Species

KNApSAcK Entry

Organism name Cocculus pendulus (Forsk.) Diels
Genus Cocculus
Family Menispermaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Cocculus
Linked NCBI taxonomy ID 13440
Linked level genus

Family

Family in NCBI taxonomy Menispermaceae
ID 3455

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (31)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00025633 External link 512 (+)-1,2-Dehydro-2'-nortelobine
/ (+)-1',2'-Didehydro-2-nortelobine
CHEMBL505958
No. 10 No. 4
C00025634 External link 512 1,2-Dehydroapateline
/ (+)-1,2-Dehydroapateline
CHEMBL390616
No. 10 No. 4
C00025635 External link 512 (+)-1,2-Dehydrokohatamine
No. 10 No. 4
C00025636 External link 512 (+)-1,2-Dehydrokohatine
No. 10 No. 4
C00025644 External link 512 (+)-5'-Hydroxytelobine
No. 10 No. 4
C00025650 External link 512 Cheratamine
/ (+)-Cheratamine
No. 10 No. 4
C00025653 External link 512 Efirine
/ Cocsulin
/ (+)-Efirine
/ Trigilletine
/ (+)-Cocsuline
/ (+)-Trigilletine
CHEMBL447886
CHEMBL2063766
No. 10 No. 4
C00025663 External link 512 Kohatamine
/ (+)-Kohatamine
No. 10 No. 4
C00025664 External link 512 Kohatine
/ (+)-Kohatine
/ 5-Hydroxy-(+)-cocsoline
No. 10 No. 4
C00025665 External link 512 Kurramine
/ (+)-Kurramine
/ O-Demethyl-1,2-dehydroapateline
No. 10 No. 4
C00025673 External link 512 1'-Epicocsuline
/ N-Methylapateline
/ (+)-N-Methylapateline
CHEMBL447886
CHEMBL2063766
No. 10 No. 4
C00025677 External link 512 (+)-Norpenduline
/ 2-Demethylpenduline
CHEMBL510273
No. 10 No. 4
C00025678 External link 512 O,O-Dimethylcocsulinine
/ (+)-O,O-Dimethylcocsulinine
No. 10 No. 4
C00025682 External link 512 Pendilinine
/ (+)-Pendilinine
/ O-Methylpendine
/ N2-Demethyl-O,O-dimethylpendulinine
/ O,O-Dimethyl-2'-N-demethylpendulinine
No. 10 No. 4
C00025683 External link 512 Penduline
/ (+)-Penduline
CHEMBL504323
CHEMBL507540
CHEMBL1198334
4 / 3 / 4 No. 10 No. 4
C00025986 External link 512 O-Methylcocsulinine
No. 10 No. 4
C00025686 External link 512 (+)-Siddiquine
No. 10 No. 4
C00025689 External link 512 Tricordatine
/ (+)-Tricordatine
CHEMBL443597
No. 10 No. 4
C00025753 External link 512 1'-Epikohatine
/ 5'-Hydroxyapateline
/ (+)-5-Hydroxyapateline
No. 10 No. 4
C00026008 External link 512 Pendine
/ (+)-Pendine
No. 10 No. 4
C00025815 External link 512 Cocsilinine
/ N,N'-Didemethylcocsulinine
No. 10 No. 4
C00025816 External link 512 Cocsoline
/ (+)-Cocsoline
/ 2'-Demethylcocsuline
No. 10 No. 4
C00025817 External link 512 Cocsulinine
No. 10 No. 4
C00025914 External link 512 Isotrilobin
/ Homotrilobin
/ Homotrilobine
/ (+)-Isotrilobine
/ N,O-Dimethylcocsoline
CHEMBL503241
CHEMBL448550
No. 10 No. 4
C00025938 External link 512 Menisarine
/ (+)-Menisarine
No. 10 No. 4
C00025965 External link 512 Nortrilobine
/ N2'-Demethyltrilobine
No. 10 No. 4
C00025685 External link 512 (+)-Siddiquamine
No. 10 No. 4
C00026144 External link 512 Sinactine
/ Tetrahydroepiberberine
No. 37 No. 4
C00025812 External link 512 Coclaurine
/ (S)-Coclaurine
/ (-)-Coclaurine
CHEMBL256448
CHEMBL453291
CHEMBL446211
C004690
8 / 17 / 10 No. 253 No. 4
C00026019 External link 512 Punjabine
/ (-)-Punjabine
No. 815
C00026101 External link 512 (+)-Ophiocarpinone
No. 820 No. 4

Human Protein / Gene in interactions

12 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P14618 Pyruvate kinase PKM Enzyme C00025812 0 / 0
P04062 Glucosylceramidase Enzyme C00025812 6 / 4
P54750 Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A PDE_1A C00025683 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00025683 0 / 0
O75496 Geminin Unclassified protein C00025812 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00025812 7 / 3
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00025683 3 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00025683 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00025812 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00025812 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00025812 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00025812 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#600274 Frontotemporal dementia; ftd P10636
#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
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#166350 Osseous heteroplasia, progressive; poh P63092
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (14)

KEGG 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)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)