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Filtered Search Results
WYE-687, MedChemExpress
MedChemExpress WYE-687 is an ATP-competitive mTOR inhibitor with an IC50 of 7 nM. WYE-687 concurrently inhibits activation of mTORC1 and mTORC2. WYE-687 also inhibits PI3Kα and PI3Kγ with IC50s of 81 nM and 3.11 μM, respectively.
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| Molecular Weight (g/mol) | 528.61 |
|---|---|
| Color | Light Yellow |
| Physical Form | Powder |
| Chemical Name or Material | WYE-687 |
| Grade | Research |
| SMILES | O=C(OC)NC1=CC=C(C2=NC(N3CCOCC3)=C4C(N(C5CCN(CC6=CC=CN=C6)CC5)N=C4)=N2)C=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.1% |
| CAS | 1062161-90-3 |
| Solubility Information | DMSO : 20.83 mg/mL (39.41 mM; ultrasonic and warming and heat to 80°C) |
| 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 | C28H32N8O3 |
| Formula Weight | 528.61 |
Reversan, MedChemExpress
MedChemExpress Reversan (CBLC4H10) is a potent and nontoxic multidrug resistance-associated protein 1 (MRP1) and P-glycoprotein (Pgp) inhibitor.
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| Molecular Weight (g/mol) | 441.52 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Reversan |
| Grade | Research |
| SMILES | O=C(C1=C2N(C(C3=CC=CC=C3)=CC(C4=CC=CC=C4)=N2)N=C1)NCCCN5CCOCC5 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 95.0% |
| CAS | 313397-13-6 |
| Solubility Information | DMSO : 15.62 mg/mL (35.38 mM; ultrasonic and warming and heat to 60°C) |
| Synonym | CBLC4H10 |
| 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 | C26H27N5O2 |
| Formula Weight | 441.52 |
Momelotinib, MedChemExpress
MedChemExpress Momelotinib (CYT387) is an ATP-competitive inhibitor of JAK1/JAK2 with IC50a of 11 nM and 18 nM,respectively. CYT387 shows much less activity against JAK3.
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| Molecular Weight (g/mol) | 414.46 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Momelotinib |
| Grade | Research |
| SMILES | O=C(C1=CC=C(C2=NC(NC3=CC=C(N4CCOCC4)C=C3)=NC=C2)C=C1)NCC#N |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 96.95% |
| CAS | 1056634-68-4 |
| Solubility Information | DMSO : 20.83 mg/mL (50.26 mM; ultrasonic and warming and heat to 80°C) |
| Synonym | CYT387 |
| 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 | C23H22N6O2 |
| Formula Weight | 414.46 |
BAY 61-3606 dihydrochloride, MedChemExpress
MedChemExpress BAY 61-3606 dihydrochloride is an orally available, ATP-competitive, reversible and highly selective Syk inhibitor with a Ki of 7.5 nM an IC50 of 10 nM.
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| Molecular Weight (g/mol) | 463.32 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | BAY 61-3606 dihydrochloride |
| Grade | Research |
| SMILES | O=C(N)C1=CC=CN=C1NC2=NC(C3=CC=C(C(OC)=C3)OC)=CC4=NC=CN24.[H]Cl.[H]Cl |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.21% |
| CAS | 648903-57-5 |
| Solubility Information | H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) |
| Purity Grade Notes | Research |
| Recommended Storage | -20°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | -20°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C20H20Cl2N6O3 |
| Formula Weight | 463.32 |
CU-CPT-8m, MedChemExpress
MedChemExpress CU-CPT-8m is a specific TLR8 antagonist, with an IC50 of 67 nM.
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| Molecular Weight (g/mol) | 252.27 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | CU-CPT-8m |
| Grade | Research |
| SMILES | O=C(C1=C2N=CC=C(C3=CC=CC(C)=C3)N2N=C1)N |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.81% |
| CAS | 125079-83-6 |
| Solubility Information | DMSO : 12.5 mg/mL (49.55 mM; ultrasonic and warming and heat to 60°C) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Synonym | TLR8-specific antagonist |
| 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 | C14H12N4O |
| Formula Weight | 252.27 |
Pictilisib, MedChemExpress
MedChemExpress Pictilisib (GDC-0941) is a potent inhibitor of PI3Kα/δ with an IC50 of 3 nM, with modest selectivity against p110β (11-fold) and p110γ (25-fold).
