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Filtered Search Results
Nifuroxazide, MedChemExpress
MedChemExpress Nifuroxazide is an effective inhibitor of STAT3, also exerts potent anti-tumor and anti-metastasis activity.
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| Molecular Weight (g/mol) | 275.22 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Nifuroxazide |
| Grade | Research |
| SMILES | O=C(N/N=C/C1=CC=C([N+]([O-])=O)O1)C2=CC=C(O)C=C2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.51% |
| CAS | 965-52-6 |
| Solubility Information | DMSO : ≥ 155 mg/mL (563.19 mM) |
| Health Hazard 1 | H302∣H312∣H332 |
| 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 | C12H9N3O5 |
| Formula Weight | 275.22 |
TM5441, MedChemExpress
MedChemExpress TM5441 is an orally bioavailable inhibitor of plasminogen activator inhibitor-1 (PAI-1), has IC50 values between 13.9 and 51.1 μM and induces intrinsic apoptosis in several human cancer cell lines. TM5441 attenuates Nω-nitro-l-arginine methyl ester-induced cardiac hypertension and vascular senescence.
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| Molecular Weight (g/mol) | 428.82 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | TM5441 |
| Grade | Research |
| SMILES | ClC1=CC=C(NC(COCC(NC2=CC=CC(C3=COC=C3)=C2)=O)=O)C(C(O)=O)=C1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.18% |
| CAS | 1190221-43-2 |
| Solubility Information | DMSO : ≥ 300 mg/mL (699.59 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 | C21H17ClN2O6 |
| Formula Weight | 428.82 |
4E2RCat, MedChemExpress
MedChemExpress 4E2RCat is an inhibitor of eIF4E-eIF4G interaction with an IC50 of 13.5 μM.
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| Molecular Weight (g/mol) | 455.93 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | 4E2RCat |
| Grade | Research |
| SMILES | O=C(O)C1=CC(C2=CC=C(/C=C(SC(N3CC4=CC=CC=C4)=S)/C3=O)O2)=CC=C1Cl |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.0% |
| CAS | 432499-63-3 |
| Solubility Information | DMSO : 23.33 mg/mL (51.17 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 | C22H14ClNO4S2 |
| Formula Weight | 455.93 |
CX-6258, MedChemExpress
MedChemExpress CX-6258 is a potent and kinase selective pan-Pim kinases inhibitor, with IC50s of 5 nM, 25 nM and 16 nM for Pim-1, Pim-2 and Pim-3, respectively.
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| Molecular Weight (g/mol) | 461.94 |
|---|---|
| Color | Orange |
| Physical Form | Solid |
| Chemical Name or Material | CX-6258 |
| Grade | Research |
| SMILES | O=C1NC2=CC=C(Cl)C=C2/C1=C\C3=CC=C(C4=CC=CC(C(N5CCCN(C)CC5)=O)=C4)O3 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.73% |
| CAS | 1202916-90-2 |
| Solubility Information | DMSO : ≥ 50 mg/mL (108.24 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 | C26H24ClN3O3 |
| Formula Weight | 461.94 |
ML167, MedChemExpress
MedChemExpress ML167 is a highly selective Cdc2-like kinase 4 (Clk4) inhibitor with IC50 of 136 nM, >10-fold selectivity for closely related kinases Clk1, Clk2, Clk3 and Dyrk1A/1B.
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| Molecular Weight (g/mol) | 335.36 |
|---|---|
| Color | Khaki |
| Physical Form | Solid |
| Chemical Name or Material | ML167 |
| Grade | Research |
| SMILES | OCC1=CC=C(C2=CC3=C(NCC4=CC=C(C)O4)N=CN=C3C=C2)O1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.08% |
| CAS | 1285702-20-6 |
| Solubility Information | DMSO : 16.67 mg/mL (49.71 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Synonym | CID44968231 NCGC00188654 |
| 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 | C19H17N3O3 |
| Formula Weight | 335.36 |
AGK2, MedChemExpress
MedChemExpress AGK2 is a selective SIRT2 inhibitor with an IC50 of 3.5 μM. AGK2 inhibits SIRT1 and SIRT3 with IC50s of 30 and 91 μM, respectively.
