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Filtered Search Results
Medchemexpress LLC HY-103107 5mg Medchemexpress, LY334370 CAS:182563-08-2 Purity:>98%
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Medchemexpress, HY-103107 5mg LY334370 CAS:182563-08-2 LY334370 is a selective 5-HT1F receptor agonist with a Ki of 1.6 nM. 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.
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MEDCHEMEXPRESS LLC PH-797804 5MG
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501872082 PH-797804 5MG
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MEDCHEMEXPRESS LLC GSK429286A 5MG
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501872274 GSK429286A 5MG
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MEDCHEMEXPRESS LLC MIVEBRESIB 5MG
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501871657 MIVEBRESIB 5MG
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MEDCHEMEXPRESS LLC BMS 299897 10MG
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501873896 BMS 299897 10MG
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MEDCHEMEXPRESS LLC ZIRITAXESTAT 5MG
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501871878 ZIRITAXESTAT 5MG
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MEDCHEMEXPRESS LLC CANERTINIB DIHYDROCHLORIDE 1
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501872062 CANERTINIB DIHYDROCHLORIDE 1
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MEDCHEMEXPRESS LLC ZAMICASTAT 5MG
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501872138 ZAMICASTAT 5MG
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eMolecules 1394820-69-9 | Medchem Express | Ningetinib | 5mg | 446259047 | HY-107145A | MFCD28502048 | 556.594 | C31H29FN4O5
ChemScene | Methyl 4-bromo-23-difluorobenzoate | 100mg | 602865666 | CS-0105524 | 1807244-07-0 | MFCD27578309 | 251.027 | C8H5BrF2O2
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Enzo Life Sciences Rucaparib (free base) (200mg). CAS: 283173-50-2
Rucaparib is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway. Purity: ≥99% (HPLC). Solubility: Soluble in DMSO. Long Term Storage: -20°C.
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Medchemexpress LLC Fbpase-1 inhibitor-1 | 883973-99-7 | 99.1% | 377.63 g/mol | C13H7Cl3N2O3S | 5 MG
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FBPase-1 inhibitor-1 is an allosteric small-molecule inhibitor of fructose-1,6-bisphosphatase (FBPase-1) intended for laboratory research use. The compound has a benzoxazole benzenesulfonamide scaffold, molecular formula C13H7Cl3N2O3S, molecular weight 377.63 g/mol, and CAS 883973-99-7. It is supplied as solids in multiple sizes and as a 10 mM solution in DMSO for in vitro studies.
- Allosteric inhibition of FBPase-1 for gluconeogenesis research.
- High purity of 99.1% suitable for biochemical assays.
- Available as solids in multiple sizes and as a DMSO solution.
- Molecular formula C13H7Cl3N2O3S and molecular weight 377.63 g/mol for reference.
- For research use only; not for human or clinical applications.
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Medchemexpress LLC (R)-GSK-3685032 | 2170140-50-6 | 99.0% | 420.53 | 50 MG
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(R)-GSK-3685032 is the R-enantiomer of GSK-3685032, a first-in-class, non-time-dependent, noncovalently, reversible DNMT1-selective inhibitor with an IC50 of 0.036 μM. It is designed to induce robust loss of DNA methylation, transcriptional activation, and inhibition of cancer cell growth.
- Selective DNMT1 inhibitor
- Target: DNMT1
- Induces loss of DNA methylation and transcriptional activation
- Inhibits cancer cell growth
- Solid storage: 4°C, sealed, away from moisture and light
- Solvent storage: -80°C for 6 months; -20°C for 1 month (sealed, away from moisture and light)
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![Medchemexpress LLC 1-{5-[(2,4-Dimethylphenoxy)methyl]-1,3,4-thiadiazol-2-yl}-3-(4-methylphenyl)urea | 428478-94-8 | 98.1% | 368.45 g/mol | C19H20N4O2S | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000262308.png-250.jpg)
Medchemexpress LLC 1-{5-[(2,4-Dimethylphenoxy)methyl]-1,3,4-thiadiazol-2-yl}-3-(4-methylphenyl)urea | 428478-94-8 | 98.1% | 368.45 g/mol | C19H20N4O2S | 5 MG
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cyt-PTPε Inhibitor-1 is a small-molecule research reagent that potently inhibits cytosolic protein tyrosine phosphatase epsilon (cyt-PTPε). It binds the enzyme's catalytic domain, prevents c-Src dephosphorylation and activation, and has reported anti-osteoclastic activity. Supplied as a white to off-white solid with high purity for laboratory use.
- Potent cytosolic protein tyrosine phosphatase epsilon inhibitor.
- Binds the catalytic domain and blocks c-Src activation.
- Reported anti-osteoclastic biological activity.
- White to off-white solid suitable for laboratory handling.
- Molecular formula C19H20N4O2S; molecular weight 368.45 g/mol.
- Intended for research use only.
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Medchemexpress LLC HY-112611 10mg Medchemexpress, H3B-5942 CAS:2052128-15-9 Purity:>98%
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Medchemexpress, HY-112611 10mg H3B-5942 CAS:2052128-15-9 H3B-5942 is a selective, irreversible and orally active estrogen receptor covalent antagonist, inactivates both wild-type and mutant ERα by targeting Cys530, with Kis of 1 nM and 0.41 nM, respectively. H3B-5942 reduces ERα target gene GREB1, shows potent antitumor activity both in multiple cell lines or animals bearing ERαWT or ERα mutations. 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.
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Medchemexpress LLC (R)-GSK-3685032 | 2170140-50-6 | 99.0% | 420.53 g·mol⁻¹ | C22H24N6OS | 5 MG
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(R)-GSK-3685032 is the R-enantiomer of GSK-3685032, a reversible, DNMT1-selective inhibitor used in epigenetics research to induce loss of DNA methylation, transcriptional activation, and cancer cell growth inhibition. The compound is characterized by a defined molecular formula and high reported purity, and it is supplied for in vitro and preclinical research use.
- Reversible DNMT1-selective inhibitor with reported low-nanomolar activity.
- Induces loss of DNA methylation and downstream transcriptional activation.
- High reported purity and fully characterized molecular properties.
- Available in small, research-scale pack sizes for preclinical studies.
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