Unsubstituted Phenols
Medchemexpress LLC HY-N1939 5mg Medchemexpress, Icariside I CAS:56725-99-6 Purity:>98%
Medchemexpress, HY-N1939 5mg Icariside I CAS:56725-99-6 Icariside I is a metabolite of Icarlin, which could regulate bone remodeling and is recognized as an effective agent for the treatment of osteoporosis. 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 Eltrombopag olamine | 496775-61-2 | ≥98.0% | 442.47 g/mol | C25H22N4O4 | 10 MG
Eltrombopag is an orally active thrombopoietin (TPO) receptor nonpeptide agonist used in research to stimulate megakaryopoiesis and study thrombocytopenia, hematology, and oncology-related mechanisms. Supplied as a research-grade compound for use in in vitro and in vivo studies.
- Stimulates thrombopoietin receptor signaling to increase platelet production.
- Suitable for in vitro and in vivo research applications.
- Available as the olamine salt for improved handling.
- Typical purity ≥98.0% by HPLC as reported by suppliers.
- Molecular formula C25H22N4O4, molecular weight 442.47 g/mol.
- CAS number 496775-61-2 for the parent compound.
Medchemexpress LLC SN-011 | 2249435-90-1 | 99.9% | C25H19FN2O4S | 100 MG
SN-011 is a potent and selective mouse and human STING inhibitor with an IC50 of 76 nM for STING signaling. It competes with cyclic dinucleotide (CDN) for the STING dimer binding pocket, blocking CDN binding and activation. This product is used for research into STING-driven autoimmune and inflammatory diseases.
- Suppresses STING stimulator-induced expression of Ifnb, Cxcl10, and Il6 mRNA in mouse embryonic fibroblasts.
- Inhibits 2′3′-cGAMP-induced Ifnb expression and STING oligomerization/phosphorylation.
- Suppresses STING ER-to-Golgi translocation.
- Inhibits inflammation and autoimmunity in vivo.
- Protects Trex1-/- mice from death, improves survival, and reduces multiorgan inflammation.
eMolecules 497063-94-2 | Medchem Express | Salmeterol-d3 | 1mg | 705860745 | HY-135119 | MFCD06658792 | 418.592 | C25H37NO4
Medchem Express | v1 integrin-IN-1 (TFA) | 5mg | 523883164 | HY-100445A | | 672.680 | C28H35F3N6O8S
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Selleck Chemical LLC Paeonol S2339-200mg
Paeonol (Peonol) a phenolic compound extracted from Chinese herbs Paeonia suffruticosa (moutan cortex) and Cynanchum paniculatum inhibits MAO with an IC50 of about 50 M
Medchemexpress LLC Darbufelone mesylate | 139340-56-0 | 99.7% | 428.57 | C19H28N2O5S2 | 25 MG
Darbufelone mesylate is a research-grade small molecule inhibitor that suppresses cellular production of PGF2α and LTB4. It potently inhibits PGHS-2 (IC50 = 0.19 μM) with substantially lower activity against PGHS-1 (IC50 = 20 μM), and is provided as the methanesulfonate salt for assay and cell-based studies.
- Potent PGHS-2 inhibition (IC50 = 0.19 μM).
- Marked selectivity over PGHS-1 (IC50 = 20 μM).
- High purity, suitable for analytical and biological use (≈99.7%).
- Provided as the mesylate salt for improved handling and stability.
- Characterized molecular weight 428.57 and formula C19H28N2O5S2.
- Intended for research use in biochemical and cell-based assays.
Medchemexpress LLC Loureirin C | 116384-24-8 | 5 MG
Loureirin C is a solid, white to off-white compound classified as a phenol and polyphenol, initially sourced from plants. It exhibits a range of biological activities.
