KCF-S cluster No. 1798 (5 metabolites)

Corresponding Phytochemical cluster No. 7


Plant Species


Cumulative plant class count

class name count
Liliopsida 3
asterids 2
eudicotyledons 1
rosids 1

Cumulative family count

class name count
Aspergillaceae 3
Orchidaceae 3
Acanthaceae 1
Brassicaceae 1
Polygonaceae 1

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Quinazoline alkaloids 1

metabolites link (1)

br08003 Category KEGG ID KNApSAcK ID
Quinazoline alkaloids C10742 C00002200

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
C00002200 External link 512 Tryptanthrin
/ Tryptanthrine
/ Couroupitine A
CHEMBL306946
C046243
20 / 22 / 23 2 / 0
C00026251 External link 512 Sclerotigenin
/ (+/-)-Sclerotigenin
CHEMBL490538
C00028055 External link 512 Circumdatin C
C00028058 External link 512 Circumdatin F
/ (-)-Circumdatin F
C00039983 External link 512 Phaitanthrin C
/ (-)-Phaitanthrin C
CHEMBL452806

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002200 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002200 0 / 3
P02545 Prelamin-A/C Unclassified protein C00002200 11 / 10
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002200 0 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002200 1 / 0
P11387 DNA topoisomerase 1 Isomerase C00002200 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00002200 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002200 0 / 0
P42858 Huntingtin Unclassified protein C00002200 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002200 2 / 0
O75496 Geminin Unclassified protein C00002200 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00002200 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002200 1 / 2
O15118 Niemann-Pick C1 protein Unclassified protein C00002200 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002200 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002200 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002200 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00002200 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002200 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002200 0 / 0

2 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00002200
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00002200

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (22)

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
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257220 Niemann-pick disease, type c1; npc1 O15118
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#275210 Restrictive dermopathy, lethal P02545
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (23)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
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)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)