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Filtered Search Results
PROTAC BET Degrader-1, MedChemExpress
MedChemExpress PROTAC BET Degrader-1 is a PROTAC connected by ligands for Cereblon and BET, decreasing BRD2, BRD3, and BRD4 protein levels at low concentration.
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| Molecular Weight (g/mol) | 871.9 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | PROTAC BET Degrader-1 |
| Grade | Research |
| SMILES | CCN1C(NC2=C3C4=CC(OC)=C(C(C(C)=NO5)=C5C)C=C4NC3=NC(C(NCCCCNC(COC6=C(C(N7C(CCC8=O)C(N8)=O)=O)C(C7=O)=CC=C6)=O)=O)=N2)=CC(C9CC9)=N1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.01% |
| CAS | 2093386-22-0 |
| Solubility Information | DMSO : ≥ 50 mg/mL (57.35 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 | C44H45N11O9 |
| Formula Weight | 871.9 |
AF64394, MedChemExpress
MedChemExpress AF64394 is a GPR3 inverse agonist, with a pIC50 of 7.3.
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| Molecular Weight (g/mol) | 393.87 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | AF64394 |
| Grade | Research |
| SMILES | ClC1=CC(OC(C)C)=C(CNC2=CC(C3=CC=CC=C3)=NC4=NC=NN42)C=C1 |
| Percent Purity | 98.02% |
| CAS | 1637300-25-4 |
| Solubility Information | DMSO : ≥ 125 mg/mL (317.36 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 | C21H20ClN5O |
| Formula Weight | 393.87 |
KDM4D-IN-1, MedChemExpress
MedChemExpress KDM4D-IN-1 is a new histone lysine demethylase 4D (KDM4D) inhibitor with an IC50 value of 0.41±0.03 μM.
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| Molecular Weight (g/mol) | 225.21 |
|---|---|
| Color | Earth Yellow |
| Physical Form | Solid |
| Chemical Name or Material | KDM4D-IN-1 |
| Grade | Research |
| SMILES | OC1=NC2=C(C#N)C(C)=NN2C3=C1C=CC=N3 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.91% |
| CAS | 2098902-68-0 |
| Solubility Information | DMSO : 7.14 mg/mL (31.70 mM; Need ultrasonic) |
| 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 | C11H7N5O |
| Formula Weight | 225.21 |
mTOR inhibitor-3, MedChemExpress
MedChemExpress mTOR inhibitor-3 is a remarkably selective mTOR inhibitor with a Ki of 1.5 nM. mTOR inhibitor-3 suppresses mTORC1 and mTORC2 in cellular and in vivo pharmacokinetic (PK)/pharmacodynamic (PD) experiments.
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| Molecular Weight (g/mol) | 474.56 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | mTOR inhibitor-3 |
| Grade | Research |
| SMILES | O=C(NC1=CC=C(C2=NC(N3[C@@H](C)COCC3)=C4C(CN(C5=NC=CC=N5)CC4)=N2)C=C1)NCC |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.58% |
| CAS | 1207358-59-5 |
| Solubility Information | DMSO : 50 mg/mL (105.36 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 | C25H30N8O2 |
| Formula Weight | 474.56 |
Lck Inhibitor, MedChemExpress
MedChemExpress Lck Inhibitor is a potent, orally active Lck (lymphocyte specific kinase) inhibitor with IC50s of 7, 2.1, 4.2 and 200 nM for Lck, Lyn, Src and Syk kinases, respectively. Lck Inhibitor shows >1000-fold selectivity for Lck over MAPK, CDK and RSK family representatives. Lck Inhibitor inhibits T cell proliferation and in vivo models of arthritis.
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| Molecular Weight (g/mol) | 530.62 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Lck Inhibitor |
| Grade | Research |
| SMILES | O=C1N(C2=C(C)C=CC=C2C)C3=NC4=CC=CC=C4N3C5=NC(NC6=CC=C(N7CCN(C)CC7)C=C6)=NC=C15 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.2% |
| CAS | 847950-09-8 |
| Solubility Information | DMSO : 100 mg/mL (188.46 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 | C31H30N8O |
| Formula Weight | 530.62 |
DMH-1, MedChemExpress
MedChemExpress DMH-1 is a potent and selective BMP inhibitor with IC50s of 27/107.9/<5/47.6 nM for ALK1/ALK2/ALK3/ALK6, respectively.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 380.44 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | DMH-1 |
| Grade | Research |
| SMILES | CC(C)OC1=CC=C(C2=CN3C(N=C2)=C(C4=CC=NC5=CC=CC=C45)C=N3)C=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.58% |
| CAS | 1206711-16-1 |
| Solubility Information | DMSO : 11.5 mg/mL (30.23 mM; Need ultrasonic and warming) |
| 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 | C24H20N4O |
| Formula Weight | 380.44 |
NIH-12848, MedChemExpress
MedChemExpress NIH-12848 is a putative phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ) inhibitor with an IC50 of 1 μM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 385.41 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | NIH-12848 |
| Grade | Research |
| SMILES | FC(C1=CC=CC=C1C2=NC(NCC3=CC=CS3)=C4C=CC=CC4=N2)(F)F |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.06% |
| CAS | 959551-10-1 |
| Solubility Information | DMSO : ≥ 100 mg/mL (259.46 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 | C20H14F3N3S |
| Formula Weight | 385.41 |
PF-4840154, MedChemExpress
MedChemExpress PF-4840154 is a potent, selective agonist of the rat and human TrpA1 channel with EC50s of 97 and 23 nM, respectively. PF-4840154 elicits TrpA1-mediated nocifensive behaviour in mouse.
