Balanophonin

Balanophonin
Identifiers
CAS Number	118916-57-7 ; (+):: 215319-47-4 ; (-):: 80286-36-8 ;
3D model (JSmol)	Interactive image ;
ChEMBL	ChEMBL253335 ;
ChemSpider	10197147 ; 10366582 ;
PubChem CID	23252258 ;
	InChI InChI=1S/C20H20O6/c1-24-17-10-13(5-6-16(17)23)19-15(11-22)14-8-12(4-3-7-21)9-18(25-2)20(14)26-19/h3-10,15,19,22-23H,11H2,1-2H3/b4-3+/t15-,19+/m0/s1 Key: GWCSSLSMGCFIFR-LNFBDUAVSA-N;
	SMILES COC1=CC(=CC2=C1O[C@@H]([C@H]2CO)C3=CC(=C(C=C3)O)OC)/C=C/C=O;
Properties
Chemical formula	C20H20O6
Molar mass	356.37 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Last updated March 18, 2025

Balanophonin is a neo-lignan. It is a bioactive compound which can be isolated from Dipteryx odorata ^[2] and Balanophora japonica .^[3]

References

↑ "KNApSAcK Metabolite Information - C00033656". www.knapsackfamily.com.
↑ Jang, DS; Park, EJ; Hawthorne, ME; Vigo, JS; Graham, JG; Cabieses, F; Santarsiero, BD; Mesecar, AD; Fong, HH; Mehta, RG; Pezzuto, JM; Kinghorn, AD (2003). "Potential cancer chemopreventive constituents of the seeds of Dipteryx odorata (tonka bean)". J Nat Prod. 66 (5): 583–7. Bibcode:2003JNAtP..66..583J. doi:10.1021/np020522n. PMID 12762787.
↑ Balanophonin, a new neo-lignan from Balanophora japonica Makino, Haruna Mitsumasa, Koube Tomoko, Ito Kazuo and Murata Hiroyuki, Chemical & Pharmaceutical Bulletin, 25-04-1982, 30(4), pages 1525-1527 (abstract)

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[1] "KNApSAcK Metabolite Information - C00033656". www.knapsackfamily.com.

[2] Jang, DS; Park, EJ; Hawthorne, ME; Vigo, JS; Graham, JG; Cabieses, F; Santarsiero, BD; Mesecar, AD; Fong, HH; Mehta, RG; Pezzuto, JM; Kinghorn, AD (2003). "Potential cancer chemopreventive constituents of the seeds of Dipteryx odorata (tonka bean)". J Nat Prod. 66 (5): 583–7. Bibcode:2003JNAtP..66..583J. doi:10.1021/np020522n. PMID 12762787.

[3] Balanophonin, a new neo-lignan from Balanophora japonica Makino, Haruna Mitsumasa, Koube Tomoko, Ito Kazuo and Murata Hiroyuki, Chemical & Pharmaceutical Bulletin, 25-04-1982, 30(4), pages 1525-1527 (abstract)

[1]

[2]

[3]

v t e Types of lignans
Lignans	Arboreol Arctigenin Chamaecypanone A and B Eudesmin Globoidnan A Gmelanone Gmelinol Gummadiol Isootobanone Lyoniresinol Macelignan Matairesinol Obtulignolide Pinoresinol Pluviatilol Podophyllotoxin Secoisolariciresinol Sesamin Sesamolin Steganacin
Lignan glycosides	Arctiin Aviculin (isolariciresinol-9'-rhamnopyranoside) Secoisolariciresinol diglucoside (SDG)
Mammalian lignans (enterolignans)	Enterodiol Enterolactone Lariciresinol Hydroxymatairesinol Syringaresinol
Neolignans	Balanophonin Eusiderin Honokiol Interiotherin Linderin A Magnolol Megaphone 4-O-Methylhonokiol Rhaphidecursinol A Rhaphidecursinol B
Flavonolignans	Cinchonain-Ib Dehydrosilybin Deoxysilycistin Deoxysilydianin Hydnocarpin Hydnowightin Neosilyhermin Palstatin Rhodiolin Salcolin A Salcolin B Scutellaprostin A, B, C, D, E and F Silandrin Silyamandin Silibinin Silybinome Silicristin Silydianin Silyhermin Tricin 4'-O-(erythro-beta-guaiacylglyceryl) ether Tricin 4'-O-(threo-beta-guaiacylglyceryl) ether

Identifiers

CAS Number	118916-57-7 (+):: 215319-47-4 (-):: 80286-36-8 ^[1]^N
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL253335
ChemSpider	10197147 10366582
PubChem CID	23252258
InChI InChI=1S/C20H20O6/c1-24-17-10-13(5-6-16(17)23)19-15(11-22)14-8-12(4-3-7-21)9-18(25-2)20(14)26-19/h3-10,15,19,22-23H,11H2,1-2H3/b4-3+/t15-,19+/m0/s1 Key: GWCSSLSMGCFIFR-LNFBDUAVSA-N
SMILES COC1=CC(=CC2=C1O[C@@H]([C@H]2CO)C3=CC(=C(C=C3)O)OC)/C=C/C=O
Properties
Chemical formula	C₂₀H₂₀O₆
Molar mass	356.37 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references