Phenols
Medchemexpress LLC Deoxybrevianamide E | 34610-68-9 | MFCD14635384 | >99.0% | 351.44 g/mol | C21H25N3O2 | 1MG
Deoxybrevianamide E is an indole alkaloid and a biosynthetic precursor for advanced metabolites isolated from marine-derived Aspergillus species. It is supplied as a research-grade small-molecule sample for natural-product and biosynthesis studies. Key identifiers include CAS 34610-68-9, molecular formula C21H25N3O2, and molecular weight 351.44 g/mol.
- Indole alkaloid biosynthetic precursor.
- Suitable for natural-product and biosynthesis research.
- CAS number 34610-68-9 and molecular formula C21H25N3O2.
- Molecular weight 351.44 g/mol.
- Available in small quantities (for example, 1 mg) for research use.
- Reported purity >99.0% by HPLC.
- Intended for research use only; not for human or veterinary use.
Medchemexpress LLC 5-bromo-3-phenyl salicylic acid | 99514-99-5 | 98.0% | 293.11 g/mol | C13H9BrO3 | 5 MG
5-Bromo-3-phenyl salicylic acid is a salicylic acid derivative for research use that acts as a selective inhibitor of human 20α-hydroxysteroid dehydrogenase (AKR1C1), with a reported Ki of 140 nM. The compound is supplied as a solid (off-white to light yellow) with a reported purity of about 98% and includes downloadable product documents (COA, SDS).
- Selective AKR1C1 inhibitor with Ki = 140 nM.
- Reported purity approximately 98.0%.
- Off-white to light yellow solid suitable for laboratory handling.
- Soluble in common organic solvents such as DMSO, ethanol, and DMF.
- Recommended storage: -20°C sealed; in solution -80°C up to 6 months or -20°C up to 1 month.
![Medchemexpress LLC 4,7-dihydro-6-(1-methylethyl)-7-oxo-5-phenyl-pyrazolo[1,5-a]pyrimidine-3-carbonitrile | 1628208-23-0 | 99.0% | 278.31 g/mol | C16H14N4O | 1 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000214795.png-250.jpg)
Medchemexpress LLC 4,7-dihydro-6-(1-methylethyl)-7-oxo-5-phenyl-pyrazolo[1,5-a]pyrimidine-3-carbonitrile | 1628208-23-0 | 99.0% | 278.31 g/mol | C16H14N4O | 1 MG
CPI-455 is a potent, cell-active pan-KDM5 (histone lysine demethylase 5 family) inhibitor used in research to increase global H3K4 trimethylation and investigate KDM5-dependent biology. It is supplied as a white to off-white solid and has documented enzymatic potency and analytical characterization suitable for laboratory studies.
- Potent pan-KDM5 inhibition with low-nanomolar biochemical activity.
- Promotes increased H3K4 trimethylation in cellular models.
- High purity appropriate for research applications.
- Solid form for convenient handling and storage.
- Documented analytical data and supporting datasheet available.
Medchemexpress LLC Rho-Kinase-IN-2 | 2573071-18-6 | C20H25FN4O2 | 25 MG
Rho-Kinase-IN-2 (Compound 23) is an orally active, selective, and CNS-penetrant Rho Kinase (ROCK) inhibitor with an IC50 of 3 nM for ROCK2. It can be used in Huntington's research. This product is for research use only and not sold to patients. It appears as a solid, light yellow to yellow in color, with a molecular weight of 372.44.
- Orally active
- Selective and CNS-penetrant Rho Kinase (ROCK) inhibitor
- ROCK2 IC50 of 3 nM
- Useful in Huntington's research
- Solid, light yellow to yellow appearance
- Molecular weight of 372.44
- CAS number: 2573071-18-6
- Chemical formula: C20H25FN4O2
Aobchem 5-Bromo-4-methoxy-2-methylpyridine | ≥95% | CAS 886372-61-8 | C7H8BrNO | 500mg
5-Bromo-4-methoxy-2-methylpyridine | ≥95% | CAS 886372-61-8 | C7H8BrNO | 500mg
Medchemexpress LLC OARV-771 | 2683008-37-7 | 98.77% | C49H59CIN8O8S2 | 100 MG
OARV-771 is a VHL-based BET degrader (PROTAC) with improved cell permeability. It demonstrates an antiproliferative effect with an EC50 value of 4 nM in MV4;11 cells.
- Exhibits DC50 values of 6 nM for Brd4, 1 nM for Brd2, and 4 nM for Brd3.
- Improved cell permeability.
- Shows antiproliferative effect in MV4;11 cells.