Tetrahydrofuran
Medchemexpress LLC N'-(4-(diethylamino)-2-hydroxybenzylidene)isonicotinohydrazide | 140405-36-3 | MFCD00542031 | 99.7% | 312.37 g/mol | C17H20N4O2 | 10 MG
RSVA405 (CAS 140405-36-3) is a small-molecule activator of AMP-activated protein kinase (AMPK) used in cellular and biochemical research. It promotes CaMKKβ-dependent AMPK activation, inhibits mTOR signaling, and can induce autophagy; supplied at high purity for research applications.
- Potent AMPK activator; reported EC50 = 1 μM.
- High purity (~99.7%).
- Molecular formula C17H20N4O2; molecular weight 312.37 g/mol.
- Soluble in DMSO; available as solid or DMSO solution.
- For research use only; not for human consumption.
Medchemexpress LLC Gsk2983559 | 99.5% | 612.63 | 100 MG
GSK2983559 is an orally active and potent receptor interacting protein 2 (RIP2) kinase inhibitor. It blocks many proinflammatory cytokine responses both in vivo and in human inflammatory bowel disease explant samples.
eMolecules 121138-01-0 | 3-Iodotetrahydrofuran | Synthonix - Stock | MFCD09878873 | 198.003 | C4H7IO | 95.000 | IC1CCOC1 | 5g | 525918605
3-Iodotetrahydrofuran | Synthonix - Stock | 121138-01-0 | MFCD09878873 | 198.003 | C4H7IO | 95.000 | IC1CCOC1 | 5g | 525918605
Medchemexpress LLC (R)-Tetrahydrofuran-2-yl-methylamine | 7202-43-9 | ≥97.0% | 101.15 | 250 MG
(R)-Tetrahydrofuran-2-yl-methylamine (1-[(2R)-tetrahydrofuran-2-yl]methanamine) is a synthetic intermediate useful for pharmaceutical synthesis. It is for research use only.
- Molecular weight: 101.15
- CAS No.: 7202-43-9
- Formula: C5H11NO
- Appearance: Liquid
- Color: Colorless to light yellow
- Purity: ≥97.0%
Medchemexpress LLC Morphiceptin | 74135-04-9 | 99.07% | 521.61 | 5 MG
Morphiceptin is a potent and specific agonist for morphine (μ) receptors. This synthetic peptide is the amide of a fragment of the milk protein β-casein. It exhibits morphinelike activities and is highly specific for morphine (μ) receptors.
- Potent and specific agonist for morphine (μ) receptors
- Synthetic peptide derived from β-casein
- Exhibits morphinelike activities
- Inhibits binding of [3H]dihydromorphine, 125I-labeled FK33824, and [3H]naloxone to rat brain membrane preparations with an IC50 of approximately 20 nM
Medchemexpress LLC Morphiceptin | 74135-04-9 | 99.1% | 521.61 | 1 MG
Morphiceptin is a potent and specific agonist for morphine (μ) receptors. It is a synthetic peptide, derived from β-casein. It exhibits morphinelike activities and shows high specificity for morphine (μ) receptors, inhibiting the binding of [3H]dihydromorphine, 125I-labeled FK33824, and [3H]naloxone to rat brain membrane preparations with an IC50 of about 20 nM.
- Potent and specific agonist for morphine (μ) receptors
- Synthetic peptide derived from β-casein
- White to off-white solid appearance
- Soluble in water and DMSO
Medchemexpress LLC SU5214 | 186611-04-1 | 251.28 | 100 MG
SU5214 is a potent VEGFR2 inhibitor. It is extracted from patent US5834504A and is suitable for research use. It acts on Protein Tyrosine Kinase/RTK pathway.
- Potent VEGFR2 inhibitor
- Target for VEGFR
- Inhibits FLK-1 with an IC50 of 14.8 μM
- Inhibits EGFR with an IC50 of 36.7 μM
Medchemexpress LLC Ceftaroline 100mg | 189345-04-8 | 100MG
T-91825 (PPI-0903M) an N-phosphono-type cephalosporin is the active form of TAK-599 T-91825 is active against both gram-positive and gram-negative bacteria[1 [2
Medchemexpress LLC PF-00446687 free bas 100mg | 862281-92-3 | 100MG
PF-00446687 is a potent selective melanocortin-4 receptor (MC4R) agonist with EC50 of 12 1 nM[1 Pf-446687 is brain penetrant[2
Medchemexpress LLC Kinase, Natto fermentation | 133876-92-3 | 27728 Da | 10 MG
Kinase, Natto fermentation is a potent fibrinolytic enzyme that breaks down blood clots by directly hydrolyzing fibrin and plasmin substrate. It is primarily used for cardiovascular disease research.
