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Filtered Search Results
eMolecules 308246-57-3 | Medchem Express | LMP744 (hydrochloride) | 1mg | 459606997 | HY-U00248A | 488.92 | C24H25ClN2O7
AstaTech | AI3-29759 | 0.25g | 718059714 | F20445 | 90.000 | 754-91-6 | MFCD03094345 | 499.140 | C8H2F17NO2S
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Medchemexpress LLC BRD4 Inhibitor-24 | 309951-18-6 | 99.3% | 262.26 | 100 MG
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BRD4 Inhibitor-24 (compound 3U) is a potent BRD4 inhibitor that exhibits antitumor activity against MCF7 and K652 cells. This compound is for research use only and is presented as a solid, white to off-white substance with the molecular formula C13H14N2O4.
- Potent BRD4 inhibitor
- Antitumor activity against MCF7 and K652 cells (IC50 values of 33.7 and 45.9 μM)
- Solid, white to off-white appearance
- Molecular formula C13H14N2O4
- Recommended storage at 4°C, protected from light
- In solvent, storage at -80°C for 6 months or -20°C for 1 month (protected from light)
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eMolecules 24088-59-3 | 3-(3-Phenyl-1,2,4-oxadiazol-5-yl)propanoic acid | MFCD05130956 | 25g
Ambeed | 3-(Pyrrolidin-2-yl)pyridine | 250mg | 552713526 | A348497 | 5746-86-1 | MFCD00016913 | 148.209 | C9H12N2
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eMolecules 1024448-59-6 | Medchem Express | RN-1747 | 5mg | 552386777 | HY-19976 | MFCD04154169 | 395.86 | C17H18ClN3O4S
Ambeed | (2R3R4R5R6R)-3-Acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-245-triyl triacetate | 1g | 595927945 | A1246619 | 10385-50-9 | MFCD15144916 | 389.357 | C16H23NO10
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eMolecules 209860-87-7 | Medchem Express | Tafluprost | 5mg | 446273054 | HY-B0600 | MFCD08062150 | 452.539 | C25H34F2O5
Ambeed | (2-Amino-4-chlorophenyl)(phenyl)methanone | 1g | 600851335 | A354534 | 4076-50-0 | MFCD00179566 | 231.680 | C13H10ClNO
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eMolecules 54924-78-6 | 5-BROMO-2-ETHOXYBENZAMIDE | AstaTech | MFCD07551819 | 244.088 | C9H10BrNO2 | 95.000 | CCOc1ccc(Br)cc1C(N)=O | 0.1g | 696739802
5-BROMO-2-ETHOXYBENZAMIDE | AstaTech | 54924-78-6 | MFCD07551819 | 244.088 | C9H10BrNO2 | 95.000 | CCOc1ccc(Br)cc1C(N)=O | 0.1g | 696739802
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Apexbio Technology LLC Tamoxifen Citrate 54965-24-1 5g
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Tamoxifen Citrate (CAS 54965-24-1) is a small-molecule antagonist targeting estrogen receptors (ER) It is designed to competitively bind ER thereby modulating estrogen-mediated signal transduction Tamoxifen Citrate exerts its biological activity primarily by inhibiting the transcriptional activity of estrogen-responsive genes leading to reduced synthesis of factors related to cell growth and angiogenesis In in vitro studies Tamoxifen Citrate demonstrates inhibition of cell proliferation with reported IC50 values typically ranging from 3 to 7 M depending on cell line and experimental conditions Based on these pharmacological properties Tamoxifen Citrate holds research potential in studies of estrogen receptor-dependent signaling pathways and anti-tumor strategies particularly in breast cancer models
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Sigma Aldrich Fine Chemicals Biosciences CX546 >=98% (HPLC), solid | 215923-54-9 | MFCD01860868 | 10MG
CX546 >=98% (HPLC), solid | Purity: >=98% (HPLC) | Mol Wt: 247.29 | 215923-54-9 | MFCD01860868 | 10MG
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eMolecules 488847-28-5 | Medchem Express | ORM-10103 | 5mg | 482204317 | HY-128678 | MFCD28016589 | 348.358 | C20H16N2O4
Medchem Express | GB-110 (hydrochloride) | 5mg | 495800024 | HY-120528A | | 645.240 | C33H49ClN6O5
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Medchemexpress LLC PND-1186 hydrochloride | 1356154-94-3 | 99.9% | C25H27ClF3N5O3 | 10MG
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PND-1186 hydrochloride is the hydrochloride salt of a potent, selective, and reversible focal adhesion kinase (FAK) inhibitor supplied for laboratory research. It exhibits nanomolar potency (IC50 = 1.5 nM) and selectively promotes tumor cell apoptosis. Supplied as a high-purity solid with defined solubility and storage recommendations for controlled experimental use.
- Potent FAK inhibition with IC50 of 1.5 nM.
- High purity (99.9%).
- Molecular formula C25H27ClF3N5O3; molecular weight 537.96.
- Soluble in DMSO (100 mg/mL) and water (20 mg/mL).
- Recommended storage: 4°C for solid; in solvent -80°C up to 6 months.
- Intended for research use only; not for human or veterinary use.
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Sigma Aldrich Fine Chemicals Biosciences Iguratimod >=98% (HPLC) | 123663-49-0 | MFCD00882374 | 25MG
Iguratimod >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 374.37 | 123663-49-0 | MFCD00882374 | 25MG
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![eMolecules 100286-90-6 | Irinotecan HCl | Broadpharm590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502461873.JPG-250.jpg)
eMolecules 100286-90-6 | Irinotecan HCl | Broadpharm590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162
Irinotecan HCl | Broadpharm | 100286-90-6590.721 | C33H42N4O6 | 0.000 | CCc1c2CN3C(CC4C(COC(=O)[C@]4(O)CC)C3=O)c2nc2ccc(OC(=O)N3CCC(CC3)N3CCCCC3)cc12 | 100mg | 724438162
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Aobchem AOBCHEM
5001042213 1 4-DIPROPOXYBENZENE 100G
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Chem-Impex International, Inc. 1,2-Dimethoxybenzene | MFCD00008357 | 1KG
1,2-Dimethoxybenzene, MFCD00008357, 1KG
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Selleck Chemical LLC Amuvatinib (MP-470) S1244-2mg
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Amuvatinib (MP-470 HPK 56) is a potent and multi-targeted inhibitor of c-Kit PDGFR and Flt3 with IC50 of 10 nM 40 nM and 81 nM respectively Amuvatinib suppresses c-MET and c-RET Amuvatinib is also active as a DNA repair protein Rad51 inhibitor with antineoplastic activity Phase 2
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