Karanjin

Karanjin
Chemical structure of karanjin
Names
IUPAC name
3-Methoxyfuro[2′′,3′′:7,8]flavone
Systematic IUPAC name
3-Methoxy-2-phenyl-4H-furo[2,3-h][1]benzopyran-4-one
Identifiers
CAS Number
  • 521-88-0 checkY
3D model (JSmol)
  • Interactive image
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ChEMBL
  • ChEMBL208484 checkY
ChemSpider
  • 90925 checkY
ECHA InfoCard 100.007.565 Edit this at Wikidata
PubChem CID
  • 100633
UNII
  • WV7IM0I02M checkY
CompTox Dashboard (EPA)
  • DTXSID20200106 Edit this at Wikidata
InChI
  • InChI=1S/C18H12O4/c1-20-18-15(19)13-7-8-14-12(9-10-21-14)17(13)22-16(18)11-5-3-2-4-6-11/h2-10H,1H3 checkY
    Key: LKPQNZRGGNOPPU-UHFFFAOYSA-N checkY
  • C1(=C(OC2=C(C1=O)C=CC3=C2C=CO3)C4=CC=CC=C4)OC
  • O=C2C(\OC)=C(/Oc3c1ccoc1ccc23)c4ccccc4
Properties
Chemical formula
C18H12O4
Molar mass 292.290 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

Karanjin is a furanoflavonol, a type of flavonoid. It is obtained from the seeds of the karanja tree (Millettia pinnata or Pongamia glabra Vent.), a tree growing wild in south India. Karanjin is an acaricide and insecticide.[citation needed] Karanjin is reported to have nitrification inhibitory properties.[1]

References

  1. ^ Majumdar, Deepanjan; Pandya, Bhavesh; Arora, Anu; Dhara, Soni (2004). "Potential use of karanjin (3-methoxy furano-2′,3′,7,8-flavone) as a nitrification inhibitor in different soil types". Archives of Agronomy and Soil Science. 50 (4–5): 455. doi:10.1080/03650340410001689406. S2CID 96706313.
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Flavonols and their conjugates
Backbone
Aglycones
Flavonols
Aglycones
Conjugates
Glycosides of herbacetin
Glycosides of kaempferol
  • Afzelin (Kaempferol 3-rhamnoside)
  • Astragalin (kaempferol 3-O-glucoside)
  • Kaempferitrin (kaempferol 3,7-dirhamnoside)
  • Juglanin (Kaempferol 3-O-arabinoside)
  • Kaempferol 3-alpha-L-arabinopyranoside
  • Kaempferol 3-alpha-D-arabinopyranoside
  • Kaempferol 7-alpha-L-arabinoside
  • Kaempferol 7-O-glucoside
  • Kaempferol 3-lathyroside
  • Kaempferol 4'-rhamnoside
  • Kaempferol 5-rhamnoside
  • Kaempferol 7-rhamnoside
  • Kaempferol 7-O-alpha-L-rhamnofuranoside
  • Kaempferol 3-xyloside
  • Kaempferol 7-xyloside
  • Robinin (kaempferol-3-O-robinoside-7-O-rhamnoside)
  • Kaempferol 3-O-rutinoside
  • Sophoraflavonoloside (Kaempferol 3-O-sophoroside)
  • Trifolin (Kaempferol 3-O-beta-D-galactoside)
Glycosides of myricetin
Conjugates of quercetin
Sulfates
Glycosides
O-Methylated flavonols
Aglycones
Glycosides
of isorhamnetin
  • Narcissin (Isorhamnetin 3-O-rutinoside)
  • Isorhamnetin 3-O-glucoside
  • Tamarixetin 7-rutinoside
other
  • Azalein (Azaleatin 3-O-α-L-rhamnoside)
  • Centaurein (Centaureidin 7-O-glucoside)
  • Eupalin (Eupalitin 3-0-rhamnoside)
  • Eupatolin (Eupatolitin 3-O-rhamnoside)
  • Jacein (Jaceidin 7-O-glucoside)
  • Patulitrin (Patuletin 7-O-glucoside
  • Xanthorhamnin (Rhamnetin glycoside)
Derivative flavonols
Aglycones
  • Noricaritin
  • Dihydronoricaritin
Glycosides
  • Amurensin
  • Icariin
  • Phelloside
  • Dihydrophelloside
  • Rutin S
Pyranoflavonols
Aglycones
Furanoflavonols
Aglycones
  • Karanjin
Glycosides
  • Pongamoside A, B and C
Semisynthetic
Glycosides


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