class name | count |
---|---|
asterids | 9 |
eudicotyledons | 4 |
rosids | 3 |
Liliopsida | 2 |
class name | count |
---|---|
Apocynaceae | 9 |
Ranunculaceae | 4 |
Moraceae | 2 |
Asparagaceae | 2 |
Brassicaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Cardanolide | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Cardanolide | C19988 | C00032213 |
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 |
---|---|---|---|---|---|---|
C00030013
![]() |
Coroglaucigenin
|
CHEMBL495179
|
![]() |
|||
C00032213
![]() |
Strophanthidin
/ Strophanthidine / Strophanthidin K |
CHEMBL111743
CHEMBL368773 CHEMBL1437139 CHEMBL1516802 |
D013327
|
28 / 48 / 65 | 0 / 1 |
![]() |
C00032214
![]() |
Strophanthidol
|
CHEMBL1628279
|
![]() |
|||
C00032469
![]() |
Uzarigenin
|
CHEMBL21214
CHEMBL1453 CHEMBL1591205 |
33 / 41 / 58 |
![]() |
||
C00032536
![]() |
Xysmalogenin
/ 5,6-Dehydrouzarigenin |
![]() |
||||
C00034103
![]() |
Periforgenin A
|
![]() |
||||
C00038847
![]() |
Coroglaucigenin 3-O-sulfate
/ (+)-Coroglaucigenin 3-O-sulfate |
![]() |
||||
C00038848
![]() |
Corotoxigenin 3-O-sulfate
/ (+)-Corotoxigenin 3-O-sulfate |
![]() |
||||
C00040609
![]() |
Uzarigenin 3-O-sulfate
/ (+)-Uzarigenin 3-O-sulfate |
![]() |
||||
C00042202
![]() |
Afrogenin
|
![]() |
||||
C00049578
![]() |
Proceragenin
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00032213 C00032469 | 1 / 0 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00032213 C00032469 | 1 / 2 |
P04637 | Cellular tumor antigen p53 | Transcription Factor | C00032213 C00032469 | 7 / 37 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00032213 C00032469 | 4 / 1 |
Q99700 | Ataxin-2 | Unclassified protein | C00032213 C00032469 | 1 / 1 |
P02545 | Prelamin-A/C | Unclassified protein | C00032213 C00032469 | 11 / 10 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00032213 C00032469 | 3 / 2 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00032213 C00032469 | 0 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00032213 C00032469 | 1 / 0 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00032213 C00032469 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00032213 C00032469 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00032213 C00032469 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00032213 C00032469 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00032213 C00032469 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00032213 C00032469 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00032213 C00032469 | 0 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00032213 C00032469 | 1 / 1 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00032213 C00032469 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00032213 C00032469 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00032213 C00032469 | 0 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00032213 C00032469 | 1 / 1 |
P11308 | Transcriptional regulator ERG | Unclassified protein | C00032213 | 1 / 2 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00032213 | 7 / 3 |
P54707 | Potassium-transporting ATPase alpha chain 2 | Potassium-transporting P-type ATPase alpha subunit | C00032469 | 0 / 0 |
P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00032213 | 4 / 2 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00032213 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00032469 | 0 / 0 |
O60755 | Galanin receptor type 3 | Galanin receptor | C00032213 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00032213 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00032213 | 1 / 2 |
Q6ZQN7 | Solute carrier organic anion transporter family member 4C1 | Unclassified protein | C00032469 | 0 / 0 |
P05023 | Sodium/potassium-transporting ATPase subunit alpha-1 | Hydrolase | C00032469 | 0 / 0 |
P14415 | Sodium/potassium-transporting ATPase subunit beta-2 | potassium_sodium | C00032469 | 0 / 0 |
P13637 | Sodium/potassium-transporting ATPase subunit alpha-3 | Hydrolase | C00032469 | 2 / 1 |
Q13733 | Sodium/potassium-transporting ATPase subunit alpha-4 | Hydrolase | C00032469 | 0 / 0 |
P54710 | Sodium/potassium-transporting ATPase subunit gamma | potassium_sodium | C00032469 | 1 / 1 |
P54709 | Sodium/potassium-transporting ATPase subunit beta-3 | potassium_sodium | C00032469 | 0 / 0 |
P50993 | Sodium/potassium-transporting ATPase subunit alpha-2 | Hydrolase | C00032469 | 2 / 2 |
P05026 | Sodium/potassium-transporting ATPase subunit beta-1 | potassium_sodium | C00032469 | 0 / 0 |
