Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
inhibit the prion protein conversion from PrPC to PrPSc
| ALogP | 3.738 |
|---|---|
| Conteggio HBD | 1 |
| Legame rotabile | 5 |
| Pubchem Sid | 528768273 |
|---|---|
| Sorrisi canonici | CCC(C)C(C(=O)N1CCC2=CC=CC=C21)NC(=O)C3=CC=CC=C3 |
| IUPAC Name | N-[1-(2,3-dihydroindol-1-yl)-3-methyl-1-oxopentan-2-yl]benzamide |
| InChIKey | ZVJMRPCDQIPYRL-UHFFFAOYSA-N |
| INCHI | 1S/C21H24N2O2/c1-3-15(2)19(22-20(24)17-10-5-4-6-11-17)21(25)23-14-13-16-9-7-8-12-18(16)23/h4-12,15,19H,3,13-14H2,1-2H3,(H,22,24) |
| Isomeri SMILES | CCC(C)C(C(=O)N1CCC2=CC=CC=C21)NC(=O)C3=CC=CC=C3 |
| PubChem CID | 4877803 |
| Peso molecolare | 336.43 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Classe | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | Isoleucine and derivatives |
| Alternative Parents | N-acyl-alpha amino acids and derivatives Hippuric acids and derivatives Alpha amino acid amides Indoles and derivatives Benzoyl derivatives Tertiary carboxylic acid amides Secondary carboxylic acid amides Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Isoleucine or derivatives - Hippuric acid or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Benzamide - Benzoic acid or derivatives - Indole or derivatives - Benzoyl - Monocyclic benzene moiety - Benzenoid - Tertiary carboxylic acid amide - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as isoleucine and derivatives. These are compounds containing isoleucine or a derivative thereof resulting from reaction of isoleucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. |
| External Descriptors | Not available |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| DMSO (mM) Solubilità massima | 10 |
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