KCF-S cluster No. 203 (30 metabolites)

Corresponding Phytochemical cluster No. 41


KEGG BRITE br08003 External link 512


Categories (2)

br08003 Category # of metabolite
Aphidicolane 1
Tiglianes 1

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
Aphidicolane C06088 C00000873
Tiglianes C09087 C00003423
Aphidicolane C06088 C00023944

Metabolite list (30)

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
C00000873 External link 512 Aphidicolin
CHEMBL12500
CHEMBL29711
CHEMBL485469
CHEMBL2006768
D016590
11 / 24 / 14 7 / 2
C00000887 External link 512 Helifulvanic acid
C00000898 External link 512 Stemarin
C00003423 External link 512 Diterpenoid SP-II
CHEMBL490353
CHEMBL517155
CHEMBL519801
CHEMBL482613
C00023944 External link 512 Aphidicolin
/ Aphidicolane-3alpha,16,17,18-tetraol
CHEMBL12500
CHEMBL29711
CHEMBL485469
CHEMBL2006768
D016590
11 / 24 / 14 7 / 2
C00023945 External link 512 3-Deoxyaphidicolin
C037612
C00035038 External link 512 Abbeokutone
CHEMBL437293
C00035596 External link 512 Doianoterpene D
/ (-)-Doianoterpene D
C00037369 External link 512
/ Kauranol
/ (-)-Kauran-16alpha-ol
C00037922 External link 512 Trachyloban-18-oic acid
/ (-)-Trachyloban-18-oic acid
CHEMBL511801
CHEMBL463698
CHEMBL1164460
1 / 0 / 0
C00037923 External link 512 Trachyloban-19-oic acid
/ (-)-Trachyloban-19-oic acid
CHEMBL511801
CHEMBL463698
CHEMBL1164460
C039978
1 / 0 / 0
C00038650 External link 512 Broussonetone A
/ (-)-Broussonetone A
CHEMBL574312
CHEMBL574535
C00038651 External link 512 Broussonetone B
/ (-)-Broussonetone B
CHEMBL574312
CHEMBL574535
C00038652 External link 512 Broussonetone C
/ (-)-Broussonetone C
C00040103 External link 512 Pterokaurane M3
/ (-)-Pterokaurane M3
C00043944 External link 512 Suremulol A
/ (-)-Suremulol A
C00044314 External link 512 Siegesbeckiol
C00045520 External link 512 16alpha,17-Dihydroxy-ent-kauran-19-oic acid
/ (-)-16alpha,17-Dihydroxy-ent-kauran-19-oic acid
CHEMBL490353
CHEMBL517155
CHEMBL519801
CHEMBL482613
C00045642 External link 512 Annosquamosin B
/ (-)-Annosquamosin B
CHEMBL516819
C00045643 External link 512 Annosquamosin C
/ (-)-Annosquamosin C
C00045647 External link 512 Annosquamosin G
C00046613 External link 512 Annoglabasin E
/ (-)-Annoglabasin E
CHEMBL1288269
C00047366 External link 512 6beta,7beta,16alpha,17-Tetrahydroxy-ent-kauranoic acid
/ ent-6alpha,7alpha,16beta,17-Tetrahydroxykauranoic acid
/ (-)-6beta,7beta,16alpha,17-Tetrahydroxy-ent-kauranoic acid
C00048380 External link 512 Epiadejone
C00048562 External link 512 Vierol
CHEMBL1760128
C00049686 External link 512 (-)-16alpha-Hydroxykauran-19-oic acid
CHEMBL207260
CHEMBL480070
CHEMBL604095
CHEMBL1760135
C060419
1 / 0 / 0
C00049687 External link 512 (-)-17-Hydroxy-16alpha-kauran-19-oic acid
CHEMBL511892
CHEMBL481645
CHEMBL448617
CHEMBL456957
C00049689 External link 512 16alpha,19-Dihydroxy-ent-kaurane
CHEMBL1760128
C00049850 External link 512 16alpha,17-Dihydroxy-ent-kauran-19-oic acid
/ (-)-16alpha,17-Dihydroxy-ent-kauran-19-oic acid
CHEMBL490353
CHEMBL517155
CHEMBL519801
CHEMBL482613
C00049852 External link 512 Annoglabasin B
CHEMBL490145
CHEMBL1288242

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000873 C00023944 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00000873 C00023944 4 / 1
P06746 DNA polymerase beta Enzyme C00000873 C00023944 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000873 C00023944 11 / 10
P54098 DNA polymerase subunit gamma-1 Enzyme C00000873 C00023944 6 / 2
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00000873 C00023944 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000873 C00023944 0 / 0
P09884 DNA polymerase alpha catalytic subunit Transferase C00000873 C00023944 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000873 C00023944 0 / 0
P28340 DNA polymerase delta catalytic subunit Transferase C00000873 C00023944 2 / 0
Q07817 Bcl-2-like protein 1 Other cytosolic protein C00037922 C00037923 0 / 0
P42858 Huntingtin Unclassified protein C00000873 C00023944 1 / 1
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00049686 0 / 0

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
890 CCNA2, CCN1, CCNA cyclin A2 C00000873 C00023944
11200 CHEK2, CDS1, CHK2, HuCds1, LFS2, PP1425, RAD53, hCds1 checkpoint kinase 2 (EC:2.7.11.1) C00000873 C00023944
3014 H2AFX, H2A.X, H2A/X, H2AX H2A histone family, member X C00000873 C00023944
5591 PRKDC, DNA-PKcs, DNAPK, DNPK1, HYRC, HYRC1, XRCC7, p350 protein kinase, DNA-activated, catalytic polypeptide (EC:2.7.11.1) C00000873 C00023944
6256 RXRA, NR2B1 retinoid X receptor, alpha C00000873 C00023944
943 TNFRSF8, CD30, D1S166E, Ki-1 tumor necrosis factor receptor superfamily, member 8 C00000873 C00023944
7518 XRCC4 X-ray repair complementing defective repair in Chinese hamster cells 4 C00000873 C00023944

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (24)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#612591 Colorectal cancer, susceptibility to, 10; crcs10 P28340
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#256000 Leigh syndrome; ls P54098
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#615381 Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome; mdpl P28340
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#203700 Mitochondrial dna depletion syndrome 4a (alpers type); mtdps4a P54098
#613662 Mitochondrial dna depletion syndrome 4b (mngie type); mtdps4b P54098
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#157640 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1; peoa1 P54098
#258450 Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive; peob P54098
#275210 Restrictive dermopathy, lethal P02545
#607459 Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis; sando P54098
#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

KEGG DISEASE (14)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00469 Mitochondrial DNA depletion syndrome (MDS) P54098 (related)
H01118 Progressive external ophthalmoplegia (PEO) P54098 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002471 Cell Transformation, Neoplastic C00000873
C00023944
D048629 Micronuclei, Chromosome-Defective C00000873
C00023944