Tetrahydrofuran
Medchemexpress LLC Protogracillin | 54848-30-5 | 1 MG
Protogracillin is a steroidal saponin isolated from the plant Dioscorea zingiberensis Wright. Steroidal saponins found in the rhizomes of this plant have the potential to reduce the risk of cardiovascular diseases through anti-thrombotic action. It is intended for research use only and not for sale to patients.
- It is a steroidal saponin.
- It is isolated from Dioscorea zingiberensis Wright.
- It has potential anti-thrombotic action.
- It has shown cytotoxicity against human CCRF-CEM cells with an IC50 of 1.77 μM.
- Its purity is 99.00%.
Medchemexpress LLC DS96432529 | 2871872-79-4 | 99.9% | C18H26N4O3S | 100 MG
DS96432529 is a potent and orally active bone anabolic agent, acting through CDK8 inhibition. It is for research use only.
- Potent and orally active bone anabolic agent
- Acts through CDK8 inhibition
- Solid appearance
- Color: Off-white to pink
- Molecular weight: 378.49
- Chemical formula: C18H26N4O3S
- CAS number: 2871872-79-4
- For research use only
Medchemexpress LLC CIL62 | 117593-36-9 | 97.0% | 382.45 | 100 MG
CIL62 is a caspase-3/7-independent cell death inducer. Its mechanism of action is Necrostatin-1 dependent cell death.
- COLO 205: IC50 28 μM (Compound: 3f) for antiproliferative activity after 24 hrs by MTT assay.
- IMR-32: IC50 41 μM (Compound: 3f) for antiproliferative activity after 24 hrs by MTT assay.
- K562: IC50 36 μM (Compound: 3f) for antiproliferative activity after 24 hrs by MTT assay.
- Necrostatin-1 suppresses CIL62 at 19 μM (5 μg/mL).
Medchemexpress LLC SU5214 | 186611-04-1 | 98.0% | 251.28 | 5 MG
SU5214 is a potent VEGFR2 inhibitor. It has been extracted from patent US5834504A and exhibits IC50s of 14.8 μM for FLK-1 and 36.7 μM for EGFR.
- Potent VEGFR2 inhibitor.
- Targets VEGFR.
- Acts on the Protein Tyrosine Kinase/RTK pathway.
- Soluble in DMSO at 100 mg/mL.
- Suitable for research purposes.
Medchemexpress LLC Phosphatidylinositols, soya, sodium salts | 383907-36-6 | 99.2% | 1 MG
Phosphatidylinositols, soya, sodium salts, is a mixture of phosphatidylinositols. Phosphoinositides are lipids involved in the vesicular transport of proteins and lipids between the different compartments of eukaryotic cells. They function by recruiting and/or activating effector proteins.
- Involved in regulating various cellular functions
- Regulates vesicular budding
- Regulates membrane fusion
- Regulates cytoskeleton dynamics
Medchemexpress LLC Su 5214 | 186611-04-1 | MFCD01595259 | >98.0% | 10 MG
SU5214 is a small-molecule tyrosine kinase inhibitor reported to inhibit vascular endothelial growth factor receptor 2 (VEGFR2/FLK-1) and epidermal growth factor receptor (EGFR) in cell-free assays. It is used for biochemical studies and target validation involving VEGFR2/EGFR signaling pathways.
- Reported IC50 of 14.8 μM for VEGFR2 (cell-free assay).
- Reported IC50 of 36.7 μM for EGFR (cell-free assay).
- CAS number 186611-04-1.
- Molecular weight 251.285 g·mol⁻¹.
- Purity greater than 98% (HPLC) as supplied by chemical vendors.
- Supplied in small milligram quantities suitable for in vitro assays.
Medchemexpress LLC N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide | 2922283-38-1 | 98.0% | C93H177N3O3 | 100 MG
N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide is an analogue of TT3 (HY-148049). TT3 is an ionizable lipid-like material used for mRNA delivery.
- Analogue of TT3, an ionizable lipid-like material for mRNA delivery.
- Available in various quantities.
- For research use only.
Medchemexpress LLC Ambroxide | 6790-58-5 | 236.39 | 100 MG
Ambroxide is a naturally occurring terpenoid, known as a key constituent of ambergris. This compound is widely utilized in the manufacture of high-end perfumes to enhance aroma quality and extend fragrance lasting time.
