Species

KNApSAcK Entry

Organism name Garcinia cowa
Genus Garcinia
Family Clusiaceae / Clusiaceae-Guttiferae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Garcinia cowa
Linked NCBI taxonomy ID 180103
Linked level species

Family

Family in NCBI taxonomy Clusiaceae
ID 55961

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (26)

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
C00029358 External link 512 1,3,5-Trihydroxy-6-methoxyxanthone
No. 3 No. 15
C00030726 External link 512 Mangostinone
CHEMBL481310
1 / 2 / 2 No. 14 No. 15
C00002963 External link 512 Mangostin
/ alpha-Mangostin
CHEMBL323197
C021053
25 / 27 / 58 0 / 3 No. 14 No. 15
C00035277 External link 512 Cowagarcinone A
No. 14 No. 15
C00029819 External link 512 beta-Mangostin
CHEMBL261706
3 / 0 / 0 No. 14 No. 15
C00034845 External link 512 Fuscaxanthone C
CHEMBL464524
1 / 0 / 0 No. 14 No. 15
C00034828 External link 512 Cowaxanthone E
No. 14 No. 15
C00035280 External link 512 Cowagarcinone E
No. 14 No. 15
C00030834 External link 512 Norcowanin
CHEMBL463409
No. 14 No. 15
C00031249 External link 512 Rubraxanthone
CHEMBL458846
C472155
No. 14 No. 15
C00034825 External link 512 Cowaxanthone B
No. 14 No. 15
C00034823 External link 512 Cowaxanthone
CHEMBL517161
No. 14 No. 15
C00034778 External link 512 7-O-Methylgarcinone E
CHEMBL463410
No. 14 No. 15
C00034822 External link 512 Cowanol
CHEMBL463408
No. 14 No. 15
C00034821 External link 512 Cowanin
CHEMBL458845
No. 14 No. 15
C00035278 External link 512 Cowaxanthone A
/ Cowagarcinone C
No. 15 No. 15
C00034824 External link 512 Cowaxanthone A
No. 15 No. 15
C00034759 External link 512 Cowagarcinone B
/ 1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)xanthone
No. 15 No. 15
C00030161 External link 512 Dulxanthone A
No. 15 No. 15
C00034827 External link 512 Cowaxanthone D
/ Dulcisxanthone F
No. 18 No. 15
C00034826 External link 512 Cowaxanthone C
No. 44
C00035279 External link 512 Cowagarcinone D
No. 44
C00034776 External link 512 6-O-Methylmangostanin
/ (+)-6-O-Methylmangostanin
No. 47 No. 15
C00030721 External link 512 Mangostanin
/ (-)-Mangostanin
CHEMBL1080698
2 / 0 / 0 No. 47 No. 15
C00002968 External link 512 Norathyriol
/ 1,3,6,7-Tetrahydroxyxanthoene
CHEMBL187265
C069053
9 / 10 / 7 4 / 0 No. 71 No. 15
C00029364 External link 512 Euxanthone
/ 1,7-Dihydroxyxanthone
CHEMBL389166
C404221
1 / 0 / 0 No. 76 No. 15

Human Protein / Gene in interactions

34 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q04206 Transcription factor p65 Transcription Factor C00002963 C00029819 C00030721 C00034845 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00002963 C00029819 C00030721 0 / 0
P49327 Fatty acid synthase Transferase C00002963 C00002968 C00029819 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00002963 C00030726 2 / 2
P28482 Mitogen-activated protein kinase 1 Erk C00002963 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002963 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002968 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002963 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002963 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00002963 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002963 2 / 2
P03956 Interstitial collagenase M10A C00002968 0 / 1
P39900 Macrophage metalloelastase M10A C00002968 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00002963 7 / 37
O60906 Sphingomyelin phosphodiesterase 2 Enzyme C00002963 0 / 0
P45452 Collagenase 3 M10A C00002968 1 / 1
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00002963 2 / 0
P14780 Matrix metalloproteinase-9 M10A C00002968 2 / 2
P08253 72 kDa type IV collagenase M10A C00002968 1 / 3
Q00987 E3 ubiquitin-protein ligase Mdm2 Other nuclear protein C00002963 1 / 5
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002963 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002963 2 / 2
O14763 Tumor necrosis factor receptor superfamily member 10B Unclassified protein C00002963 1 / 0
P12821 Angiotensin-converting enzyme M2 C00002968 4 / 2
P35610 Sterol O-acyltransferase 1 Enzyme C00029364 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00002963 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002963 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002963 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00002963 4 / 3
P08254 Stromelysin-1 M10A C00002968 1 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002963 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002963 0 / 0
O00255 Menin Unclassified protein C00002963 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002963 1 / 2

4 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00002968
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00002968
5467 PPARD, FAAR, NR1C2, NUC1, NUCI, NUCII, PPARB peroxisome proliferator-activated receptor delta C00002968
5468 PPARG, CIMT1, GLM1, NR1C3, PPARG1, PPARG2, PPARgamma peroxisome proliferator-activated receptor gamma C00002968

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (37)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#614401 Accelerated tumor formation, susceptibility to; actfs Q00987
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#300615 Brunner syndrome P21397
#114500 Colorectal cancer; crc P18054
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#133239 Esophageal cancer P04637
P18054
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#614519 Hemorrhage, intracerebral, susceptibility to; ich P12821
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#603932 Intervertebral disc disease; idd P14780
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#211980 Lung cancer P04637
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#612624 Microvascular complications of diabetes, susceptibility to, 3; mvcd3 P12821
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#267430 Renal tubular dysgenesis; rtd P12821
#602111 Spondyloepimetaphyseal dysplasia, missouri type P45452
#275355 Squamous cell carcinoma, head and neck; hnscc O14763
P04637
#601367 Stroke, ischemic P12821
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (63)

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)
H00028 Choriocarcinoma P03956 (related)
P04637 (related)
P08253 (related)
Q00987 (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)
P08253 (related)
P14780 (related)
Q00987 (related)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
Q00987 (related)
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)
Q00987 (related)
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)
H00472 Torg-Winchester syndrome P08253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00083 Allograft rejection P12821 (related)
H00575 Renal tubular dysgenesis P12821 (related)
H00479 Metaphyseal dysplasias P14780 (related)
P45452 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00548 Brunner syndrome P21397 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00037 Alveolar rhabdomyosarcoma Q00987 (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)
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)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D058186 Acute Kidney Injury C00002963
D009202 Cardiomyopathies C00002963
D009203 Myocardial Infarction C00002963