- Anti-bacterial activity
- Anti-spasmodic activity
- Anti-inflammatory activity
- Analgesic activity
- Anti-diabetic activity
- Anti-tumor activity
eMolecules 5786-54-9 | Medchem Express | Hispidol | 5mg | 446257621 | HY-102040 | MFCD00135406 | 254.241 | C15H10O4
Medchem Express | Hispidol | 5mg | 446257621 | HY-102040 | 5786-54-9 | MFCD00135406 | 254.241 | C15H10O4
Medchemexpress LLC Luteolin 5-O-glucoside | 20344-46-1 | MFCD11656133 | ≥98.0% | 448.38 g·mol⁻¹ | C21H20O11 | 10 MG
Luteolin 5-O-glucoside is a flavonoid O-glycoside used in research to study anti-inflammatory and antioxidant mechanisms. It inhibits LPS-induced nitric oxide production and t-BHP-induced reactive oxygen species generation, and is supplied as a high-purity solid for biochemical and cell-based assays.
- Flavonoid glycoside with anti-inflammatory activity.
- Inhibits LPS-induced NO production and t-BHP-induced ROS generation.
- High purity suitable for biochemical and cell-based assays.
- Solid, light yellow to yellow appearance for easy handling.
- Packaged as a small research vial (10 mg) for screening and exploratory studies.
Cayman Chemical Phenol-13C6 1g
A building block; has been used in the synthesis of 13C6-labeled metabolites of (±)-asenapine
Medchemexpress LLC HY-N0828 25mg Medchemexpress, Pterostilbene CAS:537-42-8 Purity:>98%
Medchemexpress, HY-N0828 25mg Pterostilbene CAS:537-42-8 Pterostilbene is a stilbenoid isolated from blueberries and Pterocarpus marsupium [1] . Shows anti-oxidant, anti-inflammatory, anti-carcinogenic, anti-diabetic and anti-obesity properties [1] [4] . Pterostilbene blocks ROS production [3] , also exhibits inhibitory activity against various free radicals such as DPPH, ABTS, hydroxyl, superoxide and hydrogen peroxide [4] . 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 56317-21-6 | Medchem Express | Moracin M | 10mg | 527574308 | HY-122942 | MFCD17166969 | 242.23 | C14H10O4
Medchem Express | Moracin M | 10mg | 527574308 | HY-122942 | 56317-21-6 | MFCD17166969 | 242.230 | C14H10O4
Medchemexpress LLC Isoflavone | 574-12-9 | 222.24 | 500 MG
Isoflavone is an orally available bioactive component of soy phytoestrogen with lipid-lowering and antioxidant activities. It prevents various chronic diseases by regulating fatty acid oxidation in the liver and gene expression in adipose tissue. Additionally, isoflavone is valuable in cancer and cardiovascular disease research.
- Orally available bioactive component of soy phytoestrogen
- Exhibits lipid-lowering and antioxidant activities
- Prevents chronic diseases by regulating fatty acid oxidation and gene expression
- Valuable for cancer and cardiovascular disease research
- Solid appearance
- Light brown to brown color
- Ships at room temperature in continental US
Medchemexpress LLC Suzetrigine phenol | 2649467-91-2 | 99.4% | 459.37 | 50 MG
Suzetrigine phenol is the phenolate form of the sodium channel modulator Suzetrigine (HY-148800). Suzetrigine (VX-548) is an orally active and highly selective inhibitor of NaV1.8.
- Sodium channel modulator
- Orally active
- Highly selective inhibitor of NaV1.8
- For research use only
Medchemexpress LLC RKI-1447 dihydrochloride | 1782109-09-4 | 99.9% | 399.29 | 100 MG
RKI-1447 dihydrochloride is a potent and selective ROCK inhibitor with IC50s of 14.5 and 6.2 nM for ROCK1 and ROCK2, respectively. It suppresses colorectal carcinoma cell growth and promotes apoptosis.
- Potent and selective ROCK inhibitor
- Suppresses colorectal carcinoma cell growth
- Promotes apoptosis
- Suppresses phosphorylation of the ROCK substrates MLC-2 and MYPT-1 in human cancer cells
- Exhibits effective anticancer activity in colorectal carcinoma (CRC)
- Inhibits mammary tumor growth in vivo
- Does not exert physiological toxicity on mice in vivo