Organism name | Cocculus pendulus (Forsk.) Diels |
---|---|
Genus | Cocculus |
Family | Menispermaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Cocculus |
---|---|
Linked NCBI taxonomy ID | 13440 |
Linked level | genus |
Family in NCBI taxonomy | Menispermaceae |
---|---|
ID | 3455 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | eudicotyledons |
---|---|
ID | 71240 |
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
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(+)-1,2-Dehydro-2'-nortelobine
/ (+)-1',2'-Didehydro-2-nortelobine |
CHEMBL505958
|
No. 10 | No. 4 |
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|||
C00025634
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1,2-Dehydroapateline
/ (+)-1,2-Dehydroapateline |
CHEMBL390616
|
No. 10 | No. 4 |
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|||
C00025635
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(+)-1,2-Dehydrokohatamine
|
No. 10 | No. 4 |
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||||
C00025636
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(+)-1,2-Dehydrokohatine
|
No. 10 | No. 4 |
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||||
C00025644
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(+)-5'-Hydroxytelobine
|
No. 10 | No. 4 |
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||||
C00025650
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Cheratamine
/ (+)-Cheratamine |
No. 10 | No. 4 |
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||||
C00025653
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Efirine
/ Cocsulin / (+)-Efirine / Trigilletine / (+)-Cocsuline / (+)-Trigilletine |
CHEMBL447886
CHEMBL2063766 |
No. 10 | No. 4 |
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|||
C00025663
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Kohatamine
/ (+)-Kohatamine |
No. 10 | No. 4 |
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||||
C00025664
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Kohatine
/ (+)-Kohatine / 5-Hydroxy-(+)-cocsoline |
No. 10 | No. 4 |
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||||
C00025665
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Kurramine
/ (+)-Kurramine / O-Demethyl-1,2-dehydroapateline |
No. 10 | No. 4 |
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||||
C00025673
![]() |
1'-Epicocsuline
/ N-Methylapateline / (+)-N-Methylapateline |
CHEMBL447886
CHEMBL2063766 |
No. 10 | No. 4 |
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|||
C00025677
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(+)-Norpenduline
/ 2-Demethylpenduline |
CHEMBL510273
|
No. 10 | No. 4 |
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|||
C00025678
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O,O-Dimethylcocsulinine
/ (+)-O,O-Dimethylcocsulinine |
No. 10 | No. 4 |
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||||
C00025682
![]() |
Pendilinine
/ (+)-Pendilinine / O-Methylpendine / N2-Demethyl-O,O-dimethylpendulinine / O,O-Dimethyl-2'-N-demethylpendulinine |
No. 10 | No. 4 |
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||||
C00025683
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Penduline
/ (+)-Penduline |
CHEMBL504323
CHEMBL507540 CHEMBL1198334 |
4 / 3 / 4 | No. 10 | No. 4 |
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||
C00025986
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O-Methylcocsulinine
|
No. 10 | No. 4 |
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||||
C00025686
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(+)-Siddiquine
|
No. 10 | No. 4 |
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||||
C00025689
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Tricordatine
/ (+)-Tricordatine |
CHEMBL443597
|
No. 10 | No. 4 |
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|||
C00025753
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1'-Epikohatine
/ 5'-Hydroxyapateline / (+)-5-Hydroxyapateline |
No. 10 | No. 4 |
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||||
C00026008
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Pendine
/ (+)-Pendine |
No. 10 | No. 4 |
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||||
C00025815
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Cocsilinine
/ N,N'-Didemethylcocsulinine |
No. 10 | No. 4 |
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||||
C00025816
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Cocsoline
/ (+)-Cocsoline / 2'-Demethylcocsuline |
No. 10 | No. 4 |
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||||
C00025817
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Cocsulinine
|
No. 10 | No. 4 |
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||||
C00025914
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Isotrilobin
/ Homotrilobin / Homotrilobine / (+)-Isotrilobine / N,O-Dimethylcocsoline |
CHEMBL503241
CHEMBL448550 |
No. 10 | No. 4 |
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|||
C00025938
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Menisarine
/ (+)-Menisarine |
No. 10 | No. 4 |
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||||
C00025965
![]() |
Nortrilobine
/ N2'-Demethyltrilobine |
No. 10 | No. 4 |
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||||
C00025685
![]() |
(+)-Siddiquamine
|
No. 10 | No. 4 |
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||||
C00026144
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Sinactine
/ Tetrahydroepiberberine |
No. 37 | No. 4 |
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||||
C00025812
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Coclaurine
/ (S)-Coclaurine / (-)-Coclaurine |
CHEMBL256448
CHEMBL453291 CHEMBL446211 |
C004690
|
8 / 17 / 10 | No. 253 | No. 4 |
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|
C00026019
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Punjabine
/ (-)-Punjabine |
No. 815 |
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|||||
C00026101
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(+)-Ophiocarpinone
|
No. 820 | No. 4 |
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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 |
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 | 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)
|