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| Molecular Weight (g/mol) | 434.27 |
|---|---|
| Color | Green Yellow |
| Physical Form | Solid |
| Chemical Name or Material | AGK2 |
| Grade | Research |
| SMILES | O=C(NC1=C2C=CC=NC2=CC=C1)/C(C#N)=C/C3=CC=C(C4=CC(Cl)=CC=C4Cl)O3 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 97.0% |
| CAS | 304896-28-4 |
| Solubility Information | DMSO : 12.5 mg/mL (28.78 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 | C23H13Cl2N3O2 |
| Formula Weight | 434.27 |
C646, MedChemExpress
MedChemExpress C646 is a selective and competitive histone acetyltransferase p300 inhibitor with Ki of 400 nM, and is less potent for other acetyltransferases.
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| Molecular Weight (g/mol) | 445.42 |
|---|---|
| Color | Red Brown |
| Physical Form | Solid |
| Chemical Name or Material | C646 |
| Grade | Research |
| SMILES | O=C(O)C1=CC=C(N2N=C(C)/C(C2=O)=C\C3=CC=C(C4=CC(C)=C(C)C=C4[N+]([O-])=O)O3)C=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.0% |
| CAS | 328968-36-1 |
| Solubility Information | DMSO : 16.67 mg/mL (37.43 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣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 | C24H19N3O6 |
| Formula Weight | 445.42 |
4E1RCat, MedChemExpress
MedChemExpress 4E1RCat is an inhibitor of cap-dependent translation, and inhibits eIF4E:eIF4GI interaction, with an IC50 an of ∼4 μM.
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| Molecular Weight (g/mol) | 478.45 |
|---|---|
| Color | Dark Brown |
| Physical Form | Solid |
| Chemical Name or Material | 4E1RCat |
| Grade | Research |
| SMILES | O=C(O)C1=CC=C(N2C(/C(C=C2C3=CC=CC=C3)=C\C4=CC=C(C5=CC=C([N+]([O-])=O)C=C5)O4)=O)C=C1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.0% |
| CAS | 328998-25-0 |
| Solubility Information | DMSO : 18.33 mg/mL (38.31 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣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 | C28H18N2O6 |
| Formula Weight | 478.45 |
Leukadherin-1, MedChemExpress
MedChemExpress Leukadherin-1, a specific agonist of the leukocyte surface integrin CD11b/CD18, increases CD11b/CD18-dependent cell adhesion to fibrinogen with an EC50 of 4 μM. Leukadherin-1 enhances leukocyte adhesion to ligands (such as ICAM-1) and vascular endothelium and thus reduces leukocyte transendothelial migration and influx to the injury sites. Leukadherin-1 suppresses innate inflammatory signaling.
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| Molecular Weight (g/mol) | 421.49 |
|---|---|
| Color | Orange |
| Physical Form | Solid |
| Chemical Name or Material | Leukadherin-1 |
| Grade | Research |
| SMILES | O=C(O)C1=CC=C(C2=CC=C(/C=C(SC(N3CC4=CC=CC=C4)=S)/C3=O)O2)C=C1 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.0% |
| CAS | 344897-95-6 |
| Solubility Information | DMSO : 5 mg/mL (11.86 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H410 |
| 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 | C22H15NO4S2 |
| Formula Weight | 421.49 |
NSC59984, MedChemExpress
MedChemExpress NSC59984 induces mutant p53 protein degradation via MDM2 and the ubiquitin-proteasome pathway. NSC59984 acts by targeting GOF-mutant p53 and stimulates p73 to restore the p53 pathway signaling.
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| Molecular Weight (g/mol) | 265.27 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | NSC59984 |
| Grade | Research |
| SMILES | O=C(N1CCN(C)CC1)/C=C/C2=CC=C([N+]([O-])=O)O2 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.76% |
| CAS | 803647-40-7 |
| Solubility Information | DMSO : 33.33 mg/mL (125.65 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 | C12H15N3O4 |
| Formula Weight | 265.27 |
PYR-41, MedChemExpress
MedChemExpress PYR-41 is a selective and cell permeable inhibitor of ubiquitin-activating enzyme E1 with an IC50 of < 10 μM, with little activity at E2 and E3.
