Tetrahydrofuran
![eMolecules 20881-04-3 | Ambeed | (3aR3bS7aR8aR)-2255-Tetramethyltetrahydro-7H-[13]dioxolo[4545]furo[32-d][13]dioxine | 5g | 572926723 | A181940 | MFCD00063224 | 230.26 | C11H18O5](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502484654.JPG-250.jpg)
eMolecules 20881-04-3 | Ambeed | (3aR3bS7aR8aR)-2255-Tetramethyltetrahydro-7H-[13]dioxolo[4545]furo[32-d][13]dioxine | 5g | 572926723 | A181940 | MFCD00063224 | 230.26 | C11H18O5
Pharmablock | 24-dichloro-8-methyl-quinazoline | 25mg | 714320911 | PBXA269 | 39576-83-5 | MFCD11849266 | 213.060 | C9H6Cl2N2
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eMolecules 96-47-9 | 2-Methyltetrahydrofuran | Oakwood Chemicals | MFCD00005367 | 86.134 | C5H10O | 99.000 | CC1CCCO1 | 2kg | 480143995
2-Methyltetrahydrofuran | Oakwood Chemicals | 96-47-9 | MFCD00005367 | 86.134 | C5H10O | 99.000 | CC1CCCO1 | 2kg | 480143995
Medchemexpress LLC Rhodojaponin III | 26342-66-5 | MFCD01714943 | 99.8% | 368.46 | C20H32O6 | 10 MG
Rhodojaponin III is a grayanane-type diterpenoid isolated from the leaves of Rhododendron molle. It is supplied as a high-purity research reagent for in vitro studies of anti-inflammatory activity and related biochemical research. For research use only; not for human or clinical use.
- High purity suitable for research applications.
- Reported anti-inflammatory biological activity.
- Available in small quantities for assay development and screening.
- Provided as a solid powder for laboratory handling.
eMolecules 121138-01-0 | 3-Iodotetrahydrofuran | Ambeed | MFCD09878873 | 198.003 | C4H7IO | 98.000 | IC1CCOC1 | 1g | 600842500
3-Iodotetrahydrofuran | Ambeed | 121138-01-0 | MFCD09878873 | 198.003 | C4H7IO | 98.000 | IC1CCOC1 | 1g | 600842500
Medchemexpress LLC D-α-tocopherylquinone | 7559-04-8 | MFCD00135657 | 98.9% | 446.71 | C29H50O3 | 10 MG
- Oxidation product of α-tocopherol with quinone structure.
- Exhibits antioxidant and anticoagulant activity.
- Reduces oxidative damage from oxidized lipids.
- Interacts with glutathione-S-transferase (GST).
- Used in reactive oxygen species (ROS) and lipid peroxidation research.
- Molecular formula C29H50O3; MW 446.71 Da.
Medchemexpress LLC Smyrindioloside | 87592-77-6 | 424.40 | 1 MG
Smyrindioloside is a natural product isolated from the bark of *Streblus indicus*. It is for research use only and not sold to patients.
- High purity: 99.32%
- White to off-white solid appearance
- Available in various quantities, including 1 mg, 5 mg, 10 mg, and 50 mg
- In-stock availability for 1 mg size
- Detailed documentation available, including data sheet, COA, and SDS
![Medchemexpress LLC 2-[[4-(diethylamino)-2-hydroxyphenyl]methylene]hydrazide-4-pyridinecarboxylic acid | 140405-36-3 | 99.7% | 312.37 | C17H20N4O2 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000247220.png-250.jpg)
Medchemexpress LLC 2-[[4-(diethylamino)-2-hydroxyphenyl]methylene]hydrazide-4-pyridinecarboxylic acid | 140405-36-3 | 99.7% | 312.37 | C17H20N4O2 | 25 MG
RSVA405 is a potent, orally active activator of AMP-activated protein kinase (AMPK) used in preclinical research. It facilitates CaMKKβ-dependent AMPK activation, inhibits mTOR, promotes autophagy and lysosomal degradation of Aβ, and exhibits anti-inflammatory effects via STAT3 inhibition. Activity is observed in vitro (EC50 ≈ 1 μM) and in vivo in metabolic and renal models.
