Organometallic Compounds
![Medchemexpress LLC Silane, [[(1a,3b,5E,7E,22E)-9,10-secoergosta-5,7,10(19),22-tetraene-1,3-diyl]bis(oxy)]bis | 111594-58-2 | C40H72O2Si2 | 1 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Medchemexpress LLC Silane, [[(1a,3b,5E,7E,22E)-9,10-secoergosta-5,7,10(19),22-tetraene-1,3-diyl]bis(oxy)]bis | 111594-58-2 | C40H72O2Si2 | 1 G
Silane, [[(1a,3b,5E,7E,22E)-9,10-secoergosta-5,7,10(19),22-tetraene-1,3-diyl]bis(oxy)]bis[(1,1-dimethylethyl)dimethyl- is a drug intermediate for synthesis of various active compounds.
Medchemexpress LLC RS-79948 hydrochloride hemihydrate | 186002-54-0 | 99.5% | 400.96 | C19H29ClN2O3S | 5 MG
RS-79948-197 hemihydrate is the hemihydrate salt of RS-79948, a selective non-imidazoline α2-adrenoceptor antagonist used in adrenergic receptor pharmacology research. Supplied as a white to off-white, high-purity solid in milligram quantities, it is intended for ligand binding, receptor characterization, and related in vitro or in vivo studies.
- High purity (99.5%) suitable for sensitive assays.
- Hemihydrate solid form for stable handling and storage.
- Selective α2-adrenoceptor antagonist activity reported across species.
- Small mg packaging appropriate for tracer and ligand studies.
- Certificate of analysis and safety data available for each batch.
Selleck Chemical LLC Pimavanserin tartrate
Pimavanserin tartrate(ACP-103) is a potent and selective serotonin 5-HT2A inverse agonist with pIC50 of 8 73 used to treat psychosis associated with Parkinson s disease
Medchemexpress LLC (S,R,S)-AHPC-C2-amide-benzofuranylmethyl-pyridine | 2347517-69-3 | 98.6% | 750.91 | 50 MG
(S,R,S)-AHPC-C2-amide-benzofuranylmethyl-pyridine is a dual target PROTAC that can target the ubiquitination and degradation of Smad3, and also improve the HIF-α protein level. It possesses a multi-path anti-fibrosis function and a renal protection function for research of renal anemia. This compound can be utilized for research on prostate cancer and other cancers.
- Targets ubiquitination and degradation of Smad3
- Improves HIF-α protein level
- Possesses multi-path anti-fibrosis function
- Provides renal protection function for research of renal anemia
- Degrades Smad3 protein in a concentration-dependent manner
- Significantly upregulates HIF-2α protein level in rat renal fibroblasts
- Can degrade Smad3 protein levels and downregulate the androgen receptor (AR) pathway in CWR22Rv1 cells
- Suitable for research on prostate cancer and other cancers
![Medchemexpress LLC [2-[[5-[(4-fluorophenyl)carbamoyl]pyrimidin-2-yl]sulfanylmethyl]-4-(trifluoromethoxy)phenyl]boronic acid | 1648843-04-2 | 98.7% | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000233653.png-250.jpg)
Medchemexpress LLC [2-[[5-[(4-fluorophenyl)carbamoyl]pyrimidin-2-yl]sulfanylmethyl]-4-(trifluoromethoxy)phenyl]boronic acid | 1648843-04-2 | 98.7% | 1 ML
SX-682 is a small-molecule allosteric inhibitor of chemokine receptors CXCR1 and CXCR2. It has been investigated preclinically and in clinical trials for reducing tumor myeloid-derived suppressor cell recruitment and enhancing anti-tumor immune responses.
- Potent CXCR1/2 allosteric inhibitor used in research.
- Investigated in immuno-oncology and tumor microenvironment studies.
- Reported to reduce myeloid-derived suppressor cell recruitment.
- Supplied for laboratory research, often as concentrated solutions or milligram-scale powders.
- Soluble in DMSO at high concentrations for in vitro use.
C)C(C)C | 25g | 410168138](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000170491.jpg-250.jpg)
eMolecules 6485-79-6 | Triisopropylsilane | AA Blocks LLC | MFCD00009657 | 158.360 | C9H22Si | 0.000 | CC(C)[SiH](C(C)C)C(C)C | 25g | 410168138
Triisopropylsilane | AA Blocks LLC | 6485-79-6 | MFCD00009657 | 158.360 | C9H22Si | 0.000 | CC(C)[SiH](C(C)C)C(C)C | 25g | 410168138
Medchemexpress LLC Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate | 632-93-9 | MFCD00005950 | 99.8% | 267.32 | C14H21NO4 | 1 ML
Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate is a dihydropyridine derivative used in research as a porphyrin inducer and ferrochelatase inhibitor. It is applied in preclinical studies to disrupt heme biosynthesis and to model cholestatic liver injury. The compound is supplied as concentrated DMSO solutions and as solid material for laboratory use.
- Orally active porphyrin inducer and ferrochelatase inhibitor.
- Used to model cholestatic liver injury and study heme biosynthesis disruption.
- Available as 10 mM solution in DMSO and as solids in multiple sizes.
- Reported purity approximately 99.8%.
- Molecular weight 267.32 and formula C14H21NO4.
- Powder and solution storage conditions available for long-term stability.