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Filtered Search Results
eMolecules EMOLECULES INC
5000491110 5-CHLORO-2-METHYLPYRIMIDINE 5G
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Chem-Impex International, Inc. Guanosine | 118-00-3 | MFCD00010182 | 100G
Guanosine, 118-00-3, MFCD00010182, 100G
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eMolecules EMOLECULES INC
5000190218 PYRIMIDIN-4-OL 250MG
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Medchemexpress LLC HY-12664 5mg Medchemexpress, AF64394 CAS:1637300-25-4 Purity:>98%
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Medchemexpress, HY-12664 5mg AF64394 CAS:1637300-25-4 AF64394 is a GPR3 inverse agonist, with a pIC50 of 7.3. 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 2-(3,5-Dibromophenyl)ethanol | 75894-93-8 | MFCD11617976 | 1g
Oakwood Chemical | 2-(3,5-Dibromophenyl)ethanol | 1g | 537711235 | 104747 | | 75894-93-8 | MFCD11617976 | 279.959 | C8H8Br2O
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eMolecules Pharmablock / tert-butyl cis-N-(3-formylcyclobutyl)carbamate / 25mg / 596622463 / PBLJ3618 / 0.000 / 171549-91-0 / MFCD28403245 / 199.250 / C10H17NO3
Pharmablock / tert-butyl cis-N-(3-formylcyclobutyl)carbamate / 25mg / 596622463 / PBLJ3618 / 0.000 / 171549-91-0 / MFCD28403245 / 199.250 / C10H17NO3
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eMolecules Medchem Express / LDN193189 (Tetrahydrochloride) / 5mg / 446260708 / HY-12071A / / 2310134-98-4 / MFCD30207834 / 552.330 / C25H26Cl4N6
Medchem Express / LDN193189 (Tetrahydrochloride) / 5mg / 446260708 / HY-12071A / / 2310134-98-4 / MFCD30207834 / 552.330 / C25H26Cl4N6
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Medchemexpress LLC HY-101420 5mg Medchemexpress, VUF10460 CAS:1028327-66-3 Purity:>98%
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Medchemexpress, HY-101420 5mg VUF10460 CAS:1028327-66-3 VUF10460 is a non-imidazole histamine H4 receptor agonist; binds to rat H4 receptor with a pK i of 7.46. 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 PKI-166 10mg | 187724-61-4 | 330.38 | C20H18N4O | 10 MG
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PKI-166 is a potent, selective, and orally bioavailable epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor with a reported IC50 of 0.7 nM. It is provided for research use only and has molecular formula C20H18N4O and high purity by HPLC.
- Potent EGFR kinase inhibition (IC50 ≈ 0.7 nM).
- High chemical purity (≥98% by HPLC).
- Suitable for in vitro and in vivo research applications.
- Orally bioavailable in preclinical studies.
- Well-characterized molecular properties for experimental reproducibility.
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Apexbio Technology LLC BAY 61-3606 732983-37-8 5mg
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BAY 61-3606 (CAS 732983-37-8) is a selective orally bioavailable inhibitor of spleen tyrosine kinase (SYK) displaying an IC50 of 10 nM and a Ki of 7 5 nM for SYK by competitively binding ATP This compound shows minimal activity against other tyrosine kinases such as Src Fyn Lyn Btk and Itk at concentrations up to 4 7 M BAY 61-3606 suppresses Fc RI-mediated degranulation and mediator release in mast cells and basophils as well as Fc R-driven responses in macrophages and neutrophils In preclinical models BAY 61-3606 attenuates inflammatory cell functions and reduces allergic and asthmatic responses supporting its utility in investigating SYK-mediated signaling and inflammation
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Medchemexpress LLC HY-101117 10mg Medchemexpress, EED226 CAS:2083627-02-3 Purity:>98%
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Medchemexpress, HY-101117 10mg EED226 CAS:2083627-02-3 EED226 is a polycomb repressive complex 2 (PRC2) inhibitor, which binds to the K27me3-pocket on embryonic ectoderm development (EED) and shows strong antitumor activity in xenograft mice model. EED226 is a potent, selective, and orally bioavailable EED inhibitor[2]. EED226 inhibits PRC2 with an IC50 of 23.4 nM when the H3K27me0 peptide is used as a substrate in the in vitro enzymatic assays[3]. 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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Sigma Aldrich Fine Chemicals Biosciences WYE-125132 >=97% (HPLC) | 1144068-46-1 | 5MG
WYE-125132 >=97% (HPLC) | Purity: >=97% (HPLC) | Mol Wt: 519.6 | 1144068-46-1 | 5MG
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Medchemexpress LLC Org41841 | 301847-37-0 | 99.8% | 402.53 g/mol | C19H22N4O2S2 | 25 MG
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Org41841 is a small-molecule partial agonist of the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and the thyroid-stimulating hormone receptor (TSHR), used for receptor pharmacology research. It exhibits EC50 values of 0.2 μM (LHCGR) and 7.7 μM (TSHR).
- Partial agonist at LHCGR and TSHR with EC50s of 0.2 μM and 7.7 μM.
- High purity (99.77%) appropriate for biochemical assays.
- Molecular weight 402.53 g/mol.
- Chemical formula C19H22N4O2S2.
- CAS number 301847-37-0 for unambiguous identification.
- Available in multiple milligram quantities and DMSO solution formats for screening.
- Intended for research use only and not for human or clinical use.
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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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![Medchemexpress LLC 5-amino-N-tert-butyl-4-(3-methoxyphenyl)-2-methylsulfanylthieno[2,3-d]pyrimidine-6-carboxamide | 301847-37-0 | MFCD18633223 | 99.8% | 402.53 g·mol⁻¹ | C19H22N4O2S2 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000214231.png-250.jpg)
Medchemexpress LLC 5-amino-N-tert-butyl-4-(3-methoxyphenyl)-2-methylsulfanylthieno[2,3-d]pyrimidine-6-carboxamide | 301847-37-0 | MFCD18633223 | 99.8% | 402.53 g·mol⁻¹ | C19H22N4O2S2 | 50 MG
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Org41841 is a small-molecule partial agonist of the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and the thyroid-stimulating hormone receptor (TSHR), with reported EC50 values of 0.2 μM (LHCGR) and 7.7 μM (TSHR). Supplied as a solid for research use; refer to the safety data sheet for handling and storage instructions.
- Partial agonist at LHCGR and TSHR with defined EC50 values.
- High chemical purity suitable for biochemical and cellular assays.
- Molecular weight 402.53 g·mol⁻¹ and formula C19H22N4O2S2.
- Available in multiple milligram pack sizes for research workflows.
- Stable as a powder under recommended storage; consult SDS for solvent stability.
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