Bioorganic & medicinal chemistry letters 20070801

• Carbonic anhydrase activators: an activation study of the human mitochondrial isoforms VA and VB with amino acids and amines.

  Bioorganic & medicinal chemistry letters 20070301

• Prevention of severe menorrhagia in oncology patients with treatment-induced thrombocytopenia by luteinizing hormone-releasing hormone agonist and depo-medroxyprogesterone acetate.

  Cancer 20061001

• The enantiospecific, stereospecific total synthesis of the ring-A oxygenated sarpagine indole alkaloids (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine, as well as the total synthesis of the alstonia bisindole alkaloid macralstonidine.

  The Journal of organic chemistry 20030808

• Comparison of the responses of the chorda tympani and glossopharyngeal nerves to taste stimuli in C57BL/6J mice.

  BMC neuroscience 20030101

• Expression cloning of a Na+-independent aromatic amino acid transporter with structural similarity to H+/monocarboxylate transporters.

  The Journal of biological chemistry 20010518