Species

KNApSAcK Entry

Organism name Sideritis nutans
Genus Sideritis
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Sideritis nutans
Linked NCBI taxonomy ID 403027
Linked level species

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (4)

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
C00004607 External link 512 Penduletin 4'-methyl ether
/ 5-Hydroxy-3,6,7,4'-tetramethoxyflavone
/ 6-Hydroxykaempferol-3,6,7,4'-tetramethyl ether
/ 5-Hydroxy-3,6,7-trimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL521934
No. 8 No. 15
C00022269 External link 512 3alpha-Hydroxygomeric acid
No. 70
C00022298 External link 512 Gomerol
No. 70
C00023427 External link 512 (-)-Sclareolide
/ ent-Norambreinolide
CHEMBL304461
CHEMBL1437047
6 / 4 / 5 No. 1139

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P16473 Thyrotropin receptor Glycohormone receptor C00023427 3 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00023427 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00023427 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00023427 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00023427 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00023427 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#609535 Drug metabolism, poor, cyp2c19-related P33261
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473

KEGG DISEASE (5)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)