2. Natural Products
  3. Plants Phenylpropanoids
  4. Compositae Umbelliferae Coumarins
  5. Chrysanthemum × morifolium (Ramat.) Hemsl.
  6. Isopropylidenylacetyl-marmesin

Isopropylidenylacetyl-marmesin  (Synonyms: (±)-Prantschimgin)

Cat. No.: HY-N4178
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Isopropylidenylacetyl-marmesin ((±)-Prantschimgin) is a coumarin isolated from the roots of F. bracteata.

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

Isopropylidenylacetyl-marmesin Chemical Structure

Isopropylidenylacetyl-marmesin Chemical Structure

CAS No. : 35178-20-2

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Isopropylidenylacetyl-marmesin Related Antibodies

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Description

Isopropylidenylacetyl-marmesin ((±)-Prantschimgin) is a coumarin isolated from the roots of F. bracteata[1].

Molecular Weight

328.36

Formula

C19H20O5
CAS No.
SMILES

C/C(C)=C\C(OC(C)(C(O1)CC2=C1C=C(O3)C(C=CC3=O)=C2)C)=O
Structure Classification
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
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Isopropylidenylacetyl-marmesin Related Classifications

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This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Isopropylidenylacetyl-marmesin35178-20-2(±)-PrantschimginOthersInhibitorinhibitorinhibit

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