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Filtered Search Results
Ambeed AMBEED
5000892144 4-PYRIMIDIN-2-YLMORPHOLI 100MG
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Ambeed AMBEED
5000895041 1-PYRIMIDIN-4-YLETHANONE 250MG
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Medchemexpress LLC Benzoic acid, 4-[5-[(2-furanylmethyl)amino]-1,2,4-triazolo[4,3-c]pyrimidin-8-yl]- | 2467965-71-3 | MFCD32701933 | 99.9% | C17H13N5O3 | 10MG
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EED226-COOH is an EED-targeting ligand derived from EED226 designed for PROTAC development. It binds the EED subunit of PRC2 and is intended for conjugation to E3 ligase ligands to generate targeted protein degraders. The compound is supplied as an off-white to light-yellow solid and is provided with analytical characterization for biochemical and cell-based research.
- Purity 99.9% (analytical).
- Molecular formula C17H13N5O3.
- Molecular weight 335.32 g·mol-1.
- Solubility in DMSO 125 mg/mL (requires ultrasonic treatment).
- Storage powder: -20°C (long-term) or 4°C (shorter term).
- Includes datasheet, 1H NMR, LC-MS, COA, and SDS documentation.
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eMolecules 1123231-07-1 | (1-(4-(Naphthalen-2-yl)pyrimidin-2-yl)piperidin-4-yl)methanamine | MFCD20527803 | 50mg
Medchem Express | ADRA1D receptor antagonist 1 | 5mg | 778475771 | HY-135270 | 1191908-14-1 | 337.200 | C15H14Cl2N4O
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eMolecules 2649372-20-1 | Medchem Express | B-Raf IN 2 | 5mg | 713704836 | HY-145120 | 461.44 | C20H17F2N5O4S
Medchem Express | Alternariol | 1mg | 536984959 | HY-N6714 | 641-38-3 | MFCD00133068 | 258.229 | C14H10O5
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Medchemexpress LLC TBK1/IKKε-IN-5 | 1893397-65-3 | 100.0% | 50 MG
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This product is an orally active dual inhibitor for two specific kinases, with very low nanomolar inhibitory concentrations. It is designed for use in cancer research, particularly in the field of tumor immunity.
- Potent dual inhibition against targeted kinases (IC50: 1 nM, 5.6 nM).
- Enhances immune response to anti-PD-L1 treatments, inducing immune memory in animal models.
- Demonstrates antitumor activity and prolongs survival in animal models with anti-PD-L1 combination.
- Induces immunologic memory in tumor cells when combined with anti-PD-L1.
- Promotes IL-2 and IFN-γ secretion in T cells and IL-2 in Jurkat cells.
- Blocks immunosuppressive cytokine production by spheroid cell lines without cytotoxicity.
- Orally active for convenient administration.
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eMolecules 1381930-17-1 | Medchem Express | TBK1/IKK-IN-4 | 5mg | 673358836 | HY-124652 | 533.633 | C28H35N7O4
Medchem Express | C-021 (dihydrochloride) | 1mg | 495799537 | HY-103364A | 1784252-84-1 | MFCD16618393 | 540.570 | C27H43Cl2N5O2
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eMolecules 2467965-71-3 | EED226-COOH | AstaTech335.323 | C17H13N5O3 | 95.000 | OC(=O)c1ccc(cc1)-c1cnc(NCc2ccco2)n2cnnc12 | 0.1g | 562552109
EED226-COOH | AstaTech | 2467965-71-3335.323 | C17H13N5O3 | 95.000 | OC(=O)c1ccc(cc1)-c1cnc(NCc2ccco2)n2cnnc12 | 0.1g | 562552109
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eMolecules 54376-50-0 | 5-fluoro-2-methyl-pyrimidine | Pharmablock | MFCD16611294 | 112.107 | C5H5FN2 | 97.000 | Cc1ncc(F)cn1 | 25mg | 788564172
5-fluoro-2-methyl-pyrimidine | Pharmablock | 54376-50-0 | MFCD16611294 | 112.107 | C5H5FN2 | 97.000 | Cc1ncc(F)cn1 | 25mg | 788564172
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eMolecules 94222-07-8 | 1-(2-Chloro-4-pyrimidinyl)-4-piperidinol | Synthonix | MFCD09743694 | 213.670 | C9H12ClN3O | 95.000 | OC1CCN(CC1)c1ccnc(Cl)n1 | 500mg | 786490886
1-(2-Chloro-4-pyrimidinyl)-4-piperidinol | Synthonix | 94222-07-8 | MFCD09743694 | 213.670 | C9H12ClN3O | 95.000 | OC1CCN(CC1)c1ccnc(Cl)n1 | 500mg | 786490886
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eMolecules 2757804-89-8 | Medchem Express | PI3K | Akt | mTOR-IN-2 | 5mg | 742367738 | HY-146751 | 285.294 | C17H13F2NO
Ambeed | 10-Ethyl-378-trimethylbenzo[g]pteridine-24(3H10H)-dione | 50mg | 666597797 | A1219873 | 67767-38-8 | 284.319 | C15H16N4O2
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Medchemexpress LLC Methyl-4-(6-{4-[(methoxycarbonyl)amino]phenyl}-4-morpholin-4-yl-1H-pyrazolo[3,4-d]pyrimidin-1-yl) | 1062169-56-5 | 98.0% | 5 MG
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WYE-354 is an ATP-competitive mTOR inhibitor used in research to block mTORC1 and mTORC2 signaling and to study PI3K/mTOR pathway modulation in vitro. It is supplied as a high-purity small molecule in solid form or as a ready-to-use DMSO solution for laboratory assays.
- ATP-competitive mTOR inhibitor with IC50 ≈ 5 nM.
- High purity suitable for biochemical and cell-based assays.
- Available as solid and as a 10 mM solution in DMSO for convenience.
- Molecular weight 495.53 g·mol⁻¹ and formula C24H29N7O5.
- Commonly used for pathway, signaling, and autophagy research in vitro.
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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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eMolecules 1609960-30-6 | Medchem Express | TH287 | 5mg | 446267994 | HY-16965 | MFCD29035111 | 269.13 | C11H10Cl2N4
Medchem Express | E7766 (diammonium salt) | 1mg | 694124877 | HY-111999A | 2242635-03-4 | 780.660 | C24H32F2N12O8P2S2
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eMolecules 271-70-5 | 7H-pyrrolo[2,3-d]pyrimidine | Pharmablock | MFCD08234403 | 119.127 | C6H5N3 | 97.000 | c1cc2cncnc2[nH]1 | 25g | 551185312
7H-pyrrolo[2,3-d]pyrimidine | Pharmablock | 271-70-5 | MFCD08234403 | 119.127 | C6H5N3 | 97.000 | c1cc2cncnc2[nH]1 | 25g | 551185312
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