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| Molecular Weight (g/mol) | 466.62 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | PF-4840154 |
| Grade | Research |
| SMILES | O=C(C1=CN=C(N2CCN(CC3COCCC3)CC2)N=C1NCC(C)C)NCC4=CC=CC=C4 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.0% |
| CAS | 1332708-14-1 |
| Solubility Information | DMSO : 50 mg/mL (107.15 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 | C26H38N6O2 |
| Formula Weight | 466.62 |
UNC2881, MedChemExpress
MedChemExpress UNC2881 is a potent and specific Mer kinase inhibitor; inhibits steady-state Mer kinase phosphorylation with an IC50 value of 22 nM.
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| Molecular Weight (g/mol) | 463.58 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | UNC2881 |
| Grade | Research |
| SMILES | CCCCNC1=NC(N[C@H]2CC[C@H](O)CC2)=C(C(NCC3=CC=C(N4C=NC=C4)C=C3)=O)C=N1 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.91% |
| CAS | 1493764-08-1 |
| Solubility Information | DMSO : ≥ 44 mg/mL (94.91 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 | C25H33N7O2 |
| Formula Weight | 463.58 |
EPZ015666, MedChemExpress
MedChemExpress EPZ015666 (GSK3235025) is an orally available inhibitor of PRMT5 with an IC50 of 22 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 383.44 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | EPZ015666 |
| Grade | Research |
| SMILES | O=C(NC[C@H](O)CN1CCC(C=CC=C2)=C2C1)C3=CC(NC4COC4)=NC=N3 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.96% |
| CAS | 1616391-65-1 |
| Solubility Information | DMSO : 100 mg/mL (260.80 mM; Need ultrasonic) |
| Synonym | GSK3235025 |
| 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 | C20H25N5O3 |
| Formula Weight | 383.44 |
Pyrimethamine, MedChemExpress
MedChemExpress Pyrimethamine(RP4753) is a medication used for protozoal infections; interferes with tetrahydrofolic acid synthesis from folic acid by inhibiting the enzyme dihydrofolate reductase (DHFR).
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| Molecular Weight (g/mol) | 248.71 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Pyrimethamine |
| Grade | Research |
| SMILES | NC1=NC(N)=C(C2=CC=C(Cl)C=C2)C(CC)=N1 |
| For Use With (Application) | COVID-19-anti-virus |
| Percent Purity | 99.9% |
| CAS | 58-14-0 |
| Solubility Information | DMSO : 20 mg/mL (80.41 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Synonym | Pirimecidan Pirimetamin RP 4753 |
| 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 | C12H13ClN4 |
| Formula Weight | 248.71 |
GDC-0349, MedChemExpress
MedChemExpress GDC-0349 is a potent and selective ATP-competitive mTOR inhibitor with a Ki of 3.8 nM. GDC-0349 inhibits of both mTORC1 and mTORC2 complexes.
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| Molecular Weight (g/mol) | 452.55 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | GDC-0349 |
| Grade | Research |
| SMILES | O=C(NCC)NC(C=C1)=CC=C1C2=NC3=C(CCN(C4COC4)C3)C(N5[C@@H](C)COCC5)=N2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 95.0% |
| CAS | 1207360-89-1 |
| Solubility Information | DMSO : ≥ 100 mg/mL (220.97 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 | C24H32N6O3 |
| Formula Weight | 452.55 |
ALLO-2, MedChemExpress
MedChemExpress ALLO-2 is a potent drug-resistant Smoothened (Smo) mutant antagonist that inhibits Smo agonist Hh-Ag1.5-induced luciferase expression in TM3-Gli-Luc cells with IC50 of 6 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 371.32 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | ALLO-2 |
| Grade | Research |
| SMILES | FC(F)(OC1=CC=C(C=C1)C2=NC(NC3=CC4=C(C=C3)NN=C4)=NC=C2)F |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.58% |
| CAS | 1357350-60-7 |
| Solubility Information | DMSO : 125 mg/mL (336.64 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| 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 | C18H12F3N5O |
| Formula Weight | 371.32 |
WAY-600, MedChemExpress
MedChemExpress WAY-600 is a potent, ATP-competitive, and selective mTOR inhibitor with an IC50 of 9 nM for recombinant mTOR enzyme. WAY-600 blocks mTOR complex 1/2 (mTORC1/2) assemble and activation.
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| Molecular Weight (g/mol) | 494.59 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | WAY-600 |
| Grade | Research |
| SMILES | C1(C=CN2)=C2C=CC(C3=NC(N(C4CCN(CC5=CC=CN=C5)CC4)N=C6)=C6C(N7CCOCC7)=N3)=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 95.12% |
| CAS | 1062159-35-6 |
| Solubility Information | DMSO : 50 mg/mL (101.09 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 | C28H30N8O |
| Formula Weight | 494.59 |
PRT-060318, MedChemExpress
MedChemExpress PRT-060318 (PRT318) is a novel selective inhibitor of the tyrosine kinase Syk with an IC50 of 4 nM.
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| Molecular Weight (g/mol) | 340.42 |
|---|---|
| Color | Earth Yellow |
| Physical Form | Solid |
| Chemical Name or Material | PRT-060318 |
| Grade | Research |
| SMILES | O=C(C1=CN=C(N[C@H]2[C@@H](N)CCCC2)N=C1NC3=CC=CC(C)=C3)N |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.04% |
| CAS | 1194961-19-7 |
| Solubility Information | H2O : 5.6 mg/mL (16.45 mM; Need ultrasonic and warming) |
| Synonym | PRT318 |
| 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 | C18H24N6O |
| Formula Weight | 340.42 |