N(6)-(2,4-dinitrophenyl)-L-lysine

chemical compound

C₁₂H₁₆N₄O₆

N(6)-(2,4-dinitrophenyl)-L-lysine is …
instance of (P31):
type of chemical entityQ113145171

sublass of (P279):
N(6)-(2,4-dinitrophenyl)lysineQ27123948

External links are
P233canonical SMILESC1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])NCCCCC(C(=O)O)N
P231CAS Registry Number1094-76-4
P683ChEBI ID53080
P592ChEMBL IDCHEMBL2028905
P661ChemSpider ID58579
P8494DSSTOX compound identifierDTXCID201340192
P3117DSSTox substance IDDTXSID10911153
P4168IEDB Epitope ID114088
P234InChIInChI=1S/C12H16N4O6/c13-9(12(17)18)3-1-2-6-14-10-5-4-8(15(19)20)7-11(10)16(21)22/h4-5,7,9,14H,1-3,6,13H2,(H,17,18)/t9-/m0/s1
P235InChIKeyOFKKPUNNTZKBSR-VIFPVBQESA-N
P2017isomeric SMILESC1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])NCCCC[C@@H](C(=O)O)N
P662PubChem CID65068
40488045
P1579Reaxys registry number2822998
P652UNIIS6TD66F98C

P2067mass312.107

Reverse relations

main subject (P921)
Q28330114Induction of immune tolerance by free unreactive haptens
Q42248842Intestinal absorption of dinitrophenyl-lysine and effect of immunization with dinitrophenylated bovine serum albumin
Q39714498Rapid detoxification of epsilon-dinitrophenylated-lysine of dinitrophenylated leucocytes, the anti-leukaemic immunogen
Q34178850Real-time measurement of spontaneous antigen-antibody dissociation
Q73877065The conversion from the dehydrogenase type to the oxidase type of rat liver xanthine dehydrogenase by modification of cysteine residues with fluorodinitrobenzene
Q43205446The specificity of cross‐reactivity: Promiscuous antibody binding involves specific hydrogen bonds rather than nonspecific hydrophobic stickiness

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