Species

KNApSAcK Entry

Organism name Agrimonia eupatoria
Genus Agrimonia
Family Rosaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Agrimonia eupatoria
Linked NCBI taxonomy ID 57912
Linked level species

Family

Family in NCBI taxonomy Rosaceae
ID 3745

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Natural Activity

List (23)

Species Activity
Agrimonia eupatoria L. Aggregant
Agrimonia eupatoria L. Antibacterial
Agrimonia eupatoria L. Antidiabetic
Agrimonia eupatoria L. Antiinflammatory
Agrimonia eupatoria L. Antipyretic
Agrimonia eupatoria L. Antiseptic
Agrimonia eupatoria L. Antiviral
Agrimonia eupatoria L. Astringent
Agrimonia eupatoria L. Candidicide
Agrimonia eupatoria L. Cholagogue
Agrimonia eupatoria L. Depurative
Agrimonia eupatoria L. Diuretic
Agrimonia eupatoria L. Emmenagogue
Agrimonia eupatoria L. Fungicide
Agrimonia eupatoria L. Hemostat
Agrimonia eupatoria L. Hypoglycemic
Agrimonia eupatoria L. Litholytic
Agrimonia eupatoria L. Sedative
Agrimonia eupatoria L. Stomachic
Agrimonia eupatoria L. Tonic
Agrimonia eupatoria L. Uricolytic
Agrimonia eupatoria L. Vermifuge
Agrimonia eupatoria L. Vulnerary

Metabolite list (3)

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
C00005138 External link 512 Astragalin
/ Kaempferol 3-glucoside
/ Kaempferol 3-O-beta-D-glucoside
/ Kaempferol 3-O-beta-D-glucopyranoside
CHEMBL233930
CHEMBL453290
CHEMBL1572115
C001579
10 / 6 / 7 0 / 1 No. 2 No. 15
C00005140 External link 512 Afzelin
/ Kaempferol 3-O-alpha-rhamnoside
/ Kaempferol 3-O-alpha-L-rhamnopyranoside
CHEMBL240528
CHEMBL515798
C477954
4 / 2 / 2 No. 2 No. 15
C00005288 External link 512 Kaempferide 3-rhamnoside
/ Kaempferol 4'-methyl ether 3-rhamnoside
/ 3-[(6-Deoxy-alpha-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL1642201
No. 2 No. 15

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00005140 1 / 0
Q99700 Ataxin-2 Unclassified protein C00005138 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00005138 0 / 0
P07237 Protein disulfide-isomerase Enzyme C00005138 0 / 0
P15121 Aldose reductase Enzyme C00005138 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00005138 1 / 1
P14679 Tyrosinase Oxidoreductase C00005138 4 / 2
P16083 Ribosyldihydronicotinamide dehydrogenase [quinone] Enzyme C00005140 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00005138 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00005140 0 / 1
P98170 E3 ubiquitin-protein ligase XIAP Other cytosolic protein C00005140 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00005138 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005138 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00005138 0 / 3

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#608902 Drug metabolism, poor, cyp2d6-related P10635
#300635 Lymphoproliferative syndrome, x-linked, 2; xlp2 P98170
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (9)

KEGG name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00036 Osteosarcoma P08684 (marker)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00107 Other well-defined immunodeficiency syndromes P98170 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003876 Dermatitis, Atopic C00005138