≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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.
Information
PFI-90 PFI-90 is a selective inhibitor of the histone demethylase KDM3B . PFI-90 induces apoptosis and cell differentiation resulting in delayed tumor progression in vivo.
| Pubchem Sid | 488198136 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488198136 |
| Sorrisi canonici | C1=CC=NC(=C1)C(=O)NNC2=CC=CC=N2 |
| IUPAC Name | N'-pyridin-2-ylpyridine-2-carbohydrazide |
| InChIKey | GCZPXNWBXDWHKM-UHFFFAOYSA-N |
| INCHI | 1S/C11H10N4O/c16-11(9-5-1-3-7-12-9)15-14-10-6-2-4-8-13-10/h1-8H,(H,13,14)(H,15,16) |
| Isomeri SMILES | C1=CC=NC(=C1)C(=O)NNC2=CC=CC=N2 |
| PubChem CID | 12499590 |
| Peso molecolare | 214.22 |
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 | Organoheterocyclic compounds |
| Classe | Pyridines and derivatives |
| Subclass | Pyridinecarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Pyridinecarboxylic acids and derivatives |
| Alternative Parents | Imidolactams Heteroaromatic compounds Carboxylic acid hydrazides Azacyclic compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Pyridine carboxylic acid or derivatives - Imidolactam - Heteroaromatic compound - Carboxylic acid hydrazide - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as pyridinecarboxylic acids and derivatives. These are compounds containing a pyridine ring bearing a carboxylic acid group or a derivative thereof. |
| External Descriptors | Not available |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 C23031063 | Certificate of Analysis | Dec 12, 2025 | P414503 |
| C23031068 | Certificate of Analysis | Dec 12, 2025 | P414503 |
| C23031079 | Certificate of Analysis | Dec 12, 2025 | P414503 |
| C23031084 | Certificate of Analysis | Dec 12, 2025 | P414503 |
| C23031086 | Certificate of Analysis | Dec 12, 2025 | P414503 |
| C23031111 | Certificate of Analysis | Dec 12, 2025 | P414503 |
| I2222063 | Certificate of Analysis | Jul 10, 2025 | P414503 |
| I2222073 | Certificate of Analysis | Jul 10, 2025 | P414503 |
| Solubilità | Solubility (25°C) In vitro DMSO: 43 mg/mL (200.72 mM); Ethanol: 22 mg/mL (102.69 mM); Water: Insoluble; |
|---|---|
| Peso molecolare | 214.220 g/mol |
| XLogP3 | 1.600 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 214.085 Da |
| Monoisotopic Mass | 214.085 Da |
| Topological Polar Surface Area | 66.900 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 234.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