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| Molecular Weight (g/mol) | 513.64 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Pictilisib |
| Grade | Research |
| SMILES | CS(N1CCN(CC2=CC3=C(C(N4CCOCC4)=NC(C5=CC=CC6=C5C=NN6)=N3)S2)CC1)(=O)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.03% |
| CAS | 957054-30-7 |
| Solubility Information | DMSO : 100 mg/mL (194.69 mM; ultrasonic and warming and heat to 60°C) |
| Synonym | GDC-0941 |
| 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 | C23H27N7O3S2 |
| Formula Weight | 513.64 |
PI-103 Hydrochloride, MedChemExpress
MedChemExpress PI-103 Hydrochloride is a dual PI3K and mTOR inhibitor with IC50s of 8 nM, 88 nM, 48 nM, 150 nM, 20 nM, and 83 nM for p110α, p110β, p110δ, p110γ, mTORC1, and mTORC2. PI-103 Hydrochloride also inhibits DNA-PK with an IC50 of 2 nM. PI-103 Hydrochloride induces autophagy.
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| Molecular Weight (g/mol) | 384.82 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | PI-103 Hydrochloride |
| Grade | Research |
| SMILES | OC1=CC(C2=NC3=C(OC4=C3C=CC=N4)C(N5CCOCC5)=N2)=CC=C1.[H]Cl |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 96.37% |
| CAS | 371935-79-4 |
| Solubility Information | DMSO : 4.1 mg/mL (10.65 mM; Need ultrasonic and warming) ∣H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) |
| 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 | C19H17ClN4O3 |
| Formula Weight | 384.82 |
GNF-2, MedChemExpress
MedChemExpress GNF-2 is a highly selective, allosteric, non-ATP competitive inhibitor of Bcr-Abl. GNF-2 inhibits Ba/F3.p210 proliferation with an IC50 of 138 nM .
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| Molecular Weight (g/mol) | 374.32 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | GNF-2 |
| Grade | Research |
| SMILES | O=C(C1=CC=CC(C2=CC(NC3=CC=C(OC(F)(F)F)C=C3)=NC=N2)=C1)N |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.73% |
| CAS | 778270-11-4 |
| Solubility Information | DMSO : ≥ 100 mg/mL (267.15 mM) ∣H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) |
| Health Hazard 1 | 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 | C18H13F3N4O2 |
| Formula Weight | 374.32 |
SSD114 hydrochloride, MedChemExpress
MedChemExpress SSD114 hydrochloride is a novel GABAB receptor positive allosteric modulator.
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| Molecular Weight (g/mol) | 387.83 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | SSD114 hydrochloride |
| Grade | Research |
| SMILES | FC(C1=CC=C(C2=CC(OC)=NC(NC3CCCCC3)=N2)C=C1)(F)F.[H]Cl |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.68% |
| CAS | 2319790-02-6 |
| Solubility Information | DMSO : 130 mg/mL (335.20 mM; Need ultrasonic) ∣H2O : 2 mg/mL (5.16 mM; ultrasonic and warming and heat to 60°C) |
| 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 | C18H21ClF3N3O |
| Formula Weight | 387.83 |
CRT0066101 dihydrochloride, MedChemExpress
MedChemExpress CRT0066101 dihydrochloride is a potent and specific PKD inhibitor with IC50 values of 1, 2.5 and 2 nM for PKD1, 2, and 3 respectively.
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| Molecular Weight (g/mol) | 411.33 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | CRT0066101 dihydrochloride |
| Grade | Research |
| SMILES | OC1=CC=C(C2=CN(C)N=C2)C=C1C3=NC=CC(NC[C@H](N)CC)=N3.[H]Cl.[H]Cl |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.53% |
| CAS | 1883545-60-5 |
| Solubility Information | H2O : 50 mg/mL (121.56 mM; Need ultrasonic) ∣DMSO : 11.36 mg/mL (27.62 mM; ultrasonic and warming and heat to 60°C) |
| 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 | C18H24Cl2N6O |
| Formula Weight | 411.33 |
Dorsomorphin, MedChemExpress
MedChemExpress Dorsomorphin (Compound C) is a selective and ATP-competitive AMPK inhibitor (Ki=109 nM in the absence of AMP). Dorsomorphin (BML-275) selectively inhibits BMP type I receptors ALK2, ALK3, and ALK6. Dorsomorphin induces autophagy.
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| Molecular Weight (g/mol) | 399.49 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Dorsomorphin |
| Grade | Research |
| SMILES | C12=C(C3=CC=NC=C3)C=NN1C=C(C4=CC=C(OCCN5CCCCC5)C=C4)C=N2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.0% |
| CAS | 866405-64-3 |
| Solubility Information | 1M HCl : 50 mg/mL (125.16 mM; ultrasonic and adjust pH to 1 with HCl) ∣DMSO : 5 mg/mL (12.52 mM; ultrasonic and warming and heat to 60°C) ∣Ethanol : 3.33 mg/mL (8.34 mM; Need ultrasonic) ∣H2O : < 0.1 mg/mL (insoluble) |
| Synonym | Compound C BML-275 |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Shelf Life | 4°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Molecular Formula | C24H25N5O |
| Formula Weight | 399.49 |