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Filtered Search Results
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 |
Ginkgolide B, MedChemExpress
MedChemExpress Ginkgolide B (BN-52021), an important active terpenoid from Ginkgo biloba leaves, is reported to increase cell viability and decrease cell apoptosis.
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| Molecular Weight (g/mol) | 424.4 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Ginkgolide B |
| Grade | Research |
| SMILES | O[C@@H]1C(C2([C@H]3O)[C@](OC3=O)([H])O4)([C@@](O5)([H])C[C@H]2C(C)(C)C)C4(C5=O)[C@@](O)([C@@H]6C)[C@@]1([H])OC6=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.0% |
| CAS | 15291-77-7 |
| Solubility Information | DMSO : ≥ 100 mg/mL (235.63 mM) |
| Synonym | BN-52021 |
| 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 | C20H24O10 |
| Formula Weight | 424.4 |
PSI-6206, MedChemExpress
MedChemExpress PSI-6206 (RO 2433) is the deaminated derivative of PSI-6130, which is a potent and selective inhibitor of HCV NS5B polymerase. PSI-6206 low potently inhibits HCV replicon with EC90 of >100 μM.
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| Molecular Weight (g/mol) | 260.22 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | PSI-6206 |
| Grade | Research |
| SMILES | O=C(NC1=O)C=CN1[C@H]2[C@](F)([C@@H]([C@H](O2)CO)O)C |
| For Use With (Application) | COVID-19-anti-virus |
| Percent Purity | 99.04% |
| CAS | 863329-66-2 |
| Solubility Information | DMSO : 100 mg/mL (384.29 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H332∣H335 |
| Synonym | RO 2433 GS-331007 |
| 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 | C10H13FN2O5 |
| Formula Weight | 260.22 |
6'-O-Apiosyl-5-O-Methylvisammioside, MedChemExpress
MedChemExpress 6'-O-Apiosyl-5-O-Methylvisammioside is one of the components of the traditional Chinese medicine Kang-Jing.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 584.57 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | 6'-O-Apiosyl-5-O-Methylvisammioside |
| Grade | Research |
| SMILES | COC1=C(C[C@@H](C(C)(C)O[C@@H]([C@@H]([C@@H](O)[C@@H]2O)O)O[C@@H]2CO[C@H](OC[C@]3(O)CO)[C@@H]3O)O4)C4=CC(OC(C)=C5)=C1C5=O |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.87% |
| CAS | 139446-82-5 |
| 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 | C27H36O14 |
| Formula Weight | 584.57 |
Astragaloside IV, MedChemExpress
MedChemExpress Astragaloside IV, an active component isolated from Astragalus membranaceus, suppresses the activation of ERK1/2 and JNK, and downregulates matrix metalloproteases (MMP)-2, (MMP)-9 in MDA-MB-231 breast cancer cells.
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| Molecular Weight (g/mol) | 784.97 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Astragaloside IV |
| Grade | Research |
| SMILES | O[C@H]1[C@H](O)[C@@H](O)[C@]([H])(O[C@@H]2C(C)(C)[C@@]([C@@H](O[C@]3([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C[C@]4([H])[C@@]56CC[C@@]7(C)[C@@]4(C)C[C@H](O)[C@]7([H])[C@]8(C)O[C@H](C(C)(O)C)CC8)([H])[C@]5(C6)CC2)OC1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.0% |
| CAS | 84687-43-4 |
| Solubility Information | DMSO : ≥ 100 mg/mL (127.39 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 | C41H68O14 |
| Formula Weight | 784.97 |
PSI-6130, MedChemExpress
MedChemExpress PSI-6130 is a potent and selective inhibitor of HCV NS5B polymerase, and inhibits HCV replication with a mean IC50 of 0.6 μM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 259.23 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | PSI-6130 |
| Grade | Research |
| SMILES | O=C1N=C(C=CN1[C@@H]([C@@](C)([C@@H]2O)F)O[C@@H]2CO)N |
| For Use With (Application) | COVID-19-anti-virus |
| Percent Purity | 95.0% |
| CAS | 817204-33-4 |
| Solubility Information | DMSO : 25 mg/mL (96.44 mM; Need ultrasonic) |
| Synonym | R 1656 |
| 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 | C10H14FN3O4 |
| Formula Weight | 259.23 |
UDP-GlcNAc Disodium Salt, MedChemExpress
MedChemExpress UDP-GlcNAc Disodium Salt (UDP-α-D-N-Acetylglucosamine Disodium Salt) is a donor substrate of O-GlcNAc transferase (OGT).
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Sofosbuvir impurity M, MedChemExpress
MedChemExpress Sofosbuvir impurity M, 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) | 527.46 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity M |
| Grade | Research |
| SMILES | O=[P@@](N[C@@H](C)C(OC(C)C)=O)(OC[C@@H]1[C@@H](O)[C@@](O)(C)[C@H](N2C=CC(NC2=O)=O)O1)OC3=CC=CC=C3 |
| For Use With (Application) | COVID-19-anti-virus |
| Percent Purity | 99.04% |
| CAS | 2095551-10-1 |
| 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 | C22H30N3O10P |
| Formula Weight | 527.46 |
Citicoline sodium, MedChemExpress
MedChemExpress Citicoline sodium salt is an intermediate in the synthesis of phosphatidylcholine which is a component of cell membranes and also exerts neuroprotective effects.
