top of page

Barleria lupilina LINDL  

Common name : Hophead

Frequently asked questions

S.No
Phytochemical Name
Phytochemical ID
Synonym
2D structure
3D structure
1
8-O-acetyl-6-O-(p-methoxy-cis-cinnamoyl)shanzhiside
N.A
2
8-O-acetyl-6-O-(p-methoxy-transcinnamoyl)shanzhiside
N.A
3
6-O-p-methoxy-cis-cinnamoyl-8-O-acetylshanzhiside methyl ester
N.A
4
6-O-p-methoxy-trans-cinnamoyl-8-O- acetylshanzhiside methyl ester
N.A
5
8-O-acetylipolamiidic acid
N.A
6
6-O-p-cis-coumaroyl-8-O-acetylshanzhiside methyl ester
N.A
7
6-O-p-trans-coumaroyl-8-O-acetylshanzhiside methyl ester
N.A
8
Ipolamiide
CID_442425
N.A
10
Shanzhiside
CID_11948668
Shanziside
9
Ipolamiidoside
CID_10321418
N.A
11
Shanzhiside methyl ester
CID_13892722
N.A
12
8-O-acetylshanzhiside
N.A
13
Barlerin
CID_162823
8-O-Acetyl shanzhiside methyl ester
14
6-O-acetylshanzhiside methyl ester
CID_24150641
N.A
15
Acetylbarlerin
CID_6453480
N.A
16
Mussaenosidic acid
CID_21633105
N.A
17
Phlorigidoside
N.A
18
Lupulinoside
N.A
19
Forsythoside
CID_76005395
N.A
20
Poliumoside
CID_6442411
N.A
21
(+)-lyoniresinol 3 α-O- β-glucopyranoside
CID_10483388
(+)-Lyoniresinol 9'-O-glucoside pteleifoside G lyoniresinol glucoside
22
1-octen-3-yl- β -primeveroside
N.A
23
Benzyl β -primeveroside
CID_348296141
N.A

lupulina exhibited the highest selective index (SI) (781.5) with lowest 50% inhibitory concentration (IC50) dose (0.02 µg/mL) against HSV-2 cells as reported by Wirotesangthong and Rattanakiat.

Source : Gangaram et al.,2021

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.

​

bottom of page