PCIDB

KNApSAcK Metabolite C00002456

Metabolite

KNApSAcK Entry

id C00002456
Name Chalepensin
CAS RN 13164-03-9
Standard InChI InChI=1S/C16H14O3/c1-4-16(2,3)12-8-11-7-10-5-6-18-13(10)9-14(11)19-15(12)17/h4-9H,1H2,2-3H3
Standard InChI (Main Layer) InChI=1S/C16H14O3/c1-4-16(2,3)12-8-11-7-10-5-6-18-13(10)9-14(11)19-15(12)17/h4-9H,1H2,2-3H3

Cluster

Phytochemical cluster No. 25
KCF-S cluster No. 3930

Link

ChEMBL

By standard InChI CHEMBL1333931
By standard InChI Main Layer CHEMBL1333931

KEGG

By LinkDB C09165

CTD

By CAS RN C020740

Human Protein / Gene in interaction

7 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme CHEMBL1333931 CHEMBL1613818 (1)
6 / 4
P42858 Huntingtin Unclassified protein CHEMBL1333931 CHEMBL1613918 (1)
1 / 1
O75496 Geminin Unclassified protein CHEMBL1333931 CHEMBL2114780 (1)
0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL1333931 CHEMBL1794401 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL1333931 CHEMBL1794483 (1)
0 / 0
O75164 Lysine-specific demethylase 4A Enzyme CHEMBL1333931 CHEMBL1737991 (1)
0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein CHEMBL1333931 CHEMBL2354287 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#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
#143100 Huntington disease; hd P42858
#168600 Parkinson disease, late-onset; pd P04062

KEGG DISEASE (6)

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)
H00059 Huntington's disease (HD) P42858 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)