Species

KNApSAcK Entry

Organism name Catha edulis
Genus Catha
Family Celastraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Catha edulis
Linked NCBI taxonomy ID 123405
Linked level species

Family

Family in NCBI taxonomy Celastraceae
ID 4305

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Natural Activity

List (20)

Species Activity
Catha edulis (vahl) Forrsk. Ex Endl. Anorectic
Catha edulis (vahl) Forrsk. Ex Endl. Aperitif
Catha edulis (vahl) Forrsk. Ex Endl. Aphrodisiac
Catha edulis (vahl) Forrsk. Ex Endl. Astringent
Catha edulis (vahl) Forrsk. Ex Endl. Cardiotonic
Catha edulis (vahl) Forrsk. Ex Endl. Cardiotoxic
Catha edulis (vahl) Forrsk. Ex Endl. Carminative
Catha edulis (vahl) Forrsk. Ex Endl. CNS-Stimulant
Catha edulis (vahl) Forrsk. Ex Endl. Euphoriant
Catha edulis (vahl) Forrsk. Ex Endl. Hypertensive
Catha edulis (vahl) Forrsk. Ex Endl. Inebrian
Catha edulis (vahl) Forrsk. Ex Endl. Insecticide
Catha edulis (vahl) Forrsk. Ex Endl. Mutagenic
Catha edulis (vahl) Forrsk. Ex Endl. Mydriatic
Catha edulis (vahl) Forrsk. Ex Endl. Myodepressant
Catha edulis (vahl) Forrsk. Ex Endl. Narctotic
Catha edulis (vahl) Forrsk. Ex Endl. Neurotonic
Catha edulis (vahl) Forrsk. Ex Endl. Stimulant
Catha edulis (vahl) Forrsk. Ex Endl. Sympathomimetic
Catha edulis (vahl) Forrsk. Ex Endl. Tonic

Metabolite list (16)

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
C00008722 External link 512 Ampelopsin 3-rhamnoside
No. 12 No. 14
C00013112 External link 512 Cathedulin K 6
/ Catheduline K 6
No. 43
C00013110 External link 512 Cathedulin K 1
/ Catheduline K 1
No. 43
C00013111 External link 512 Cathedulin K 2
/ Catheduline K 2
No. 43
C00013114 External link 512 Cathedulin K 15
/ Catheduline K 15
No. 43
C00001967 External link 512 Catheduline E2
No. 168
C00013133 External link 512 Cathidine D
No. 168
C00013167 External link 512 Cathedulin 8
/ Cathedulin E 8
/ Catheduline E 8
/ (3alpha,4alpha,5beta,5aalpha,6alpha,7alpha,9alpha,9aalpha)-[6,7-bis(Acetyloxy)-5-(benzoyloxy)octahydro-4-hydroxy-2,2,9-trimethyl-5aH-3,9a-methano-1-benzoxepin-5a-yl]methyl ester 3-pyridinecarboxylic acid
No. 168
C00003753 External link 512 Pristimerin
CHEMBL54804
CHEMBL227090
CHEMBL1486063
C009043
13 / 21 / 47 No. 403 No. 51
C00013113 External link 512 Cathedulin K 12
/ Catheduline K 12
No. 1988
C00013108 External link 512 Cathedulin 5
/ Catheduline 5
/ Catheduline E 5
/ Catheduline E 6 6-acetate
No. 1988
C00013109 External link 512 Cathedulin E6
No. 1988
C00013116 External link 512 Cathedulin K 20
/ Catheduline K 20
No. 1988
C00013115 External link 512 Cathedulin K 19
/ Catheduline K 19
No. 1988
C00001405 External link 512 D-Cathine
CHEMBL61006
CHEMBL136560
CHEMBL1412041
CHEMBL1574804
CHEMBL1616525
CHEMBL1788114
CHEMBL2092846
13 / 13 / 13 No. 2149 No. 9
C00001406 External link 512 D-Cathinone
CHEMBL1124
CHEMBL2104047
1 / 0 / 0 No. 2578 No. 9

Human Protein / Gene in interactions

25 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001405 C00003753 0 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001405 C00003753 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00003753 2 / 0
P02545 Prelamin-A/C Unclassified protein C00001405 11 / 10
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001405 0 / 1
P11473 Vitamin D3 receptor NR1I1 C00003753 2 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00003753 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001405 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001405 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00001405 0 / 0
P35348 Alpha-1A adrenergic receptor Adrenergic receptor C00001405 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00003753 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00003753 4 / 1
P28482 Mitogen-activated protein kinase 1 Erk C00003753 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001405 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00003753 2 / 2
P16050 Arachidonate 15-lipoxygenase Enzyme C00003753 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001405 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001405 1 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00003753 4 / 3
P04637 Cellular tumor antigen p53 Transcription Factor C00003753 7 / 37
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003753 1 / 1
P35368 Alpha-1B adrenergic receptor Adrenergic receptor C00001405 0 / 0
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00001405 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001406 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (34)

OMIM preferred title UniProt
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P18054
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
P18054
#600274 Frontotemporal dementia; ftd P10636
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#211980 Lung cancer P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#275210 Restrictive dermopathy, lethal P02545
#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
#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
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (59)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (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)
H00033 Adrenal carcinoma 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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)