Species

KNApSAcK Entry

Organism name Grindelia squarrosa
Genus Grindelia
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Grindelia squarrosa
Linked NCBI taxonomy ID 1114761
Linked level species

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

Natural Activity

List (13)

Species Activity
Grindelia squarrosa (Pursh) Dunal Abortifacient
Grindelia squarrosa (Pursh) Dunal Antibacterial
Grindelia squarrosa (Pursh) Dunal Antidote
Grindelia squarrosa (Pursh) Dunal Antiedemic
Grindelia squarrosa (Pursh) Dunal Antiinflammatory
Grindelia squarrosa (Pursh) Dunal Antiseptic
Grindelia squarrosa (Pursh) Dunal Antispasmodic
Grindelia squarrosa (Pursh) Dunal Antitussive
Grindelia squarrosa (Pursh) Dunal Contraceptive
Grindelia squarrosa (Pursh) Dunal Expectorant
Grindelia squarrosa (Pursh) Dunal Fungicide
Grindelia squarrosa (Pursh) Dunal Sedative
Grindelia squarrosa (Pursh) Dunal Stimulant

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
C00001096 External link 512 Santin
CHEMBL161957
C104803
9 / 7 / 5 No. 3 No. 15
C00004596 External link 512 6-Methoxykaempferol 3-methyl ether
/ 5,7,4'-Trihydroxy-3,6-dimethoxyflavone
/ 5,7-Dihydroxy-2-(4-hydroxyphenyl)-3,6-dimethoxy-4H-1-benzopyran-4-one
CHEMBL351607
C014868
No. 3 No. 15
C00004646 External link 512 Pachypodol
/ Quercetin 3,3',7-trimethyl ether
/ 5,4'-Dihydroxy-3,7,3'-trimethoxyflavone
/ 5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-1-benzopyran-4-one
CHEMBL165180
C008751
1 / 2 / 0 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

Human Protein / Gene in interactions

27 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00004646 C00004647 2 / 0
P68366 Tubulin alpha-4A chain Structural C00004647 0 / 0
Q99700 Ataxin-2 Unclassified protein C00001096 1 / 1
P14618 Pyruvate kinase PKM Enzyme C00001096 0 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00001096 1 / 1
P08183 Multidrug resistance protein 1 drug C00004647 1 / 0
O75496 Geminin Unclassified protein C00001096 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00001096 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00001096 0 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00004647 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001096 4 / 3
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00001096 1 / 0
Q13748 Tubulin alpha-3C/D chain Structural C00004647 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001096 0 / 0
Q9H4B7 Tubulin beta-1 chain Structural C00004647 1 / 0
P04350 Tubulin beta-4A chain Structural C00004647 2 / 0
Q3ZCM7 Tubulin beta-8 chain Structural C00004647 0 / 0
P07437 Tubulin beta chain Structural C00004647 0 / 0
Q71U36 Tubulin alpha-1A chain Structural C00004647 1 / 1
P68371 Tubulin beta-4B chain Structural C00004647 0 / 0
Q13509 Tubulin beta-3 chain Structural C00004647 2 / 1
P68363 Tubulin alpha-1B chain Unclassified protein C00004647 0 / 0
Q13885 Tubulin beta-2A chain Structural C00004647 0 / 0
Q6PEY2 Tubulin alpha-3E chain Unclassified protein C00004647 0 / 0
Q9BQE3 Tubulin alpha-1C chain Unclassified protein C00004647 0 / 0
Q9BUF5 Tubulin beta-6 chain Structural C00004647 0 / 0
Q9BVA1 Tubulin beta-2B chain Structural C00004647 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

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
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#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
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#610031 Polymicrogyria, symmetric or asymmetric; pmgysa Q9BVA1
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#278300 Xanthinuria, type i P47989

KEGG DISEASE (7)

KEGG name UniProt
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00192 Xanthinuria P47989 (related)
H00838 Congenital fibrosis of the extraocular muscles (CFEOM) Q13509 (related)
H00268 Lissencephaly (LIS) Q71U36 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)