Unsubstituted Phenols
Medchemexpress LLC HY-W008772 5mg Medchemexpress, 4-Hydroxymephenytoin CAS:61837-65-8 Purity:>98%
Medchemexpress, HY-W008772 5mg 4-Hydroxymephenytoin CAS:61837-65-8 4-Hydroxymephenytoin is a metabolism of an antiepileptic drug mephenytoin, which is used as a CYP2C19 substrate. 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 693288-97-0 | Medchem Express | CPPHA | 5mg | 446264375 | HY-14612 | MFCD12912405 | 406.82 | C22H15ClN2O4
Medchem Express | CPPHA | 5mg | 446264375 | HY-14612 | 693288-97-0 | MFCD12912405 | 406.820 | C22H15ClN2O4
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.
eMolecules 1600515-49-8 | Medchem Express | Tilfrinib | 5mg | 482203923 | HY-110244 | MFCD30011871 | 275.311 | C17H13N3O
Medchem Express | GLP-1 receptor agonist 2 | 5mg | 446260394 | HY-112679 | 2230197-64-3 | 580.060 | C30H31ClFN5O4
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Medchemexpress LLC Suzetrigine phenol | 2649467-91-2 | 99.4% | 459.37 | 5 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.
- Phenolate form of sodium channel modulator
- Orally active
- Highly selective inhibitor of NaV1.8
Medchemexpress LLC HY-B0882 500mg , Edrophonium (chloride) CAS:116-38-1 Purity:98%
Medchemexpress, HY-B0882 500mg Edrophonium (chloride) CAS:116-38-1 Formula:C10H16ClNO 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 (+)-Tyrphostin B44 | 133550-37-5 | MFCD00209855 | 97.0% | 308.33 g/mol | C18H16N2O3 | 50 MG
(+)-Tyrphostin B44 is a small-molecule EGFR inhibitor used in preclinical research to study EGFR-dependent signaling and antitumor activity. It is supplied as a solid and as DMSO solutions for biochemical and cellular assays, and includes formulation guidance for in vivo studies.
- High purity (97.0%) suitable for research assays.
- Molecular formula C18H16N2O3, molecular weight 308.33 g/mol.
- Available as solid (multiple milligram pack sizes) and 10 mM solutions in DMSO.
- Soluble in DMSO ≥ 100 mg/mL; in vivo formulation protocols provided.
- Storage recommendations provided for powder and solvent formulations to preserve stability.
Selleck Chemical LLC 2 6-Dihydroxybenzoic acid
2 6-Dihydroxybenzoic acid ( -resorcylic acid 2-Carboxyresorcinol 2 6-Resorcylic acid) is a phenolic compound which is known to have poor biological performance such as DPPH scavenging activity and microbial growth inhibition
Medchemexpress LLC Hesperetin 7-O-glucoside | 31712-49-9 | 99.4% | 464.42 g·mol⁻¹ | C22H24O11 | 5MG
Hesperetin 7-O-glucoside is a flavanone monoglucoside provided for laboratory research with reported anti-inflammatory and antihypertensive activity. It is intended for research use only and not for human or clinical applications. The product is supplied with supporting documentation including a datasheet, certificate of analysis, and safety data sheet.
- Flavanone monoglucoside structure with molecular formula C22H24O11.
- Molecular weight 464.42 g·mol⁻¹.
- High purity (~99.4%) as indicated on the COA.
- Supplied in small research pack sizes suitable for assay development.
- Includes datasheet, certificate of analysis, and safety data sheet.
- Commonly used in studies of flavonoid metabolism and enzyme inhibition.
Medchemexpress LLC RKI-1447 dihydrochloride | 1782109-09-4 | 99.9% | 399.29 | 50 MG
RKI-1447 dihydrochloride is a potent and selective ROCK inhibitor, effectively targeting ROCK1 and ROCK2. It has been shown to suppress colorectal carcinoma cell growth and promote apoptosis, exhibiting antitumor activity both in vitro and in vivo.
- Potent and selective ROCK inhibitor (IC50s of 14.5 nM for ROCK1 and 6.2 nM for ROCK2).
- Suppresses colorectal carcinoma cell growth.
- Promotes apoptosis.
- Inhibits phosphorylation of ROCK substrates MLC-2 and MYPT-1 in human cancer cells.
- Demonstrates antitumor activity in vivo in models of mammary tumor and colorectal carcinoma.
Medchemexpress LLC VL285 Phenol | 1448188-69-9 | C29H32N4O5S | 100 MG
VL285 Phenol is a phenol-based analog of VL285, which functions as an E3 ubiquitin ligase VHL ligand. It can be utilized in the synthesis of HaloPROTAC3 to degrade HaloTag7 fusion protein with an IC50 of 0.34 μM. This product targets Ligands for E3 Ligase and VHL, and is involved in the PROTAC pathway.
- Phenol-based analog of VL285
- Functions as an E3 ubiquitin ligase VHL ligand
- Utilized in the synthesis of HaloPROTAC3
- Degrades HaloTag7 fusion protein (IC50=0.34 μM)
- Targets ligands for E3 ligase and VHL
- Involved in the PROTAC pathway
Medchemexpress LLC Suzetrigine phenol | 2649467-91-2 | 99.4% | 459.37 | 100 MG
Suzetrigine phenol is the phenolate form of the sodium channel modulator Suzetrigine. It is an orally active and highly selective inhibitor of NaV1.8.
- Phenolate form of suzetrigine
- Sodium channel modulator
- Orally active
- Highly selective inhibitor of NaV1.8
- Relevant for neurological and eye or ear diseases
Medchemexpress LLC Kuwanon E | 68401-05-8 | 5 MG
Kuwanon E is a flavonoid isolated from Morus alba.
- Cytotoxic to human monocytic leukemic cell lines.
- Reduces the level of IL-1β.
- Shows cytotoxic activity against THP-1 human monocytic leukemic cell line, with an IC50 of 4.0±0.08 μM.
- Inhibits SERCA1 in New Zealand rabbit skeletal muscle SR vesicles.
Medchemexpress LLC Procyanidin B3 | 23567-23-9 | 5 MG
Procyanidin B3 is a natural product that exhibits antioxidant activity and oral bioavailability. It has good blood-brain barrier penetration and acts as a selective inhibitor of histone acetyltransferase (HAT). It inhibits p300 HAT-mediated acetylation of the androgen receptor and can alleviate intervertebral disc degeneration (IVDD) by inhibiting the formation of the TLR4/MD-2 complex. Procyanidin B3 is suitable for research related to prostate cancer and arthritis.
- Natural product
- Antioxidant activity
- Oral bioavailability
- Good blood-brain barrier penetration
- Selective inhibitor of histone acetyltransferase (HAT)
- Inhibits p300 HAT-mediated acetylation of the androgen receptor
- Alleviates intervertebral disc degeneration (IVDD) by inhibiting the formation of the TLR4/MD-2 complex
- Can be used in research on prostate cancer and arthritis
Medchemexpress LLC HY-B0167A 10g Medchemexpress, Sodium Salicylate CAS:54-21-7 Purity:>98%
Medchemexpress, HY-B0167A 10g Sodium Salicylate CAS:54-21-7 Sodium Salicylate inhibits cyclo-oxygenase-2 ( COX-2 ) activity independently of transcription factor (NF-κB) activation. 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.