Unsubstituted Phenols
eMolecules 4-Isopropylpyrimidin-2-amine | 5782-70-7 | MFCD11847654 | 1g
Combi-Blocks | 4-Isopropylpyrimidin-2-amine | 1g | 517033093 | QW-8660 | 95.000 | 5782-70-7 | MFCD11847654 | 137.186 | C7H11N3
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Medchemexpress LLC Navarixin | 473727-83-2 | 99.3% | 397.42 g/mol | C21H23N3O5 | 10 MG
Navarixin is an orally active, allosteric antagonist of CXCR1 and CXCR2 used as a research compound to study chemokine receptor signaling, neutrophil recruitment, and inflammatory responses in vitro and in vivo.
- Potent, allosteric antagonist of CXCR1 and CXCR2.
- Suitable for in vitro and in vivo pharmacology studies.
- High purity (99.3%) for consistent experimental results.
- Soluble in DMSO at ≥50 mg/mL; several in vivo vehicle formulations reported.
- Recommended storage supports long-term stability of powder and solutions.
- Available in small research quantities for dosing flexibility.
Medchemexpress LLC HY-18719B 10mg Medchemexpress, Endoxifen (hydrochloride) CAS:1197194-41-4 Purity:>98%
Medchemexpress, HY-18719B 10mg Endoxifen (hydrochloride) CAS:1197194-41-4 Endoxifen hydrochloride is a key active metabolite of Tamoxifen (TAM) with higher affinity and specificity to estrogen receptor that also inhibits aromatase activity. Endoxifen hydrochloride has the potential for breast cancer study. 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.
Medchemexpress LLC HY-13704 500mg , SN-38 NK012 CAS:86639-52-3 Purity:98%
Medchemexpress, HY-13704 500mg SN-38 NK012 CAS:86639-52-3 Formula:C22H20N2O5 Topoisomerase I Purity:98% SN-38 is an active metabolite of the Topoisomerase I inhibitor Irinotecan. 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.
![Medchemexpress LLC N-[5-amino-1,2,3,4-tetrahydro-1-[4-(trifluoromethyl)phenyl]-3-quinolinyl]-2-propenamide | 2766575-48-6 | MFCD22417285 | 99.8% | 361.36 | C19H18F3N3O | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000285876.png-250.jpg)
Medchemexpress LLC N-[5-amino-1,2,3,4-tetrahydro-1-[4-(trifluoromethyl)phenyl]-3-quinolinyl]-2-propenamide | 2766575-48-6 | MFCD22417285 | 99.8% | 361.36 | C19H18F3N3O | 10 MG
SWTX-143 is a covalent, irreversible inhibitor of the YAP/TAZ-TEAD transcriptional complex developed for research. It binds the palmitoylation pocket of TEAD isoforms and suppresses YAP/TAZ-TEAD transcriptional activity, and has demonstrated oral activity in preclinical studies. The compound is supplied as a high-purity solid intended for biochemical and cell-based research applications.
- Covalent, irreversible inhibitor of YAP/TAZ-TEAD.
- Binds the palmitoylation pocket of TEAD isoforms.
- Inhibits YAP/TAZ-TEAD transcriptional activity.
- Demonstrated oral activity in preclinical studies.
- High reported purity (about 99.8%).
- Supplied as a white to off-white solid.
- Available in milligram-scale packages for laboratory research.
- Suitable for biochemical and cell-based assays.
