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4,10-Dioxatricyclo[5.2.1.0(2,6)]decan-8-en-3-one 97.0+%, TCI America™
CAS: 72150-22-2 Molecular Formula: C8H8O3 Molecular Weight (g/mol): 152.149 InChI Key: KIAQKKYOUVIGII-UHFFFAOYSA-N Synonym: 4,7-Epoxy-3a,4,7,7a-tetrahydroisobenzofuran-1(3H)-one PubChem CID: 331417 SMILES: C1C2C3C=CC(C2C(=O)O1)O3
| PubChem CID | 331417 |
|---|---|
| CAS | 72150-22-2 |
| Molecular Weight (g/mol) | 152.149 |
| SMILES | C1C2C3C=CC(C2C(=O)O1)O3 |
| Synonym | 4,7-Epoxy-3a,4,7,7a-tetrahydroisobenzofuran-1(3H)-one |
| InChI Key | KIAQKKYOUVIGII-UHFFFAOYSA-N |
| Molecular Formula | C8H8O3 |
4,9,11-Trioxatetracyclo[5.3.1.0(2,6).0(8,10)]undecan-3-one 98.0+%, TCI America™
CAS: 632339-23-2 Molecular Formula: C8H8O4 Molecular Weight (g/mol): 168.15 MDL Number: MFCD10566937 InChI Key: UAFDSOCDQRHNCL-UHFFFAOYNA-N Synonym: 2,6-Epoxy-2,2a,5,5a,6,6a-hexahydrooxireno[f]isobenzofuran-3(1aH)-one PubChem CID: 20632532 IUPAC Name: 4,9,11-trioxatetracyclo[5.3.1.0²,⁶.0⁸,¹⁰]undecan-3-one SMILES: O=C1OCC2C3OC(C4OC34)C12
| PubChem CID | 20632532 |
|---|---|
| CAS | 632339-23-2 |
| Molecular Weight (g/mol) | 168.15 |
| MDL Number | MFCD10566937 |
| SMILES | O=C1OCC2C3OC(C4OC34)C12 |
| Synonym | 2,6-Epoxy-2,2a,5,5a,6,6a-hexahydrooxireno[f]isobenzofuran-3(1aH)-one |
| IUPAC Name | 4,9,11-trioxatetracyclo[5.3.1.0²,⁶.0⁸,¹⁰]undecan-3-one |
| InChI Key | UAFDSOCDQRHNCL-UHFFFAOYNA-N |
| Molecular Formula | C8H8O4 |
Norcantharidin 98.0+%, TCI America™
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, exo-7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic Anhydride 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, exo-7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic Anhydride |
| InChI Key | JAABVEXCGCXWRR-GUCUJZIJSA-N |
| Molecular Formula | C8H8O4 |
Cantharidin 98.0+%, TCI America™
CAS: 56-25-7 Molecular Formula: C10H12O4 Molecular Weight (g/mol): 196.202 MDL Number: MFCD00134968 InChI Key: DHZBEENLJMYSHQ-XCVPVQRUSA-N Synonym: cantharidin,cantharone,cantharidine,kantaridin,kantharidin,cantharides camphor,kantharidin german,caswell no. 157,1,2-dimethyl-3,6-epoxyperhydrophthalic anhydride,unii-igl471wq8p PubChem CID: 5944 ChEBI: CHEBI:64213 SMILES: CC12C3CCC(C1(C(=O)OC2=O)C)O3
| PubChem CID | 5944 |
|---|---|
| CAS | 56-25-7 |
| Molecular Weight (g/mol) | 196.202 |
| ChEBI | CHEBI:64213 |
| MDL Number | MFCD00134968 |
| SMILES | CC12C3CCC(C1(C(=O)OC2=O)C)O3 |
| Synonym | cantharidin,cantharone,cantharidine,kantaridin,kantharidin,cantharides camphor,kantharidin german,caswell no. 157,1,2-dimethyl-3,6-epoxyperhydrophthalic anhydride,unii-igl471wq8p |
| InChI Key | DHZBEENLJMYSHQ-XCVPVQRUSA-N |
| Molecular Formula | C10H12O4 |
Cantharidin, 98%, Thermo Scientific Chemicals
CAS: 56-25-7 Molecular Formula: C10H12O4 Molecular Weight (g/mol): 196.202 MDL Number: MFCD00134968 InChI Key: DHZBEENLJMYSHQ-XCVPVQRUSA-N Synonym: cantharidin,cantharone,cantharidine,kantaridin,kantharidin,cantharides camphor,kantharidin german,caswell no. 157,1,2-dimethyl-3,6-epoxyperhydrophthalic anhydride,unii-igl471wq8p PubChem CID: 5944 ChEBI: CHEBI:64213 SMILES: CC12C3CCC(C1(C(=O)OC2=O)C)O3
| PubChem CID | 5944 |
|---|---|
| CAS | 56-25-7 |
| Molecular Weight (g/mol) | 196.202 |
| ChEBI | CHEBI:64213 |
| MDL Number | MFCD00134968 |
| SMILES | CC12C3CCC(C1(C(=O)OC2=O)C)O3 |
| Synonym | cantharidin,cantharone,cantharidine,kantaridin,kantharidin,cantharides camphor,kantharidin german,caswell no. 157,1,2-dimethyl-3,6-epoxyperhydrophthalic anhydride,unii-igl471wq8p |
| InChI Key | DHZBEENLJMYSHQ-XCVPVQRUSA-N |
| Molecular Formula | C10H12O4 |
Medchemexpress LLC AT-9010 tetrasodium | 1621884-18-1 | 99.7% | 627.13 | 1 MG
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AT-9010 tetrasodium, a triphosphate active metabolite of AT-527, is a potent inhibitor of NiRAN (a function essential for viral replication). It can inhibit SARS-CoV-2 replication.
