Species

KNApSAcK Entry

Organism name Heterotheca inuloides
Genus Heterotheca
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Heterotheca
Linked NCBI taxonomy ID 71056
Linked level genus

Family

Family in NCBI taxonomy Asteraceae
ID 4210

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (7)

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
C00004597 External link 512 5,6,4'-Trihydroxy-3,7-dimethoxyflavone
/ 6-Hydroxykaempferol 3,7-dimethyl ether
/ 5,6-Dihydroxy-2-(4-hydroxyphenyl)-3,7-dimethoxy-4H-1-benzopyran-4-one
No. 3 No. 15
C00004640 External link 512 Quercetin 3,4'-dimethyl ether
/ 5,7,3'-Trihydroxy-3,4'-dimethoxyflavone
/ 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-methoxy-4H-1-benzopyran-4-one
CHEMBL309263
16 / 8 / 2 No. 3 No. 15
C00004647 External link 512 Ayanin
/ 3,7,4'-Tri-O-methylquercetin
/ 5,3'-Dihydroxy-3,7,4'-trimethoxyflavone
/ 5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,7-dimethoxy-4H-1-benzopyran-4-one
CHEMBL74898
18 / 10 / 2 No. 3 No. 15
C00020113 External link 512 4,7-Dimethyl-2-(1-methylethyl)-1-naphthalenol
No. 647 No. 38
C00020068 External link 512 3-Hydroxy-alpha-calacorene
CHEMBL452210
No. 1859
C00020160 External link 512 1,2,8,8a-Tetrahydro-4,6-dimethyl-1-(1-methylethyl)-2-naphthalenol
No. 4919
C00017516 External link 512 4-Hydroxy-2-isopropyl-4,7-dimethyl-1(4H)-naphthalenone
CHEMBL459411
No. 7167

Human Protein / Gene in interactions

19 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9BVA1 Tubulin beta-2B chain Structural C00004640 C00004647 1 / 0
Q9BUF5 Tubulin beta-6 chain Structural C00004640 C00004647 0 / 0
Q9BQE3 Tubulin alpha-1C chain Unclassified protein C00004640 C00004647 0 / 0
Q6PEY2 Tubulin alpha-3E chain Unclassified protein C00004640 C00004647 0 / 0
Q13748 Tubulin alpha-3C/D chain Structural C00004640 C00004647 0 / 0
P68366 Tubulin alpha-4A chain Structural C00004640 C00004647 0 / 0
Q9H4B7 Tubulin beta-1 chain Structural C00004640 C00004647 1 / 0
P04350 Tubulin beta-4A chain Structural C00004640 C00004647 2 / 0
Q3ZCM7 Tubulin beta-8 chain Structural C00004640 C00004647 0 / 0
Q13885 Tubulin beta-2A chain Structural C00004640 C00004647 0 / 0
Q71U36 Tubulin alpha-1A chain Structural C00004640 C00004647 1 / 1
P68371 Tubulin beta-4B chain Structural C00004640 C00004647 0 / 0
Q13509 Tubulin beta-3 chain Structural C00004640 C00004647 2 / 1
P68363 Tubulin alpha-1B chain Unclassified protein C00004640 C00004647 0 / 0
P07437 Tubulin beta chain Structural C00004640 C00004647 0 / 0
O14763 Tumor necrosis factor receptor superfamily member 10B Unclassified protein C00004640 1 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00004647 2 / 0
P08183 Multidrug resistance protein 1 drug C00004647 1 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00004647 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#614490 Blood group, junior system; jr Q9UNQ0
#614039 Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 Q13509
#128101 Dystonia 4, torsion, autosomal dominant; dyt4 P04350
#600638 Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a Q13509
#612244 Inflammatory bowel disease 13; ibd13 P08183
#612438 Leukodystrophy, hypomyelinating, 6; hld6 P04350
#611603 Lissencephaly 3; lis3 Q71U36
#613112 Macrothrombocytopenia, autosomal dominant, tubb1-related Q9H4B7
#610031 Polymicrogyria, symmetric or asymmetric; pmgysa Q9BVA1
#275355 Squamous cell carcinoma, head and neck; hnscc O14763
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0

KEGG DISEASE (2)

KEGG name UniProt
H00838 Congenital fibrosis of the extraocular muscles (CFEOM) Q13509 (related)
H00268 Lissencephaly (LIS) Q71U36 (related)