![eMolecules Medchem Express / (-)-DHMEQ / 2mg / 446264401 / HY-14645 / / 287194-40-5 / [null] / 261.233 / C13H11NO5](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502460449.PNG-250.jpg)
eMolecules Medchem Express / (-)-DHMEQ / 2mg / 446264401 / HY-14645 / / 287194-40-5 / [null] / 261.233 / C13H11NO5
Medchem Express / (-)-DHMEQ / 2mg / 446264401 / HY-14645 / / 287194-40-5 / [null] / 261.233 / C13H11NO5
Sigma Aldrich Fine Chemicals Biosciences Isoprenaline hydrochloride British Pharmacopoeia (BP) Reference Standard | 51-30-9 | MFCD00012603 |
Isoprenaline hydrochloride British Pharmacopoeia (BP) Reference Standard | Mol Wt: 247.72 | 51-30-9 | MFCD00012603 |
eMolecules Medchem Express / AG126 / 5mg / 446259300 / HY-108330 / / 118409-62-4 / MFCD00236448 / 215.168 / C10H5N3O3
Medchem Express / AG126 / 5mg / 446259300 / HY-108330 / / 118409-62-4 / MFCD00236448 / 215.168 / C10H5N3O3
Medchemexpress LLC Tyrphostin AG1433 | 168835-90-3 | 99.1% | 10MG
Tyrphostin AG1433 | 168835-90-3 | 99.1% | 10MG
Medchemexpress LLC Combretastatin A-1 | 109971-63-3 | 97.0% | 100 MG
Combretastatin A-1 (CAS 109971-63-3) is a microtubule polymerization inhibitor supplied as a research-grade solid. It is used as an analytical standard and reagent for studying tubulin dynamics, cell biology assays, and biochemical experiments. Common handling involves dissolution in DMSO to prepare concentrated stock solutions for in vitro use.
- Microtubule polymerization inhibitor for tubulin-related studies.
- Suitable as an analytical standard and research reagent.
- High purity appropriate for biochemical and cell-based assays.
- Stable as a powder when stored under recommended frozen conditions.
- Soluble in DMSO for preparation of concentrated stock solutions.
Medchemexpress LLC HY-14596 500mg , Genistein NPI 031L CAS:446-72-0 Purity:98%
Medchemexpress, HY-14596 500mg Genistein NPI 031L CAS:446-72-0 Formula:C15H10O5 IC50: 0.7 μg/mL (0.6 μM) (EGFR) Purity:98% Genistein is a potent inhibitor of the protein tyrosine kinase (PTK) activity of the EGFR in vitro with an IC 50 of 0.7 μg/mL (0.6 μM). 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.
Medchemexpress LLC Honokiol dichloroacetate | 1620160-42-0 | 99.1% | 488.19 g/mol | C22H18Cl4O4 | 50MG
Honokiol DCA (honokiol dichloroacetate) is a dichloroacetate ester of honokiol used as a research reagent with reported in vitro activity against prostate cancer cell growth and androgen receptor expression. The compound is provided as a well-characterized, high-purity material suitable for laboratory studies.
- Research-grade dichloroacetate ester of honokiol.
- CAS 1620160-42-0; molecular weight 488.19 g/mol.
- Chemical formula C22H18Cl4O4.
- Purity 99.1% (manufacturer reported).
- Soluble in DMSO (100 mg/mL); in vivo formulation protocols available.
- Storage: -20°C protected from light; in solvent -80°C (6 months) or -20°C (1 month).
- Reported to inhibit prostate cancer cell growth and reduce androgen receptor levels in vitro.
Sigma Aldrich Fine Chemicals Biosciences Phenol natural, 97%, FG | 108-95-2 | MFCD00002143 | 100G
Phenol natural, 97%, FG | Purity: 97% | Mol Wt: 94.11 | 108-95-2 | MFCD00002143 | 100G
eMolecules Apigenin 7-O-neohesperidoside | 17306-46-6 | MFCD00016773 | 250mg
Chem-Impex | Apigenin 7-O-neohesperidoside | 250mg | 510432330 | 35336 | | 17306-46-6 | MFCD00016773 | 578.523 | C27H30O14
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Medchemexpress LLC (E/Z)-mirin | 299953-00-7 | 99.2% | 220.25 | C10H8N2O2S | 10 MG
(E/Z)-Mirin is a research-grade small molecule mixture of E and Z isomers that inhibits the MRN (Mre11-Rad50-Nbs1) complex and prevents MRN-dependent activation of ATM. It is intended for laboratory research use, and is provided with standard analytical documentation and storage recommendations.
- Inhibits the MRN (Mre11-Rad50-Nbs1) complex and prevents MRN-dependent activation of ATM.
- Research-grade mixture of E and Z isomers supplied for laboratory use only.
- High purity, 99.22% (as provided by manufacturer).
- Available as 10 mg solid and 10 mM solutions in DMSO for flexible dosing.
- Characterized by COA, HNMR, RP-HPLC, and LCMS documentation.
- Store sealed, away from moisture and light; in solvent store at -80°C for long-term storage.