KCF-S cluster No. 677 (11 metabolites)

Corresponding Phytochemical cluster No. 2



Metabolite list (11)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00002013 External link 512 Alexine
CHEMBL469429
CHEMBL1552977
CHEMBL2219815
2 / 4 / 2
C00002023 External link 512 Australine
CHEMBL469429
CHEMBL1552977
CHEMBL2219815
C059794
2 / 4 / 2
C00002028 External link 512 Castanospermine
CHEMBL67964
CHEMBL311226
CHEMBL421040
CHEMBL464490
CHEMBL1213468
CHEMBL1438313
CHEMBL1980354
C037806
14 / 13 / 16
C00002050 External link 512 Lentiginosine
CHEMBL63254
C063984
C00002075 External link 512 Swainsonine
/ (-)-Swainsonine
CHEMBL63139
CHEMBL292716
CHEMBL302300
CHEMBL65098
CHEMBL371197
D017026
4 / 2 / 4
C00036485 External link 512 2-Epilentiginosine
/ (-)-2-Epilentiginosine
CHEMBL63254
C00036523 External link 512 3-epi-Australine
/ 3,7a-Diepialexine
CHEMBL469429
CHEMBL1552977
CHEMBL2219815
2 / 4 / 2
C00036605 External link 512 6,7-Diepicastanospermine
/ (+)-6,7-Diepicastanospermine
CHEMBL67964
CHEMBL311226
CHEMBL421040
CHEMBL464490
CHEMBL1213468
CHEMBL1438313
CHEMBL1980354
14 / 13 / 16
C00036617 External link 512 6-Epicastanospermine
/ (+)-6-Epicastanospermine
CHEMBL67964
CHEMBL311226
CHEMBL421040
CHEMBL464490
CHEMBL1213468
CHEMBL1438313
CHEMBL1980354
14 / 13 / 16
C00036643 External link 512 7a-Epialexaflorine
C00036886 External link 512 Casuarine
/ (+)-Casuarine

Human Protein / Gene in interactions

19 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10253 Lysosomal alpha-glucosidase Hydrolase C00002013 C00002023 C00002028 C00036523 C00036605 C00036617 1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00002028 C00036605 C00036617 0 / 0
Q14697 Neutral alpha-glucosidase AB Enzyme C00002028 C00036605 C00036617 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002028 C00036605 C00036617 1 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00002013 C00002023 C00036523 3 / 1
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002028 C00036605 C00036617 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002028 C00036605 C00036617 0 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002028 C00036605 C00036617 1 / 2
O75496 Geminin Unclassified protein C00002028 C00036605 C00036617 0 / 0
P04062 Glucosylceramidase Enzyme C00002028 C00036605 C00036617 6 / 4
Q9UBT6 DNA polymerase kappa Enzyme C00002028 C00036605 C00036617 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002028 C00036605 C00036617 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002028 C00036605 C00036617 0 / 1
O00255 Menin Unclassified protein C00002028 C00036605 C00036617 2 / 5
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002028 C00036605 C00036617 0 / 0
O00754 Lysosomal alpha-mannosidase Enzyme C00002075 1 / 2
P06239 Tyrosine-protein kinase Lck Src C00002075 0 / 1
O43561 Linker for activation of T-cells family member 1 Unclassified protein C00002075 0 / 0
P43403 Tyrosine-protein kinase ZAP-70 Syk C00002075 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#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
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#248500 Mannosidosis, alpha b, lysosomal; mansa O00754
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#168600 Parkinson disease, late-onset; pd P04062
#269840 Selective t-cell defect; stcd P43403
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828

KEGG DISEASE (21)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00139 alpha-Mannosidosis O00754 (related)
H00422 Glycoproteinoses O00754 (related)
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)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
P43403 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00005 Chronic lymphocytic leukemia (CLL) P43403 (marker)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)