Pyrimidines And Derivatives
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Filtered Search Results
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 |
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 |
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 |
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 |
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.
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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 |
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 |
NIH-12848, MedChemExpress
MedChemExpress NIH-12848 is a putative phosphatidylinositol 5-phosphate 4-kinase γ (PI5P4Kγ) inhibitor with an IC50 of 1 μM.
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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 |
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 |
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 |
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.
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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 |
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.
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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 |
LDN-212854, MedChemExpress
MedChemExpress LDN-212854 is a bone morphogenetic protein (BMP) inhibitor that potently inhibits ALK2 (IC50: 1.3 nM). LDN-212854 also inhibits ALK1 (IC50: 2.40 nM). LDN-212854 can be used in the research of fibrodysplasia ossificans progressive and cancers, such as hepatocellular carcinoma (HCC).
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| Molecular Weight (g/mol) | 406.48 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | LDN-212854 |
| Grade | Research |
| SMILES | C12=C(C3=C4N=CC(C5=CC=C(N6CCNCC6)C=C5)=CN4N=C3)C=CC=C1N=CC=C2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.65% |
| CAS | 1432597-26-6 |
| Solubility Information | DMSO : ≥ 30 mg/mL (73.80 mM) |
| Health Hazard 1 | H301 |
| 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 | C25H22N6 |
| Formula Weight | 406.48 |
Citarinostat, MedChemExpress
MedChemExpress Citarinostat (ACY241) is a second generation potent, orally active and high-selective HDAC6 inhibitor with an IC50 of 2.6 nM (IC50s of 35 nM, 45 nM, 46 nM and 137 nM for HDAC1, HDAC2, HDAC3 and HDAC8, respectively). Citarinostat has anticancer effects.
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| Molecular Weight (g/mol) | 467.95 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Citarinostat |
| Grade | Research |
| SMILES | O=C(C1=CN=C(N(C2=CC=CC=C2Cl)C3=CC=CC=C3)N=C1)NCCCCCCC(NO)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 95.0% |
| CAS | 1316215-12-9 |
| Solubility Information | DMSO : ≥ 30 mg/mL (64.11 mM) |
| Synonym | ACY241 |
| 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 | C24H26ClN5O3 |
| Formula Weight | 467.95 |
HDACs/mTOR Inhibitor 1, MedChemExpress
MedChemExpress HDACs/mTOR Inhibitor 1 is a dual Histone Deacetylases (HDACs) and mammalian target of Rapamycin (mTOR) target inhibitor for treating hematologic malignancies, with IC50s of 0.19 nM, 1.8 nM, 1.2 nM and >500 nM for HDAC1, HDAC6, mTOR and PI3Kα, respectively. HDACs/mTOR Inhibitor 1 stimulates cell cycle arrest in G0/G1 phase and induce tumor cell apoptosis with low toxicity in vivo.
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| Molecular Weight (g/mol) | 566.65 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | HDACs/mTOR Inhibitor 1 |
| Grade | Research |
| SMILES | O=C(NO)CCCCCCN1C2=NC(C3=CC=C(NC(N4C[C@@H](C)OCC4)=O)C=C3)=NC(N5CCOCC5)=C2C=N1 |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 98.21% |
| CAS | 2271413-06-8 |
| Solubility Information | DMSO : 32.5 mg/mL (57.35 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 | C28H38N8O5 |
| Formula Weight | 566.65 |