Phenols
Medchemexpress LLC 2-Hydrazinobenzothiazole | 615-21-4 | 99.95% | C7H7N3S | 50 G
This product is a potent inhibitor of IDO1, with an IC50 of 8 μM. It functions by interacting with the enzyme's haem through its hydrazine component. This compound shows potential for research related to immune system diseases.
- Potent inhibitory activity against a specific enzyme.
- Interacts with the enzyme's active site via a hydrazine group.
- Suitable for investigation into immune system-related conditions.
(C)C(F)(F)F | 250g | 590288702](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000223712.jpg-250.jpg)
eMolecules 81290-20-2 | Trifluoromethyltrimethylsilane | Oakwood Chemical | MFCD00145454 | 142.196 | C4H9F3Si | 98.000 | C[Si](C)(C)C(F)(F)F | 250g | 590288702
Trifluoromethyltrimethylsilane | Oakwood Chemical | 81290-20-2 | MFCD00145454 | 142.196 | C4H9F3Si | 98.000 | C[Si](C)(C)C(F)(F)F | 250g | 590288702
Medchemexpress LLC 3,6-dichloropyridine-2-carboxylic acid | 1702-17-6 | MFCD00078655 | 98.5% | 192.00 g/mol | C6H3Cl2NO2 | 25 G
Clopyralid (3,6-dichloropyridine-2-carboxylic acid) is a selective pyridine herbicide supplied as a research-grade reagent for analytical, formulation, and experimental use. Supplied as a high-purity solid (CAS 1702-17-6), it is used in studies of herbicidal activity, environmental fate, and formulation development; consult the certificate of analysis and safety data sheet for handling and storage.
- High purity (98.52%), suitable for analytical applications.
- Confirmed identity as 3,6-dichloropyridine-2-carboxylic acid (CAS 1702-17-6).
- Available in multiple pack sizes, including 25 g.
- Appropriate for herbicide activity, toxicology, and environmental fate studies.
- Certificate of analysis and safety data sheet available for batch-specific information.
Medchemexpress LLC Animal-free FGF-8a protein, human (His) | >95.0% | 50UG
Animal-free FGF-8a protein, human (His) is a recombinant human FGF-8a isoform produced in Escherichia coli and supplied as a lyophilized powder with a C-terminal His tag. It is intended for cell culture applications, supplied as a 50 μg vial, with sequence range P55075-2 (Q23-R204), ≥95.0% purity, and an approximate molecular weight of 23.0 kDa. Reconstitute to 100-200 μg/mL as recommended.
- Recombinant human FGF-8a isoform with C-terminal His tag.
- Produced in Escherichia coli and supplied as lyophilized powder.
- High purity (≥95.0%) suitable for in vitro cell culture work.
- Approximate molecular weight ~23.0 kDa by SDS-PAGE.
- Recommended reconstitution concentration 100-200 μg/mL.
Medchemexpress LLC cis-1-Amino-9-octadecene | 112-90-3 | 90.0% | 267.49 | 500 G
cis-1-Amino-9-octadecene | 112-90-3 | 90.0% | 267.49 | 500 G
Medchemexpress LLC N-(3-tert-butyl-4-hydroxyphenyl)-2,6-dichloro-4-(cyclopentylamino)benzamide HCl | 100.0% | 457.82 | 25 MG
FXR antagonist 2 hydrochloride is a chemical compound that functions as an FXR antagonist.
- Functions as an FXR antagonist
- Tested to comply with given specifications
eMolecules 50270-27-4 | 2,4,6-Trichloropyrimidine-5-carbaldehyde | ChemScene | MFCD02257700 | 211.430 | C5HCl3N2O | 98.000 | Clc1nc(Cl)c(C=O)c(Cl)n1 | 10g | 536836811
2,4,6-Trichloropyrimidine-5-carbaldehyde | ChemScene | 50270-27-4 | MFCD02257700 | 211.430 | C5HCl3N2O | 98.000 | Clc1nc(Cl)c(C=O)c(Cl)n1 | 10g | 536836811
Cayman Chemical JWH 073 N 3hydroxybutyl meta
Expected product of the metabolism of JWH 073 by human liver microsomes in vitro, generated by the oxidation of the aminoalkyl chain; biological actions are unknown; intended for research and forensic applications
Medchemexpress LLC 2OH-BNPP1 | 833481-73-5 | MFCD28120704 | 99.7% | 297.35 g/mol | C16H19N5O | 50 MG
2OH-BNPP1 is a small-molecule inhibitor of BUB1 serine/threonine kinase used in cancer research to probe mitotic checkpoint signaling and cell-cycle regulation. The compound is supplied as a solid for laboratory research use.
- Inhibits BUB1 kinase, a serine/threonine kinase implicated in mitosis.
- High purity suitable for biochemical and cell-based assays.
- Soluble in DMSO; in vivo formulation examples are reported.
- Available in milligram-scale quantities including 50 mg.
- Powder storage at low temperature recommended for long-term stability.
Medchemexpress LLC Dolutegravir intermediate-1 | 1335210-23-5 | MFCD28978322 | 99.8% | 315.28 g/mol | C13H17NO8 | 100 G
Dolutegravir intermediate-1 is a synthetic building block used in the synthesis of the HIV integrase inhibitor dolutegravir. It is supplied as a high-purity solid or as a ready-to-use solution for research and development applications, with documentation available for safe handling and quality verification.
- High purity (99.8%) for reliable synthetic performance.
- Available as solid and as 10 mM solution in DMSO for flexible use.
- Multiple package sizes up to 500 g to support scale-up.
- Documented safety and quality data including SDS and COA.
- Suitable for research and process development workflows.
eMolecules 888318-22-7 | 6-Bromo-2,3-difluoroanisole | Combi-Blocks, Inc. | MFCD16295239 | 223.017 | C7H5BrF2O | 98.000 | COc1c(F)c(F)ccc1Br | 100g | 854189958
6-Bromo-2,3-difluoroanisole | Combi-Blocks, Inc. | 888318-22-7 | MFCD16295239 | 223.017 | C7H5BrF2O | 98.000 | COc1c(F)c(F)ccc1Br | 100g | 854189958