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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 |
Olprinone Hydrochloride, MedChemExpress
MedChemExpress Olprinone (Loprinone) Hydrochloride is a potent phosphodiesterase (PDE) 3 inhibitor, with IC50s of 150, 100, 0.35 and 14 μM for PDE1, PDE2, PDE3 and PDE4, respectively. Olprinone Hydrochloride is used for the research of heart failure due to its positive inotropic and vasodilative effects. Anti-inflammatory activity.
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| Molecular Weight (g/mol) | 286.72 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Olprinone Hydrochloride |
| Grade | Research |
| SMILES | CC(N1)=C(C=C(C#N)C1=O)C2=CN3C(C=C2)=NC=C3.[H]Cl |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.91% |
| CAS | 119615-63-3 |
| Solubility Information | H2O : ≥ 7.69 mg/mL (26.82 mM) |
| Health Hazard 1 | H315∣H319∣H335 |
| Synonym | Loprinone Hydrochloride |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C14H11ClN4O |
| Formula Weight | 286.72 |
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 |