Furofurans
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Enantiomer of Sofosbuvir, MedChemExpress
MedChemExpress Enantiomer of Sofosbuvir is an enantiomer of Sofosbuvir, a prescription medicine for the treatment of patients with chronic hepatitis C. There is no biological activity report on enantiomer of Sofosbuvir until now.
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| Molecular Weight (g/mol) | 529.45 |
|---|---|
| Color | White |
| Physical Form | Powder |
| Chemical Name or Material | Enantiomer of Sofosbuvir |
| Grade | Research |
| SMILES | O=[P@](N[C@H](C)C(OC(C)C)=O)(OC[C@H]1[C@H](O)[C@@](F)(C)[C@@H](N2C=CC(NC2=O)=O)O1)OC3=CC=CC=C3 |
| 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 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Molecular Formula | C22H29FN3O9P |
| Formula Weight | 529.45 |
Sofosbuvir impurity D, MedChemExpress
MedChemExpress Sofosbuvir impurity D is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity.
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| Molecular Weight (g/mol) | 529.45 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity D |
| Grade | Research |
| SMILES | O=[P@@](N[C@@H](C)C(OC(C)C)=O)(OC[C@H]1[C@H](O)[C@@](F)(C)[C@@H](N2C=CC(NC2=O)=O)O1)OC3=CC=CC=C3 |
| 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 | C22H29FN3O9P |
| Formula Weight | 529.45 |
Sofosbuvir impurity E, MedChemExpress
MedChemExpress Sofosbuvir impurity E is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity.
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| Molecular Weight (g/mol) | 529.45 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity E |
| Grade | Research |
| SMILES | O=[P@@](N[C@@H](C)C(OC(C)C)=O)(OC[C@@H]1[C@H](O)[C@@](F)(C)[C@H](N2C=CC(NC2=O)=O)O1)OC3=CC=CC=C3 |
| 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 | C22H29FN3O9P |
| Formula Weight | 529.45 |
Sofosbuvir impurity B, MedChemExpress
MedChemExpress Sofosbuvir impurity B is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity.
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| Molecular Weight (g/mol) | 529.45 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity B |
| Grade | Research |
| SMILES | O=[P@@](N[C@@H](C)C(OC(C)C)=O)(OC[C@@H]1[C@@H](O)[C@](F)(C)[C@@H](N2C=CC(NC2=O)=O)O1)OC3=CC=CC=C3 |
| 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 | C22H29FN3O9P |
| Formula Weight | 529.45 |
Decitabine, MedChemExpress
MedChemExpress Decitabine (NSC 127716) is an orally active deoxycytidine analogue antimetabolite and a DNA methyltransferase inhibitor. Decitabine incorporates into DNA in place of cytosine can covalently trap DNA methyltransferase to DNA causing irreversible inhibition of the enzyme. Decitabine induces cell G2/M arrest and cell apoptosis. Decitabine has potent anticancer activity.
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| Molecular Weight (g/mol) | 228.21 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Decitabine |
| Grade | Research |
| SMILES | O=C1N=C(N)N=CN1[C@H](O[C@@H]2CO)C[C@@H]2O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 95.0% |
| CAS | 2353-33-5 |
| Solubility Information | DMSO : ≥ 50 mg/mL (219.10 mM) ∣H2O : 20 mg/mL (87.64 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Synonym | 5-Aza-2'-deoxycytidine 5-AZA-CdR NSC 127716 |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Shelf Life | 4°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Molecular Formula | C8H12N4O4 |
| Formula Weight | 228.21 |
Sofosbuvir impurity N, MedChemExpress
MedChemExpress Sofosbuvir impurity N, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir (PSI-7977) is an inhibitor of HCV RNA replication, demonstrates potent anti-hepatitis C virus activity.
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| CAS | 1394157-34-6 |
|---|---|
| Molecular Weight (g/mol) | 501.4 |
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity N |
| Grade | Research |
| SMILES | O=[P@@](N[C@@H](C)C(OC)=O)(OC[C@@H]1[C@@H](O)[C@](F)(C)[C@H](N2C=CC(NC2=O)=O)O1)OC3=CC=CC=C3 |
| 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 | C20H25FN3O9P |
| Formula Weight | 501.4 |
Sofosbuvir impurity C, MedChemExpress
MedChemExpress Sofosbuvir impurity C is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity.
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| CAS | 1496552-28-3 |
|---|---|
| Molecular Weight (g/mol) | 529.45 |
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity C |
| Grade | Research |
| SMILES | O=[P@@](N[C@H](C)C(OC(C)C)=O)(OC[C@@H]1[C@@H](O)[C@](F)(C)[C@H](N2C=CC(NC2=O)=O)O1)OC3=CC=CC=C3 |
| 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 | C22H29FN3O9P |
| Formula Weight | 529.45 |
Octazamide, MedChemExpress
MedChemExpress Octazamide (ICI-US 457) is an analgesic drug.