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| Molecular Weight (g/mol) | 371.3 |
|---|---|
| Color | Red browm |
| Physical Form | Solid |
| Chemical Name or Material | PYR-41 |
| Grade | Research |
| SMILES | O=C(N1)/C(C(N1C2=CC=C(C=C2)C(OCC)=O)=O)=C/C3=CC=C([N+]([O-])=O)O3 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.0% |
| CAS | 418805-02-4 |
| Solubility Information | DMSO : ≥ 46 mg/mL (123.89 mM) |
| Health Hazard 1 | H302∣H317 |
| 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 | C17H13N3O7 |
| Formula Weight | 371.3 |
CID 2011756, MedChemExpress
MedChemExpress CID 2011756 is an ATP competitive PKD inhibitor, with an IC50 of 3.2 μM for PKD1 in cell free assay, and also shows cellular pan-PKD inhibitory activity against PKD2 and PKD3 (IC50, 0.6 and 0.7 μM, respectively). CID 2011756 also has antitumor activity.
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| Molecular Weight (g/mol) | 396.87 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | CID 2011756 |
| Grade | Research |
| SMILES | O=C(C1=CC=C(C2=CC=CC(Cl)=C2)O1)NC3=CC=C(CN4CCOCC4)C=C3 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 96.04% |
| CAS | 638156-11-3 |
| Solubility Information | DMSO : 20 mg/mL (50.39 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H319 |
| 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 | C22H21ClN2O3 |
| Formula Weight | 396.87 |
Wortmannin, MedChemExpress
MedChemExpress Wortmannin (SL-2052; KY-12420) is a potent, selective and irreversible PI3K inhibitor with an IC50 of 3 nM. Wortmannin also blocks autophagy formation, and potently inhibits Polo-like kinase 1 (PlK1) and Plk3 with IC50s of 5.8 and 48 nM, respectively.
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| Molecular Weight (g/mol) | 428.43 |
|---|---|
| Color | White |
| Physical Form | Powder |
| Chemical Name or Material | Wortmannin |
| Grade | Research |
| SMILES | O=C1C([C@@](CC2)([H])[C@@]3(C)C2=O)=C([C@H](OC(C)=O)C3)[C@]4(C)C5=C1OC=C5C(O[C@@H]4COC)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.0% |
| CAS | 19545-26-7 |
| Solubility Information | DMSO : ≥ 50 mg/mL (116.71 mM) |
| Health Hazard 1 | H300∣H310∣H330 |
| Synonym | SL-2052 KY-12420 |
| 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 | C23H24O8 |
| Formula Weight | 428.43 |
MK2-IN-1 hydrochloride, MedChemExpress
MedChemExpress MK2-IN-1 hydrochloride is a potent and selecitve MAPKAPK2(MK2) inhibitor(IC50=0.11 uM) with a non-ATP competitive binding mode.
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| Molecular Weight (g/mol) | 509.43 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | MK2-IN-1 hydrochloride |
| Grade | Research |
| SMILES | O=C(C1=CC=C(C2=CC=C(Cl)C=C2)O1)N(C3=CC=C(N4CCNCC4)C=C3)CC5=NC=CC=C5.[H]Cl |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 97.32% |
| CAS | 1314118-94-9 |
| Solubility Information | DMSO : 100 mg/mL (196.30 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (stored under nitrogen) |
| Shelf Life | 4°C, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (stored under nitrogen) |
| Molecular Formula | C27H26Cl2N4O2 |
| Formula Weight | 509.43 |
Oglemilast, MedChemExpress
MedChemExpress Oglemilast (GRC 3886) is a potent and orally active phosphodiesterase-4 (PDE4) inhibitor with an IC50 of 0.5 nM for PDE4D3. Oglemilast inhibits pulmonary cell infiltration, including eosinophilia and neutrophilia in vitro and in vivo. Oglemilast has the potential for inflammatory airway diseases.
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| Molecular Weight (g/mol) | 516.3 |
|---|---|
| Color | Khaki |
| Physical Form | Solid |
| Chemical Name or Material | Oglemilast |
| Grade | Research |
| SMILES | O=C(C1=C2C(OC3=CC=C(NS(=O)(C)=O)C=C23)=C(OC(F)F)C=C1)NC4=C(Cl)C=NC=C4Cl |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.2% |
| CAS | 778576-62-8 |
| Solubility Information | DMSO : 4 mg/mL (7.75 mM; Need ultrasonic) |
| Synonym | GRC 3886 |
| 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 | C20H13Cl2F2N3O5S |
| Formula Weight | 516.3 |