Pyrimidines And Derivatives
- (401)
- (5)
- (2)
- (3)
- (2)
- (2)
- (1)
- (4)
- (1)
- (4)
- (4)
- (5)
- (4)
- (4)
- (2)
- (2)
- (5)
- (4)
- (4)
- (5)
- (4)
- (3)
- (4)
- (2)
- (4)
- (4)
- (1)
- (3)
- (1)
- (3)
- (4)
- (3)
- (4)
- (4)
- (4)
- (5)
- (4)
- (4)
- (4)
- (2)
- (5)
- (6)
- (4)
- (4)
- (5)
- (3)
- (3)
- (4)
- (3)
- (3)
- (4)
- (3)
- (2)
- (6)
- (5)
- (5)
- (4)
- (4)
- (8)
- (2)
- (4)
- (5)
- (4)
- (1)
- (1)
- (3)
- (3)
- (2)
- (4)
- (4)
- (3)
- (4)
- (4)
- (3)
- (3)
- (4)
- (4)
- (3)
- (3)
- (5)
- (3)
- (4)
- (4)
- (3)
- (4)
- (4)
- (4)
- (4)
- (4)
- (5)
- (5)
- (3)
- (4)
- (6)
- (3)
- (3)
- (4)
- (4)
- (4)
- (3)
- (3)
- (3)
- (3)
- (5)
- (4)
- (5)
- (2)
- (4)
- (4)
- (3)
- (3)
- (4)
- (33)
- (368)
- (2)
- (5)
- (1)
- (102)
- (1)
- (68)
- (8)
- (7)
- (1)
- (15)
- (1)
- (93)
- (95)
- (2)
- (20)
- (5)
- (5)
- (3)
- (4)
- (1)
- (3)
- (5)
- (9)
- (2)
- (3)
- (5)
- (53)
- (10)
- (15)
- (5)
- (7)
- (4)
- (8)
- (3)
- (4)
- (3)
- (4)
- (4)
- (3)
- (4)
- (10)
- (4)
- (4)
- (5)
- (2)
- (4)
- (5)
- (6)
- (3)
- (7)
- (5)
- (5)
- (4)
- (4)
- (4)
- (4)
- (7)
- (5)
- (5)
- (8)
- (4)
- (3)
- (3)
- (8)
- (4)
- (4)
- (5)
- (5)
- (3)
- (3)
- (4)
- (4)
- (5)
- (4)
- (3)
- (2)
- (2)
- (4)
- (7)
- (3)
- (2)
- (4)
- (4)
- (3)
- (2)
- (7)
- (3)
Filtered Search Results
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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
PRT-060318, MedChemExpress
MedChemExpress PRT-060318 (PRT318) is a novel selective inhibitor of the tyrosine kinase Syk with an IC50 of 4 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
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).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
VUF10460, MedChemExpress
MedChemExpress VUF10460 is a non-imidazole histamine H4 receptor agonist; binds to rat H4 receptor with a pKi of 7.46.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
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).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
GSK2334470, MedChemExpress
MedChemExpress GSK2334470 is a highly specific and potent inhibitor of PDK1 with an IC50 of 10 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
AF64394, MedChemExpress
MedChemExpress AF64394 is a GPR3 inverse agonist, with a pIC50 of 7.3.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
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.
Learn More
| 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 |
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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| 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 |
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.
Learn More
| 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 |