KCF-S cluster No. 2117 (5 metabolites)

Corresponding Phytochemical cluster No. 38


Plant Species


Cumulative plant class count

class name count
asterids 11

Cumulative family count

class name count
Asteraceae 11

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Eudesmanes 3

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
Eudesmanes C09344 C00003221
Eudesmanes C02206 C00003364
Eudesmanes C09545 C00003365

Metabolite list (5)

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
C00003221 External link 512 (-)-Artemisin
/ 8-Hydroxysantonin
/ [3S-(3alpha,3aalpha,4alpha,5abeta,9bbeta)]-3a,5,5a,9b-Tetrahydro-4-hydroxy-3,5a,9-trimethylnaphtho[1,2-b]furan-2,8(3H,4H)-dione
CHEMBL158124
CHEMBL1673435
C075875
1 / 2 / 2 1 / 0
C00003364 External link 512 Semenen
/ Santonin
/ a-Santonin
/ (-)-Santonin
/ (-)-alpha-Santonin
/ [3S-(3alpha,3aalpha,5abeta,9bbeta)]-3a,5,5a,9b-Tetrahydro-3,5a,9-trimethylnaphtho[1,2-b]furan-2,8(3H,4H)-dione
CHEMBL226231
CHEMBL259254
CHEMBL1357930
CHEMBL1570028
CHEMBL1600999
CHEMBL1717567
CHEMBL2103785
D012500
14 / 11 / 8
C00003365 External link 512 beta-Santonin
/ [3R-(3alpha,3abeta,5aalpha,9balpha)]-3a,5,5a,9b-Tetrahydro-3,5a,9-trimethylnaphtho[1,2-b]furan-2,8(3H,4H)-dione
CHEMBL226231
CHEMBL259254
CHEMBL1357930
CHEMBL1570028
CHEMBL1600999
CHEMBL1717567
CHEMBL2103785
14 / 11 / 8
C00013078 External link 512 Tubiferin
/ Tuberiferin
/ (+)-Tuberiferine
/ [3aS-(3aalpha,5abeta,9alpha,9aalpha,9bbeta)]-3a,5,5a,9,9a,9b-Hexahydro-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2,8(3H,4H)-dione
C00021439 External link 512 6,7,9,10-Tetradehydroasteriscanolide

Human Protein / Gene in interactions

15 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003364 C00003365 1 / 0
Q99700 Ataxin-2 Unclassified protein C00003364 C00003365 1 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00003364 C00003365 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003364 C00003365 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003364 C00003365 0 / 1
Q92830 Histone acetyltransferase KAT2A Enzyme C00003364 C00003365 0 / 0
O75496 Geminin Unclassified protein C00003364 C00003365 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00003364 C00003365 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00003364 C00003365 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003364 C00003365 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003364 C00003365 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003364 C00003365 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00003364 C00003365 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00003364 C00003365 7 / 3
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00003221 2 / 2

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00003221

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#613688 Long qt syndrome 2; lqt2 Q12809
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#609620 Short qt syndrome 1; sqt1 Q12809
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (10)

KEGG name UniProt
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)