class name | count |
---|---|
Liliopsida | 3 |
asterids | 2 |
eudicotyledons | 1 |
rosids | 1 |
class name | count |
---|---|
Aspergillaceae | 3 |
Orchidaceae | 3 |
Acanthaceae | 1 |
Brassicaceae | 1 |
Polygonaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Quinazoline alkaloids | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Quinazoline alkaloids | C10742 | C00002200 |
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
![]() |
Tryptanthrin
/ Tryptanthrine / Couroupitine A |
CHEMBL306946
|
C046243
|
20 / 22 / 23 | 2 / 0 |
![]() |
C00026251
![]() |
Sclerotigenin
/ (+/-)-Sclerotigenin |
CHEMBL490538
|
![]() |
|||
C00028055
![]() |
Circumdatin C
|
![]() |
||||
C00028058
![]() |
Circumdatin F
/ (-)-Circumdatin F |
![]() |
||||
C00039983
![]() |
Phaitanthrin C
/ (-)-Phaitanthrin C |
CHEMBL452806
|
![]() |
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 |
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
|
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 | 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)
|