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 |
|---|
≥97% 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
H3B-6527 H3B-6527 is a highly selective covalent FGFR4 inhibitor with an IC50 value of <1.2 nM and at least 250-fold selectivity over FGFR1-3 (IC50 values of 320, 1,290 and 1,060 nM respectively).
Targets
FGFR4 (Cell-free assay) <1.2 nM
In vitro
H3B-6527 shows robust inhibition of the target kinase FGFR4 with an IC50 value of <1.2 nmol/L and at least 250-fold selectivity over FGFR1-3 (IC50 values of 320, 1,290 and 1,060 nmol/L respectively). TAOK2, JNK2, and CSF1R are also less sensitive to H3B-6527 treatment with IC50 values of 690, >10,000, and >10,000 nmol/L, respectively. H3B-6527 inhibits FGFR4 signaling, proliferation, and leads to apoptosis in a HCC cell line (Hepatocellular carcinoma). Treatment on Hep3B cells leads to robust activation of caspase-3/7, an apoptotic marker, in a concentration-dependent manner, indicating FGFR4 inhibition by H3B-6527 leads to cell death in HCC cell lines. H3B-6527 has the selectivity and the selective dependence on FGFR4 across cancer types.
In vivo
In the Hep3B human HCC xenograft mouse model, H3B-6527 shows dose-proportional plasma exposures and greater than dose-proportional tumor exposures within the dose range evaluated (30, 100, and 300 mg/kg). The H3B-6527 pharmacodynamic response as measured by CYP7A1 mRNA and pERK1/2 protein levels is dose dependent, with higher doses leading to sustained responses. Oral treatment of H3B-6527, twice daily, inhibits xenograft growth in a dose-dependent manner in nude mice, with the 300 or 100 mg/kg twice daily, significantly inhibiting tumor growth in both Hep3B subcutaneous and orthotopic xenograft model and causing tumor regressions in the subcutaneous xenograft model. Palbociclib can enhance H3B-6527 efficacy and promote tumor regression in JHH-7 model where H3B-6527 as a single agent can only lead to tumor stasis.
Cell Research(from reference)
Cell lines:Hep3B cells
Concentrations:100 and 300 nmol/L
Incubation Time:0.5, 1, 2, 4, 8, and 24 hours
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 | Diazinanes |
| Subclass | Piperazines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylpiperazines |
| Alternative Parents | N-arylpiperazines N-phenylureas Dimethoxybenzenes Methoxyanilines Anilides Phenoxy compounds N-arylamides Dichlorobenzenes Dialkylarylamines Anisoles N-alkylpiperazines Aminopyrimidines and derivatives Alkyl aryl ethers Imidolactams Aryl chlorides Heteroaromatic compounds Acrylic acids and derivatives Ureas Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Secondary amines Azacyclic compounds Organopnictogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | N-arylpiperazine - Phenylpiperazine - M-dimethoxybenzene - Dimethoxybenzene - N-phenylurea - Methoxyaniline - Anilide - Phenoxy compound - Methoxybenzene - Aniline or substituted anilines - Dialkylarylamine - N-arylamide - Tertiary aliphatic/aromatic amine - Phenol ether - 1,3-dichlorobenzene - Anisole - N-alkylpiperazine - Halobenzene - Chlorobenzene - Aminopyrimidine - Alkyl aryl ether - Imidolactam - Benzenoid - Pyrimidine - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Acrylic acid or derivatives - Heteroaromatic compound - Urea - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carbonic acid derivative - Carboxamide group - Amino acid or derivatives - Azacycle - Secondary amine - Ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Carbonyl group - Amine - Aromatic heteromonocyclic compound |
| Descrição | This compound belongs to the class of organic compounds known as phenylpiperazines. These are compounds containing a phenylpiperazine skeleton, which consists of a piperazine bound to a phenyl group. |
| 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 | Data | Item |
|---|---|---|---|
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 | |
| Certificate of Analysis | Feb 04, 2026 | H414109 |
| Solubilidade | Solubility (25°C) In vitro DMSO: 50 mg/mL (79.42 mM); Water: Insoluble; Ethanol: Insoluble; |
|---|---|
| DMSO (mg/mL) Solubilidade máxima | 50 |
| DMSO (mM) Solubilidade máxima | 79.42307081 |
| Água (mg/mL) Solubilidade máxima | <1 |
| Peso molecular | 629.500 g/mol |
| XLogP3 | 4.400 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 10 |
| Exact Mass | 628.208 Da |
| Monoisotopic Mass | 628.208 Da |
| Topological Polar Surface Area | 124.000 Ų |
| Heavy Atom Count | 43 |
| Formal Charge | 0 |
| Complexity | 913.000 |
| 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 |
No item-specific, tested application protocols are provided for this SKU. The following is general guidance for handling small-molecule research compounds in biochemical and cellular assays.
Biochemical enzyme assay (general)
Cell-based assay (general)
Analytical QC check (general)
Note: These are general, literature-style procedures and are not item-specific validations. Consult the CoA/SDS for material handling limits.
Item-specific biological target information is not provided in the product data. The following context is general/literature-based and should not be interpreted as a specification for this item.
General notes on small-molecule kinase-directed probes (literature):
Experimental considerations (general):
Important: No medical or clinical claims are made. This product is supplied strictly for research use only, as stated in the product data.
This product is not a buffering reagent and has no typical role in preparing buffer systems.
General guidance for use in buffered biological assays (not item-specific):
For bioactive screening compounds, the principal environmental considerations are solvent choice, packaging, and waste minimization rather than substitution of the active itself.
Greener handling strategies (general):
Comparison of common assay solvents (general)
Waste management
No pharmacopeial grade or excipient role is specified for this item; it is supplied strictly for research use only.
General, non-clinical context for small-molecule research standards:
Documentation recommendations:
Item-specific physico-chemical data are not provided for this catalog entry.
General, literature-based expectations for small-molecule screening solids (guidance only, not item specifications):
Important: Treat all numerical property needs (e.g., exact solubility limits, MP) as Not specified for this item unless stated on the CoA/Spec Sheet. Use batch documentation for authoritative values.
How to interpret typical quality indicators for small-molecule screening compounds (general guidance):
Recommendations
This item is a bioactive small molecule for research screening and is not typically employed as a synthetic reagent or catalyst.
Applicable research uses (general guidance, not item-specific claims):
Not commonly applicable
Practical tips
Not applicable. This product is not intended for use as a reagent or catalyst in synthetic organic reactions.
General guidance for biological assay conditions (not item-specific):
GHS and hazard classifications are not provided for this item; consult the SDS for authoritative information.
General laboratory precautions (good practice for bioactive small molecules):
Storage and transport
This product is a small-molecule intended for research screening; item-specific solubility is not provided.
General solvent strategy for bioactive small molecules (guidance, not item specifications):
Comparison (general)
Reconstitution (general guidance; not item-specific specifications):
Stability (general):
Note: If batch-specific solubility limits, extinction coefficients, or stability data are required, consult the CoA/Spec Sheet for this item.
Structural description
Identity best practices
This product is supplied as a finished small-molecule research compound and is not generally used as a synthetic intermediate or reagent.
If derivatization is desired (general considerations):
Conclusion: Treat this item as a terminal research probe rather than a building block. Consult the CoA or primary literature for structural data if synthetic campaigns are contemplated.
Item-specific target, epitope, or binding data have not been provided in the product data for this SKU.
Note: If you require definitive target specificity or kinome selectivity profiling, please contact us with the lot number to request any available internal data or references.