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Filtered Search Results
Medchemexpress LLC Farudodstat (ASLAN003) | 1035688-66-4 | 99.7% | 100 MG
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Farudodstat (ASLAN003) is an orally active and potent Dihydroorotate Dehydrogenase (DHODH) inhibitor with an IC50 of 35 nM for the human DHODH enzyme. Its mechanism of action involves inhibiting protein synthesis by activating AP-1 transcription factors. This compound induces apoptosis and significantly prolongs survival in acute myeloid leukemia (AML) xenograft mice.
- Exhibits antiproliferative activity against various human cell lines.
- Inhibits leukemic cell proliferation in vitro.
- Increases cleaved caspase 8.
- Decreases viability and induces differentiation in primary acute myeloid leukemia blasts and myelodysplastic syndrome samples.
- Inhibits protein synthesis by reducing O-propargyl-puromycin (OPP) incorporation and downregulating EIF4B and RPL6 proteins.
- Substantially reduces the number and size of disseminated tumors in vivo.
- Available as a white to off-white solid.
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eMolecules 890839-66-4 | 8-(Trifluoromethyl)chroman-4-one | ChemScene | MFCD11506686 | 216.159 | C10H7F3O2 | 97.000 | FC(F)(F)c1cccc2C(=O)CCOc12 | 100mg | 572175906
8-(Trifluoromethyl)chroman-4-one | ChemScene | 890839-66-4 | MFCD11506686 | 216.159 | C10H7F3O2 | 97.000 | FC(F)(F)c1cccc2C(=O)CCOc12 | 100mg | 572175906
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Medchemexpress LLC Dicentrine | 517-66-8 | 5 MG
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Dicentrine is a natural product isolated from the plant Stephania epigaea Lo that exhibits an antihypertensive effect. It functions as an α1-adrenoceptor antagonist and has been shown to be effective against human hyperplastic prostates.
- Isolated from the plant Stephania epigaea Lo.
- Exhibits an antihypertensive effect.
- Functions as an α1-adrenoceptor antagonist.
- Effective against human hyperplastic prostates.
- For research use only.
- High purity (99.94%).
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Medchemexpress LLC TAO Kinase inhibitor 1 | 850467-66-2 | 99.8% | 384.47 | 100 MG
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TAO Kinase inhibitor 1 (compound 43) is a selective, ATP-competitive thousand-and-one amino acid kinases (TAOK) inhibitor with IC50s of 11 to 15 nM for TAOK1 and 2. It delays mitosis and induces mitotic cell death. It is for research use only.
- Selective, ATP-competitive TAOK inhibitor.
- IC50s of 11 to 15 nM for TAOK1 and 2.
- Delays mitosis.
- Induces mitotic cell death.
- Purity: 99.81%.
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Chem-Impex International, Inc. 2-(2-Methyl-1H-indol-3-yl)ethylamine | 2731-06-8 | MFCD00130185 | 1G
2-(2-Methyl-1H-indol-3-yl)ethylamine, 2731-06-8, MFCD00130185, 1G
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Medchemexpress LLC DX3-213B | 2749555-66-4 | 99.7% | C20H28F2N2O5S2 | 100 MG
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DX3-213B is a highly potent, orally active oxidative phosphorylation (OXPHOS) complex I inhibitor with an IC50 of 3.6 nM. It effectively impairs ATP generation with an IC50 of 11 nM and blocks the growth of MIA PaCa-2 cells, also with a GI50 of 11 nM. This compound is utilized in research concerning pancreatic cancer.
- Highly potent and orally active.
- Functions as an oxidative phosphorylation (OXPHOS) complex I inhibitor.
- Impairs ATP generation.
- Blocks MIA PaCa-2 cell growth.
- Used in pancreatic cancer research.
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eMolecules 155877-83-1 | Medchem Express | LE135 | 5mg | 596366425 | HY-107436 | MFCD06798318 | 438.571 | C29H30N2O2
Ambeed | (S)-tert-Butyl 2-aminopropanoate | 1g | 572830027 | A605887 | 21691-50-9 | MFCD00270591 | 145.202 | C7H15NO2
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eMolecules 370882-66-9 | tert-butyl (1S,5R)-3,6-diazabicyclo[3.2.0]heptane-6-carboxylate | Pharmablock198.266 | C10H18N2O2 | 97.000 | CC(C)(C)OC(=O)N1C[C@@H]2CNC[C@H]12 | 25mg | 586144518
tert-butyl (1S,5R)-3,6-diazabicyclo[3.2.0]heptane-6-carboxylate | Pharmablock | 370882-66-9198.266 | C10H18N2O2 | 97.000 | CC(C)(C)OC(=O)N1C[C@@H]2CNC[C@H]12 | 25mg | 586144518
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Medchemexpress LLC Nevadensin | 10176-66-6 | MFCD08689947 | 344.32 | 20 MG
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Nevadensin is a natural flavonoid and a selective human carboxylesterase 1 (hCE1) inhibitor. It demonstrates greater selectivity for hCE1 over hCE2.
