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Filtered Search Results
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 |
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 |
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 |
Nitrofurazone, MedChemExpress
MedChemExpress Nitrofurazone (Nitrofural) is a bactericidal compound used as an antibiotic most commonly in the form of ointments.
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| Molecular Weight (g/mol) | 198.14 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Nitrofurazone |
| Grade | Research |
| SMILES | O=C(N/N=C/C1=CC=C([N+]([O-])=O)O1)N |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.04% |
| CAS | 59-87-0 |
| Solubility Information | DMSO : ≥ 155 mg/mL (782.28 mM) |
| Health Hazard 1 | H302∣H317∣H350∣H360 |
| Synonym | Nitrofural |
| 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 | C6H6N4O4 |
| Formula Weight | 198.14 |
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 |
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 |
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 |
Furaprofen, MedChemExpress
MedChemExpress Furaprofen (R803) is an effective HCV replication inhibitor. Furaprofen (R803) is substantially more potent against genotype 1a and 1b replicons (EC50, ∼30 nM) than against the genotype 2a replicon (EC50, ∼1,000 nM).
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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 |
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 |
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 |
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 |
Azimilide dihydrochloride, MedChemExpress
MedChemExpress Azimilide (NE-10064) dihydrochloride is a class III antiarrhythmic compound, inhibits I(Ks) and I(Kr) in guinea-pig cardiac myocytes and I(Ks) (minK) channels expressed in Xenopus oocytes.
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| Molecular Weight (g/mol) | 530.88 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Azimilide dihydrochloride |
| Grade | Research |
| SMILES | O=C1N(CCCCN2CCN(C)CC2)C(CN1/N=C/C3=CC=C(C4=CC=C(Cl)C=C4)O3)=O.[H]Cl.[H]Cl |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.02% |
| CAS | 149888-94-8 |
| Solubility Information | H2O : 2.22 mg/mL (4.18 mM; Need ultrasonic) ∣DMSO : 1.67 mg/mL (3.15 mM; Need ultrasonic) |
| Synonym | NE-10064 dihydrochloride |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C23H30Cl3N5O3 |
| Formula Weight | 530.88 |
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 |
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 |