| Organism name | Machilus wangchiana |
|---|---|
| Genus | Machilus |
| Family | Lauraceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Machilus wangchiana |
|---|---|
| Linked NCBI taxonomy ID | 460783 |
| Linked level | species |
| Family in NCBI taxonomy | Lauraceae |
|---|---|
| ID | 3433 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | Magnoliophyta |
|---|---|
| ID | 3398 |
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
|
C00000640
|
(+)-Eudesmin
|
CHEMBL519099
CHEMBL512865 CHEMBL523743 CHEMBL464352 CHEMBL1726879 |
C105875
|
2 / 0 / 0 | No. 38 | No. 21 |
|
|
|
C00000643
|
Kobusin
/ (+)-Kobusin / (+)-Spinescin / Methylpiperitol |
CHEMBL462822
|
No. 38 | No. 21 |
|
|||
|
C00030703
|
Machilin I
|
CHEMBL228326
CHEMBL1170325 |
1 / 0 / 1 | No. 38 | No. 21 |
|
||
|
C00021674
|
Nectandrin B
/ Malabaricanol |
CHEMBL228326
CHEMBL1170325 |
1 / 0 / 1 | No. 38 | No. 21 |
|
||
|
C00030746
|
meso-Dihydroguaiaretic acid
|
CHEMBL430464
CHEMBL375927 CHEMBL1976696 |
16 / 18 / 12 | No. 282 | No. 21 |
|
||
|
C00047968
|
Lincomolide B
|
CHEMBL509648
|
No. 329 |
|
||||
|
C00047929
|
Isomahubanolide 23
|
CHEMBL1080352
|
No. 329 |
|
||||
|
C00047969
|
Lincomolide C
|
No. 329 |
|
|||||
|
C00037221
|
Guaiacin
/ (+)-Guaiacin |
CHEMBL482239
CHEMBL1080351 |
No. 406 |
|
||||
|
C00012727
|
Costic acid
/ Costus acid |
CHEMBL486398
|
No. 978 |
|
||||
|
C00047920
|
Hamabiwalactone A
|
CHEMBL452992
|
No. 1362 |
|
||||
|
C00003429
|
Ginkgolide A
|
CHEMBL465161
CHEMBL1370614 CHEMBL1408113 CHEMBL1472160 CHEMBL1712596 CHEMBL1741996 CHEMBL2112174 |
13 / 10 / 12 | No. 2137 | No. 44 |
|
||
|
C00035830
|
Ginkgolide B
|
CHEMBL514432
CHEMBL1434825 CHEMBL1515002 CHEMBL1898434 |
17 / 21 / 17 | No. 2137 | No. 44 |
|
||
|
C00047666
|
4-(3-Methoxy-4-hydroxy)phenyl-3-methyl-3-buten-2-one
|
No. 4323 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04150 | Glucocorticoid receptor | NR3C1 | C00021674 C00030703 C00030746 | 0 / 1 |
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003429 C00035830 | 1 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00003429 C00035830 | 1 / 1 |
| P25105 | Platelet-activating factor receptor | PAF receptor | C00003429 C00035830 | 0 / 0 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00003429 C00035830 | 0 / 0 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00003429 C00035830 | 0 / 1 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00030746 C00035830 | 7 / 3 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00003429 C00035830 | 0 / 1 |
| P23415 | Glycine receptor subunit alpha-1 | GLR alpha | C00003429 C00035830 | 1 / 1 |
| O75496 | Geminin | Unclassified protein | C00030746 C00035830 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00000640 C00035830 | 0 / 0 |
| P23416 | Glycine receptor subunit alpha-2 | GLR alpha | C00003429 C00035830 | 0 / 0 |
| P00918 | Carbonic anhydrase 2 | Lyase | C00030746 | 1 / 2 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00035830 | 2 / 3 |
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00030746 | 2 / 2 |
| O75311 | Glycine receptor subunit alpha-3 | GLR alpha | C00035830 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00030746 | 2 / 0 |
| P37840 | Alpha-synuclein | Unclassified protein | C00030746 | 4 / 2 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00030746 | 0 / 0 |
| P00915 | Carbonic anhydrase 1 | Lyase | C00030746 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00030746 | 0 / 0 |
| P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00030746 | 0 / 0 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00003429 | 1 / 2 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00035830 | 0 / 0 |
| P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00003429 | 0 / 0 |
| Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00030746 | 0 / 0 |
| P04062 | Glucosylceramidase | Enzyme | C00035830 | 6 / 4 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00035830 | 3 / 3 |
| Q99700 | Ataxin-2 | Unclassified protein | C00030746 | 1 / 1 |
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00003429 | 0 / 0 |
| Q16637 | Survival motor neuron protein | Unclassified protein | C00003429 | 4 / 1 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00030746 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00035830 | 0 / 0 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00030746 | 0 / 0 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00000640 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00003429 | 2 / 5 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00030746 | 1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #127750 | Dementia, lewy body; dlb |
P37840
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #149400 | Hyperekplexia, hereditary 1; hkpx1 |
P23415
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
| #257200 | Niemann-pick disease, type a |
P17405
|
| #607616 | Niemann-pick disease, type b |
P17405
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
| #168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
| #605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
P37840 |
| #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
|
| #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
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
| KEGG | name | UniProt |
|---|---|---|
| H00033 | Adrenal carcinoma |
O00255
(related)
|
| H00034 | Carcinoid |
O00255
(related)
|
| H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
| H00246 | Primary hyperparathyroidism |
O00255
(related)
|
| H01102 | Pituitary adenomas |
O00255
(related)
|
| H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
| H00436 | Osteopetrosis |
P00918
(related)
|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
P37840 (related) |
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H00342 | Tuberculosis |
P11473
(related)
|
| H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
| H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
| H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
| H00769 | Hyperekplexia |
P23415
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00057 | Parkinson's disease (PD) |
P37840
(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)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
| H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|