Unsubstituted Phenols
Sigma Aldrich Fine Chemicals Biosciences Phenol | 108-95-2 | MFCD00002143 | 25 g
Phenol | Purity: ≥99.0% | Mol Wt: 94.11 | 108-95-2 | MFCD00002143 | 25 g
Medchemexpress LLC Eriodictyol-7-O-glucoside | 38965-51-4 | MFCD18632528 | 99.8% | 450.39 g/mol | C21H22O11 | 10 MG
Eriodictyol-7-O-glucoside is a flavonoid glycoside used as a research reagent with reported antioxidant and Nrf2-activating activity in biological assays. Typical use includes in vitro biochemical and cell-based studies.
- Flavonoid glycoside (eriodictyol-7-o-glucoside).
- Molecular formula C21H22O11.
- Molecular weight 450.39 g/mol.
- CAS number 38965-51-4.
- Purity 99.8% (manufacturer listed).
- Solubility ≥ 2.5 mg/mL (5.55 mM); clear solution.
- Supplied as 10 MG vial for laboratory use.
Medchemexpress LLC Cirsimaritin | 6601-62-3 | 99.2% | 314.29 g/mol | C17H14O6 | 10 MG
Cirsimaritin is a flavone-class natural product used as a pharmacological research tool. It binds weakly to the benzodiazepine site on GABAA receptors and has reported antidepressant, anxiolytic, and antinociceptive activities.
- High chemical purity reported at 99.23%.
- CAS number 6601-62-3 for unambiguous identification.
- Molecular weight 314.29 g/mol, formula C17H14O6.
- Soluble in DMSO (22.73 mg/mL) and formulatable in 10% DMSO/90% corn oil for in vivo use.
- Offered in small research sizes suitable for discovery work, including 10 mg and larger packs.
- Powder stable at -20°C (up to 3 years); store solutions at -80°C for long-term stability.
Medchemexpress LLC HY-U00450 5mg Medchemexpress, 4-O-Methyl honokiol CAS:68592-15-4 Purity:>98%
Medchemexpress, HY-U00450 5mg 4-O-Methyl honokiol CAS:68592-15-4 4-O-Methyl honokiol is a natural neolignan isolated from Magnolia officinalis, acts as a PPARγ agonist, and inhibtis NF-κB activity, used for cancer and inflammation research. 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.
eMolecules Icariside I | 56725-99-6 | MFCD01662755 | 25mg
Ambeed | Icariside I | 25mg | 598442438 | A473088 | | 56725-99-6 | MFCD01662755 | 530.526 | C27H30O11
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Medchemexpress LLC Ko 143 | 461054-93-3 | 100.0% | 469.57 | 25MG
Ko 143 is a potent and selective ATP-binding cassette subfamily G member 2 (ABCG2/BCRP) inhibitor. This compound demonstrates over 200-fold selectivity compared to P-gp and MRP-1 transporters.
- Potent and selective ABCG2/BCRP inhibitor.
- Shows over 200-fold selectivity compared to P-gp and MRP-1 transporters.
- Has an EC90 of 26 nM for BCRP.
eMolecules Aloin (Mixture of A and B) | 8015-61-0 | MFCD00151160 | 25g
Ambeed | Aloin (Mixture of A and B) | 25g | 600833537 | A201696 | | 8015-61-0 | MFCD00151160 | 418.398 | C21H22O9
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Medchemexpress LLC HY-N0148 10g , Rutin Rutoside;Quercetin 3-O-rutinoside CAS:153-18-4 Purity:98%
Medchemexpress, HY-N0148 10g Rutin Rutoside;Quercetin 3-O-rutinoside CAS:153-18-4 Formula:C27H30O16 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 Branaplam hydrochloride | 1562338-39-9 | 99.4% | 429.94 | 5 MG
Branaplam hydrochloride is a highly potent, selective, and orally active survival motor neuron-2 (SMN2) splicing modulator. It is for research use only, inhibiting human-ether-a-go-go-related gene (hERG) and showing potential in treating spinal muscular atrophy.
- Highly potent, selective, and orally active splicing modulator.
- Inhibits human-ether-a-go-go-related gene (hERG).
- Elevates full-length SMN protein.
- Extends survival in a severe spinal muscular atrophy (SMA) mouse model.
Medchemexpress LLC Liquiritin apioside | 74639-14-8 | MFCD09260034 | 100.0% | 550.51 g·mol⁻¹ | C26H30O13 | 10 MG
Liquiritin apioside is a flavonoid O-glycoside used as a research reagent and reported as an orally active inhibitor of the TRPV1 receptor. It selectively inhibits the laryngeal chemoreflex and is applied in studies of respiratory-related pharmacology and analytical research.
- Orally active TRPV1 receptor inhibitor.
- Suitable for respiratory-related pharmacology research.
- High chemical purity and analytical-grade quality.
- Available in multiple package sizes, including 10 mg.
- Characterized by CAS 74639-14-8 and formula C26H30O13.
Medchemexpress LLC HY-16561 500mg , Resveratrol trans-Resveratrol CAS:501-36-0 Purity:98%
Medchemexpress, HY-16561 500mg Resveratrol trans-Resveratrol CAS:501-36-0 Formula:C14H12O3 IC50: 0.8 μM (Adenylyl cyclase), 1 μM (IKKβ), 3.3 and 5 μM (DNA polymerase α and δ) Purity:98% Resveratrol is one of the numerous polyphenolic compounds found in several vegetal sources, has a wide spectrum of targets with IC 50 of 0.8, 1, 3.3 and 5 μM for adenylyl cyclase, IKKβ , DNA polymerase α and δ, respectively. 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-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 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 VL285 phenol | 1448188-69-9 | MFCD31746640 | 98.6% | 548.65 g/mol | C29H32N4O5S | 10 MG
VL285 Phenol is a phenol-based analog of a VHL E3 ligase ligand, provided as a high-purity research chemical for use as a PROTAC building block and for VHL recruitment studies. It has reported activity in degrading HaloTag7 fusion proteins (IC50 = 0.34 μM).
- Phenol-based VHL ligand analog.
- Suitable for PROTAC synthesis and VHL studies.
- High purity (98.56%).
- Molecular weight 548.65 g/mol; formula C29H32N4O5S.
- Soluble in DMSO at 100 mg/mL.
- Powder storage: -20°C (up to 3 years), 4°C (up to 2 years).