Cyclohexylphenols
Medchemexpress LLC 2-methyl-1,3-cyclohexanedione | 1193-55-1 | MFCD00001587 | 99.9% | 126.15 g/mol | C7H10O2 | 10 G
2-Methyl-1,3-cyclohexanedione is a small-molecule reagent used primarily as a drug-synthetic intermediate and laboratory research chemical. It is offered in multiple pack sizes and reported at high purity for use in organic synthesis and related applications. Listed uses include research-only applications and potential cosmetic ingredient uses where applicable.
- High reported purity (listed as 99.86% on supplier documentation).
- Molecular formula C7H10O2 and molecular weight 126.15 g/mol.
- Intended for research and synthesis applications as a building block.
- Available in a range of pack sizes suitable for laboratory use.
- Supplied with safety and datasheet documentation for laboratory handling.
eMolecules 1256834-28-2 | Methyl 4,5-dichloropicolinate | ChemScene | MFCD18257882 | 206.020 | C7H5Cl2NO2 | 98.000 | COC(=O)c1cc(Cl)c(Cl)cn1 | 100mg | 632284671
Methyl 4,5-dichloropicolinate | ChemScene | 1256834-28-2 | MFCD18257882 | 206.020 | C7H5Cl2NO2 | 98.000 | COC(=O)c1cc(Cl)c(Cl)cn1 | 100mg | 632284671
Medchemexpress LLC HY-10790 5mg Medchemexpress, Cilomilast CAS:153259-65-5 Purity:>98%
Medchemexpress, HY-10790 5mg Cilomilast CAS:153259-65-5 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC Fraxinol | 486-28-2 | 5 MG
Fraxinol is a compound isolated from *Lobelia chinensis* that acts as a Cytochrome P450 Inhibitor. It exhibits cytotoxicity against human U937 cells with a CC50 > 2 mM and growth inhibition with an IC50 > 400 μM after 48 hours.
- Isolated from Lobelia chinensis
- Identified as a Cytochrome P450 inhibitor
- High purity of 98.82%
- Cytotoxicity against human U937 cells (CC50 > 2 mM)
- Growth inhibition of human U937 cells (IC50 > 400 μM)
- Molecular formula: C11H10O5
- Molecular weight: 222.19
- Appearance: Light yellow to yellow solid
- Recommended storage: 4°C, sealed, away from moisture and light
Medchemexpress LLC ML-9 (free base) | 110448-31-2 | 99.9% | 324.83 | C15H17ClN2O2S | 50 MG
ML-9 (free base) is a small-molecule kinase inhibitor used in biochemical and cell-based research to probe myosin light-chain kinase (MLCK) and Akt-related signaling. It also modulates PKA, PKC, and STIM1 activity and can induce autophagy, making it useful for studies of cytoskeleton regulation and autophagic processes.
- Inhibits myosin light-chain kinase and Akt kinase.
- Modulates PKA, PKC, and STIM1 activity.
- Induces autophagy by promoting autophagosome formation.
- Suitable for biochemical and cell-based assays.
- Well characterized with reported chemical identifiers and molecular weight.
Medchemexpress LLC Olaquindox | 23696-28-8 | MFCD00210341 | 99.9% | 263.25 | C12H13N3O4 | 10 MG
Olaquindox is a quinoxaline-derivative antibiotic supplied as a research-grade solid. It is orally active and has been used historically as a growth promoter in swine; provided at high purity for laboratory and analytical applications.
- High purity (99.9%) suitable for analytical use.
- Orally active quinoxaline derivative with documented biological effects.
- Solid, light yellow to green-yellow appearance for easy handling.
- Suitable for research and analytical applications.
- Store protected from light at 4°C; in solvent, store at -80°C for long-term stability.
Medchemexpress LLC Estriol | 50-27-1 | 500 MG
Estriol (Oestriol) is an orally active estrogen and an ERα and ERβ agonist. It is also a potent GPR30 antagonist in estrogen receptor-negative breast cancer cells. Estriol can ameliorate disease severity through immunomodulatory mechanisms that decrease tissue inflammation and has powerful proconvulsant effects.
- Orally active estrogen
- ERα and ERβ agonist
- Potent GPR30 antagonist in estrogen receptor-negative breast cancer cells
- Ameliorates disease severity through immunomodulatory mechanisms that decrease tissue inflammation
- Has powerful proconvulsant effects
eMolecules 486-28-2 | Medchem Express | Fraxinol | 5mg | 495802714 | HY-N2372 | MFCD08693526 | 222.196 | C11H10O5
Medchem Express | AMXT-1501 tetrahydrochloride | 5mg | 475641612 | HY-124617A | | 714.770 | C32H72Cl4N6O2
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Medchemexpress LLC 2-methyl-1,3-cyclohexanedione | 1193-55-1 | MFCD00001587 | 99.9% | 126.15 g/mol | C7H10O2 | 500 G
2-Methyl-1,3-cyclohexanedione (CAS 1193-55-1) is an organic building block used as a drug-synthesis intermediate and reported for use in cosmetic ingredient syntheses. It is provided as a high-purity reagent for research and development and is suitable for multi-step organic synthesis and analytical confirmation workflows.
- High purity suitable for synthetic applications.
- Characterized by GC assay for composition confirmation.
- Available in multiple pack sizes for scalability.
- Molecular formula C7H10O2 and molecular weight 126.15 g/mol.
- Stable under recommended storage for consistent performance.
eMolecules 1189767-28-9 | Medchem Express | Osoresnontrine | 10mg | 446260430 | HY-112831 | 311.345 | C16H17N5O2
ChemScene | 1-(35-Dichloropyridin-4-yl)ethanol | 250mg | 536838406 | CS-M2092 | 1254473-66-9 | MFCD23163275 | 192.040 | C7H7Cl2NO
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Medchemexpress LLC NU9056 | 1450644-28-6 | 98.8% | 232.37 | 1 MG
NU9056 is a potent and selective Tip60 (KAT5) histone acetyltransferase inhibitor with an IC50 of 2 μM. It demonstrates over 16-fold selectivity for Tip60 compared to PCAF, p300, and GCN5. This compound is known to induce apoptosis in prostate cancer cells.
- Activates caspase 3 and caspase 9 in a time- and concentration-dependent manner.
- Decreases acetylated histone H4K16, H3K14, and H4K8 levels.
- Reduces androgen receptor, prostate-specific antigen, p53, and p21 protein levels.
- Induces apoptosis in LNCaP cells.