- Induces apoptosis and DNA damage in cancer cells.
- Possesses anti-inflammatory, anti-tumor, anti-hypertensive, anti-tubercular, antitussive, antioxidant, and anti-microbial activities.
- Inhibits hCE1 with an IC50 of 2.64 μM.
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Medchemexpress LLC SIRT-IN-2 | 1431411-66-3 | 98.1% | 383.49 | 50 MG
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SIRT-IN-2 is a potent inhibitor of SIRT1/2/3, with IC50s of 4, 4, 7 nM, respectively. It is described as one of the most potent truncated pan SIRT1/2/3 inhibitors. SIRT-IN-2 (compound 31) binds identically in the catalytic active site (RMS=0.29), occupying the nicotinamide C-pocket and acetyl lysine substrate channel.
- Potent inhibitor of SIRT1/2/3
- IC50s of 4, 4, 7 nM for SIRT1, SIRT2, and SIRT3
- Truncated pan SIRT1/2/3 inhibitor
- Binds in the catalytic active site
- Occupies nicotinamide C-pocket and acetyl lysine substrate channel
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Medchemexpress LLC Dx3-213b | 2749555-66-4 | 99.7% | 478.57 g/mol | C20H28F2N2O5S2 | 5 MG
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DX3-213B is a potent, orally active oxidative phosphorylation (OXPHOS) complex I inhibitor used in preclinical research. It disrupts mitochondrial ATP production and exhibits cellular activity in cancer models, making it useful for mechanistic studies of mitochondrial function and cancer metabolism. Not for human use.
- Highly potent complex I inhibition (IC50 = 3.6 nM)
- Impairs ATP generation in cells (IC50 = 11 nM)
- Inhibits growth of pancreatic cancer cell line (GI50 = 11 nM)
- High chemical purity suitable for biochemical assays
- Available as solid and DMSO solution for assay flexibility
- Intended for mechanistic mitochondrial and cancer metabolism research
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eMolecules 181144-66-1 | Medchem Express | Co 102862 | 5mg | 722714018 | HY-108504 | MFCD00953614 | 273.267 | C14H12FN3O2
Medchem Express | NRX-1933 | 5mg | 713706709 | HY-144984 | 2763260-30-4 | 350.261 | C14H9F3N6O2
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eMolecules 1214387-66-2 | 3-METHYL-4-(TRIFLUOROMETHYL)BENZOIC ACID ETHYL ESTER | AstaTech | MFCD14698275 | 232.202 | C11H11F3O2 | 95.000 | CCOC(=O)c1ccc(c(C)c1)C(F)(F)F | 1g | 296384189
3-METHYL-4-(TRIFLUOROMETHYL)BENZOIC ACID ETHYL ESTER | AstaTech | 1214387-66-2 | MFCD14698275 | 232.202 | C11H11F3O2 | 95.000 | CCOC(=O)c1ccc(c(C)c1)C(F)(F)F | 1g | 296384189
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eMolecules 74290-66-7 | 2-Amino-3,5-dibromo-6-methylpyrazine | ChemScene | MFCD08705764 | 266.924 | C5H5Br2N3 | 98.000 | Cc1nc(N)c(Br)nc1Br | 100mg | 801476141
2-Amino-3,5-dibromo-6-methylpyrazine | ChemScene | 74290-66-7 | MFCD08705764 | 266.924 | C5H5Br2N3 | 98.000 | Cc1nc(N)c(Br)nc1Br | 100mg | 801476141
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Medchemexpress LLC PGAM1-IN-2 | 2438637-66-0 | 98.0% | 10 MG
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PGAM1-IN-2 is a phosphoglycerate mutase 1 (PGAM1) inhibitor with an IC50 of 2.1 μM. This compound inhibits H1299 proliferation with an IC50 of 33.8±6.1 μM.
- Potent phosphoglycerate mutase 1 inhibitor
- Inhibits H1299 proliferation
- Suitable for research applications
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