(Q27105565)

Senegalensin (English)

5 October 2016

chemical formula

C₂₅H₂₈O₅

1 reference

Senegalensin (English)

5 October 2016

canonical SMILES

CC(=CCC1=C(C2=C(C(=C1O)CC=C(C)C)OC(CC2=O)C3=CC=C(C=C3)O)O)C

1 reference

Senegalensin (English)

5 October 2016

isomeric SMILES

CC(=CCC1=C(C2=C(C(=C1O)CC=C(C)C)O[C@@H](CC2=O)C3=CC=C(C=C3)O)O)C

1 reference

Flavanoids and pterocarpans from the bark of Erythrina fusca

Senegalensin (English)

5 October 2016

2 references

A New Pterocarpan from Erythrina fusca

Lupinus luteus

2 references

Prenylated flavonoids in the roots of yellow lupin

Seventeen isoflavonoids from Lupinus albus roots

Derris laxiflora

1 reference

Prenylated Flavanones fromDerris laxiflora

Sophora tetraptera

1 reference

Flavonoid compounds in roots of Sophora tetraptera

Macaranga conifera

1 reference

Prenylated flavonoids of the leaves of Macaranga conifera with inhibitory activity against cyclooxygenase-2.

Erythrina senegalensis

3 references

Senegalensein, A Novel Prenylated Flavanone from Erythrina senegalensis

A new prenylated isoflavone and long chain esters from two Erythrina species

Erysenegalenseins H and I: Two New Isoflavones from Erythrina senegalensis1.

Lonchocarpus minimiflorus

2 references

Flavanones from Lonchocarpus minimiflorus

Antibacterial activity of lonchocarpol A.

Melipotis perpendicularis

1 reference

Antibacterial activity of lonchocarpol A.

Monotes africanus

1 reference

Anti-HIV prenylated flavonoids from Monotes africanus

Monotes engleri

1 reference

Prenylated Flavanones fromMonotes engleri: On-line Structure Elucidation by LC/UV/NMR

Citrus medica

2 references

Anti-inflammatory principles from the stem and root barks of Citrus medica

Chemical Constituents and Cytotoxicity from the Stem Bark of Citrus medica

Limonia acidissima

1 reference

Antimicrobial constituents from the stem bark of Feronia limonia.

Flemingia macrophylla

1 reference

Neuroprotective flavonoids from Flemingia macrophylla

Glycyrrhiza pallidiflora

1 reference

Structures of Prenylated Dihydrochalcone, Gancaonin J and Homoisoflavonone, Gancaonin K from Glycyrrhiza pallidiflora

Humulus lupulus

2 references

Estrogens and congeners from spent hops (Humulus lupulus).

Prenylflavonoid variation in Humulus lupulus: distribution and taxonomic significance of xanthogalenol and 4'-O-methylxanthohumol

Erythrina sigmoidea

1 reference

Auriculatin 4'-O-Glucoside: A New Prenylated Isoflavone Glycoside from Erythrina eriotricha1

Erythrina suberosa

1 reference

Revised structures for senegalensin and euchrenone b(10).

Monotes africana

1 reference

Anti-HIV prenylated flavonoids from Monotes africanus

Citrus medica var. sarcodactylis

2 references

Anti-inflammatory principles from the stem and root barks of Citrus medica

Chemical Constituents and Cytotoxicity from the Stem Bark of Citrus medica

Maclura tricuspidata

1 reference

Prenylated and benzylated flavonoids from the fruits of Cudrania tricuspidata

Deguelia scandens

1 reference

Prenylated Isoflavones from Derris scandens.

Identifiers

InChI

InChI=1S/C25H28O5/c1-14(2)5-11-18-23(28)19(12-6-15(3)4)25-22(24(18)29)20(27)13-21(30-25)16-7-9-17(26)10-8-16/h5-10,21,26,28-29H,11-13H2,1-4H3/t21-/m0/s1

1 reference

Senegalensin (English)

5 October 2016

2 references

Senegalensin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

6,8-diprenylnaringenin (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=68236-11-3

9 April 2021

1 reference

(2S)-5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methyl-2-buten-1-yl)-2,3-dihydro-4H-chromen-4-one (English)

5 October 2016

2 references

Senegalensin (English)

matched by identifier from

5 October 2016

Reaxys registry number

6940246

1 reference

6,8-diprenylnaringenin (English)

5 October 2016

ChEBI ID

2156

mapping relation type

2 references

6,8-diprenylnaringenin (English)

matched by identifier from

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C25H28O5/c1-14(2)5-11-18-23(28)19(12-6-15(3)4)25-22(24(18)29)20(27)13-21(30-25)16-7-9-17(26)10-8-16/h5-10,21,26,28-29H,11-13H2,1-4H3/t21-/m0/s1

1 reference

splash10-0a4i-0000900000-b70bcc7844fc22df5b27

LONCHOCARPOL A (English)

5 October 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-0a4i-0000900000-44d2ab7f3397cb160d5b

0 references

splash10-0a4i-0000900000-59a8071756ad08d84dc9

0 references

splash10-000i-0290300000-748b87f10e198b7761d2

0 references

splash10-014i-0950000000-f783637c2d4dd348fc94

0 references

DSSTox substance ID

DTXSID20218408

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

matched by identifier from

DSSTOX compound identifier

0 references

1 reference

6,8-diprenylnaringenin (English)

5 October 2016

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

6,8-diprenylnaringenin (English)

5 October 2016

1 reference