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| Molecular Weight (g/mol) | 510.31 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Citicoline sodium |
| Grade | Research |
| SMILES | O[C@H]1[C@H](N(C=CC(N)=N2)C2=O)O[C@H](COP(OP(OCC[N+](C)(C)C)([O-])=O)(O[Na])=O)[C@H]1O |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 99.82% |
| CAS | 33818-15-4 |
| Solubility Information | H2O : ≥ 100 mg/mL (195.96 mM) ∣DMSO : 1 mg/mL (1.96 mM; ultrasonic and warming and heat to 80°C) |
| Health Hazard 1 | H302∣H315∣H319∣H332∣H335 |
| Synonym | Cytidine diphosphate-choline sodiumCDP-Choline sodiumCytidine 5'-diphosphocholine sodium |
| 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 | C14H25N4NaO11P2 |
| Formula Weight | 510.31 |
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 |
Eprinomectin, MedChemExpress
MedChemExpress Eprinomectin(MK-397) is an avermectin selected for development as a topical endectocide; has anthelmintic, insecticidal and miticidal activity.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 914.13 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Eprinomectin |
| Grade | Research |
| SMILES | C[C@H]1[C@@H](NC(C)=O)[C@@H](OC)C[C@H](O[C@@H]2[C@H](C)O[C@@H](O[C@@H](/C(C)=C/C[C@@H](C3)OC4(O[C@@H]([C@@H](CC)C)[C@H](C)C=C4)C[C@H]3OC5=O)[C@@H](/C=C/C=C6CO[C@@H]7[C@@]\6(O)[C@H]5C=C(C)[C@H]7O)C)C[C@@H]2OC)O1 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.0% |
| CAS | 123997-26-2 |
| Solubility Information | DMSO : ≥ 100 mg/mL (109.39 mM) |
| Health Hazard 1 | H225∣H302+H312+H332∣H319 |
| Synonym | MK-397 |
| 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 | C50H75NO14 |
| Formula Weight | 914.13 |
Sofosbuvir impurity J, MedChemExpress
MedChemExpress Sofosbuvir impurity J, 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 | 1334513-10-8 |
|---|---|
| Molecular Weight (g/mol) | 528.47 |
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Sofosbuvir impurity J |
| Grade | Research |
| SMILES | O[C@H]1[C@](F)(C)[C@H](N2C=CC(N)=NC2=O)O[C@@H]1CO[P@](OC3=CC=CC=C3)(N[C@@H](C)C(OC(C)C)=O)=O |
| 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 | C22H30FN4O8P |
| Formula Weight | 528.47 |
Velsecorat, MedChemExpress
MedChemExpress AZD7594 is a potent selective nonsteroidal glucocorticoid receptor modulator, with an IC50 of 0.9 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 606.62 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Velsecorat |
| Grade | Research |
| SMILES | O=C(N[C@H]1COCC1)C2=CC=CC(N3N=CC4=C3C=CC(O[C@H](C5=CC=C(OCCO6)C6=C5)[C@@H](NC(C(F)(F)C)=O)C)=C4)=C2 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.6% |
| CAS | 1196509-60-0 |
| Solubility Information | DMSO : ≥ 83.3 mg/mL (137.32 mM) |
| Synonym | AZD7594 AZ13189620 |
| 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 | C32H32F2N4O6 |
| Formula Weight | 606.62 |
Ginkgolide C, MedChemExpress
MedChemExpress Ginkgolide C is a flavone isolated from Ginkgo biloba leaves, possessing multiple biological functions, such as decreasing platelet aggregation and ameliorating Alzheimer disease.
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| Molecular Weight (g/mol) | 440.4 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Ginkgolide C |
| Grade | Research |
| SMILES | O[C@@H]1C2([C@@](O3)([H])[C@H](O)[C@H]4C(C)(C)C)C4([C@H]5O)[C@](OC5=O)([H])OC2(C3=O)[C@@](O)([C@@H]6C)[C@@]1([H])OC6=O |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 98.0% |
| CAS | 15291-76-6 |
| Solubility Information | DMSO : 250 mg/mL (567.67 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Synonym | BN-52022 Ginkgolide-C |
| 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 | C20H24O11 |
| Formula Weight | 440.4 |
3BDO, MedChemExpress
MedChemExpress 3BDO is a new mTOR activator which can also inhibit autophagy.
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| Molecular Weight (g/mol) | 327.33 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid-Liquid Mixture |
| Chemical Name or Material | 3BDO |
| Grade | Research |
| SMILES | O=C1OC(COC2=C([N+]([O-])=O)C=CC=C2)CC1CC3=CC=CC=C3 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.91% |
| CAS | 890405-51-3 |
| Solubility Information | DMSO : ≥ 100 mg/mL (305.50 mM) ∣Ethanol : 20 mg/mL (61.10 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 | C18H17NO5 |
| Formula Weight | 327.33 |