Species

KNApSAcK Entry

Organism name Vanilla planifolia
Genus Vanilla
Family Orchidaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Vanilla planifolia
Linked NCBI taxonomy ID 51239
Linked level species

Family

Family in NCBI taxonomy Orchidaceae
ID 4747

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Liliopsida
ID 4447

Natural Activity

List (27)

Species Activity
Vanilla planifolia Andrews Allergenic
Vanilla planifolia Andrews Antianemic
Vanilla planifolia Andrews Anticancer
Vanilla planifolia Andrews Anticariogenic
Vanilla planifolia Andrews Antidote
Vanilla planifolia Andrews Antimutagenic
Vanilla planifolia Andrews Antioxidant
Vanilla planifolia Andrews Antiseptic
Vanilla planifolia Andrews Antisickling
Vanilla planifolia Andrews Antispasmodic
Vanilla planifolia Andrews Aphrodisiac
Vanilla planifolia Andrews Bacteristat
Vanilla planifolia Andrews Carminative
Vanilla planifolia Andrews Choleretic
Vanilla planifolia Andrews Digestive
Vanilla planifolia Andrews Diuretic
Vanilla planifolia Andrews Emmenagogue
Vanilla planifolia Andrews Febrifuge
Vanilla planifolia Andrews Insecticide
Vanilla planifolia Andrews Insectifuge
Vanilla planifolia Andrews Larvicide
Vanilla planifolia Andrews Mosquitocide
Vanilla planifolia Andrews Piscicide
Vanilla planifolia Andrews Stimulant
Vanilla planifolia Andrews Tonic
Vanilla planifolia Andrews Vesicant
Vanilla planifolia Andrews Vulnerary

Metabolite list (1)

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
C00002683 External link 512 Vanillin
CHEMBL13883
18 / 8 / 9 No. 1003

Human Protein / Gene in interactions

18 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00002683 0 / 0
P78527 DNA-dependent protein kinase catalytic subunit Atypical serine/threonine protein kinase PIKK subfamily C00002683 0 / 0
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00002683 0 / 0
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002683 1 / 1
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00002683 0 / 0
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00002683 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002683 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00002683 0 / 0
O00519 Fatty-acid amide hydrolase 1 Enzyme C00002683 0 / 0
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002683 1 / 1
Q96RI1 Bile acid receptor NR1H4 C00002683 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002683 2 / 2
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00002683 0 / 0
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00002683 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002683 0 / 0
P10275 Androgen receptor NR3C4 C00002683 3 / 4
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002683 1 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002683 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#119900 Digital clubbing, isolated congenital P15428
#613163 Gaba-transaminase deficiency P80404
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649

KEGG DISEASE (9)

KEGG name UniProt
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H01257 GABA-transaminase deficiency P80404 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)