KCF-S cluster No. 226 (28 metabolites)

Corresponding Phytochemical cluster No. 81



Metabolite list (28)

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
C00002908 External link 512 Alnusiin
C00002909 External link 512 Casuarictin
CHEMBL305099
CHEMBL446979
C073064
C00002910 External link 512 Casuarinin
CHEMBL79244
CHEMBL507387
11 / 2 / 2
C00002911 External link 512 Chebulagic acid
CHEMBL525240
CHEMBL1970427
C076178
12 / 2 / 2
C00002912 External link 512 Chebulinic acid
CHEMBL501154
CHEMBL1159459
CHEMBL1391063
C103481
29 / 15 / 14 6 / 0
C00002926 External link 512 Geraniin
CHEMBL506069
C024603
1 / 4 / 2 0 / 1
C00002928 External link 512 Isoterchebin
C00002931 External link 512 Mallotusinic acid
C00002932 External link 512 Pedunculagin
CHEMBL292719
CHEMBL506204
1 / 1 / 0
C00031107 External link 512 Pterocarinin A
C00032196 External link 512 Stachyurin
CHEMBL79244
CHEMBL507387
11 / 2 / 2
C00035321 External link 512 Geraniinic acid B
C00035322 External link 512 Geraniinic acid C
C00035366 External link 512 Phyllanthusiin A
C00035367 External link 512 Phyllanthusiin B
C00035368 External link 512 Phyllanthusiin D
C00037605 External link 512 Pelargoniin A
C00040861 External link 512 Acalyphidin M2
C00041050 External link 512 Mallotusinin
C00042346 External link 512 Castalagin
CHEMBL288949
CHEMBL288273
CHEMBL504485
CHEMBL607711
11 / 2 / 2
C00043104 External link 512 Vescalagin
CHEMBL288949
CHEMBL288273
CHEMBL504485
CHEMBL607711
C084709
11 / 2 / 2
C00044999 External link 512 Paeonianin E
C00046303 External link 512 Phyllanemblinin C
CHEMBL501660
C00048812 External link 512 Phenazine A
C00048813 External link 512 Phenazine B
C00049290 External link 512 Carpinerin B
/ Rhoipteleanin H
C00049958 External link 512 5'-Desgalloylstachyurin
CHEMBL509562
CHEMBL488110
1 / 1 / 0
C00050033 External link 512 Casuariin
CHEMBL509562
CHEMBL488110
1 / 1 / 0

Human Protein / Gene in interactions

32 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q15139 Serine/threonine-protein kinase D1 Pkd C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 0
P41743 Protein kinase C iota type Iota C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 0
P24723 Protein kinase C eta type Eta C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 1 / 0
P05771 Protein kinase C beta type Alpha C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 0
P05129 Protein kinase C gamma type Alpha C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 1 / 1
Q05655 Protein kinase C delta type Delta C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 0
Q05513 Protein kinase C zeta type Iota C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 0
O94806 Serine/threonine-protein kinase D3 Pkd C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 0
Q02156 Protein kinase C epsilon type Eta C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 0
Q04759 Protein kinase C theta type Delta C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 1
P17252 Protein kinase C alpha type Alpha C00002910 C00002911 C00002912 C00032196 C00042346 C00043104 0 / 0
P00742 Coagulation factor X S1A C00002932 C00049958 C00050033 1 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002912 0 / 0
P12821 Angiotensin-converting enzyme M2 C00002926 4 / 2
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002912 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002912 4 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00002912 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002912 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002912 1 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00002912 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00002912 1 / 4
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002912 1 / 2
P11387 DNA topoisomerase 1 Isomerase C00002911 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002912 1 / 0
P54132 Bloom syndrome protein Enzyme C00002912 1 / 2
P10828 Thyroid hormone receptor beta NR1A2 C00002912 3 / 1
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002912 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002912 1 / 1
P06746 DNA polymerase beta Enzyme C00002912 0 / 0
P14618 Pyruvate kinase PKM Enzyme C00002912 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002912 0 / 0
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00002912 0 / 0

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
43 ACHE, ACEE, ARACHE, N-ACHE, YT acetylcholinesterase (EC:3.1.1.7) C00002912
2623 GATA1, ERYF1, GATA-1, GF-1, GF1, NF-E1, NFE1, XLANP, XLTDA, XLTT GATA binding protein 1 (globin transcription factor 1) C00002912
2624 GATA2, DCML, MONOMAC, NFE1B GATA binding protein 2 C00002912
2993 GYPA, CD235a, GPA, GPErik, GPSAT, HGpMiV, HGpMiXI, HGpSta(C), MN, MNS, PAS-2 glycophorin A (MNS blood group) C00002912
3145 HMBS, PBG-D, PBGD, PORC, UPS hydroxymethylbilane synthase (EC:2.5.1.61) C00002912
4778 NFE2, NF-E2, p45 nuclear factor, erythroid 2 C00002912

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (19)

OMIM preferred title UniProt
#210900 Bloom syndrome; blm P54132
#227600 Factor x deficiency P00742
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#614519 Hemorrhage, intracerebral, susceptibility to; ich P12821
#612624 Microvascular complications of diabetes, susceptibility to, 3; mvcd3 P12821
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#267430 Renal tubular dysgenesis; rtd P12821
#605361 Spinocerebellar ataxia 14; sca14 P05129
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P12821
P24723
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#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 (16)

KEGG name UniProt
H00063 Spinocerebellar ataxia (SCA) P05129 (related)
Q9NUW8 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00083 Allograft rejection P12821 (related)
H00575 Renal tubular dysgenesis P12821 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (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)
H00408 Type I diabetes mellitus Q04759 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D012878 Skin Neoplasms C00002926