Imidazopyridines
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Filtered Search Results
PDE10-IN-1, MedChemExpress
MedChemExpress PDE10-IN-1 is a potent PDE10-IN-1 inhibitor extracted from Patent WO 2013192273 A1, for treating CNS and metabolic disorders.
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| Molecular Weight (g/mol) | 369.42 |
|---|---|
| Color | Earth Yellow |
| Physical Form | Solid |
| Chemical Name or Material | PDE10-IN-1 |
| Grade | Research |
| SMILES | CC1=C([C@H]2[C@H](C3=NN4C(C(C)=NC=C4C)=N3)C2)N=C5C6=C(N=CC=C6)C=CN51 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 97.82% |
| CAS | 1516896-09-5 |
| Solubility Information | DMSO : 2 mg/mL (5.41 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 | C21H19N7 |
| Formula Weight | 369.42 |
Savolitinib, MedChemExpress
MedChemExpress Savolitinib (AZD-6094) is a potent, highly selective, and orally bioavailable c-Met inhibitor with IC50 s of 5 nM and 3 nM for c-Met and p-Met, respectively. Savolitinib (AZD-6094) selectively binds to and inhibits the activation of c-Met in an ATP-competitive manner, and disrupts c-Met signal transduction pathways. Antineoplastic activity.
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| Molecular Weight (g/mol) | 345.36 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Savolitinib |
| Grade | Research |
| SMILES | CN1N=CC(C2=CN=C3C(N([C@H](C4=CN5C(C=C4)=NC=C5)C)N=N3)=N2)=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.45% |
| CAS | 1313725-88-0 |
| Solubility Information | DMSO : 25 mg/mL (72.39 mM; Need ultrasonic) |
| Synonym | Volitinib HMPL-504 AZD-6094 |
| 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 | C17H15N9 |
| Formula Weight | 345.36 |
CXCR7 modulator 2, MedChemExpress
MedChemExpress CXCR7 modulator 2 is a modulator of C-X-C Chemokine Receptor Type 7 (CXCR7), with a Ki of 13 nM.
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| Molecular Weight (g/mol) | 522.68 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | CXCR7 modulator 2 |
| Grade | Research |
| SMILES | O=C([C@@H]1[C@H](O2)CC[C@H]2C1)N3CCC([C@H](CC(N)=O)N4CCCN(C5=C(CC)C=CN6C5=NC=C6)CC4)CC3 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.39% |
| CAS | 2227426-37-9 |
| Solubility Information | DMSO : 250 mg/mL (478.30 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 | C29H42N6O3 |
| Formula Weight | 522.68 |
Dipraglurant, MedChemExpress
MedChemExpress Dipraglurant (ADX48621) is a potent, selective, orally active and brain penetrant mGluR5 negative allosteric modulator (NAM), with an IC50 of 21 nM. Dipraglurant can reduce Levodopa-induced dyskinesia (LID) in vivo.
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| Molecular Weight (g/mol) | 265.29 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Dipraglurant |
| Grade | Research |
| SMILES | FC1=CN2C(C=C1)=NC(CCC#CC3=NC=CC=C3)=C2 |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 95.95% |
| CAS | 872363-17-2 |
| Solubility Information | DMSO : ≥ 40 mg/mL (150.78 mM) |
| Synonym | ADX48621 |
| 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 | C16H12FN3 |
| Formula Weight | 265.29 |
Soraprazan, MedChemExpress
MedChemExpress Soraprazan (BYK61359) is a selective, reversible K-competitive inhibitor of the H,K-ATPase (Ki=6.4 nM), with an IC50 of 0.19 μM in gastric glands. Soraprazan binds to the H,K-ATPase with a Kd of 28.27 nM. Soraprazan shows immediate inhibition of acid secretion and is more than 2000-fold selective for H,K-ATPase over Na,K- and Ca-ATPases.
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| Molecular Weight (g/mol) | 367.44 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Soraprazan |
| Grade | Research |
| SMILES | O[C@@H]1[C@@H](C2=CC=CC=C2)NC3=C(C=CN4C3=NC(C)=C4C)[C@H]1OCCOC |
| Percent Purity | 99.69% |
| CAS | 261944-46-1 |
| Solubility Information | DMSO : ≥ 150 mg/mL (408.23 mM) |
| Synonym | BYK61359 |
| 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 | C21H25N3O3 |
| Formula Weight | 367.44 |
Serabelisib, MedChemExpress
MedChemExpress Serabelisib (MLN1117) is a selective p110α inhibitor with an IC50 of 15 nM.
