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Cell Reactant:RNA(23-mer)
Syringe Reactant:BDBM19
Meas. Tech.:ITC
Entry Date:12/19/00
 
ΔG°:-4.82± (kcal/mole)
pH:7±n/a
Log10Kb:3.53± 0.0212
Temperature:298.15±n/a (K)
ΔH° :-4.82± (kcal/mole)
ΔHobs :-4.82± (kcal/mole)
Ionic Strength:n/a
Corrected for ΔHioniz:n/a
Protons Released:n/a
ΔCp :n/a
Stoich. Param.:n/a
ΔS° :0± (kcal/mole-K)
Comments:high affinity site
 
Citation Cowan, JAOhyama, TWang, DNatarajan, K Recognition of a cognate RNA aptamer by neomycin B: quantitative evaluation of hydrogen bonding and electrostatic interactions. Nucleic Acids Res28:2935-42 (2000) [PubMed]  Article
More Info.:  Get all data from this article ,  ITC RUN data ,  Solution Info
 
RNA(23-mer)
Source:in vitro transcription using T7 RNA polymerase
Purity:n/a
Prep. Method:purified using PAGE and electroeluted from the gel
Name:RNA(23-mer)
Synonyms:RNA 23mer
Type:RNA
Mol. Mass.:1388.55
Organism:n/a
Description:n/a
Residue:19
Sequence:
GGCCUGGGCGAGAAGUUUAGGCC
 
BDBM19
Source:Sigma (St. Louis, MO)
Purity:n/a
Prep. Method:n/a
NameBDBM19
Synonyms:(2S,3S,4R,5R,6R)-5-amino-2-(aminomethyl)-6-{[(2R,3S,4R,5S)-5-{[(1R,2R,3S,5R,6S)-3,5-diamino-2-{[(2R,3R,4R,5S,6R)-3-amino-6-(aminomethyl)-4,5-dihydroxyoxan-2-yl]oxy}-6-hydroxycyclohexyl]oxy}-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy}oxane-3,4-diol | KDR Kinase Inhibitor, 3 | Neomycin | Neomycin B
TypeSmall organic molecule
Emp. Form.C23H46N6O13
Mol. Mass.614.6437
SMILESNC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O |r|
Structure
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Last update November 1, 2007
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