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Sofosbuvir impurity G, MedChemExpress
MedChemExpress Sofosbuvir impurity G, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir (PSI-7977) is an inhibitor of HCV RNA replication, demonstrates potent anti-hepatitis C virus activity.
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| CAS | 1337482-15-1 |
|---|---|
| Molecular Weight (g/mol) | 529.45 |
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity G |
| Grade | Research |
| SMILES | O=[P@@](N[C@@H](C)C(OC(C)C)=O)(O[C@H]1[C@](F)(C)[C@H](N2C(NC(C=C2)=O)=O)O[C@@H]1CO)OC3=CC=CC=C3 |
| 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 |
| For Use With (Application) | COVID-19-anti-virus |
| Molecular Formula | C22H29FN3O9P |
| Formula Weight | 529.45 |
Sofosbuvir impurity H, MedChemExpress
MedChemExpress Sofosbuvir impurity H, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir (PSI-7977) is an inhibitor of HCV RNA replication, demonstrates potent anti-hepatitis C virus activity.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 633.56 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity H |
| Grade | Research |
| SMILES | O=[P@@](N[C@@H](C)C(OC(C)C)=O)(OC[C@@H]1[C@@H](OC(C2=CC=CC=C2)=O)[C@](F)(C)[C@H](N3C=CC(NC3=O)=O)O1)OC4=CC=CC=C4 |
| 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 |
| For Use With (Application) | COVID-19-anti-virus |
| Molecular Formula | C29H33FN3O10P |
| Formula Weight | 633.56 |
8-Hydroxyguanosine, MedChemExpress
MedChemExpress 8-Hydroxyguanosine is a systematic marker of oxidative stress and a marker of hydroxyl radical damage to RNA.
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Dinotefuran, MedChemExpress
MedChemExpress Dinotefuran is an insecticide of the neonicotinoid class, its mechanism of action involves disruption of the insect's nervous system by inhibiting nicotinic acetylcholine receptors.
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| Molecular Weight (g/mol) | 202.21 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Dinotefuran |
| Grade | Research |
| SMILES | O=[N+](N/C(NC)=N/CC1COCC1)[O-] |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.88% |
| CAS | 165252-70-0 |
| Solubility Information | H2O : 50 mg/mL (247.27 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Synonym | MTI-446 |
| 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 | C7H14N4O3 |
| Formula Weight | 202.21 |
Eplerenone, MedChemExpress
MedChemExpress Eplerenone (Epoxymexrenone) is a selective, competitive and oreally active aldosterone antagonist with an IC50 of 138 nM. Eplerenone has low affinity for progesterone, androgen, estrogen and glucocorticoid receptors. Eplerenone can be used for hypertension and heart failure after myocardial infarction reserch.
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| Molecular Weight (g/mol) | 414.49 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Eplerenone |
| Grade | Research |
| SMILES | O=C(CC1)O[C@@]21CC[C@@]3([H])[C@]4([H])[C@H](C(OC)=O)CC5=CC(CC[C@]5(C)[C@@]46[C@H](O6)C[C@@]32C)=O |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.68% |
| CAS | 107724-20-9 |
| Solubility Information | DMSO : 25 mg/mL (60.32 mM; Need ultrasonic) |
| Synonym | Epoxymexrenone |
| 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 | C24H30O6 |
| Formula Weight | 414.49 |
AZD5904, MedChemExpress
MedChemExpress AZD5904 is a selective and irreversible inhibitor of human Myeloperoxidase (MPO) with an IC50 of 140 nM and has similar potency in mouse and rat.
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| Molecular Weight (g/mol) | 252.29 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | AZD5904 |
| Grade | Research |
| SMILES | O=C1NC(N(C[C@@H]2OCCC2)C3=C1N=CN3)=S |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.0% |
| CAS | 618913-30-7 |
| Solubility Information | DMSO : 22.73 mg/mL (90.09 mM; Need ultrasonic) |
| Health Hazard 1 | H361 |
| 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 | C10H12N4O2S |
| Formula Weight | 252.29 |
3'-Azido-3'-deoxy-beta-L-uridine, MedChemExpress
MedChemExpress 3'-Azido-3'-deoxy-beta-L-uridine (Compound 25) is a nucleoside derivative.
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| Molecular Weight (g/mol) | 269.21 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | 3'-Azido-3'-deoxy-beta-L-uridine |
| Grade | Research |
| SMILES | O=C(N([C@H]1O[C@@H](CO)[C@H](N=[N+]=[N-])[C@@H]1O)C=C2)NC2=O |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.7% |
| CAS | 2095417-28-8 |
| Solubility Information | DMSO : 125 mg/mL (464.32 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 | C9H11N5O5 |
| Formula Weight | 269.21 |