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| Molecular Weight (g/mol) | 363.37 |
|---|---|
| Color | Gray |
| Physical Form | Solid |
| Chemical Name or Material | Serabelisib |
| Grade | Research |
| SMILES | O=C(C1=CN=C2C=CC(C3=CC=C(OC(N)=N4)C4=C3)=CN21)N5CCOCC5 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.1% |
| CAS | 1268454-23-4 |
| Solubility Information | DMSO : 6.4 mg/mL (17.61 mM; Need ultrasonic and warming) |
| Synonym | MLN1117 INK1117 TAK-117 |
| 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 | C19H17N5O3 |
| Formula Weight | 363.37 |
JK184, MedChemExpress
MedChemExpress JK184 is a potent Hedgehog (Hh) pathway inhibitor with IC50 of 30 nM in mammalian cells.
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| Molecular Weight (g/mol) | 350.44 |
|---|---|
| Color | Pink |
| Physical Form | Solid |
| Chemical Name or Material | JK184 |
| Grade | Research |
| SMILES | CC1=C(C2=CSC(NC3=CC=C(OCC)C=C3)=N2)N4C=CC=CC4=N1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.37% |
| CAS | 315703-52-7 |
| Solubility Information | DMSO : ≥ 50 mg/mL (142.68 mM) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| 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 | C19H18N4OS |
| Formula Weight | 350.44 |
Pumaprazole, MedChemExpress
MedChemExpress Pumaprazole is a reversible proton pump antagonist.
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| Molecular Weight (g/mol) | 338.4 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Pumaprazole |
| Grade | Research |
| SMILES | O=C(OC)NC1=CC=CC(C)=C1CNC2=CC=CN3C2=NC(C)=C3C |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.9% |
| CAS | 158364-59-1 |
| Solubility Information | DMSO : 100 mg/mL (295.51 mM; Need ultrasonic) |
| Synonym | BY-841 |
| 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 | C19H22N4O2 |
| Formula Weight | 338.4 |
IRAK inhibitor 1, MedChemExpress
MedChemExpress IRAK inhibitor 1 is a potent IRAK-4 inhibitor with IC50 of 216 nM, is poorly active against JNK-1 and JNK-2 with IC50 of 3.801 μM, and >10 μM, respectively.
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| Molecular Weight (g/mol) | 293.37 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | IRAK inhibitor 1 |
| Grade | Research |
| SMILES | C1(C2=CN=C3N2C=CC=C3)=CC=CC(NC4CCNCC4)=N1 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.05% |
| CAS | 1042224-63-4 |
| Solubility Information | DMSO : 16.67 mg/mL (56.82 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 | C17H19N5 |
| Formula Weight | 293.37 |
Linaprazan, MedChemExpress
MedChemExpress Linaprazan (AZD0865) inhibits gastric H+,K+-ATPase by K+-competitive binding.
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| Molecular Weight (g/mol) | 366.46 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Linaprazan |
| Grade | Research |
| SMILES | O=C(C1=CN2C(C(NCC3=C(C)C=CC=C3C)=C1)=NC(C)=C2C)NCCO |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.8% |
| CAS | 248919-64-4 |
| Solubility Information | DMSO : ≥ 35 mg/mL (95.51 mM) |
| Synonym | AZD0865 |
| 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 | C21H26N4O2 |
| Formula Weight | 366.46 |
DGAT1-IN-1, MedChemExpress
MedChemExpress DGAT1-IN-1 is a potent DGAT1 inhibitor with IC50 of < 10 nM(cell lysate from Hep3B cells overexpressing human DGAT1).
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| Molecular Weight (g/mol) | 551.56 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | DGAT1-IN-1 |
| Grade | Research |
| SMILES | OC(C[C@H]1CC[C@H](C2=CC=C(C3=CN4C=C(C(NCC5=CC=C(OC(F)(F)F)C=C5)=O)N=C4C=C3)C=C2)CC1)=O |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 95.0% |
| CAS | 1449779-49-0 |
| Solubility Information | DMSO : 20 mg/mL (36.26 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 | C30H28F3N3O4 |
| Formula Weight | 551.56 |
Antitumor agent-3, MedChemExpress
MedChemExpress Antitumor agent-3 is a potent compound which comprises a new imidazopyridine having excellent antitumor activity as an active ingredient.
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| Molecular Weight (g/mol) | 428.35 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Antitumor agent-3 |
| Grade | Research |
| SMILES | FC(C1=CC=C(NC2=NC(C3=C(C(F)(F)F)N=C4C=CC=CN43)=CS2)C=C1)(F)F |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.71% |
| CAS | 420126-30-3 |
| Solubility Information | DMSO : ≥ 59 mg/mL (137.74 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 | C18H10F6N4S |
| Formula Weight | 428.35 |