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Filtered Search Results
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 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 |
Sofosbuvir impurity A, MedChemExpress
MedChemExpress Sofosbuvir impurity A, 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 | 1496552-16-9 |
|---|---|
| Molecular Weight (g/mol) | 529.45 |
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity A |
| 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 |
| For Use With (Application) | COVID-19-anti-virus |
| 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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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 |
Octazamide, MedChemExpress
MedChemExpress Octazamide (ICI-US 457) is an analgesic drug.
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Actein, MedChemExpress
MedChemExpress Actein is a triterpene glycoside isolated from the rhizomes of Cimicifuga foetida. Actein suppresses cell proliferation, induces autophagy and apoptosis through promoting ROS/JNK activation, and blunting AKT pathway in human bladder cancer. Actein has little toxicity in vivo.
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Magnolin, MedChemExpress
MedChemExpress Magnolin, a major component of Magnolia flos (Shin-Yi), inhibits the Ras/ERKs/RSK2 signaling axis by targeting the active pocket of ERK1 and ERK2 with IC50s of 87 nM and 16.5 nM, respectively.
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| Molecular Weight (g/mol) | 416.46 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Magnolin |
| Grade | Research |
| SMILES | COC1=C(OC)C(OC)=CC([C@H]2OC[C@]3([H])[C@@H](C4=CC=C(OC)C(OC)=C4)OC[C@@]32[H])=C1 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.85% |
| CAS | 31008-18-1 |
| Solubility Information | DMSO : 100 mg/mL (240.12 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 | C23H28O7 |
| Formula Weight | 416.46 |
Bilobalide, MedChemExpress
MedChemExpress Bilobalide, a sesquiterpene trilactone constituent of Ginkgo biloba, inhibits the NMDA-induced efflux of choline with an IC50 value of 2.3 μM. Bilobalide prevents apoptosis through activation of the PI3K/Akt pathway in SH-SY5Y cells. Exerts protective and trophic effects on neurons.
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| Molecular Weight (g/mol) | 326.3 |
|---|---|
| Color | White |
| Physical Form | Powder |
| Chemical Name or Material | Bilobalide |
| Grade | Research |
| SMILES | O=C(O1)C[C@@]2([C@]1([H])C[C@]3(C(C)(C)C)O)[C@@]34[C@](OC([C@@H]4O)=O)([H])OC2=O |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 98.0% |
| CAS | 33570-04-6 |
| Solubility Information | DMSO : ≥ 100 mg/mL (306.47 mM) |
| Synonym | (-)-Bilobalide |
| 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 | C15H18O8 |
| Formula Weight | 326.3 |
Saridegib, MedChemExpress
MedChemExpress Saridegib is a potent and specific inhibitor of Smoothened (Smo), a key signaling transmembrane protein in the Hedgehog (Hh) pathway.
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| Molecular Weight (g/mol) | 504.77 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Saridegib |
| Grade | Research |
| SMILES | CC1=C(C[C@@]2([H])[C@@]3([H])CC[C@@]4([H])[C@]2(C)CC[C@@H](NS(C)(=O)=O)C4)[C@@]3([H])CC[C@@]([C@@H]5C)(C1)O[C@@]6([H])[C@@]5([H])NC[C@@H](C)C6 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.0% |
| CAS | 1037210-93-7 |
| Synonym | IPI-926 Patidegib |
| 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 | C29H48N2O3S |
| Formula Weight | 504.77 |
Dehydroascorbic acid, MedChemExpress
MedChemExpress Dehydroascorbic acid, a blood-brain barrier transportable form of vitamin C, mediates potent cerebroprotection in experimental stroke.
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M3258, MedChemExpress
MedChemExpress M3258 is an orally bioavailable, potent, reversible and highly selective immunoproteasome subunit LMP7 (β5i) inhibitor.
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| Molecular Weight (g/mol) | 329.16 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | M3258 |
| Grade | Research |
| SMILES | O=C(N[C@@H](CC1=COC2=C1C=CC=C2)B(O)O)[C@H]3[C@@H]4CC[C@@H](O4)C3 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.0% |
| CAS | 2285330-15-4 |
| Solubility Information | DMSO : 250 mg/mL (759.51 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 | C17H20BNO5 |
| Formula Weight | 329.16 |
Tegafur, MedChemExpress
MedChemExpress Tegafur (FT 207; NSC 148958) is a chemotherapeutic 5-FU prodrug used in the treatment of cancers; is a component of tegafur-uracil.
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| Molecular Weight (g/mol) | 200.17 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Tegafur |
| Grade | Research |
| SMILES | O=C1NC(C(F)=CN1C2OCCC2)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.74% |
| CAS | 17902-23-7 |
| Solubility Information | DMSO : ≥ 48 mg/mL (239.80 mM) |
| Health Hazard 1 | H301∣H311∣H331 |
| Synonym | FT 207 NSC 148958 |
| 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 | C8H9FN2O3 |
| Formula Weight | 200.17 |
Zylofuramine, MedChemExpress
MedChemExpress Zylofuramine is a psychomotor stimulant.
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| Molecular Weight (g/mol) | 219.32 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Zylofuramine |
| Grade | Research |
| SMILES | CCN[C@@H]([C@@]1([H])CCCO1)CC2=CC=CC=C2 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.87% |
| CAS | 3563-92-6 |
| Solubility Information | DMSO : ≥ 100 mg/mL (455.95 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 | C14H21NO |
| Formula Weight | 219.32 |
Drospirenone, MedChemExpress
MedChemExpress Drospirenone(Dihydrospirorenone) is a synthetic progestin that is an analog to spironolactone.
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| Molecular Weight (g/mol) | 366.49 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Drospirenone |
| Grade | Research |
| SMILES | C[C@@]12[C@](OC3=O)(CC3)[C@@H](C4)[C@@H]4[C@@]1([H])[C@@]([C@@H]5[C@H]6C5)([H])[C@]([C@](C6=CC7=O)(CC7)C)([H])CC2 |
| Percent Purity | 98.0% |
| CAS | 67392-87-4 |
| Solubility Information | DMSO : 50 mg/mL (136.43 mM; Need ultrasonic) |
| Health Hazard 1 | H360 |
| Synonym | Dihydrospirorenone |
| 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 | C24H30O3 |
| Formula Weight | 366.49 |