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AZD3839 free base, MedChemExpress
MedChemExpress AZD3839 free base is a potent and selective orally active, brain-permeable BACE1 inhibitor (Ki=26 nM).
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| Molecular Weight (g/mol) | 431.41 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | AZD3839 free base |
| Grade | Research |
| SMILES | FC1=C2C([C@](C3=CC=CC(C4=CN=CN=C4)=C3)(C5=CC(C(F)F)=NC=C5)N=C2N)=CC=C1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.89% |
| CAS | 1227163-84-9 |
| Solubility Information | DMSO : 125 mg/mL (289.75 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C24H16F3N5 |
| Formula Weight | 431.41 |
Gefitinib-based PROTAC 3, MedChemExpress
MedChemExpress Gefitinib-based PROTAC 3, conjugating an EGFR binding element to a von Hippel-Lindau ligand via a linker, induces EGFR degradation with DC50s of 11.7 nM and 22.3 nM in HCC827(exon 19 del) and H3255 (L858R mutantion) cells, respectively.
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| Molecular Weight (g/mol) | 934.51 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Gefitinib-based PROTAC 3 |
| Grade | Research |
| SMILES | O=C([C@H]1N(C([C@@H](NC(CCOCCOCCCCCOC2=CC3=C(NC4=CC=C(F)C(Cl)=C4)N=CN=C3C=C2OC)=O)C(C)(C)C)=O)C[C@H](O)C1)NCC5=CC=C(C6=C(C)N=CS6)C=C5 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.24% |
| CAS | 2230821-27-7 |
| Solubility Information | DMSO : ≥ 60 mg/mL (64.20 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture and light∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture and light) |
| Shelf Life | 4°C, sealed storage, away from moisture and light∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture and light) |
| Molecular Formula | C47H57ClFN7O8S |
| Formula Weight | 934.51 |
AV-412 free base, MedChemExpress
MedChemExpress AV-412 free base (MP-412 free base) is an EGFR inhibitor with IC50s of 0.75, 0.5, 0.79, 2.3, 19 nM for EGFR, EGFRL858R, EGFRT790M, EGFRL858R/T790M and ErbB2, respectively.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 507.0 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | AV-412 free base |
| Grade | Research |
| SMILES | O=C(C=C)NC1=CC2=C(NC3=CC=C(C(Cl)=C3)F)N=CN=C2C=C1C#CC(C)(C)N(CC4)CCN4C |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.33% |
| CAS | 451492-95-8 |
| Solubility Information | DMSO : 50 mg/mL (98.62 mM; Need ultrasonic) |
| Synonym | MP-412 free base |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C27H28ClFN6O |
| Formula Weight | 507.0 |
Nelonemdaz, MedChemExpress
MedChemExpress Nelonemdaz (Salfaprodil free base) is an NR2B-selective and uncompetitive antagonist of N-methyl-D-aspartate (NMDA). Nelonemdaz is also a free radical scavenger. Nelonemdaz has excellent neuroprotection against NMDA- and free radical-induced cell death.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 383.22 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Nelonemdaz |
| Grade | Research |
| SMILES | OC(C1=C(O)C=CC(NCC2=C(C(F)=C(C(F)(F)F)C(F)=C2F)F)=C1)=O |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 98.15% |
| CAS | 640290-67-1 |
| Solubility Information | DMSO : ≥ 112.5 mg/mL (293.57 mM) |
| Synonym | Salfaprodil free base Neu2000 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C15H8F7NO3 |
| Formula Weight | 383.22 |
Vonoprazan, MedChemExpress
MedChemExpress Vonoprazan (TAK-438 free base), a proton pump inhibitor (PPI), is a potent and orally active potassium-competitive acid blocker (P-CAB), with antisecretory activity.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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