Species

KNApSAcK Entry

Organism name Machilus wangchiana
Genus Machilus
Family Lauraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Machilus wangchiana
Linked NCBI taxonomy ID 460783
Linked level species

Family

Family in NCBI taxonomy Lauraceae
ID 3433

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

Metabolite list (14)

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 External link 512 (+)-Eudesmin
CHEMBL519099
CHEMBL512865
CHEMBL523743
CHEMBL464352
CHEMBL1726879
C105875
2 / 0 / 0 No. 38 No. 21
C00000643 External link 512 Kobusin
/ (+)-Kobusin
/ (+)-Spinescin
/ Methylpiperitol
CHEMBL462822
No. 38 No. 21
C00030703 External link 512 Machilin I
CHEMBL228326
CHEMBL1170325
1 / 0 / 1 No. 38 No. 21
C00021674 External link 512 Nectandrin B
/ Malabaricanol
CHEMBL228326
CHEMBL1170325
1 / 0 / 1 No. 38 No. 21
C00030746 External link 512 meso-Dihydroguaiaretic acid
CHEMBL430464
CHEMBL375927
CHEMBL1976696
16 / 18 / 12 No. 282 No. 21
C00047968 External link 512 Lincomolide B
CHEMBL509648
No. 329
C00047929 External link 512 Isomahubanolide 23
CHEMBL1080352
No. 329
C00047969 External link 512 Lincomolide C
No. 329
C00037221 External link 512 Guaiacin
/ (+)-Guaiacin
CHEMBL482239
CHEMBL1080351
No. 406
C00012727 External link 512 Costic acid
/ Costus acid
CHEMBL486398
No. 978
C00047920 External link 512 Hamabiwalactone A
CHEMBL452992
No. 1362
C00003429 External link 512 Ginkgolide A
CHEMBL465161
CHEMBL1370614
CHEMBL1408113
CHEMBL1472160
CHEMBL1712596
CHEMBL1741996
CHEMBL2112174
13 / 10 / 12 No. 2137 No. 44
C00035830 External link 512 Ginkgolide B
CHEMBL514432
CHEMBL1434825
CHEMBL1515002
CHEMBL1898434
17 / 21 / 17 No. 2137 No. 44
C00047666 External link 512 4-(3-Methoxy-4-hydroxy)phenyl-3-methyl-3-buten-2-one
No. 4323

Human Protein / Gene in interactions

37 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (38)

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 DISEASE (33)

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)