Tetrahydrofuran
Medchemexpress LLC Ro5-3335 | 30195-30-3 | 99.5% | 259.69 | 10 MG
Ro5-3335 | 30195-30-3 | 99.5% | 259.69 | 10 MG
eMolecules 89160-04-3 | Ambeed | 21-Hydroxyhenicosanoic acid | 1g | 660582704 | A1195099 | 342.564 | C21H42O3
Ambeed | 21-Hydroxyhenicosanoic acid | 1g | 660582704 | A1195099 | 89160-04-3 | 342.564 | C21H42O3
Medchemexpress LLC Zectivimod | 1623066-63-6 | 99.4% | 528.47 | 100 MG
Zectivimod is a sphingosine-1-phosphate receptor agonist. It is intended for research applications related to autoimmune diseases, chronic inflammatory diseases, and immunoregulation disorders.
- Sphingosine-1-phosphate receptor agonist
- Suitable for research on autoimmune diseases
- Suitable for research on chronic inflammatory diseases
- Suitable for research on immunoregulation disorders
- Solid appearance, white to off-white color
- Purity of 99.35%
- Store at 4°C, sealed, away from moisture and light
- Store in solvent at -80°C for 6 months or -20°C for 1 month, sealed, away from moisture and light
- Target LPL receptor
- Part of the GPCR/G protein pathway
- Solubility in DMSO: 100 mg/mL
Medchemexpress LLC 2-((5-((4-fluorophenyl)carbamoyl)pyrimidinyl)sulfanylmethyl)-4-(trifluoromethoxy)phenyl boronic acid | 1648843-04-2 | 98.7% | 25 MG
SX-682 (CAS 1648843-04-2) is an orally bioavailable small-molecule allosteric inhibitor of CXCR1 and CXCR2 investigated for oncology research. It blocks recruitment of immunosuppressive myeloid-derived suppressor cells to the tumor microenvironment and can enhance the activity of checkpoint inhibitors.
- Oral bioavailability and potent CXCR1/2 antagonism
- Useful for preclinical and clinical oncology research
- Blocks myeloid-derived suppressor cell recruitment to tumors
- Well-characterized chemical identity: CAS 1648843-04-2, C19H14BF4N3O4S
- Analytical purity typically >98% and supplied as a 25 MG vial
Medchemexpress LLC MST-312, chemically modified derivative of epigallocatechin gallate | 368449-04-1 | 98.6% | 100 MG
MST-312 is a small-molecule telomerase inhibitor derived from epigallocatechin gallate (EGCG), intended for research use in oncology and cellular studies. It is available both as a solid and as a DMSO solution for in vitro assays.
- Telomerase inhibitor used in cancer research.
- Purity 98.6%.
- Molecular formula C20H16N2O6.
- Molecular weight 380.35 g/mol.
- CAS number 368449-04-1.
- Available as solid (5-500 mg) and 10 mM solution in DMSO.
Medchemexpress LLC VPC-70619 | 2361742-30-3 | 99.93% | C16H8ClF3N4O | 100 MG
VPC-70619 is a potent N-Myc inhibitor that blocks the binding of the N-Myc-Max heterocomplex to the DNA E-box and shows strong inhibitory activity against N-Myc-dependent cell lines. It can partially reverse paclitaxel resistance in cells by reducing MYCN expression and can be used for cancer research, including neuroblastoma and thyroid cancer.
- Potent N-Myc inhibitor
- Blocks the binding of the N-Myc-Max heterocomplex to the DNA E-box
- Shows strong inhibitory activity against N-Myc-dependent cell lines
- Partially reverses paclitaxel resistance by reducing MYCN expression
- Can be used for cancer research, including neuroblastoma and thyroid cancer
- Demonstrates high inhibition rates in certain cell types
- Highly stable in liver microsomes
- Regulates MYCN signaling pathway
- Inhibits proliferation, migration, and aggressiveness of cancer cells
Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran | 109-99-9 | MFCD00005356 | 1 L
Tetrahydrofuran | Purity: ≥99.9% | Mol Wt: 72.11 | 109-99-9 | MFCD00005356 | 1 L
Sigma Aldrich Fine Chemicals Biosciences 2-Methyltetrahydrofuran BioRenewable, anhydrous, >=99%, Inhibitor-free | 96-47-9 | MFCD00005367 | 100ML
2-Methyltetrahydrofuran BioRenewable, anhydrous, >=99%, Inhibitor-free | Purity: >=99% | Mol Wt: 86.13 | 96-47-9 | MFCD00005367 | 100ML
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
Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran | 109-99-9 | MFCD00005356 | 4l
Tetrahydrofuran | Purity: 99% | Mol Wt: 72.11 | 109-99-9 | MFCD00005356 | 4l
eMolecules 1207727-04-5 | Medchem Express | Broflanilide | 5mg | 559839407 | HY-108689 | 663.285 | C25H14BrF11N2O2
ChemScene | 3-Chloro-2-fluoro-5-(trifluoromethyl)benzoic acid | 1g | 536808729 | CS-0108802 | 129931-45-9 | MFCD01631509 | 242.550 | C8H3ClF4O2
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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).
Sigma Aldrich Fine Chemicals Biosciences Linalool oxide natural, >=95% | 60047-17-8 | MFCD00053543 |
Linalool oxide natural, >=95% | Purity: >=95% | Mol Wt: 170.25 | 60047-17-8 | MFCD00053543 |