PCIDB

KNApSAcK Metabolite C00032389

Metabolite

KNApSAcK Entry

id C00032389
Name Tricalysioside B / (-)-Tricalysioside B
CAS RN 438632-44-1
Standard InChI InChI=1S/C26H38O9/c1-24-6-5-16-14(8-19(29)33-16)15(24)4-7-25-9-13(2-3-18(24)25)26(11-25,12-28)35-23-22(32)21(31)20(30)17(10-27)34-23/h8,13,15-18,20-23,27-28,30-32H,2-7,9-12H2,1H3/t13-,15-,16-,17-,18+,20-,21+,22-,23+,24-,25+,26+/m1/s1
Standard InChI (Main Layer) InChI=1S/C26H38O9/c1-24-6-5-16-14(8-19(29)33-16)15(24)4-7-25-9-13(2-3-18(24)25)26(11-25,12-28)35-23-22(32)21(31)20(30)17(10-27)34-23/h8,13,15-18,20-23,27-28,30-32H,2-7,9-12H2,1H3

Cluster

Phytochemical cluster
KCF-S cluster No. 1528

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL1448560

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
asterids 1

Family

family name count
Rubiaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Tricalysia dubia OHWI 58438 Rubiaceae 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)
P04062 Glucosylceramidase Enzyme CHEMBL1448560 CHEMBL1613818 (1)
6 / 4
O75496 Geminin Unclassified protein CHEMBL1448560 CHEMBL2114843 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#168600 Parkinson disease, late-onset; pd P04062

KEGG DISEASE (4)

KEGG disease name UniProt
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)