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Murraya paniculata L. 

Common name : Orange jasmine, Kamini 

Frequently asked questions

S.No
Phytochemical Name
Phytochemical ID
synonym
Part
2D structure
3D structure
1
Yuehcukene
N.A
Leaves
2
1β-(3,-indolyl-7,9α,9β-trimethyl-5β,8,9,10β-tetrahydroindano-[2,3-b] indole
N.A
leaves
3
murrayacarine
CID_11977126
N.A
Root bark Flowers
4
murrayaculatine
CID_101416188
N.A
Root bark flowers
5
3’,4’,5,5’,7,8-hexa-methoxyflavone
N.A
Leaves
6
3,3’, 4’,5,5’,7,8-heptamethoxyflavone
N.A
Leaves
7
3,5,7,3’,4’,5’- hexamethoxyflavone
CID_634113
Hexa-O-methylmyricitin Myricetin hexamethyl ether
Flower
8
meranzin hydrate
CID_5070783
8-(2,3-dihydroxy-3-methylbutyl)-7-methoxychromen-2-one Meranzin (hydrate)
Leaves
9
murpanidin
CID_6426907
8-[(1S,2S)-1,2-dihydroxy-3-methylbut-3-enyl]-7-methoxychromen-2-one
Leaves
10
murragatin
N.A
Leaves
11
3-formylindole,omphalocar-pin,5,7-dimethoxy-8-(3’-methyl-2’- oxobuty coumarin
N.A
Root bark
12
coumurrayin
CID_176911
5,7-dimethoxy-8-(3-methylbut-2-enyl)chromen-2-one
Root bark

The cytotoxic activity exhibited a prominent selective effect against hepatoma cancer cells (IC50 value =63.7 μg/mL) compared with normal fibroblasts (IC50 value =195.0 μg/mL), whereas the β-caryophyllene showed low cytotoxicity.

Source : Sayar et al.,2014

Disclaimer: The main motive behind the construction of this database is to compile information from the scientific literature on Indian medicinal plants to aid ongoing research efforts in the field of computational drug discovery.The curated data should be used only for research purposes and not for any self-diagnosis or any medical treatment.

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