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Filtered Search Results
Medchemexpress LLC BMS-986094 50 mg
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BMS-986094 50MG
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Medchemexpress LLC PI3KA-IN-4 50 mg
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PI3KA-IN-4 50MG
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eMolecules 86569-86-0 | Ambeed | Ethyl 245-trichlorobenzoate | 25g | 632810321 | A1213555 | MFCD02149442 | 253.5 | C9H7Cl3O2
Ambeed | Ethyl 245-trichlorobenzoate | 25g | 632810321 | A1213555 | 86569-86-0 | MFCD02149442 | 253.500 | C9H7Cl3O2
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000742844 5-METHOXYTRYPTAMINE- 5MG
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Ambeed AMBEED
5000887798 1-BOC-TRYPTAMINE 100MG
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eMolecules 241146-66-7 | Ethyl 2,8-dimethylimidazo[1,2-a]pyridine-3-carboxylate | ChemScene | MFCD00139511 | 218.256 | C12H14N2O2 | 98.000 | CCOC(=O)c1c(C)nc2c(C)cccn12 | 1g | 712801680
Ethyl 2,8-dimethylimidazo[1,2-a]pyridine-3-carboxylate | ChemScene | 241146-66-7 | MFCD00139511 | 218.256 | C12H14N2O2 | 98.000 | CCOC(=O)c1c(C)nc2c(C)cccn12 | 1g | 712801680
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eMolecules 103628-48-4 | SUMATRIPTAN SUCCINATE | AstaTech | MFCD00902856 | 413.490 | C18H27N3O6S | 98.000 | OC(=O)CCC(O)=O.CNS(=O)(=O)Cc1ccc2[nH]cc(CCN(C)C)c2c1 | 1g | 551677402
SUMATRIPTAN SUCCINATE | AstaTech | 103628-48-4 | MFCD00902856 | 413.490 | C18H27N3O6S | 98.000 | OC(=O)CCC(O)=O.CNS(=O)(=O)Cc1ccc2[nH]cc(CCN(C)C)c2c1 | 1g | 551677402
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Medchemexpress LLC 1-[(6,8-dimethyl-2-oxo-1H-quinolin-3-yl)methyl]-3-(4-ethoxyphenyl)-1-(2-hydroxyethyl)thiourea | 484006-66-8 | 98.2% | 425.54 g/mol | C23H27N3O3S | 5 MG
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β-Glucuronidase-IN-1 is a potent, selective, uncompetitive inhibitor of E. coli bacterial β-glucuronidase used in biochemical and cellular research. It exhibits an IC50 of 283 nM and a Ki of 164 nM, and is supplied as a high-purity solid for assay development and inhibitor characterization.
- Potent, selective uncompetitive inhibitor of E. coli β-glucuronidase.
- Biochemical potency: IC50 283 nM; Ki 164 nM.
- High purity solid suitable for research assays (≈98.2%).
- Good solubility in DMSO (100 mg/mL) for convenient stock preparation.
- Available as small-scale solid and as a DMSO solution for convenience.
- Stable when stored as powder at -20°C (recommended storage conditions).
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Medchemexpress LLC Sisunatovir hydrochloride | 1903763-83-6 | 98.6% | 482.90 g/mol | C23H23ClF4N4O | 50MG
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Sisunatovir hydrochloride is the hydrochloride salt of sisunatovir (RV521), a small-molecule inhibitor of the respiratory syncytial virus fusion (RSV-F) protein. Supplied as a solid research chemical (50 mg), it exhibits low-nanomolar antiviral activity and is intended for in vitro and preclinical studies.
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eMolecules 343-94-2 | Medchem Express | Tryptamine (hydrochloride) | 1g | 786489644 | HY-W014971 | MFCD00012682 | 196.68 | C10H13ClN2
Medchem Express | CRA-026440 (hydrochloride) | 5mg | 769193615 | HY-19754A | 847459-98-7 | 456.930 | C23H25ClN4O4
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eMolecules 196205-07-9 | 7-Bromo-1H-indol-5-amine | Oakwood Chemical | MFCD09753942 | 211.062 | C8H7BrN2 | 95.000 | Nc1cc(Br)c2[nH]ccc2c1 | 250mg | 537694424
7-Bromo-1H-indol-5-amine | Oakwood Chemical | 196205-07-9 | MFCD09753942 | 211.062 | C8H7BrN2 | 95.000 | Nc1cc(Br)c2[nH]ccc2c1 | 250mg | 537694424
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Medchemexpress LLC Farudodstat | 1035688-66-4 | 99.7% | 10 MG
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Farudodstat is an orally active and potent Dihydroorotate Dehydrogenase (DHODH) inhibitor with an IC50 of 35 nM for the human DHODH enzyme. It inhibits protein synthesis by activating AP-1 transcription factors, induces apoptosis, and significantly prolongs survival in acute myeloid leukemia (AML) xenograft mice.
- Potent Dihydroorotate Dehydrogenase (DHODH) inhibitor
- IC50 of 35 nM for human DHODH enzyme
- Inhibits protein synthesis via activation of AP-1 transcription factors
- Induces apoptosis
- Substantially prolongs survival in acute myeloid leukemia (AML) xenograft mice
- Inhibits leukemic cell proliferation
- Increases cleaved caspase 8
- Decreases viability and induces differentiation in primary acute myeloid leukemia blasts and myelodysplastic syndrome samples
- Causes downregulation of EIF4B and RPL6 proteins
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Medchemexpress LLC Tryptamine guanosine carbamate | 1414808-96-0 | 99.8% | 469.45 | 100 MG
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Tryptamine guanosine carbamate (TpGc) is a selective HINT1 (histidine triad nucleotide-binding protein 1) inhibitor with a Ki of 34 μM and a Kd of 3.65 μM. It significantly enhances morphine antinociception while preventing the development of tolerance.
- Enhances morphine antinociception in 129 HINT1+/+ mice and has no effect in HINT1-/- mice.
- Significantly reduces the development of acute antinociceptive tolerance in HINT1+/+ mice but not in HINT1-/- animals.
- Reduces the recruitment of NMDAR activity promoted by morphine.
- Attenuates NMDAR function and alleviates mechanical allodynia in mice with chronic constriction injury.
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Medchemexpress LLC Navocaftor | 2159103-66-7 | 99.2% | 416.33 | 50 MG
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Navocaftor (GLPG 3067) is a protein modulator acting as a cystic fibrosis transmembrane regulator (CFTR), intended for research use only. Identified as a laboratory chemical for substance manufacturing, it has been tested and complies with specifications. Its chemical, physical, and toxicological properties are not fully investigated, and it is not validated for medical applications.
- Acts as a cystic fibrosis transmembrane regulator (CFTR)
- Functions as a protein modulator
- For research use only
- Solid, light yellow to yellow appearance
- Purity of 99.2%
- Molecular weight of 416.33
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Cambridge Isotope Laboratories 5-Methoxytryptamine HCl (A A B B-D4 98%) 0 01 g
5-Methoxytryptamine HCl (A A B B-D4 98%) 0 01 g
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