AMORPHISPIRONONE

Structure

2D structure of AMORPHISPIRONONE
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 3086653

Names and identifiers

Name

AMORPHISPIRONONE

IUPAC name

(1R,7a'R,10a'S)-3,4-dimethoxy-3',3'-dimethyl-10',10a'-dihydro-3'H-spiro[cyclohexane-1,8'-furo[3,4-b]pyrano[2,3-h]chromene]-2,4-diene-6,7'(7a'H)-dione

SMILES

CC1(C=CC2=C(O1)C=CC3=C2O[C@@H]4CO[C@@]5([C@@H]4C3=O)C=C(C(=CC5=O)OC)OC)C

General information

Molecular formula

C23H22O7

Molecular weight

410.42 g/mol

Monoisotopic mass

410.1366 Da

Classification

Pathway:
Superclass:
-
Class:
-
Glycoside:
No

Chemical classification: NPClassifier (Kim et al., 2021)

Plants with the compound

Plant Plant part Amount Reference
Amorpha fruticosa L. aerial parts -
Li, L.P., Wang, H.K., Chang, J.J., Mcphail, A.T., Mcphaildr, Terada, H., Konoshima, T., Kokumai, M., Kozuka, M., Estes, J.R., Lee, K.H. (1993). Antitumor agents, 138. rotenoids and isoflavones as cytotoxic constituents from Amorpha fruticosa. J Nat Prod, 56(5), 690-698 doi:10.1021/np50095a005
Amorpha fruticosa L. leaf -
Dat, N.T., Lee, J.H., Lee, K., Hong, Y.S., Kim, Y.H., Lee, J.J. (2008). Phenolic constituents of Amorpha fruticosa that inhibit nf-kb activation and related gene expression J Nat Prod, 71(10), 1696-1700 doi:10.1021/np800383q
Amorpha fruticosa L. leaf -
Terada, H., Kokumai, M., Konoshima, T., Kozuka, M., Haruna, M., Ito, K., Lee, K.H., Li, L.P., Wang, H.K. (1992). A novel rotenoid from Amorpha fruticosa. Tennen Yuki Kagobutsu Toronkai Koen Yoshishu, 34, 502-509