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Filtered Search Results
IU1-47, MedChemExpress
MedChemExpress IU1-47 is a potent and specific USP14 inhibitor with an IC50 of 0.6 μM. IU1-47 inhibits IsoT/USP5 with an IC50 of 20 μM. IU1-47 induces tau elimination in cultured neurons.
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| Molecular Weight (g/mol) | 330.85 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | IU1-47 |
| Grade | Research |
| SMILES | CC1=CC(C(CN2CCCCC2)=O)=C(N1C3=CC=C(C=C3)Cl)C |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 99.92% |
| CAS | 670270-31-2 |
| Solubility Information | DMSO : 16.67 mg/mL (50.39 mM; Need ultrasonic) |
| 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 | C19H23ClN2O |
| Formula Weight | 330.85 |
Vinburnine, MedChemExpress
MedChemExpress Vincamone is a vinca alkaloid and a metabolite of vincamine, is a vasodilator.
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Metergoline, MedChemExpress
MedChemExpress Metergoline is a serotonin (5-HT) receptor and dopamine receptors antagonist, with pKis of 8.64, 8.75 and 8.75 for 5-HT2A, 5-HT2B and 5-HT2C, respectively. Metergoline is a high-affinity ligand for the h5-HT7 receptor, with a Ki of 16 nM. Metergoline is also a reversible neural Na+ channels inhibitor. Metergoline is commonly used for the research of seasonal affective disorder, prolactin hormone regulation.
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| Molecular Weight (g/mol) | 403.52 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Metergoline |
| Grade | Research |
| SMILES | O=C(OCC1=CC=CC=C1)NC[C@H](C[C@@]23[H])CN(C)[C@]2([H])CC4=CN(C)C5=CC=CC3=C54 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.62% |
| CAS | 17692-51-2 |
| Solubility Information | DMSO : 125 mg/mL (309.77 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H312∣H332 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C25H29N3O2 |
| Formula Weight | 403.52 |
GSK2606414, MedChemExpress
MedChemExpress GSK2606414 is a cell-permeable and orally available protein kinase R-like endoplasmic reticulum (ER) kinase (PERK) inhibitor with an IC50 of 0.4 nM.
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| Molecular Weight (g/mol) | 451.44 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | GSK2606414 |
| Grade | Research |
| SMILES | NC1=C2C(N(C)C=C2C3=CC4=C(N(C(CC5=CC=CC(C(F)(F)F)=C5)=O)CC4)C=C3)=NC=N1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.59% |
| CAS | 1337531-36-8 |
| Solubility Information | DMSO : ≥ 100 mg/mL (221.51 mM) |
| 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 | C24H20F3N5O |
| Formula Weight | 451.44 |
SB269652, MedChemExpress
MedChemExpress SB269652 is the first drug-like allosteric modulator of the dopamine D2 receptor (D2R); a new chemical probe that can differentiate D2R monomers from dimers or oligomers depending on the observed pharmacology.
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GSK2018682, MedChemExpress
MedChemExpress GSK2018682 is an agonist for S1P1 and S1P5 receptor with pEC50s of 7.7 and 7.2, respectively, and has no agonist activity towards human S1P2, S1P3, or S1P4. GSK2018682 is used in the research of multiple sclerosis.
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| Molecular Weight (g/mol) | 440.88 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | GSK2018682 |
| Grade | Research |
| SMILES | O=C(O)CCCN1C=CC2=C1C=CC=C2C3=NOC(C4=CC(Cl)=C(OC(C)C)N=C4)=N3 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.25% |
| CAS | 1034688-30-6 |
| Solubility Information | DMSO : ≥ 125 mg/mL (283.52 mM) |
| 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 | C22H21ClN4O4 |
| Formula Weight | 440.88 |
EHop-016, MedChemExpress
MedChemExpress EHop-016 is a potent and selective Rac GTPase Rac1 and Rac3 inhibitor. EHop-016 inhibits Rac1 activity with an IC50 of 1.1 μM in MDA-MB-435 cells. EHop-016 inhibits Vav2 interaction with Rac, Rac-activated PAK1, lamellipodia formation, and cell migration.
