41989
DD-2,6-Diaminopimelic acid
≥95.0% (TLC)
Synonym(s):
(2R,6R)-2,6-Diaminoheptanedioic acid, D,D-α,ε-Diaminopimelic acid, D-DAP, NSC 206278
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About This Item
Empirical Formula (Hill Notation):
C7H14N2O4
CAS Number:
Molecular Weight:
190.20
UNSPSC Code:
12352204
PubChem Substance ID:
MDL number:
assay
≥95.0% (TLC)
optical purity
enantiomeric excess: ≥98.0%
SMILES string
OC([C@H](N)CCC[C@@H](N)C(O)=O)=O
InChI
1S/C7H14N2O4/c8-4(6(10)11)2-1-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)/t4-,5-/m1/s1
InChI key
GMKMEZVLHJARHF-RFZPGFLSSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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The stereoisomers of alpha epsilon-diaminopimelic acid. II. Their distribution in the bacterial order Actinomycetales and in certain Eubacteriales.
D S HOARE et al.
The Biochemical journal, 65(3), 441-447 (1957-03-01)
L K Lam et al.
The Journal of biological chemistry, 263(24), 11814-11819 (1988-08-25)
Analogs 1-8 of diaminopimelic acid (DAP) were synthesized and tested for inhibition of purified meso-DAP D-dehydrogenase from Bacillus sphaericus and of LL-DAP epimerase from Escherichia coli. The dehydrogenase was assayed by monitoring NADPH formation spectrophotometrically at 340 nm. N-Hydroxy DAP
The stereoisomers of alpha epsilon-diaminopimelic acid: their distribution in nature and behaviour towards certain enzyme preparations.
D S HOARE et al.
The Biochemical journal, 61(4), 562-568 (1955-12-01)
Limin Zhang et al.
International journal of systematic and evolutionary microbiology, 62(Pt 2), 272-278 (2011-03-15)
An actinomycete, strain FXJ6.011(T), was isolated from a cup-shaped sponge collected at Dachan reef, Yangpu in the South China Sea. The strain had morphological characteristics of members of the family Micromonosporaceae. Phylogenetic analysis of the 16S rRNA gene sequence of
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