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D-Histidine

CAS No.:
351-50-8
Catalog Number:
AG0034P0
Molecular Formula:
C6H9N3O2
Molecular Weight:
155.1546
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$19
- +
25g
98%
In Stock USA
United States
$57
- +
100g
98%
In Stock USA
United States
$138
- +
500g
98%
In Stock USA
United States
$650
- +
Product Description
Catalog Number:
AG0034P0
Chemical Name:
D-Histidine
CAS Number:
351-50-8
Molecular Formula:
C6H9N3O2
Molecular Weight:
155.1546
MDL Number:
MFCD00065963
IUPAC Name:
(2R)-2-amino-3-(1H-imidazol-5-yl)propanoic acid
InChI:
InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m1/s1
InChI Key:
HNDVDQJCIGZPNO-RXMQYKEDSA-N
SMILES:
N[C@@H](C(=O)O)Cc1c[nH]cn1
EC Number:
206-513-8
Properties
Complexity:
151  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
155.069g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
155.157g/mol
Monoisotopic Mass:
155.069g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
92A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-3.2  
Literature
Title Journal
Bacillus anthracis spore interactions with mammalian cells: relationship between germination state and the outcome of in vitro. BMC microbiology 20110101
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
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
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: 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
Carbonic anhydrase activators. Activation of isozymes I, II, IV, VA, VII, and XIV with l- and d-histidine and crystallographic analysis of their adducts with isoform II: engineering proton-transfer processes within the active site of an enzyme. Chemistry (Weinheim an der Bergstrasse, Germany) 20060918
The mitochondrial ornithine transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms. The Journal of biological chemistry 20030829
Novel spermine-amino acid conjugates and basic tripeptides enhance cleavage of the hairpin ribozyme at low magnesium ion concentration. Bioorganic & medicinal chemistry letters 20011203
Effects of intravenous infusion of amino acids and glucose on the yield and concentration of milk protein in dairy cows. The Journal of dairy research 20010201
Properties