Halomethanes
Medchemexpress LLC Tenuazonic acid | 610-88-8 | 5 MG
Tenuazonic acid is a nonhost-selective mycotoxin belonging to the tetramic acids family. It inhibits protein biosynthesis on ribosomes by suppressing the release of new protein. It is acutely toxic and functions as a photosystem II (PSII) inhibitor. Additionally, it exhibits antiviral effects on measles virus, enterovirus, and respiratory virus, and has an inhibitory effect on skin cancer.
- Nonhost-selective mycotoxin
- Belongs to the tetramic acids family
- Inhibits protein biosynthesis on ribosomes
- Blocks electron transport beyond the primary quinone receptor (QA)
- Acts as a photosystem II (PSII) inhibitor
- Has antiviral effects on measles virus, enterovirus, and respiratory virus
- Has an inhibitory effect on skin cancer
eMolecules 593-71-5 | Chloroiodomethane | Combi-Blocks | MFCD00001078 | 176.380 | CH2ClI | 98.000 | ClCI | 5g | 117541117
Chloroiodomethane | Combi-Blocks | 593-71-5 | MFCD00001078 | 176.380 | CH2ClI | 98.000 | ClCI | 5g | 117541117
eMolecules 3518-88-5 | Ambeed | Diethyl 33-azanediyldipropanoate | 250mg | 600841193 | A474093 | MFCD14705114 | 217.265 | C10H19NO4
Ambeed | 2-(Bromomethyl)-14-dichlorobenzene | 1g | 532081552 | A710824 | 85482-13-9 | MFCD00236034 | 239.920 | C7H5BrCl2
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Medchemexpress LLC Aryl Hydrocarbon Receptor Antibody (YA610) | Predicted band size: 96 kDa; Observed band size: 105 kDa | 50 UL
Aryl Hydrocarbon Receptor Antibody (YA610) is a rabbit-derived, non-conjugated IgG monoclonal antibody, specifically targeting the Aryl Hydrocarbon Receptor. It is for research use only and not intended for patient use.
- Rabbit-derived recombinant monoclonal antibody
- Targets human Aryl Hydrocarbon Receptor
- Validated for Western Blot and Immunocytochemistry/Immunofluorescence
- Supplied as a liquid in TBS with BSA, glycerol, and sodium azide preservative
- Store at -20°C for up to 1 year
- Plays a role in development, immunity, and cancer
- Regulates angiogenesis, hematopoiesis, and metabolism
- Functions as a ligand-activated transcription factor
- Subcellular localization in cytoplasm and nucleus
eMolecules 593-71-5 | Chloroiodomethane | Combi-Blocks | MFCD00001078 | 176.380 | CH2ClI | 98.000 | ClCI | 500g | 228814127
Chloroiodomethane | Combi-Blocks | 593-71-5 | MFCD00001078 | 176.380 | CH2ClI | 98.000 | ClCI | 500g | 228814127
eMolecules 558-13-4 | Carbon tetrabromide | Oakwood Chemicals | MFCD00000117 | 331.627 | CBr4 | 99.000 | BrC(Br)(Br)Br | 5g | 480153916
Carbon tetrabromide | Oakwood Chemicals | 558-13-4 | MFCD00000117 | 331.627 | CBr4 | 99.000 | BrC(Br)(Br)Br | 5g | 480153916
![Medchemexpress LLC 3-{[(3,4-dichlorophenyl)amino]carbonyl}bicyclo[2.2.1]hept-5-ene-2-carboxylic acid | 199735-88-1 | MFCD00167693 | >98.0% | 326.17 g·mol⁻¹ | C15H13Cl2NO3 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000242454.png-250.jpg)
Medchemexpress LLC 3-{[(3,4-dichlorophenyl)amino]carbonyl}bicyclo[2.2.1]hept-5-ene-2-carboxylic acid | 199735-88-1 | MFCD00167693 | >98.0% | 326.17 g·mol⁻¹ | C15H13Cl2NO3 | 50 MG
CADD522 is a small-molecule inhibitor of RUNX2-DNA binding used in research to downregulate RUNX2-mediated transcription. It has demonstrated antiproliferative and antimetastatic effects in cell-based and animal cancer studies and is supplied as a solid for laboratory use.
- Inhibits RUNX2-DNA binding with reported IC50 ≈ 10 nM.
- Demonstrated activity in in vitro and in vivo cancer models.
- High purity appropriate for biochemical and cell-based assays.
- Provided in small research quantities for screening and mechanistic studies.
- Stable solid form; store at -20 °C under recommended conditions.
Medchemexpress LLC 1-Propanone, 3,3,3-trifluoro-2-methoxy-1-[(7R)-7-(2-methoxyphenyl)-3,9-diazaspiro[5.5]undec-3-yl]-2-phenyl-, (2R)- | 2413020-56-9 | 99.9% | 476.53 | 25 MG
BAY-593 is an orally active GGTase-I inhibitor. It can block YAP1/TAZ signaling in animals and has antitumor activity.
