| 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)
|