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Filtered Search Results
Aobchem 5-(4-Fluorophenyl)pyrimidin-2-amine | ≥97% | CAS 31408-40-9 | C10H8FN3 | 500mg
5-(4-Fluorophenyl)pyrimidin-2-amine | ≥97% | CAS 31408-40-9 | C10H8FN3 | 500mg
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Aobchem AOBCHEM
5000916180 5- 4-BROMOPHENYL PYRIMIDIN-2-A
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Chemscene CHEMSCENE
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5000575620 7H-PYRROLO 2 3-D PYRIMIDIN- 1G
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Aobchem AOBCHEM
5000914989 5- 4-BROMOPHENYL PYRIMIDIN-2-A
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Selleck Chemical LLC Dorsomorphin 2HCl
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Dorsomorphin 2HCl is a potent reversible selective AMPK inhibitor with Ki of 109 nM in cell-free assays exhibiting no significant inhibition of several structurally related kinases including ZAPK SYK PKC PKA and JAK3 Also inhibits type BMP receptor activity Dorsomorphin induces autophagy in cancer cell line
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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](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000259799.png-250.jpg)
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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Medchemexpress LLC Org41841 | 301847-37-0 | 99.8% | 402.53 g/mol | C19H22N4O2S2 | 100 MG
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Org41841 is a small-molecule partial agonist of the luteinizing hormone/choriogonadotropin receptor (LHCGR) and the thyroid-stimulating hormone receptor (TSHR), provided for research use in studies of GPCR signaling and cAMP-mediated receptor responses.
- Partial agonist of LHCGR and TSHR, suitable for receptor pharmacology studies.
- Molecular weight 402.53 g/mol.
- Molecular formula C19H22N4O2S2.
- CAS number 301847-37-0.
- Purity 99.77% with supporting analytical data (COA, LCMS).
- Available in multiple solid sizes and as a DMSO solution format for in vitro use.
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eMolecules 907604-62-0 | Ambeed | Potassium trifluoro(5-formylfuran-2-yl)borate | 1g | 672523275 | A446781 | MFCD11052668 | 201.98 | C5H3BF3KO2
Ambeed | Potassium trifluoro(5-formylfuran-2-yl)borate | 1g | 672523275 | A446781 | 907604-62-0 | MFCD11052668 | 201.980 | C5H3BF3KO2
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Medchemexpress LLC HY-10942 5mg Medchemexpress, VER-82576 CAS:847559-80-2 Purity:>98%
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Medchemexpress, HY-10942 5mg VER-82576 CAS:847559-80-2 VER-82576 (NVP-BEP800) is a potent, orally available and selective Hsp90 inhibitor, with an IC50 of 58 nM for Hsp90β; VER-82576 also slightly blocks Grp94 and Trap-1, with IC50s of 4.1 and 5.5 μM, respectively. 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 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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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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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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