Reaction Details | |
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Cell Reactant: | BDBM36127 |
Syringe Reactant: | BDBM50216627 |
Meas. Tech.: | ITC |
Entry Date: | 12/08/10 |
ΔG°: | -24.9±0.0900 (kJ/mole) |
pH: | 7±0 |
Log10Kb: | 4.29± 2.85 |
Temperature: | 303.25±0 (K) |
ΔH° : | -25.0±0.130 (kJ/mole) |
ΔHobs: | n/a |
Ionic Strength: | n/a |
n/a | |
Protons Released: | n/a |
ΔCp : | n/a |
Stoich. Param.: | n/a |
ΔS° : | -0.0005±0.000500 (kJ/mole-K) |
Comments: | First trial |
Citation | Carrazana, J; Jover, A; Meijide, F; Soto, VH; Vazquez Tato, J Complexation of adamantyl compounds by beta-cyclodextrin and monoaminoderivatives. J Phys Chem B109:9719-26 (2005) [PubMed] Article |
More Info.: | Get all data from this article , ITC RUN data , Solution Info , Instrument Info |
BDBM36127 | |
Source: | n/a |
Purity: | n/a |
Prep. Method: | n/a |
Name | BDBM36127 |
Synonyms: | 6-Amino-6-deoxy-beta-cyclodextrin (am-beta-CD) | 6-NH2-beta-cyclodextrin | mono(6-amino-6-deoxy)-beta-cyclodextrin |
Type | Molecular Host |
Emp. Form. | C42H72NO34 |
Mol. Mass. | 1135.0068 |
SMILES | [NH3+]C[C@H]1O[C@@H]2O[C@@H]3[C@@H](CO)O[C@H](O[C@@H]4[C@@H](CO)O[C@H](O[C@@H]5[C@@H](CO)O[C@H](O[C@@H]6[C@@H](CO)O[C@H](O[C@@H]7[C@@H](CO)O[C@H](O[C@@H]8[C@@H](CO)O[C@H](O[C@H]1[C@H](O)[C@H]2O)[C@H](O)[C@H]8O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)[C@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O |
Structure | |
BDBM50216627 | |
Source: | n/a |
Purity: | n/a |
Prep. Method: | n/a |
Name | BDBM50216627 |
Synonyms: | (alpha-methyl-1-adamantyl)methylamine | 1-Adamantan-1-yl-ethylamine | CHEMBL959 | RIMANTADINE | US11241393, Rimantadine | rimantadin | rimantidin |
Type | Small organic molecule |
Emp. Form. | C12H21N |
Mol. Mass. | 179.3018 |
SMILES | CC(N)C12CC3CC(CC(C3)C1)C2 |TLB:10:5:12:9.8.11,10:9:12:6.5.4,THB:4:5:8:12.3.11,4:3:6.5.10:8,1:3:6.5.10:8| |
Structure |
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