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Filtered Search Results
eMolecules 288315-03-7 | 3?3-Difluoroazetidine hydrochloride | AA Blocks LLC | MFCD05663714 | 129.530 | C3H6ClF2N | 0.000 | Cl.FC1(F)CNC1 | 250mg | 433193862
3?3-Difluoroazetidine hydrochloride | AA Blocks LLC | 288315-03-7 | MFCD05663714 | 129.530 | C3H6ClF2N | 0.000 | Cl.FC1(F)CNC1 | 250mg | 433193862
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000759026 2-AZIDOTEREPHTHALIC 250MG
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eMolecules 1599440-06-8 | [2-(Fmoc-amino)acetamido]methyl Acetate | Broadpharm368.389 | C20H20N2O5 | 0.000 | CC(=O)OCNC(=O)CNC(=O)OCC1c2ccccc2-c2ccccc12 | 250mg | 761707258
[2-(Fmoc-amino)acetamido]methyl Acetate | Broadpharm | 1599440-06-8368.389 | C20H20N2O5 | 0.000 | CC(=O)OCNC(=O)CNC(=O)OCC1c2ccccc2-c2ccccc12 | 250mg | 761707258
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5000759293 5 5 -2 2 -BITH 250MG
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Medchemexpress LLC N-[3-(1H-indol-4-yl)-5-(2-methoxypyridine-4-carbonyl)phenyl]methanesulfonamide | 915412-67-8 | MFCD18782727 | 99.9% | C22H19N3O4S | 10MG
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LP-261 is an orally active antimitotic small-molecule research compound that inhibits tubulin polymerization and has demonstrated in vivo efficacy against human non-small-cell lung tumor xenografts. It is supplied as a high-purity solid and is documented with analytical files for research use.
- Inhibits tubulin polymerization (EC50 3.2 μM).
- Demonstrated in vivo antitumor activity in xenograft models.
- High purity solid with available COA, LC-MS, and SDS documentation.
- Molecular formula C22H19N3O4S; molecular weight 421.47 g·mol⁻¹.
- Soluble in DMSO (≈33.33 mg/mL) for stock solution preparation.
- Storage recommendations provided for powder and solution formats.
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eMolecules 1353016-70-2 | 11,12-Didehydro-?-oxodibenz[b,f]azocine-5(6H)-butanoic acid | AA Blocks LLC | MFCD28064336 | 305.333 | C19H15NO3 | 0.000 | OC(=O)CCC(=O)N1Cc2ccccc2C#Cc2ccccc12 | 250mg | 713340033
11,12-Didehydro-?-oxodibenz[b,f]azocine-5(6H)-butanoic acid | AA Blocks LLC | 1353016-70-2 | MFCD28064336 | 305.333 | C19H15NO3 | 0.000 | OC(=O)CCC(=O)N1Cc2ccccc2C#Cc2ccccc12 | 250mg | 713340033
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Accela Chembio Inc 1 | 3-dimethyluracil | 100g | 874-14-6 | MFCD00038065 | 98% | Shelf Life: 1620 Days | Light Sensitive
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1 | 3-dimethyluracil | 100g | 874-14-6 | MFCD00038065 | 98% | Shelf Life: 1620 Days | Light Sensitive
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000759386 5-BROMOPENTYLOXY 250MG
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5000759387 TETRAFLUOROISOPHTHAL 250MG
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Medchemexpress LLC 2,3-dihydroxybenzoic acid | 303-38-8 | MFCD00002446 | 99.6% | 154.12 | C7H6O4 | 250mg
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Pyrocatechuic acid (Standard) is the analytical standard of Pyrocatechuic acid This product is intended for research and analytical applications Pyrocatechuic acid is a normal human benzoic acid metabolite found in plasma and has increased levels after aspirin ingestion
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5000759422 1 1 4 1 4 1 250MG
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eMolecules 87573-88-4 | 1-(2-HYDROXYPYRIMIDIN-5-YL)ETHANONE | AstaTech | MFCD29921801 | 138.126 | C6H6N2O2 | 95.000 | CC(=O)c1cnc(O)nc1 | 1g | 384830342
1-(2-HYDROXYPYRIMIDIN-5-YL)ETHANONE | AstaTech | 87573-88-4 | MFCD29921801 | 138.126 | C6H6N2O2 | 95.000 | CC(=O)c1cnc(O)nc1 | 1g | 384830342
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Medchemexpress LLC HY-114414 5mg Medchemexpress, HDACs/mTOR Inhibitor 1 CAS:2271413-06-8 Purity:>98%
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Medchemexpress, HY-114414 5mg HDACs/mTOR Inhibitor 1 CAS:2271413-06-8 HDACs/mTOR Inhibitor 1 is a dual Histone Deacetylases (HDACs) and mammalian target of Rapamycin (mTOR) target inhibitor for treating hematologic malignancies, with IC 50 s of 0.19 nM, 1.8 nM, 1.2 nM and >500 nM for HDAC1, HDAC6, mTOR and PI3Kα, respectively. HDACs/mTOR Inhibitor 1 stimulates cell cycle arrest in G0/G1 phase and induce tumor cell apoptosis with low toxicity in vivo [1] . 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 PROTAC BET DEGRADER-2 5MG
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501872511 PROTAC BET DEGRADER-2 5MG
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5000383172 AZIDO-PEG9-S-METHYL 25MG
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