KCF-S cluster No. 6166 (1 metabolites)

Corresponding Phytochemical cluster No. 44


Plant Species


Cumulative plant class count

class name count
Spermatophyta 1

Cumulative family count

class name count
Ginkgoaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Ginkgolides 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Ginkgolides C07605 C00011512

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
figure
C00011512 External link 512 Bilobalide
CHEMBL133266
CHEMBL1318117
C073710
11 / 18 / 15 3 / 1

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00011512 4 / 1
P10828 Thyroid hormone receptor beta NR1A2 C00011512 3 / 1
O75496 Geminin Unclassified protein C00011512 0 / 0
P23416 Glycine receptor subunit alpha-2 GLR alpha C00011512 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00011512 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00011512 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00011512 0 / 0
O00255 Menin Unclassified protein C00011512 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00011512 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00011512 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00011512 1 / 4

3 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
351 APP, AAA, ABETA, ABPP, AD1, APPI, CTFgamma, CVAP, PN-II, PN2 amyloid beta (A4) precursor protein C00011512
1385 CREB1, CREB cAMP responsive element binding protein 1 C00011512
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00011512

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828

KEGG DISEASE (15)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D009410 Nerve Degeneration C00011512