Species

KNApSAcK Entry

Organism name Cocculus laurifolius DC.
Genus Cocculus
Family Menispermaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Cocculus laurifolius
Linked NCBI taxonomy ID 152359
Linked level species

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
C00025653 External link 512 Efirine
/ Cocsulin
/ (+)-Efirine
/ Trigilletine
/ (+)-Cocsuline
/ (+)-Trigilletine
CHEMBL447886
CHEMBL2063766
No. 10 No. 4
C00025313 External link 512 Isotetrandrine
/ Isosinomenine A
/ O-Methylberbamine
/ O,O-Dimethylobamegine
/ O,O'-Dimethylobamegine
/ O,O-Dimethylstepholine
/ O,O'-Dimethylstepholine
CHEMBL176045
CHEMBL367260
CHEMBL445477
CHEMBL449690
CHEMBL504958
CHEMBL504757
26 / 23 / 48 No. 10 No. 4
C00025962 External link 512 Norisoboldine
/ Laurelliptine
/ (+)-Norisoboldine
/ (+)-Laurelliptine
/ (+)-N-Norisoboldine
/ (S)-(+)-Laurelliptine
CHEMBL375902
No. 20 No. 4
C00026094 External link 512 Stepholidine
/ (-)-Stepholidine
CHEMBL487387
CHEMBL2334890
C010513
7 / 4 / 0 0 / 1 No. 37 No. 4
C00026102 External link 512 (+)-Sinactine
No. 37 No. 4
C00025812 External link 512 Coclaurine
/ (S)-Coclaurine
/ (-)-Coclaurine
CHEMBL256448
CHEMBL453291
CHEMBL446211
C004690
8 / 17 / 10 No. 253 No. 4
C00025869 External link 512 Erythramide
No. 273 No. 4
C00025868 External link 512 Erythlaurine
No. 273 No. 4
C00025850 External link 512 Dihydroerysodine
No. 273 No. 4
C00025870 External link 512 Erythroculine
No. 273 No. 4
C00025807 External link 512 Cocculitinine
No. 273 No. 4
C00025802 External link 512 Cocculidine
C015083
No. 273 No. 4
C00025805 External link 512 Kokuline
/ Cocculine
/ (+)-Coculine
No. 273 No. 4
C00025806 External link 512 Cocculitine
No. 273 No. 4
C00024888 External link 512 Garryfoline
/ Laurifoline
/ 15-Epiveatchine
/ (20S)-Garryfoline
No. 274 No. 10
C00025667 External link 512 (+)-Laurifoline
CHEMBL235429
No. 286 No. 4
C00025674 External link 512 N-Methylcorydine
/ (+)-N-Methylcorydine
CHEMBL1617951
No. 286 No. 4
C00001918 External link 512 Cucoline
/ Kukoline
/ Sinomenine
CHEMBL248095
CHEMBL1551847
CHEMBL1555036
CHEMBL1589951
CHEMBL1591798
C009271
9 / 8 / 8 No. 346 No. 4
C00025988 External link 512 Sebiferine
/ (9R)-Sebiferine
/ O-Methylflavinantine
/ (+)-O-Methylflavinanthine
/ (+)-O-Methylflavinantine
CHEMBL224744
CHEMBL490139
C024736
No. 426 No. 4
C00025810 External link 512 Coccuvine
C013447
No. 446 No. 4
C00025811 External link 512 Coccuvinine
/ O-Methylcoccuvine
No. 446 No. 4
C00025272 External link 512 Stepharine
/ (+)-Stepharine
CHEMBL463957
CHEMBL1975436
C009320
No. 688
C00001905 External link 512 Milthanthine
/ Pronuciferine
/ (+)-Pronuciferine
/ N-Methylstepharine
/ N,O-Dimethylcrotonosine
CHEMBL237766
No. 688
C00025799 External link 512 Coccoline
No. 948
C00025800 External link 512 Coccolinine
/ O-Methylcoccoline
No. 948
C00025925 External link 512 Laurifinine
No. 2029
C00025926 External link 512 Laurifonine
/ (+/-)-Laurifonine
No. 2029
C00025904 External link 512 Isococculine
No. 3755 No. 4
C00025804 External link 512 Cocculimine
No. 3755 No. 4
C00025803 External link 512 Cocculidinone
No. 4375
C00025801 External link 512 Coccudienone
No. 4375

Human Protein / Gene in interactions

44 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001918 C00025313 1 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001918 C00025812 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001918 C00025812 4 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001918 C00025313 0 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001918 C00025313 0 / 0
O75496 Geminin Unclassified protein C00025313 C00025812 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00025313 0 / 0
P01375 Tumor necrosis factor Secreted protein C00001918 3 / 4
P04062 Glucosylceramidase Enzyme C00025812 6 / 4
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00025313 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00025313 0 / 0
P21918 D(1B) dopamine receptor Dopamine receptor C00026094 1 / 0
P08183 Multidrug resistance protein 1 drug C00025313 1 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00001918 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00025313 0 / 1
P14416 D(2) dopamine receptor Dopamine receptor C00026094 2 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00025313 0 / 0
P39748 Flap endonuclease 1 Enzyme C00025313 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001918 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00025313 2 / 0
P14618 Pyruvate kinase PKM Enzyme C00025812 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00026094 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00026094 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00025812 7 / 3
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001918 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00025313 0 / 0
P06280 Alpha-galactosidase A Enzyme C00025313 1 / 1
P13726 Tissue factor Membrane receptor C00026094 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00025313 0 / 0
Q99700 Ataxin-2 Unclassified protein C00025313 1 / 1
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00026094 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00025313 1 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00025313 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00025313 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00025313 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00025313 4 / 1
P08908 5-hydroxytryptamine receptor 1A Serotonin receptor C00026094 1 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00025313 7 / 37
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00025812 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00025313 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00025313 1 / 0
O00255 Menin Unclassified protein C00025313 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00025313 1 / 2
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00025812 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (47)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103780 Alcohol dependence P14416
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#606798 Blepharospasm, benign essential P21918
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#133239 Esophageal cancer P04637
#301500 Fabry disease P06280
#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
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610424 Hepatitis b virus, susceptibility to P01375
#145000 Hyperparathyroidism 1; hrpt1 O00255
#612244 Inflammatory bowel disease 13; ibd13 P08183
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#611162 Malaria, susceptibility to P01375
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#159900 Myoclonic dystonia P14416
#166350 Osseous heteroplasia, progressive; poh P63092
#260500 Papilloma of choroid plexus; cpp P04637
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#614674 Periodic fever, menstrual cycle-dependent P08908
#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
#607507 Psoriatic arthritis, susceptibility to P01375
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (62)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00079 Asthma P01375 (related)
H00080 Systemic lupus erythematosus P01375 (related)
P01375 (marker)
H00083 Allograft rejection P01375 (related)
H00084 Graft-versus-host disease P01375 (related)
P01375 (marker)
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)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00125 Fabry disease P06280 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D004409 Dyskinesia, Drug-Induced C00026094