Pyrimidines And Derivatives
Filtered Search Results
Emapunil, MedChemExpress
MedChemExpress Emapunil (AC-5216), an orally active and selective TSPO (a mitochondrial benzodiazepine receptor) ligand, produces anti-anxiety and antidepressant-like effects in various animal models.
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| Molecular Weight (g/mol) | 401.46 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Emapunil |
| Grade | Research |
| SMILES | O=C(N(CC)CC1=CC=CC=C1)CN2C(N(C)C3=CN=C(C4=CC=CC=C4)N=C23)=O |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.26% |
| CAS | 226954-04-7 |
| Solubility Information | DMSO : 33.33 mg/mL (83.02 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Synonym | AC-5216 XBD-173 |
| 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 | C23H23N5O2 |
| Formula Weight | 401.46 |
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 |
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 |
PF-06928215, MedChemExpress
MedChemExpress PF-06928215 is a cGAS (cyclic GMP-AMP Synthase) inhibitor with an IC50 of 4.9 μμ. PF-06928215 has a high binding affinity of 0.2 μM (Kd).
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G-749, MedChemExpress
MedChemExpress G-749 is a potent, oral active and ATP competitive FLT3 inhibitor, with IC50s of 0.4 nM and 0.6 nM for FLT3 wild type and FLT3-D835Y, respectively. G-749 can be used for the research of drug resistance for acute myeloid leukemia (AML).
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| Molecular Weight (g/mol) | 521.41 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | G-749 |
| Grade | Research |
| SMILES | O=C1C2=C(N=C(NC3CCN(C)CC3)N=C2NC4=CC=C(OC5=CC=CC=C5)C=C4)C(Br)=CN1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.0% |
| CAS | 1457983-28-6 |
| Solubility Information | DMSO : 25 mg/mL (47.95 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 | C25H25BrN6O2 |
| Formula Weight | 521.41 |
AZ20, MedChemExpress
MedChemExpress AZ20 is a potent and selective inhibitor of ATR with an IC50 of 5 nM, and has 8-fold selectivity against mTOR (IC50=38 nM).
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| Molecular Weight (g/mol) | 412.51 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | AZ20 |
| Grade | Research |
| SMILES | O=S(C1(C2=CC(N3[C@H](C)COCC3)=NC(C4=CC=CC5=C4C=CN5)=N2)CC1)(C)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.92% |
| CAS | 1233339-22-4 |
| Solubility Information | DMSO : ≥ 100 mg/mL (242.42 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 | C21H24N4O3S |
| Formula Weight | 412.51 |
ML347, MedChemExpress
MedChemExpress ML347 (LDN193719) is a highly selective ALK1/ALK2 inhibitor. ML347 has IC50 values of 46 and 32 nM against ALK1 and ALK2, respectively, >300-fold selective over ALK3. ML347 block the phosphorylation of Smad1/5 by TGF-β1.
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| Molecular Weight (g/mol) | 352.39 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | ML347 |
| Grade | Research |
| SMILES | COC1=CC=C(C2=CN3C(N=C2)=C(C4=C5C=CC=NC5=CC=C4)C=N3)C=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.85% |
| CAS | 1062368-49-3 |
| Solubility Information | DMSO : 10 mg/mL (28.38 mM; Need ultrasonic) |
| Synonym | LDN 193719 |
| 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 | C22H16N4O |
| Formula Weight | 352.39 |
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 |
EED226, MedChemExpress
MedChemExpress EED226 is a polycomb repressive complex 2 (PRC2) inhibitor, which binds to the K27me3-pocket on embryonic ectoderm development (EED) and shows strong antitumor activity in xenograft mice model. EED226 is a potent, selective, and orally bioavailable EED inhibitor. EED226 inhibits PRC2 with an IC50 of 23.4 nM when the H3K27me0 peptide is used as a substrate in the in vitro enzymatic assays.
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| Molecular Weight (g/mol) | 369.4 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | EED226 |
| Grade | Research |
| SMILES | O=S(C1=CC=C(C2=CN=C(NCC3=CC=CO3)N4C2=NN=C4)C=C1)(C)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.61% |
| CAS | 2083627-02-3 |
| Solubility Information | DMSO : ≥ 29 mg/mL (78.51 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 | C17H15N5O3S |
| Formula Weight | 369.4 |
GSK2334470, MedChemExpress
MedChemExpress GSK2334470 is a highly specific and potent inhibitor of PDK1 with an IC50 of 10 nM.
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| Molecular Weight (g/mol) | 462.59 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | GSK2334470 |
| Grade | Research |
| SMILES | O=C([C@@H]1CN(C2=NC(NC)=NC(C3=CC4=C(C=C3)C(N)=NN4)=C2)[C@H](C)CC1)NC5CCCCC5 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 95.73% |
| CAS | 1227911-45-6 |
| Solubility Information | DMSO : ≥ 50 mg/mL (108.09 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 | C25H34N8O |
| Formula Weight | 462.59 |
HJB97, MedChemExpress
MedChemExpress HJB97 is a high-affinity BET inhibitor with Kis of 0.9 nM (BRD2 BD1), 0.27 nM (BRD2 BD2), 0.18 nM (BRD3 BD1), 0.21 nM (BRD3 BD2), 0.5 nM (BRD4 BD1), 1.0 nM (BRD4 BD2), respectively. HJB97 is employed for the design of potential PROTAC BET degrader and has antitumor activity.
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| Molecular Weight (g/mol) | 500.55 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | HJB97 |
| Grade | Research |
| SMILES | O=C(C1=NC(NC2=CC(C3CC3)=NN2CC)=C4C(NC5=C4C=C(OC)C(C6=C(C)ON=C6C)=C5)=N1)NC |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.24% |
| CAS | 2093391-24-1 |
| Solubility Information | DMSO : 30 mg/mL (59.93 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 | C26H28N8O3 |
| Formula Weight | 500.55 |
VUF10460, MedChemExpress
MedChemExpress VUF10460 is a non-imidazole histamine H4 receptor agonist; binds to rat H4 receptor with a pKi of 7.46.
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| Molecular Weight (g/mol) | 269.34 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | VUF10460 |
| Grade | Research |
| SMILES | NC1=NC(C2=CC=CC=C2)=CC(N3CCN(C)CC3)=N1 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.0% |
| CAS | 1028327-66-3 |
| Solubility Information | DMSO : 50 mg/mL (185.64 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 | C15H19N5 |
| Formula Weight | 269.34 |
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 |
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 |