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| Molecular Weight (g/mol) | 430.55 |
|---|---|
| Color | Pink |
| Physical Form | Solid |
| Chemical Name or Material | EHop-016 |
| Grade | Research |
| SMILES | CCN1C2=C(C3=C1C=CC=C3)C=C(NC4=NC(NCCCN5CCOCC5)=NC=C4)C=C2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.43% |
| CAS | 1380432-32-5 |
| Solubility Information | DMSO : ≥ 32 mg/mL (74.32 mM) |
| 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 | C25H30N6O |
| Formula Weight | 430.55 |
JMS-17-2, MedChemExpress
MedChemExpress JMS-17-2 is a potent and selective CX3CR1 antagonist with an IC50 of 0.32 nM. JMS-17-2 impairs metastatic seeding and colonization of breast cancer cells.
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Lestaurtinib, MedChemExpress
MedChemExpress Lestaurtinib (CEP-701) is an orally active and selective RPTKs (receptor protein tyrosine kinase) inhibitor, competitively inhibits ATP binding to the TrkA/B/C domain. Lestaurtinib inhibits RPTKs phosphorylation, with IC50s of 2, 25 and 0.9 nM for FLT3, TrkA and JAK2, respectively. Lestaurtinib induces apoptosis and cycle arrest, also can inhibit growth of tumor.
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UBCS039, MedChemExpress
MedChemExpress UBCS039 is the first synthetic, specific Sirtuin 6 (SIRT6) activator, inducing autophagy in human tumor cells, with an EC50 of 38 μM.
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| Molecular Weight (g/mol) | 247.29 |
|---|---|
| Color | Light Yellow |
| Physical Form | Powder |
| Chemical Name or Material | UBCS039 |
| Grade | Research |
| SMILES | N12C(C(C3=CC=CN=C3)NC4=C2C=CC=C4)=CC=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.13% |
| CAS | 358721-70-7 |
| Solubility Information | DMSO : 100 mg/mL (404.38 mM; Need ultrasonic) |
| 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 | C16H13N3 |
| Formula Weight | 247.29 |
Dirlotapide, MedChemExpress
MedChemExpress Dirlotapide (CP742033) is a gut-selective inhibitor of microsomal triglyceride transfer protein (MTP) that reliably produces weight loss in obese dogs.
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Mutated EGFR-IN-1, MedChemExpress
MedChemExpress Mutated EGFR-IN-1 (Osimertinib analog) is a useful intermediate for the inhibitors design for mutated EGFR, such as L858R EGFR, Exonl9 deletion activating mutant and T790M resistance mutant.
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| Molecular Weight (g/mol) | 445.56 |
|---|---|
| Color | Pale Purple |
| Physical Form | Solid |
| Chemical Name or Material | Mutated EGFR-IN-1 |
| Grade | Research |
| SMILES | NC1=CC(NC2=NC=CC(C3=CN(C)C4=C3C=CC=C4)=N2)=C(OC)C=C1N(CCN(C)C)C |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.59% |
| CAS | 1421372-66-8 |
| Solubility Information | DMSO : ≥ 75 mg/mL (168.33 mM) |
| Synonym | Osimertinib analog |
| 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 | C25H31N7O |
| Formula Weight | 445.56 |
Vincamine, MedChemExpress
MedChemExpress Vincamine is a monoterpenoid indole alkaloid extracted from the Madagascar periwinkle.
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| Molecular Weight (g/mol) | 354.44 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Vincamine |
| Grade | Research |
| SMILES | O=C(OC)[C@@]1(O)C[C@@]2(CC)[C@@]3([H])C(N1C4=CC=CC=C54)=C5CCN3CCC2 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.76% |
| CAS | 1617-90-9 |
| Solubility Information | DMSO : 25 mg/mL (70.53 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 | C21H26N2O3 |
| Formula Weight | 354.44 |
MBQ-167, MedChemExpress
MedChemExpress MBQ-167 is a dual Rac/Cdc42 inhibitor, with IC50s of 103 nM for Rac 1/2/3 and 78 nM for Cdc42 in MDA-MB-231 cells, respectively.
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| Molecular Weight (g/mol) | 338.41 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | MBQ-167 |
| Grade | Research |
| SMILES | CCN1C2=C(C3=C1C=CC=C3)C=C(N4N=NC=C4C5=CC=CC=C5)C=C2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.26% |
| CAS | 2097938-73-1 |
| Solubility Information | DMSO : 155 mg/mL (458.02 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 | C22H18N4 |
| Formula Weight | 338.41 |
Ecopladib, MedChemExpress
MedChemExpress Ecopladib is a sub-micromolar inhibitor of cytosolic phospholipase A2α (cPLA2α), with IC50s of 0.15 μM and 0.11 μM in the GLU micelle and rat whole blood assays, respectively.
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