- Breaks down blood clots by directly hydrolyzing fibrin and plasmin substrate.
- Dissolves 94% of blood clots within ten minutes in vitro.
- Degrades fibrin clots after two hours of incubation in vitro.
- Exhibits fibrinolytic activity and dissolves blood clots in vivo.
- Stable in neutral or alkaline environments (pH 7.0-12.0).
- Stability improved when mixed with boiled rice extract, broth, serum protein, or gastric juice protein.
- Retains enzyme activity under acidic conditions with stabilizing agents.
- Better stability below 37°C.
- Retains 95% of original activity after 5 freeze-thaw cycles.
eMolecules 121138-01-0 | 3-Iodotetrahydrofuran | Ambeed | MFCD09878873 | 198.003 | C4H7IO | 98.000 | IC1CCOC1 | 5g | 600842501
3-Iodotetrahydrofuran | Ambeed | 121138-01-0 | MFCD09878873 | 198.003 | C4H7IO | 98.000 | IC1CCOC1 | 5g | 600842501
eMolecules 121138-01-0 | 3-Iodotetrahydrofuran | Ambeed | MFCD09878873 | 198.003 | C4H7IO | 98.000 | IC1CCOC1 | 25g | 582615058
3-Iodotetrahydrofuran | Ambeed | 121138-01-0 | MFCD09878873 | 198.003 | C4H7IO | 98.000 | IC1CCOC1 | 25g | 582615058
Medchemexpress LLC SJ10542 | 2789678-92-6 | 99.3% | C41H46N12O5S | 50 MG
SJ10542 is a potent and selective JAK2/3 PROTAC degrader. In PDX cells lSJBALL020589, SJ10542 has DC50 values of 14 and 11 nM for JAK2 and JAK3, respectively. It exhibits antitumor activity and can be used for the research of hematological malignancies and autoimmune diseases.
- Potent and selective JAK2/3 PROTAC degrader
- Exhibits antitumor activity
- Useful for research of hematological malignancies and autoimmune diseases
- Degrades JAK2 (DC50: 24 nM), JAK3, and GSPT1 in MHH-CALL-4 cells
- JAK2 DC50: 14 nM
- JAK3 DC50: 11 nM
- JAK2-fusion ALL DC50: 24 nM
- CRBN recruiter
Medchemexpress LLC Ralaniten triacetate | 1637573-04-6 | 98.8% | 521.00 | C27H33ClO8 | 50MG
Ralaniten triacetate (EPI-506) is a research-stage prodrug of ralaniten that inhibits the androgen receptor N-terminal domain (NTD). It is intended for preclinical biochemical and cellular research into AR signaling and prostate cancer models.
- CAS number: 1637573-04-6.
- Purity: 98.8% (reported by supplier).
- Molecular formula: C27H33ClO8.
- Molecular weight: 521.00 Da.
- Physical state: colorless to light yellow liquid; density ≈1.188 g/cm3.
- Storage: pure form -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- Pack sizes: available in milligram quantities for research use (including 50 mg).
Medchemexpress LLC Tmx-4100 | 2367619-63-2 | 98.2% | C11H10N4O2S | 10MG
TMX-4100 is a research small-molecule described as a PDE6D degrader. It is supplied as a solid and as a DMSO solution, with molecular formula C11H10N4O2S and a reported purity of 98.18%. Intended for laboratory research use; consult the datasheet and COA for handling, storage, and batch-specific information.
- PDE6D degrader activity useful for protein degradation studies.
- Available as solid powder and as a 10 mM solution in DMSO.
- High reported purity (98.2%) for consistent experimental results.
- Comes with datasheet and certificate of analysis for batch verification.
- White to off-white solid appearance; suitable for standard laboratory handling.