- Potent AMPK activator with an EC50 of approximately 1 μM.
- Promotes autophagy and lysosomal degradation of Aβ.
- Inhibits mTOR and modulates adipocyte differentiation.
- Exhibits anti-inflammatory effects through STAT3 inhibition.
- Demonstrated in vitro and in vivo activity in metabolic and renal models.
- Supplied as a light yellow to yellow solid with high purity.
Medchemexpress LLC Ganodermanontriol | 106518-63-2 | 472.70 | 1 MG
Ganodermanontriol is a sterol isolated from *Ganoderma lucidum* that induces anti-inflammatory activity in tert-butyl hydroperoxide (t-BHP)-damaged hepatic cells through the expression of HO-1. It also exhibits hepatoprotective activity and antiproliferative activity against human MCF7 and MDA-MB-231 breast cancer cells.
- Induces anti-inflammatory activity.
- Exhibits hepatoprotective activity.
- Suppresses growth of colon cancer cells through β-catenin signaling.
- Exhibits anti-melanogenic effects through regulation of CREB and MAPK signaling pathways.
- Inhibits breast cancer cell lines MCF-7 and MDA-MB-231.
Medchemexpress LLC Nerigliatin | 1245603-92-2 | 99.9% | 432.43 g/mol | C22H20N6O4 | 10 MG
Nerigliatin is a small-molecule glucokinase activator used for laboratory research into glucose-lowering mechanisms. It has demonstrated glucose-lowering efficacy in preclinical studies but has been associated with peripheral nerve degeneration in reported results. Intended for research use only and not for human or clinical applications.
- Glucokinase activator for glucose-lowering research.
- High purity (99.94%).
- Molecular weight 432.43 g/mol.
- Soluble in DMSO at 100 mg/mL with ultrasonic assistance.
- Available in multiple small-scale solid quantities suitable for lab studies.
- Not intended for clinical or human use; handle with appropriate safety precautions.
![eMolecules 87151-60-8 | 1-oxaspiro[4.5]decan-8-one | MFCD09759212 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502136139.JPG-250.jpg)
eMolecules 87151-60-8 | 1-oxaspiro[4.5]decan-8-one | MFCD09759212 | 1g
Pharmablock | 1-oxaspiro[4.5]decan-8-one | 1g | 551144307 | PBP11073 | 87151-60-8 | MFCD09759212 | 154.209 | C9H14O2
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Medchemexpress LLC CSF1R-IN-1 | 2095849-04-8 | 98.0% | 479.45 g/mol | C25H20F3N5O2 | 25 MG
CSF1R-IN-1 is a potent small-molecule inhibitor of the colony stimulating factor 1 receptor (CSF1R) used for research into macrophage biology, tumor-associated macrophages, cancer, inflammation, and neurodegeneration. The compound has an IC50 of 0.5 nM against CSF1R, a molecular weight of 479.45 g/mol, and is supplied as a white to off-white solid with reported purity of 98.04%.
- Potent CSF1R inhibition (IC50 0.5 nM).
- High purity suitable for research (≈98.0%).
- Defined molecular properties: C25H20F3N5O2, 479.45 g/mol.
- Solid, white to off-white appearance for easy handling.
- Stable under recommended storage: powder -20°C (up to 3 years).
- Available in small research quantities including 25 MG.
Medchemexpress LLC Linzagolix | 935283-04-8 | 99.7% | 508.42 | 100 MG
Linzagolix is a potent, non-peptide, and orally active GnRH antagonist. It can be used for uterine fibroids, endometriosis, and adenomyosis research. For research use only, not for sale to patients.
- Potent GnRH antagonist
- Non-peptide compound
- Orally active
- Used for uterine fibroids research
- Used for endometriosis research
- Used for adenomyosis research
Supply Solutions Burdick & Jackson - Filter Column 8ml (50/PK)
Burdick & Jackson - Filter Column 8ml (50/PK)