Tetrahydrofuran
Medchemexpress LLC Ecliptasaponin D | 206756-04-9 | 5 MG
Ecliptasaponin D is a triterpenoid glucoside isolated from Eclipta alba (L.) Hassk, which is the aerial part of Eclipta prostrate. Eclipta prostrate is considered a nourishing herbal medicine with pleiotropic effects, including anti-inflammatory, hepatoprotective, antioxidant, and immunomodulatory properties.
- Triterpenoid glucoside
- Isolated from Eclipta alba (L.) Hassk
- Anti-inflammatory properties
- Hepatoprotective properties
- Antioxidant properties
- Immunomodulatory properties
Medchemexpress LLC Remdesivir metabolite | 1911579-04-8 | 99.6% | C15H19N6O8P | 10MG
GS-704277 is an alanine metabolite of remdesivir used as a research reference standard for antiviral metabolism and analytical studies. It is intended for metabolite identification, pharmacokinetic investigations, and development or validation of chromatographic and mass-spectrometric assays.
- High stated purity suitable for analytical applications.
- Molecular formula and weight provided for confirmation and reporting.
- Available in small research-scale pack sizes for bench studies.
- Useful for metabolite identification and pharmacokinetic work.
- Compatible with LC-MS and HPLC analytical workflows.
Medchemexpress LLC CCT369260 | 2647503-57-7 | 99.7% | 50 MG
CCT369260 is a chemical probe and an orally active B-cell lymphoma 6 (BCL6) inhibitor with anti-tumor activity, exhibiting an IC50 of 520 nM for BCL6.
- Chemical probe and orally active B-cell lymphoma 6 (BCL6) inhibitor
- Exhibits anti-tumor activity
- IC50 of 520 nM for BCL6
- Significantly inhibits BCL6 in OCI-Ly1 DLBCL xenograft model
- Demonstrates moderate clearance with a mean oral bioavailability of 54%
- Induces BCL6 degradation in human OCI-LY1 cells
- Shows antiproliferative activity against OCI-LY1, OCI-LY3, and SUDHL4 cells
- Storage as powder: -20°C for 3 years, 4°C for 2 years
- Storage in solvent: -80°C for 6 months, -20°C for 1 month
Medchemexpress LLC ETZ (C3-CA-DTZ) | 2989379-61-3 | 99.8% | C34H28N6O6 | 100 MG
ETZ (C3-CA-DTZ) is a promising luciferase substrate, acting as a prosubstrate that can be activated in vivo by non-specific esterase. This activation enhances the brain delivery of luciferin, making it a valuable tool for research applications. It has a molecular weight of 616.62 and a purity of 99.84%.
- Promising luciferase substrate
- Activated in vivo by non-specific esterase
- Enhances brain delivery of luciferin
- For research use only
Medchemexpress LLC Rhamnocitrin | 569-92-6 | 300.26 | 5 MG
Rhamnocitrin is an anti-inflammatory and antioxidant agent that targets STIM-1, NFATc3, and MAPK pathways. It selectively inhibits oxidative stress and inflammatory responses in vascular endothelial cells and neurons by regulating miR-185, STIM-1, NFATc3, and ERK/p38 MAPK pathways. It can be used in the study of endothelial-related inflammatory diseases and neuroprotection.
- Functions as an anti-inflammatory and antioxidant agent.
- Targets STIM-1, NFATc3, and MAPK pathways.
- Inhibits oxidative stress and inflammatory responses.
- Useful for studying endothelial-related inflammatory diseases.
- Useful for neuroprotection research.
Medchemexpress LLC L-homopropargylglycine (2S)-2-amino-5-hexynoic acid | 98891-36-2 | MFCD11052896 | 98.0% | 127.14 g/mol | C6H9NO2 | 5 MG
L-homopropargylglycine is an alkyne-bearing amino acid analog used as a PROTAC linker and for bioorthogonal click chemistry. The compound contains a terminal alkyne for azide-alkyne cycloaddition and is supplied as a small, crystalline reagent suitable for synthetic and conjugation workflows.
- Alkyne-functional amino acid ideal for click chemistry applications.
- Suitable as a PROTAC linker or for probe conjugation.
- High purity of 98.0% supports reliable synthesis.
- Low molecular weight (127.14 g/mol) simplifies handling and analysis.
- Stable when stored sealed at recommended cold temperatures.
- Available in small pack sizes for research-scale use.
Medchemexpress LLC Mpt0b392 | 1346169-92-3 | 99.6% | 404.44 | C19H20N2O6S | 5 MG
This research compound is a quinoline-derived microtubule-depolymerizing agent that activates c-Jun N-terminal kinase (JNK), induces mitotic arrest, and promotes apoptosis. Intended for preclinical in-vitro and in-vivo research.
- High purity (99.6%) for reproducible results.
- Mechanism: microtubule depolymerization and JNK activation.
- Suitable for in vitro and in vivo preclinical studies.
- Soluble in DMSO; sonication recommended for full dissolution.
- Powder stable at -20°C; follow solvent storage recommendations.
