about
The role of surface charge on the uptake and biocompatibility of hydroxyapatite nanoparticles with osteoblast cells.Identification of novel transaminases from a 12-aminododecanoic acid-metabolizing Pseudomonas strain.Efficient production of the Nylon 12 monomer ω-aminododecanoic acid methyl ester from renewable dodecanoic acid methyl ester with engineered Escherichia coli.Emtricitabine prodrugs with improved anti-HIV activity and cellular uptake.Aminoalkanoic Acids as Alternatives to Mercaptoalkanoic Acids for the Linker-Assisted Attachment of Quantum Dots to TiO2.Synthesis and biological evaluation of fatty acyl ester derivatives of 2',3'-didehydro-2',3'-dideoxythymidine.A β-Alanine Catabolism Pathway Containing a Highly Promiscuous ω-Transaminase in the 12-Aminododecanate-Degrading Pseudomonas sp. Strain AAC.Novel Bradykinin Analogues Modified in the N-Terminal Part of the Molecule with a Variety of Acyl Substituents.Star-like oligo-arginyl-maltotriosyl derivatives as novel cell-penetrating enhancers for the intracellular delivery of colloidal therapeutic systems.High yield synthesis of 12-aminolauric acid by "enzymatic transcrystallization" of omega-laurolactam using omega-laurolactam hydrolase from Acidovorax sp. T31.A unidirectional crosslinking strategy for HIV-1 protease dimerization inhibitors.The screening, characterization, and use of omega-laurolactam hydrolase: a new enzymatic synthesis of 12-aminolauric acid.Poly(ethylene terephthalate)/clay nanocomposites based on aminododecanoic acid-modified clay: effect of compatibilizer reactivity on clay dispersion.Adsorption of fluorescently labeled protein residues on poly(ethylene-co-acrylic acid) films modified with affinity functionalities.Self-assembled monolayers of alkanoic acids on the native oxide surface of SS316L by solution deposition
P921
Q35131094-3CBD01C6-633E-4A66-94CB-54FF49CE6AFFQ35767646-2D1527AF-0B23-4D87-AA59-7437ECE82CA1Q38896309-57F4674A-2C2D-4679-90FB-7F51E9F32E4CQ39292170-DC16FBB7-5444-4C62-99D7-CD43C6ED6D2DQ39473448-7E02FA19-D617-4E65-AC24-5CFA854DEB56Q39580043-F53C43CD-2CC3-45D6-AABE-88635CD72E03Q42118120-3AF95B1C-B8D6-4013-9DC1-5257A5F0E5D0Q42535719-E99704EB-AEF4-4FED-AD31-9EC4562F3F0FQ42833688-22D9E559-1F09-4992-B884-CE734B82334AQ43745935-9825701C-E444-4C4C-A929-723F7C2C5BE7Q44984444-D4609915-CFC2-4285-B343-306A37D80A64Q45029544-F4A6E9EB-181D-4AE9-AFA0-5C149EFB8426Q51080195-F1193189-9EE0-4F65-AE77-65B629A18361Q51187914-E6378BBB-FDFF-4EF8-AA3F-7EFEBD164393Q79697264-A0A29EED-0620-4B50-9E25-BBCE4FD9D503
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
12-aminododecanoic acid
@en
type
label
12-aminododecanoic acid
@en
prefLabel
12-aminododecanoic acid
@en
P638
P592
P661
P662
P683
P2063
LMFA01100005
P2067
P231
P232
P233
C(CCCCCC(=O)O)CCCCCN
P234
1S/C12H25NO2/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15/h1-11,13H2,(H,14,15)
P235
PBLZLIFKVPJDCO-UHFFFAOYSA-N
P2566
100.010.687
P274
P3117
DTXSID3040803
P592
CHEMBL371701
P638
P652
9042RP777G