- Potent inhibitor of NiRAN
- Inhibits SARS-CoV-2 replication
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Selleck Chemical LLC L-Gulono-1 4-lactone
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L-Gulono-1 4-lactone (L-Gulonolactone L-Gulono-gamma-lactone reduced ascorbic acid) is the substrate of the enzyme L-gulono-1 4-lactone oxidoreductase which catalyzes the last step of the biosynthesis of L-ascorbic acid (vitamin C) in plants and animals
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Research Products International Corp Calcium Chloride Anhydrous, 1 Kilogram
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CAS Number: 10043-52-4
Molecular Formula: CaCl2
Molecular Weight: 110.98
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Medchemexpress LLC Jujuboside A | 55466-04-1 | 1207.35 | 100 MG
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Jujuboside A | 55466-04-1 | 1207.35 | 100 MG
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Medchemexpress LLC Jujuboside A | 55466-04-1 | 1207.35 | 50 MG
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Jujuboside A is a glycoside extracted from Semen Ziziphi Spinosae, a Chinese herbal medicine traditionally used to address insomnia and anxiety. It appears as a white to off-white solid and its structure is classified under Terpenoids and Triterpenes. It is initially sourced from plants like Actaea dahurica Turcz. ex Fisch. & C. A. Mey. and plants from the Rhamnaceae family.
- Acts as an agonist for the GABA receptor.
- Targets mTOR, PI3K, and Akt pathways.
- Increases total sleep and REM sleep during daytime.
- Increases total sleep and NREM sleep during nighttime.
- Neuroprotective agent against behavioral disorders in dementia mouse models.
- Mitigates learning and memory impairment.
- Reduces Aβ1-42 levels in the hippocampus.
- Protects H9C2 cells from isoproterenol-induced injury.
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Medchemexpress LLC Astragaloside I | 84680-75-1 | 869.04 | 100 MG
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Astragaloside I is a main active ingredient in Astragalus membranaceus that possesses osteogenic properties. It stimulates osteoblast differentiation by activating the Wnt/β-catenin signaling pathway. This product is for research use only.
- Possesses osteogenic properties
- Stimulates osteoblast differentiation
- Activates the Wnt/β-catenin signaling pathway
- Upregulates expression of osteogenesis marker genes
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Medchemexpress LLC Astragaloside II | 84676-89-1 | 827.01 | 50 MG
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Astragaloside II is an orally active Cycloartane-type triterpene glycoside extracted from Astragalus membranaceus. It inhibits Autophagy, decreases pro-inflammatory cytokines (IL-6, IL-1β), HIF-α, p-p65, p-IκB, and increases SOD. It regulates immunity and reduces inflammatory responses. This compound can be used in research for diseases like liver cancer, osteoporosis, immunosuppressive diseases, and ulcerative colitis.
- Purity: 99.45%
- Molecular weight: 827.01
- Formula: C43H70O15
- Appearance: Solid
- Color: White to off-white
- Structure classification: Terpenoids, Triterpenes
- Initial source: Plants, Leguminosae, Astragalus membranaceus var. mongholicus (Bunge)P.K.Hsiao
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Medchemexpress LLC Astragaloside I | 84680-75-1 | 869.04 | 50 MG
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Astragaloside I, one of the main active ingredients in Astragalus membranaceus, possesses osteogenic properties. It stimulates osteoblast differentiation through activating the Wnt/β-catenin signaling pathway.
- Main active ingredient in Astragalus membranaceus.
- Has osteogenic properties.
- Stimulates osteoblast differentiation by activating the Wnt/β-catenin signaling pathway.
- Upregulates expression of β-catenin, Runx2, BGP, and OPG, RANKL (osteogenesis marker genes) in MC3T3-E1 cells at concentrations of 10-40 μM.
- No obvious cytotoxic effect observed in MC3T3-E1 cells at 10-40 μM.
- Purity: 99.81%.
- Appearance: Solid.
- Color: White to off-white.
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Medchemexpress LLC Astragaloside II | 84676-89-1 | 827.01 | 100 MG
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Astragaloside II is an orally active Cycloartane-type triterpene glycoside extracted from *Astragalus membranaceus*. It is used in the research of diseases such as liver cancer, osteoporosis, immunosuppressive diseases, and ulcerative colitis. It functions by inhibiting autophagy, decreasing pro-inflammatory cytokines (IL-6, IL-1β), HIF-α, p-p65, and p-IκB, and increasing superoxide dismutase (SOD). It also regulates immunity and reduces inflammatory responses.
- Promotes cell viability of rat primary osteoblasts.
- Enhances proliferation of primary splenocytes.
- Sensitizes cells to 5-fluorouracil-induced cell death.
- Inhibits levels of HIF-α, p-p65, and p-IκB, demonstrating an anti-inflammatory effect.
- Alleviates symptoms of DSS-induced ulcerative colitis in mice.
- Reduces DAI score and prevents body weight loss in vivo.
- Increases colon length and superoxide dismutase in colon tissues.
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Medchemexpress LLC UDP-GlcNAc disodium | 91183-98-1 | 99.9% | 651.32 | 10 MG
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UDP-GlcNAc Disodium Salt is a donor substrate of O-GlcNAc transferase (OGT). OGT is a nucleocytoplasmic glycosyltransferase that modifies thousands of proteins by adding a unique N-acetylglucosamine residue onto acceptor substrates mainly confined within the cytosol and nucleus.
- Donor substrate of O-GlcNAc transferase (OGT).
- For research use only.
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