![eMolecules benzyl N-(1-oxaspiro[2.3]hexan-5-ylmethyl)carbamate | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502160061.JPG-250.jpg)
eMolecules benzyl N-(1-oxaspiro[2.3]hexan-5-ylmethyl)carbamate | 1g
Pharmablock - Stock | benzyl N-(1-oxaspiro[2.3]hexan-5-ylmethyl)carbamate | 1g | 534153255 | PBHW351 | 247.294 | C14H17NO3
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Medchemexpress LLC Ganodermanontriol | 106518-63-2 | 472.70 | 5 MG
Ganodermanontriol is a sterol isolated from Ganoderma lucidum that induces anti-inflammatory activity in tert-butyl hydroperoxide (t-BHP)-damaged hepatic cells by expressing HO-1. It also exhibits hepatoprotective activity. It has been shown to inhibit breast cancer cell lines MCF-7 and MDA-MB-231 with IC50 values of 5.8 and 9.7 μM, respectively.
- Induces anti-inflammatory activity in damaged hepatic cells.
- Exhibits hepatoprotective activity.
- Inhibits breast cancer cell lines MCF-7 and MDA-MB-231.
Medchemexpress LLC Tenuifoliside B | 139726-36-6 | MFCD00915287 | 99.2% | 668.60 g/mol | C30H36O17 | 10 MG
Tenuifoliside B is a natural glycoside isolated from Polygala tenuifolia and supplied as a high-purity solid for laboratory research. It is reported to have neuroprotective and cognition-enhancing effects in preclinical studies and is intended for research use only.
- Natural glycoside isolated from Polygala tenuifolia
- White to yellow solid powder suitable for analytical and biological studies
- Molecular formula C30H36O17 and molecular weight 668.60 g/mol
- High purity (approx. 99.2%) for research applications
- Reported biological activities include inhibition of KCN-induced hypoxia and protection against scopolamine-induced memory impairment
- For research use only; not for human or clinical use
Medchemexpress LLC N-Vanillyldecanamide | 31078-36-1 | MFCD01233545 | 50 MG
N-Vanillyldecanamide is a capsaicinoid isolated from the fruits of Capsicum annuum. It significantly reduced the radical length of Lactuca sativa seedling in a dose-dependent manner. This product is for research use only.
- Purity of 99.86%
- Molecular weight of 307.43
- Molecular formula C18H29NO3
- Appears as a white to off-white solid
- Exhibits agonist activity at rat TRPV1 in CHO cells with an EC50 of 83 nM
Medchemexpress LLC (S)-Tetrahydrofuran-3-ol | 86087-23-2 | MFCD00064327 | 99.9% | C4H8O2 | 25 G
(S)-Tetrahydrofuran-3-ol is the (S)-enantiomer of Tetrahydrofuran-3-ol. This chemical serves as a significant precursor for the creation of HIV protease inhibitors and can be manufactured through chemical synthesis or enzymatic hydrolysis.
- High purity of 99.94%
- Appears as a colorless to light yellow liquid
- Stable in pure form for 3 years at -20°C or 2 years at 4°C
- Stable in solvent for 6 months at -80°C or 1 month at -20°C
Medchemexpress LLC AVJ16 | 2775241-92-2 | 99.6% | C28H27N3O4 | 50 MG
AVJ16 is an inhibitor of insulin-like growth factor 2 mRNA binding protein (IGF2BP1), which shows a strong affinity with a Kd of 1.4 μM. It acts as a cancer cell migration inhibitor by interfering with IGF2BP1's ability to bind target mRNA, thereby regulating gene expression and translation.
- Specifically targets IGF2BP1 with a Kd of 1.4 μM.
- Interferes with IGF2BP1 binding to target mRNA, regulating gene expression and translation.
- Inhibits proliferation, invasion, and migration of IGF2BP1-expressing lung adenocarcinoma cells.
- Suppresses colony formation and spheroid growth, and induces apoptosis in H1299 and LKR-M-FI cells.
- Exhibits antitumor activity in xenograft mouse models.
Medchemexpress LLC ABD957 | 3007772-60-0 | 98.1% | C27H36F3N7O5S | 50 MG
ABD957 is a potent and selective covalent inhibitor of the ABHD17 family of depalmitoylases. This compound can block N-Ras signaling and inhibit the growth of NRAS-mutant AML cells. It is intended for research use only.
- Potent and selective covalent inhibitor of ABHD17 family depalmitoylases
- Blocks N-Ras signaling
- Inhibits the growth of NRAS-mutant AML cells (OCI-AML3, THP1, HL60)
- Attenuates N-Ras depalmitoylation in AML cells at 500 nM
- Has an IC50 of 0.21 μM for ABHD17B
Strem, An Ascensus Company CAS 920-39-8. 0.25mole. i-Propylmagnesium bromide 2.9M (35wt% 1wt%) in 2-methyltetrahydrofuran. MFCD00672110
CAS 920-39-8. 0.25mole. i-Propylmagnesium bromide 2.9M (35wt% 1wt%) in 2-methyltetrahydrofuran. MFCD00672110. Molecular Weight 147.30. Molecular Formula (CH3)2CHMgBr. Color/form liq. Strem 12-0825. http//www.strem.com/catalog/v/12-0825/