- Orally active GGTase-I inhibitor
- Blocks YAP1/TAZ signaling in animals
- Exhibits antitumor activity
- Inhibits proliferation of HT-1080 and MDA-MB-231 cells with IC50 values of 0.038 and 0.564 μM, respectively
- Shows dose-dependent antitumor activity in HT-1080 fibrosarcoma and MDA-MB-231 triple negative breast cancer xenotransplantation mouse models
Medchemexpress LLC Methylene blue | 61-73-4 | 95.0% | C16H18ClN3S | 10 MM * 1 ML
Methylene blue is an inhibitor of guanylyl cyclase (sGC), monoamine oxidase A (MAO-A), and NO synthase (NOS). It acts as a vasopressor and is commonly used as a dye in medical procedures. This REDOX cycling compound crosses the blood-brain barrier, functions as a Tau aggregation inhibitor, and has been shown to reduce cerebral edema, attenuate microglial activation, and decrease neuroinflammation.
- Inhibits guanylyl cyclase (sGC), monoamine oxidase A (MAO-A), and NO synthase (NOS)
- Acts as a vasopressor and dye in medical procedures
- REDOX cycling compound; crosses the blood-brain barrier
- Inhibits Tau aggregation
- Reduces cerebral edema and attenuates microglial activation
- Decreases neuroinflammation
![eMolecules 1128-88-7 | 1-(BENZO[B]THIOPHEN-5-YL)ETHANONE | AstaTech | MFCD16619666 | 176.230 | C10H8OS | 95.000 | CC(=O)c1ccc2sccc2c1 | 0.25g | 381448158](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502457283.PNG-250.jpg)
eMolecules 1128-88-7 | 1-(BENZO[B]THIOPHEN-5-YL)ETHANONE | AstaTech | MFCD16619666 | 176.230 | C10H8OS | 95.000 | CC(=O)c1ccc2sccc2c1 | 0.25g | 381448158
1-(BENZO[B]THIOPHEN-5-YL)ETHANONE | AstaTech | 1128-88-7 | MFCD16619666 | 176.230 | C10H8OS | 95.000 | CC(=O)c1ccc2sccc2c1 | 0.25g | 381448158
eMolecules 1343722-88-2 | ChemScene | 4-Chloro-2-fluorobenzothioamide | 250mg | 572194186 | CS-0114061 | MFCD17290209 | 189.63 | C7H5ClFNS
ChemScene | Sodium tetrahydrofuran-3-sulfinate | 250mg | 801476584 | CS-0530358 | 1622013-59-5 | MFCD28124335 | 158.150 | C4H7NaO3S
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Medchemexpress LLC MPP+ (iodide) | 36913-39-0 | 99.96% | 297.14 | 25 MG
MPP+ iodide is a toxic metabolite of the neurotoxin MPTP. It causes symptoms of Parkinson's disease in animal models by selectively destroying dopaminergic neurons in the substantia nigra. The compound is taken up by the dopamine transporter into dopaminergic neurons, where it exerts its neurotoxic action on mitochondria by affecting complex I of the respiratory chain. It is also a high-affinity substrate for the serotonin transporter (SERT).
- Toxic metabolite of neurotoxin MPTP
- Causes Parkinson's disease symptoms in animal models
- Selectively destroys dopaminergic neurons in the substantia nigra
- Taken up by the dopamine transporter
- Exerts neurotoxic action on mitochondria by affecting complex I of the respiratory chain
- High-affinity substrate for the serotonin transporter (SERT)
eMolecules 1211591-88-6 | 5-(Trifluoromethyl)pyridazin-3-amine | ChemScene | MFCD20726836 | 163.103 | C5H4F3N3 | 98.000 | Nc1cc(cnn1)C(F)(F)F | 50mg | 582640721
5-(Trifluoromethyl)pyridazin-3-amine | ChemScene | 1211591-88-6 | MFCD20726836 | 163.103 | C5H4F3N3 | 98.000 | Nc1cc(cnn1)C(F)(F)F | 50mg | 582640721
Medchemexpress LLC CCL4 Human 100ug
CCL4 Protein Human is a small cytokine of the CC chemokine subfamily that binds to the CCR5 chemokine receptor on the cell surface promotes leukocyte aggregation under various inflammatory conditions and contributes to immune protection against human immunodeficiency virus type 1 CCL4 Protein Human is a recombinant human CCL4 (A24-N92) expressed by E coli[1]
![eMolecules 914780-95-3 | Ambeed | 14-Dioxa-10-azadispiro[4.2.4.2]tetradecan-11-one | 1g | 600846241 | A713387 | MFCD24566289 | 211.261 | C11H17NO3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502464824.JPG-250.jpg)
eMolecules 914780-95-3 | Ambeed | 14-Dioxa-10-azadispiro[4.2.4.2]tetradecan-11-one | 1g | 600846241 | A713387 | MFCD24566289 | 211.261 | C11H17NO3
Ambeed | 14-Dioxa-10-azadispiro[4.2.4.2]tetradecan-11-one | 1g | 600846241 | A713387 | 914780-95-3 | MFCD24566289 | 211.261 | C11H17NO3