P22310 | UDP-glucuronosyltransferase 1-4 | Enzyme | C00032469 | 3 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
#104290 | Alternating hemiplegia of childhood 1; ahc1 |
P50993
|
#614820 | Alternating hemiplegia of childhood 2; ahc2 |
P13637
|
#614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 |
P04637
|
#114480 | Breast cancer |
P38398
|
#604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
#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
|
#218800 | Crigler-najjar syndrome, type i |
P22310
|
#606785 | Crigler-najjar syndrome, type ii |
P22310
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#128235 | Dystonia 12; dyt12 |
P13637
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#133239 | Esophageal cancer |
P04637
|
#612219 | Ewing sarcoma; es |
P11308
|
#143500 | Gilbert syndrome |
P22310
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#154020 | Hypomagnesemia 2, renal; homg2 |
P54710
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#151623 | Li-fraumeni syndrome 1; lfs1 |
P04637
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#211980 | Lung cancer |
P04637
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#602481 | Migraine, familial hemiplegic, 2; fhm2 |
P50993
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#167000 | Ovarian cancer |
P38398
|
#614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
#260500 | Papilloma of choroid plexus; cpp |
P04637
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#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
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#275355 | Squamous cell carcinoma, head and neck; hnscc |
P04637
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
P04637 (related) |
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
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)
|
H00004 | Chronic myeloid leukemia (CML) |
P04637
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
P04637
(related)
|
H00006 | Hairy-cell leukemia |
P04637
(related)
|
H00008 | Burkitt lymphoma |
P04637
(related)
|
H00009 | Adult T-cell leukemia |
P04637
(related)
|
H00010 | Multiple myeloma |
P04637
(related)
|
H00013 | Small cell lung cancer |
P04637
(related)
|
H00014 | Non-small cell lung cancer |
P04637
(related)
|
H00015 | Malignant pleural mesothelioma |
P04637
(related)
|
H00016 | Oral cancer |
P04637
(related)
P04637 (marker) |
H00017 | Esophageal cancer |
P04637
(related)
P04637 (marker) |
H00018 | Gastric cancer |
P04637
(related)
|
H00019 | Pancreatic cancer |
P04637
(related)
P04637 (marker) |
H00020 | Colorectal cancer |
P04637
(related)
P04637 (marker) |
H00022 | Bladder cancer |
P04637
(related)
|
H00025 | Penile cancer |
P04637
(related)
P04637 (marker) |
H00026 | Endometrial Cancer |
P04637
(related)
|
H00027 | Ovarian cancer |
P04637
(related)
P38398 (related) |
H00028 | Choriocarcinoma |
P04637
(related)
|
H00029 | Vulvar cancer |
P04637
(related)
|
H00031 | Breast cancer |
P04637
(related)
P38398 (related) |
H00032 | Thyroid cancer |
P04637
(related)
Q06710 (related) |
H00036 | Osteosarcoma |
P04637
(related)
P08684 (marker) |
H00038 | Malignant melanoma |
P04637
(related)
|
H00039 | Basal cell carcinoma |
P04637
(related)
|
H00040 | Squamous cell carcinoma |
P04637
(related)
|
H00041 | Kaposi's sarcoma |
P04637
(related)
|
H00042 | Glioma |
P04637
(related)
P04637 (marker) |
H00044 | Cancer of the anal canal |
P04637
(related)
|
H00046 | Cholangiocarcinoma |
P04637
(related)
|
H00047 | Gallbladder cancer |
P04637
(related)
|
H00048 | Hepatocellular carcinoma |
P04637
(related)
|
H00055 | Laryngeal cancer |
P04637
(related)
P04637 (marker) |
H00881 | Li-Fraumeni syndrome |
P04637
(related)
|
H01007 | Choroid plexus papilloma |
P04637
(related)
|
H00021 | Renal cell carcinoma |
P04637
(marker)
|
H00024 | Prostate cancer |
P11308
(related)
|
H00035 | Ewing's sarcoma |
P11308
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00831 | Primary dystonia |
P13637
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
Q06710 (related) |
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00775 | Familial or sporadic hemiplegic migraine |
P50993
(related)
|
H00998 | Alternating hemiplegia of childhood |
P50993
(related)
|
H01210 | Hypomagnesemia |
P54710
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(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)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|