Metabolite

KNApSAcK Entry

id C00036467
Name Leonuriside A / 2,6-Dimethoxy-p-hydroquinone 1-O-beta-glucopyranoside
CAS RN 121748-12-7
Standard InChI InChI=1S/C14H20O9/c1-20-7-3-6(16)4-8(21-2)13(7)23-14-12(19)11(18)10(17)9(5-15)22-14/h3-4,9-12,14-19H,5H2,1-2H3/t9-,10-,11+,12-,14+/m1/s1
Standard InChI (Main Layer) InChI=1S/C14H20O9/c1-20-7-3-6(16)4-8(21-2)13(7)23-14-12(19)11(18)10(17)9(5-15)22-14/h3-4,9-12,14-19H,5H2,1-2H3

Cluster

Phytochemical cluster No. 6
KCF-S cluster No. 678

Link

ChEMBL

By standard InChI CHEMBL464406
By standard InChI Main Layer CHEMBL464406

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
asterids 2

Family

family name count
Acanthaceae 1
Lamiaceae 1

List (2)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Acanthus ilicifolius 328098 Acanthaceae asterids Viridiplantae
Clerodendrum inerme 49994 Lamiaceae asterids Viridiplantae

Human Protein / Gene in interaction

2 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr CHEMBL464406 CHEMBL980220 (1)
0 / 0
P00734 Prothrombin S1A CHEMBL464406 CHEMBL976587 (1)
4 / 2

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (2)

KEGG disease name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)