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Filtered Search Results
exo-7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic anhydride, 98%, Thermo Scientific Chemicals
CAS: 29745-04-8 Molecular Formula: C8H8O4 Molecular Weight (g/mol): 168.148 MDL Number: MFCD00213361 InChI Key: JAABVEXCGCXWRR-GUCUJZIJSA-N Synonym: exo-3,6-Epoxyhexahydrophthalic anhydride; Norcantharadin PubChem CID: 12251906 SMILES: C1CC2C3C(C1O2)C(=O)OC3=O
PubChem CID | 12251906 |
---|---|
CAS | 29745-04-8 |
Molecular Weight (g/mol) | 168.148 |
MDL Number | MFCD00213361 |
SMILES | C1CC2C3C(C1O2)C(=O)OC3=O |
Synonym | exo-3,6-Epoxyhexahydrophthalic anhydride; Norcantharadin |
InChI Key | JAABVEXCGCXWRR-GUCUJZIJSA-N |
Molecular Formula | C8H8O4 |
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 |
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 |
Timosaponin A1, MedChemExpress
MedChemExpress Timosaponin A1 is a coprostane type steroidal saponin isolated from Rhizoma Anemarrhenae.
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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 |
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 |
Alfuzosin, MedChemExpress
MedChemExpress Alfuzosin is an α1 adrenergic receptor antagonist used to treat benign prostatic hyperplasia (BPH).
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Molecular Weight (g/mol) | 389.45 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Alfuzosin |
Grade | Research |
SMILES | O=C(C1OCCC1)NCCCN(C2=NC(N)=C3C=C(OC)C(OC)=CC3=N2)C |
Percent Purity | 99.67% |
CAS | 81403-80-7 |
Solubility Information | DMSO : ≥ 50 mg/mL (128.39 mM) |
Synonym | SL 77499 |
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 | C19H27N5O4 |
Formula Weight | 389.45 |
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 |
Jujuboside A, MedChemExpress
MedChemExpress Jujuboside A is a glycoside extracted from Semen Ziziphi Spinosae, a Chinese herbal medicine used to treat insomnia and anxiety.
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Molecular Weight (g/mol) | 1207.35 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Jujuboside A |
Grade | Research |
SMILES | C[C@]([C@]1([H])CC2)(CC[C@]3([H])[C@@]1(CC[C@H](O[C@@](OC[C@H](O)[C@@H]4O[C@@](O[C@H](CO[C@@H]([C@@H]([C@@H](O)[C@@H]5O)O)O[C@@H]5CO)[C@@H](O)[C@@H]6O)([H])[C@@H]6O[C@@](OC[C@@H](O)[C@@H]7O)([H])[C@@H]7O)([H])[C@@H]4O[C@@](O[C@@H](C)[C@H](O)[C@H]8O)([H])[C@@H]8O)C3(C)C)C)[C@@]9(CO%10)[C@@]2([H])[C@]([C@]%11(O)C)([H])[C@@]%10(O[C@@H](/C=C(C)/C)C%11)C9 |
For Use With (Application) | Neuroscience-Neurodegeneration |
Percent Purity | 98.0% |
CAS | 55466-04-1 |
Solubility Information | DMSO : 100 mg/mL (82.83 mM; Need ultrasonic) ∣H2O : 50 mg/mL (41.41 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 | C58H94O26 |
Formula Weight | 1207.35 |
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 |
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 |
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 |
L-Gulono-1,4-lactone, MedChemExpress
MedChemExpress L-Gulono-1,4-lactone is a substrate of L-gulono-1,4-lactone oxidoreductase, which catalyzes the last step of the biosynthesis of L-ascorbic (Vatamin) C. In other words, L-Gulono-1,4-lactone is a direct precursor of vitamin C in animals, in plants and in some protists.
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Gemcitabine elaidate, MedChemExpress
MedChemExpress Gemcitabine elaidate (CP-4126) is lipophilic pro-drug of Gemcitabine. Gemcitabine elaidate is converted to Gemcitabine by esterases in order to be phosphorylated. Gemcitabine elaidate exhibits anti-tumor activity.
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Molecular Weight (g/mol) | 527.64 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Gemcitabine elaidate |
Grade | Research |
SMILES | O[C@@H](C(F)(F)[C@H](N1C(N=C(C=C1)N)=O)O2)[C@H]2COC(CCCCCCC/C=C/CCCCCCCC)=O |
For Use With (Application) | Cancer-Kinase/protease |
Percent Purity | 97.42% |
CAS | 210829-30-4 |
Solubility Information | DMSO : ≥ 26 mg/mL (49.28 mM) |
Synonym | CP-4126 CO-101 Gemcitabine 5'-elaidate |
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 | C27H43F2N3O5 |
Formula Weight | 527.64 |
Ginkgolide A, MedChemExpress
MedChemExpress Ginkgolide A (BN-52020) is an extract from in Ginkgo biloba and a g-aminobutyric acid (GABA) antagonist.
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Molecular Weight (g/mol) | 408.4 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Ginkgolide A |
Grade | Research |
SMILES | O=C1[C@@H](C)[C@]2(O)[C@@]3(C4=O)C(C5([C@@H](O)C(O6)=O)C6O3)([C@H](O4)C[C@H]5C(C)(C)C)C[C@]2([H])O1 |
For Use With (Application) | COVID-19-immunoregulation |
Percent Purity | 98.0% |
CAS | 15291-75-5 |
Solubility Information | DMSO : 100 mg/mL (244.86 mM; Need ultrasonic) |
Health Hazard 1 | H315∣H319∣H335 |
Synonym | BN-52020 |
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 | C20H24O9 |
Formula Weight | 408.4 |