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Cat. No.: HY-135492

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O-Methylmoschatoline

(Synonyms: Liridine; Homomoschatoline)

O-Methylmoschatoline (Liridine) is a compound with notable bioactivity, exhibiting potential applications in medicinal chemistry.

For research use only. We do not sell to patients.

CAS No.: 5140-38-5
Formula: C₁₉H₁₅NO₄
Molecular Weight:321.33

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (271 KB)

O-Methylmoschatoline Chemical Structure

CAS No.: 5140-38-5

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- Cellular Effect
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

O-Methylmoschatoline (Liridine) is a compound with notable bioactivity, exhibiting potential applications in medicinal chemistry.

All Endogenous Metabolite Isoforms :

Cellular Effect

Cell Line	Type	Value	Description	References
B-cell	IC₅₀	>100 μM Compound: 22	Inhibition of LPS-induced BALB/c mouse B cell proliferation Inhibition of LPS-induced BALB/c mouse B cell proliferation	[PMID: 17081761]
KB	ED₅₀	>10 μg/mL Compound: homomoschatoline	Cytotoxicity against human KB cells Cytotoxicity against human KB cells	10.1021/np50019a011
RAW264.7	IC₅₀	>50 μM Compound: 12	Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay	[PMID: 33939429]
T-cell	IC₅₀	>100 μM Compound: 22	Inhibition of ConA-induced BALB/c mouse T cell proliferation Inhibition of ConA-induced BALB/c mouse T cell proliferation	[PMID: 17081761]

Chemical Information

CAS No. 5140-38-5
Molecular Weight 321.33
Formula C₁₉H₁₅NO₄
SMILES

O=C1C2=NC=CC3=C(C(OC)=C(C(C4=C1C=CC=C4)=C23)OC)OC
Synonyms

Liridine; Homomoschatoline
Structure Classification
- Alkaloids
- Other Alkaloids
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (271 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Novel total syntheses of oxoaporphine alkaloids enabled by mild Cu-catalyzed tandem oxidation/aromatization of 1-Bn-DHIQs

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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Biological Activity
- Description
Chemical Information
Purity & Documentation
References

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O-Methylmoschatoline

All Endogenous Metabolite Isoforms

Biological Activity

Chemical Information

Purity & Documentation

References

Calculators

Help & FAQs

O-Methylmoschatoline Related Classifications

HY-135492 Related Classifications