Noscapine
CAS No. 128-62-1
Noscapine( (SR)-Noscapine | Narcotine )
Catalog No. M21130 CAS No. 128-62-1
Noscapine is a Non-addictive Opioid and Microtubule-Inhibitor in Potential Treatment of Glioblastoma.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 28 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | 58 | Get Quote |
|
| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameNoscapine
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NoteResearch use only, not for human use.
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Brief DescriptionNoscapine is a Non-addictive Opioid and Microtubule-Inhibitor in Potential Treatment of Glioblastoma.
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DescriptionNoscapine is a Non-addictive Opioid and Microtubule-Inhibitor in Potential Treatment of Glioblastoma.
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In Vitro——
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In Vivo——
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Synonyms(SR)-Noscapine | Narcotine
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PathwayAutophagy
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TargetSigma receptor
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Recptorσ-receptor
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Research Areacancer
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IndicationNon-Hodgkin's LymphomaChronic Lymphocytic Leukemia
Chemical Information
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CAS Number128-62-1
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Formula Weight413.42
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Molecular FormulaC22H23NO7
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Purity>98% (HPLC)
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SolubilityDMSO:30 mg/mL (72.57 mM)
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SMILESCOc1ccc2c(c1OC)C(=O)OC2C1c2c(cc3c(c2OC)OCO3)CCN1C
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Chemical Name(S)-67-dimethoxy-3-((R)-4-methoxy-6-methyl-5678-tetrahydro-[13]dioxolo[45-g]isoquinolin-5-yl)isobenzofuran-1(3H)-one
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Glycerol phenylbutyr...
Glycerol phenylbutyrate (GPB) is a new generation ammonia scavenger drug and it also is a sigma-2 (σ2) receptor ligand (pKi: 8.02).Glycerol phenylbutyrate may have therapeutic potential in additional conditions such as chronic hepatic encephalopathy or other inherited metabolic disorders. Glycerol phenylbutyrate also has the potential for the treatment of hyperammonemia.
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KSK67
KSK67 is a selective dual antagonist of sigma-2 and histamine H3 receptors with inhibitory effects on H3 receptors, sigma-1, and sigma-2 receptors, with Ki values of 3.2, 1531, and 101 nM, respectively.
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NE-100
A potent, selective, and orally active sigma-1 receptor antagonist with Ki of 1.03 nM.
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