Determine the necessary mass, volume, or concentration for preparing a solution.
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Chidamide is an HDAC (histone deacetylase) inhibitor that increases histone H3 acetylation levels in LoVo and HT29 colon cancer cells at concentrations as low as 4 μM.
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Anilides |
| Intermediate Tree Nodes | Aromatic anilides |
| Direct Parent | Benzanilides |
| Alternative Parents | Benzamides Benzoyl derivatives Aniline and substituted anilines Fluorobenzenes Pyridines and derivatives Aryl fluorides Heteroaromatic compounds Secondary carboxylic acid amides Amino acids and derivatives Azacyclic compounds Primary amines Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Benzanilide - Benzamide - Benzoic acid or derivatives - Benzoyl - Aniline or substituted anilines - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Pyridine - Heteroaromatic compound - Amino acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organofluoride - Organohalogen compound - Organic oxide - Carbonyl group - Amine - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Primary amine - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as benzanilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with a benzene ring. They have the general structure RNC(=O)R', where R,R'= benzene. |
| External Descriptors | Not available |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 | |
| Certificate of Analysis | Mar 27, 2024 | C338042 |
| Solubilidad | Soluble in DMSO (~20 mg/ml), DMF (~20 mg/ml), and 1: 1 DMSO: PBS(pH 7.2) (~0.5 mg/ml). |
|---|---|
| Índice de refracción | n20D1.69 (Predicted) |
| Punto de ebullición (°C) | ~600.16° C at 760 mmHg (Predicted) |
| Punto de fusión (°C) | 284.63° C (Predicted) |
| Peso molecular | 390.400 g/mol |
| XLogP3 | 2.300 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 6 |
| Exact Mass | 390.149 Da |
| Monoisotopic Mass | 390.149 Da |
| Topological Polar Surface Area | 97.100 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 577.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
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