KCF-S cluster No. 401 (19 metabolites)

Corresponding Phytochemical cluster No. 41


Plant Species


Cumulative plant class count

class name count
rosids 24

Cumulative family count

class name count
Thymelaeaceae 19
Euphorbiaceae 5

Metabolite list (19)

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
C00003430 External link 512 Gnidicin
CHEMBL49689
CHEMBL2023370
C010459
C00003431 External link 512 Gnididin
C010460
C00003432 External link 512 Gnididilatin
CHEMBL454006
C00003433 External link 512 Gniditrin
CHEMBL1159653
C010461
C00003435 External link 512 Huratoxin
CHEMBL470375
CHEMBL1978920
C044222
C00003454 External link 512 Mezerein
CHEMBL126750
CHEMBL1468786
CHEMBL2007127
C011309
14 / 16 / 11 4 / 3
C00003455 External link 512 Montanin
CHEMBL451572
C024716
C00003482 External link 512 Simplexin
CHEMBL444290
C011110
C00003490 External link 512 Terpenoid EA-I
CHEMBL453030
CHEMBL447856
C00039258 External link 512 Genkwadaphnin
/ (+)-Genkwadaphnin
C036412
C00039283 External link 512 Gnidilatidin
CHEMBL504425
C048261
C00044232 External link 512 Mellerin B
/ (+)-Mellerin B
C00047057 External link 512 Kirkinine
/ (+)-Kirkinine
CHEMBL502037
C00047922 External link 512 Hirsein A
/ (+)-Hirsein A
CHEMBL553900
C00047923 External link 512 Hirsein B
CHEMBL562784
C00049027 External link 512 Wikstroelide A
/ (+)-Wikstroelide A
CHEMBL499462
C00049028 External link 512 Wikstroelide B
/ (+)-Wikstroelide B
C00049032 External link 512 Wikstroelide H
/ (+)-Wikstroelide H
C00049035 External link 512 Wikstroelide L
/ (+)-Wikstroelide L
CHEMBL499462

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00003454 1 / 1
P37840 Alpha-synuclein Unclassified protein C00003454 4 / 2
P17405 Sphingomyelin phosphodiesterase Enzyme C00003454 2 / 2
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00003454 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00003454 7 / 3
P11021 78 kDa glucose-regulated protein Unclassified protein C00003454 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00003454 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00003454 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00003454 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00003454 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003454 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00003454 1 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00003454 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00003454 0 / 3

4 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00003454
5578 PRKCA, AAG6, PKC-alpha, PKCA, PRKACA protein kinase C, alpha (EC:2.7.11.13) C00003454
5579 PRKCB, PKC-beta, PKCB, PRKCB1, PRKCB2 protein kinase C, beta (EC:2.7.11.13) C00003454
5582 PRKCG, PKC-gamma, PKCC, PKCG, SCA14 protein kinase C, gamma (EC:2.7.11.13) C00003454

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (16)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#127750 Dementia, lewy body; dlb P37840
#137800 Glioma susceptibility 1; glm1 O75874
#174800 Mccune-albright syndrome; mas P63092
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#166350 Osseous heteroplasia, progressive; poh P63092
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (11)

KEGG name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002471 Cell Transformation, Neoplastic C00003454
D010212 Papilloma C00003454
D012878 Skin Neoplasms C00003454