- Naturally occurring terpenoid
- Key constituent of ambergris
- Utilized in high-end perfumes
- Enhances aroma quality
- Extends fragrance lasting time
- High purity (98.0%)
- Appears as a white to off-white solid
- Molecular formula: C16H28O
Medchemexpress LLC PF-00446687 free base | 862281-92-3 | 98.0% | 470.59 g/mol | C28H36F2N2O2 | 50 MG
PF-00446687 free base is a non-peptide, brain-penetrant small-molecule agonist of the melanocortin-4 receptor (MC4R) used in research on melanocortin signaling and central nervous system pharmacology. It is supplied as a powder for in vitro and in vivo studies and demonstrates low-nanomolar potency and selectivity.
- Selective melanocortin-4 receptor agonist with EC50 12 ± 1 nM.
- Binding affinity (Ki) approximately 27 ± 4 nM.
- Brain-penetrant, suitable for central nervous system studies.
- Provided as a powder with solubility in DMSO 62.5 mg/mL (ultrasonic recommended).
- Molecular formula C28H36F2N2O2 and molecular weight 470.59 g/mol.
- High purity by HPLC (≈98.0% per COA).
- Storage: powder -20°C (long-term) or 4°C (short-term).
Medchemexpress LLC Tienilic acid (Ticrynafen) | 40180-04-9 | 99.7% | 331.18 | 5 MG
Tienilic acid (Ticrynafen; ANP 3624) acts as a diuretic hypotensive agent, but it induces hepatotoxicity. It is converted into electrophilic metabolites by cytochrome P450 (CYP) in vitro.
- Functions as a diuretic hypotensive agent.
- Known to induce hepatotoxicity.
- Converted into electrophilic metabolites by cytochrome P450 (CYP) in vitro.
eMolecules 24808-04-6 | Medchem Express | (-)-Epiafzelechin | 5mg | 713705081 | HY-N0943 | MFCD20260428 | 274.272 | C15H14O5
Ambeed | 9-(4-Bromophenyl)-36-di-tert-butyl-9H-carbazole | 1g | 525197143 | A363941 | 601454-33-5 | MFCD11617971 | 434.421 | C26H28BrN
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eMolecules 1192-30-9 | TETRAHYDROFURFURYL BROMIDE | AstaTech | MFCD00016894 | 165.030 | C5H9BrO | 95.000 | BrCC1CCCO1 | 100g | 449775922
TETRAHYDROFURFURYL BROMIDE | AstaTech | 1192-30-9 | MFCD00016894 | 165.030 | C5H9BrO | 95.000 | BrCC1CCCO1 | 100g | 449775922
Medchemexpress LLC Naz2329 | 2809469-05-2 | 99.0% | 501.56 g/mol | C21H18F3NO4S3 | 25 MG
NAZ2329 is a small-molecule inhibitor of PTPRZ and PTPRG intended for research use. It is supplied as a 25 mg research sample and is characterized by high purity and defined physicochemical properties suitable for biochemical and in vivo studies.
- Inhibits PTPRZ and PTPRG activity.
- High purity: 99.02%.
- Molecular formula: C21H18F3NO4S3; molecular weight: 501.56 g/mol.
- Soluble in DMSO; in vitro solubility reported at 100 mg/mL.
- Provided as a 25 mg sample suitable for preliminary biochemical and in vivo assays.
Medchemexpress LLC Onjisaponin B | 35906-36-6 | 99.1% | 10 MG
Onjisaponin B is a natural triterpenoid saponin isolated from Polygala tenuifolia with reported neuroprotective and autophagy-enhancing activity. It is used in cell-based and preclinical studies investigating protein aggregation, neurodegeneration, and inflammatory signaling.
- Natural triterpenoid saponin derived from Polygala tenuifolia.
- Inhibits NF-κB p65 and modulates inflammatory signaling.
- Enhances autophagy and promotes degradation of mutant α-synuclein and huntingtin.
- High purity solid powder (99.1%).
- Supplied as a 10 mg quantity suitable for research-scale assays.
- Intended for mechanistic studies and preclinical pharmacology models.
Medchemexpress LLC Rifalazil 100mg | 129791-92-0 | 100MG
Rifalazil (KRM-1648 ABI-1648) a rifamycin derivative inhibits the bacterial DNA-dependent RNA polymerase and kills bacterial cells by blocking off the -subunit in RNA polymerase[1 Rifalazil (KRM-1648 ABI-1648) is an antibiotic exhibits high potency against mycobacteria gram-positive bacteria Helicobacter pylori C pneumoniae and C trachomatis with MIC values from 0 00025 to 0 0025 g/ml[3 Rifalazil (KRM-1648 ABI-1648) has the potential for the treatment of Chlamydia infection Clostridium difficile associated diarrhea (CDAD) and tuberculosis (TB)[2