Species

KNApSAcK Entry

Organism name Hypericum geminiflorum
Genus Hypericum
Family Hypericaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Hypericum geminiflorum
Linked NCBI taxonomy ID 860794
Linked level species

Family

Family in NCBI taxonomy Hypericaceae
ID 629714

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (18)

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
C00036379 External link 512 1,3,8-Trihydroxy-2-methoxyxanthone
No. 3 No. 15
C00049558 External link 512 4-Hydroxy-1,2-dimethoxy-xanthone
CHEMBL2029865
No. 3 No. 15
C00049557 External link 512 6,7-Dihydroxy-1,3-dimethoxyxanthone
No. 3 No. 15
C00038114 External link 512 1,5-Dihydroxy-6-methoxyxanthone
No. 3 No. 15
C00038112 External link 512 1,3,8-Trihydroxy-4-methoxyxanthone
No. 3 No. 15
C00038200 External link 512 2,3-Dimethoxyxanthone
CHEMBL1434162
14 / 16 / 16 No. 35 No. 15
C00029364 External link 512 Euxanthone
/ 1,7-Dihydroxyxanthone
CHEMBL389166
C404221
1 / 0 / 0 No. 76 No. 15
C00038192 External link 512 1-Hydroxyxanthone
CHEMBL187368
C478872
1 / 1 / 1 No. 76 No. 15
C00039394 External link 512 Hyperielliptone HD
CHEMBL465510
No. 338
C00039393 External link 512 Hyperielliptone HC
No. 338
C00038677 External link 512 Cadensin D
CHEMBL465511
No. 338
C00049588 External link 512 Gemixanthone A
No. 338
C00039392 External link 512 Hyperielliptone HB
/ (-)-Hyperielliptone HB
CHEMBL511791
CHEMBL2023366
1 / 1 / 1 No. 1011
C00014453 External link 512 Gemichalcone A
/ 3'-(4-Feruloyloxy-3-methylbutyl-2(Z)-enyl)-4,2',4'-trihydroxychalcone
CHEMBL2164984
CHEMBL2164987
No. 1706
C00014483 External link 512 Gemichalcone C
/ 3'-(4-Feruloyloxy-3-methylbutyl-2(Z)-enyl)-2,4,2',4'-tetrahydroxychalcone
CHEMBL463638
CHEMBL499860
1 / 2 / 2 No. 1706
C00014451 External link 512 Isogemichalcone B
/ 3'-(4-Coumaroyloxy-3-methylbutyl-2(E)-enyl)-4,2',4'-trihydroxychalcone
CHEMBL497716
CHEMBL517334
2 / 0 / 3 No. 1706
C00014452 External link 512 Gemichalcone B
/ 3'-(4-Coumaroyloxy-3-methylbutyl-2(Z)-enyl)-4,2',4'-trihydroxychalcone
CHEMBL497716
CHEMBL517334
2 / 0 / 3 No. 1706
C00039391 External link 512 Hyperielliptone HA
/ (-)-Hyperielliptone HA
No. 7669

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00014451 C00014452 0 / 3
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00014451 C00014452 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00038200 0 / 0
P37840 Alpha-synuclein Unclassified protein C00038200 4 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00039392 1 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00038192 1 / 1
P35610 Sterol O-acyltransferase 1 Enzyme C00029364 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00038200 2 / 2
P39748 Flap endonuclease 1 Enzyme C00038200 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00038200 0 / 0
P04062 Glucosylceramidase Enzyme C00038200 6 / 4
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00014483 2 / 2
O15118 Niemann-Pick C1 protein Unclassified protein C00038200 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00038200 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00038200 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00038200 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00038200 0 / 0
O00255 Menin Unclassified protein C00038200 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00038200 1 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00038200 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#300615 Brunner syndrome P21397
#127750 Dementia, lewy body; dlb P37840
#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
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P04062
P37840
#278300 Xanthinuria, type i P47989

KEGG DISEASE (23)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00066 Lewy body dementia (LBD) P04062 (related)
P37840 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (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)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00192 Xanthinuria P47989 (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)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)