Home Other Building Blocks D-Tryptophan

D-Tryptophan

CAS No.:
153-94-6
Catalog Number:
AG0034OJ
Molecular Formula:
C11H12N2O2
Molecular Weight:
204.2252
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$25
- +
100g
98%
In Stock USA
United States
$75
- +
500g
98%
In Stock USA
United States
$300
- +
Product Description
Catalog Number:
AG0034OJ
Chemical Name:
D-Tryptophan
CAS Number:
153-94-6
Molecular Formula:
C11H12N2O2
Molecular Weight:
204.2252
MDL Number:
MFCD00005647
IUPAC Name:
(2R)-2-amino-3-(1H-indol-3-yl)propanoic acid
InChI:
InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m1/s1
InChI Key:
QIVBCDIJIAJPQS-SECBINFHSA-N
SMILES:
OC(=O)[C@@H](Cc1c[nH]c2c1cccc2)N
EC Number:
205-819-9
UNII:
7NS97N9H1G
NSC Number:
97942
Properties
Complexity:
245  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
204.09g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
204.229g/mol
Monoisotopic Mass:
204.09g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
79.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.1  
Literature
Title Journal
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
Properties