class name | count |
---|---|
asterids | 55 |
class name | count |
---|---|
Apocynaceae | 55 |
Diclidophoridae | 1 |
br08003 Category | # of metabolite |
---|---|
Indole alkaloids | 3 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Indole alkaloids | C09035 | C00001688 |
Indole alkaloids | C09146 | C00001713 |
Indole alkaloids | C09149 | C00001714 |
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 |
---|---|---|---|---|---|---|
C00001688
![]() |
Apovincamine
|
CHEMBL1163488
|
C063621
|
![]() |
||
C00001713
![]() |
Eburnamine
/ (-)-Eburnamine |
CHEMBL2104946
|
![]() |
|||
C00001714
![]() |
Eburnamonine
|
CHEMBL1318553
CHEMBL1553441 CHEMBL1733074 CHEMBL1892145 |
14 / 20 / 16 |
![]() |
||
C00024535
![]() |
Goniomitine
/ (-)-Goniomitine |
![]() |
||||
C00025041
![]() |
(-)-11-Methoxyeburnamonine
|
![]() |
||||
C00025047
![]() |
Vincamenine
/ (-)-Eburnamenine / cis-Vincamenine |
CHEMBL1097688
|
![]() |
|||
C00025051
![]() |
O-Methyleburnamine
/ (-)-O-Methyleburnamine / O-Methyl-(-)-eburnamine |
CHEMBL1097360
CHEMBL1164562 |
![]() |
|||
C00025061
![]() |
(+)-Eburnamenine
|
CHEMBL1097688
|
![]() |
|||
C00025062
![]() |
(+)-Isoeburnamine
|
CHEMBL2104946
|
![]() |
|||
C00025071
![]() |
16-Epivincanol
|
CHEMBL2104946
|
![]() |
|||
C00025075
![]() |
(+)-O-methylisoeburnamine
|
CHEMBL1097360
CHEMBL1164562 |
![]() |
|||
C00025079
![]() |
20-Oxoeburnamenine
|
![]() |
||||
C00027619
![]() |
(+)-19-Oxoeburnamine
|
![]() |
||||
C00027628
![]() |
(+)-Vincamone
/ d-Eburnamonine / (+)-Eburnamonine / (+)-cis-Vincamone / (+)-cis-Eburnamonine |
CHEMBL1318553
CHEMBL1553441 CHEMBL1733074 CHEMBL1892145 |
C016422
|
14 / 20 / 16 | 2 / 0 |
![]() |
C00042577
![]() |
Hecubine
|
![]() |
||||
C00047264
![]() |
Kopsiyunnanine D
/ (-)-Kopsiyunnanine D |
CHEMBL564146
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001714 C00027628 | 1 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00001714 C00027628 | 1 / 1 |
P02545 | Prelamin-A/C | Unclassified protein | C00001714 C00027628 | 11 / 10 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00001714 C00027628 | 3 / 2 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001714 C00027628 | 0 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00001714 C00027628 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00001714 C00027628 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00001714 C00027628 | 0 / 0 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00001714 C00027628 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001714 C00027628 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001714 C00027628 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001714 C00027628 | 0 / 1 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00001714 C00027628 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00001714 C00027628 | 1 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
1129 | CHRM2, HM2 | cholinergic receptor, muscarinic 2 |
C00027628
|
1132 | CHRM4, HM4, M4R | cholinergic receptor, muscarinic 4 |
C00027628
|
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
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#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
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
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)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|