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Filtered Search Results
Aobchem 6-Bromo-4-chloro-1H-indazole | ≥95% | CAS 885518-99-0 | C7H4BrClN2 | 5g
6-Bromo-4-chloro-1H-indazole | ≥95% | CAS 885518-99-0 | C7H4BrClN2 | 5g
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eMolecules 204716-17-6 | 4-(Aminocarbonyl)-N-Fmoc-L-phenylalanine | Acrotein ChemBio Inc. | MFCD01317021 | 430.460 | C25H22N2O5 | 97.000 | NC(=O)c1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc23)C(O)=O)cc1 | 1g | 570931260
4-(Aminocarbonyl)-N-Fmoc-L-phenylalanine | Acrotein ChemBio Inc. | 204716-17-6 | MFCD01317021 | 430.460 | C25H22N2O5 | 97.000 | NC(=O)c1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc23)C(O)=O)cc1 | 1g | 570931260
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eMolecules 1227374-66-4 | Ambeed | (11bR)-N-(26-Di(naphthalen-1-yl)-4-oxido-89101112131415-octahydrodinaphtho[21-d12-f][132]dioxaphosphepin-4-yl)-111-trifluoromethanesulfonamide | 50mg | 633658969 | A1006129 | 739.75 | C41H33F3NO5PS
Ambeed | 1-(Chloro(pyrrolidin-1-yl)methylene)pyrrolidin-1-ium hexafluorophosphate(V) | 5g | 600846473 | A723618 | 135540-11-3 | MFCD00191333 | 332.660 | C9H16ClF6N2P
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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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Medchemexpress LLC Strophanthidin | 5MG
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Strophanthidin is a naturally available cardiac glycoside[1] Strophanthidin 0 1 and 1 nmol/L increases and 1 100 mol/L inhibits the Na /K -ATPase activities but Strophanthidin 10 and 100 nmol/L does not affect Na /K -ATPase activities in cardiac sarcolemmal[2] Strophanthidin increases both diastolic and systolic intracellular Ca2 concentration[3]
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eMolecules 816449-66-8 | METHYL 2-FLUORO-3-(HYDROXYMETHYL)BENZOATE | AstaTech | MFCD23709598 | 184.166 | C9H9FO3 | 95.000 | COC(=O)c1cccc(CO)c1F | 0.25g | 532135240
METHYL 2-FLUORO-3-(HYDROXYMETHYL)BENZOATE | AstaTech | 816449-66-8 | MFCD23709598 | 184.166 | C9H9FO3 | 95.000 | COC(=O)c1cccc(CO)c1F | 0.25g | 532135240
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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 | 0.25g | 551677401
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 | 0.25g | 551677401
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eMolecules 1379324-66-9 | 2-CHLOROBENZO[D]THIAZOLE-7-CARBOXYLIC ACID | AstaTech | MFCD13195420 | 213.640 | C8H4ClNO2S | 95.000 | OC(=O)c1cccc2nc(Cl)sc12 | 0.25g | 233628241
2-CHLOROBENZO[D]THIAZOLE-7-CARBOXYLIC ACID | AstaTech | 1379324-66-9 | MFCD13195420 | 213.640 | C8H4ClNO2S | 95.000 | OC(=O)c1cccc2nc(Cl)sc12 | 0.25g | 233628241
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Medchemexpress LLC Strophanthidin 25mg | 66-28-4 | 25 MG
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Strophanthidin is a naturally occurring cardiac glycoside used as a research standard and Na+/K+-ATPase modulator. It is supplied as a solid suitable for analytical, in vitro, and in vivo studies, with recommended solvents and storage guidance to maintain stability.
- Naturally occurring cardiac glycoside and Na+/K+-ATPase modulator.
- High purity suitable for analytical and biological assays.
- Offered in small research quantities for assay development.
- Soluble in ethanol; in vivo formulation protocols are provided for clear dosing solutions.
- Store solid at 4°C and protect from moisture and light to preserve integrity.
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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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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 159730-12-8 | 6-Methyltryptamine hydrochloride | Chem-Impex | MFCD01074517 | 210.710 | C11H15ClN2 | 99.000 | Cl.Cc1ccc2c(CCN)c[nH]c2c1 | 1g | 112755382
6-Methyltryptamine hydrochloride | Chem-Impex | 159730-12-8 | MFCD01074517 | 210.710 | C11H15ClN2 | 99.000 | Cl.Cc1ccc2c(CCN)c[nH]c2c1 | 1g | 112755382
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Medchemexpress LLC Parp-2-in-1 | 2115698-83-2 | 99.6% | 465.40 g/mol | C21H19F4N5O3 | 5 MG
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A potent, selective small-molecule inhibitor of poly(ADP-ribose) polymerase 2 (PARP-2) with a reported IC50 of 11.5 nM. The compound has molecular formula C21H19F4N5O3, molecular weight 465.40 g/mol, and is supplied as a white to off-white solid for use in biochemical and cellular research.
- Potent PARP-2 inhibition (IC50 11.5 nM).
- High chemical purity (99.6%).
- Molecular formula C21H19F4N5O3 and molecular weight 465.40 g/mol for easy reference.
- Supplied as a solid suitable for handling and storage.
- Manufacturer documentation available: data sheet, COA, and SDS for characterization.
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eMolecules 116751-24-7 | 3-Hydroxy-2,4,5-trifluorobenzoic acid | Ambeed | MFCD00800378 | 192.093 | C7H3F3O3 | 98.000 | OC(=O)c1cc(F)c(F)c(O)c1F | 1g | 632809333
3-Hydroxy-2,4,5-trifluorobenzoic acid | Ambeed | 116751-24-7 | MFCD00800378 | 192.093 | C7H3F3O3 | 98.000 | OC(=O)c1cc(F)c(F)c(O)c1F | 1g | 632809333
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Medchemexpress LLC Sphondin | 483-66-9 | 5 MG
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Sphondin is a compound that demonstrates an inhibitory effect on the increase of COX-2 protein levels and PGE2 release induced by IL-1β in A549 cells. It is intended for research use only and not sold to patients. It is an off-white to light yellow solid with a molecular weight of 216.19 and a purity of 99.70%.
- Inhibits COX-2 protein expression and PGE2 release
- Off-white to light yellow solid appearance
- High purity of 99.70%
- Suitable for research applications
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