Species

KNApSAcK Entry

Organism name Siparuna pauciflora
Genus Siparuna
Family Monimiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Siparuna pauciflora
Linked NCBI taxonomy ID 141960
Linked level species

Family

Family in NCBI taxonomy Siparunaceae
ID 104773

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

Metabolite list (8)

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
C00027150 External link 512 Nantenine
/ (+)-Domestine
/ (+)-Nantenine
CHEMBL179440
CHEMBL467094
C041615
38 / 10 / 2 No. 20 No. 4
C00027304 External link 512 Boldine
/ d-Boldine
/ (+)-Boldine
CHEMBL388342
CHEMBL1321247
CHEMBL1437753
C011686
34 / 32 / 35 No. 20 No. 4
C00027409 External link 512 Laurotetanin
/ Laurotetanine
/ (+)-Laurotetanine
CHEMBL464098
C008256
No. 20 No. 4
C00027433 External link 512 Laurolitsine
/ (+)-Norboldine
/ (+)-Laurolitsine
CHEMBL487388
C109133
No. 20 No. 4
C00028728 External link 512 Noroliveroline
/ Nor-Oliveroline
/ (-)-Noroliveroline
/ (-)-Nor-Oliveroline
CHEMBL464657
CHEMBL1618042
No. 553
C00037825 External link 512 Sipaucin A
No. 4928
C00037827 External link 512 Sipaucin C
No. 4928
C00037826 External link 512 Sipaucin B
/ (+)-Sipaucin B
No. 8257

Human Protein / Gene in interactions

72 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00027304 1 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00027304 0 / 0
Q99700 Ataxin-2 Unclassified protein C00027304 1 / 1
P21728 D(1A) dopamine receptor Dopamine receptor C00027150 0 / 0
Q9Y5N1 Histamine H3 receptor Histamine receptor C00027150 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00027304 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00027304 0 / 0
P02545 Prelamin-A/C Unclassified protein C00027304 11 / 10
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00027150 0 / 1
P25021 Histamine H2 receptor Histamine receptor C00027150 0 / 0
P28222 5-hydroxytryptamine receptor 1B Serotonin receptor C00027150 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00027150 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00027150 1 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00027150 0 / 0
P21918 D(1B) dopamine receptor Dopamine receptor C00027150 1 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00027150 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00027150 0 / 0
P47898 5-hydroxytryptamine receptor 5A Serotonin receptor C00027150 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00027304 0 / 1
P17787 Neuronal acetylcholine receptor subunit beta-2 CHRN beta C00027304 1 / 1
P43681 Neuronal acetylcholine receptor subunit alpha-4 CHRN alpha C00027304 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00027304 1 / 0
P14416 D(2) dopamine receptor Dopamine receptor C00027150 2 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00027150 0 / 0
P28566 5-hydroxytryptamine receptor 1E Serotonin receptor C00027150 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00027304 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00027304 0 / 0
P39748 Flap endonuclease 1 Enzyme C00027304 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00027304 0 / 0
O75496 Geminin Unclassified protein C00027304 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00027150 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00027150 0 / 0
P35348 Alpha-1A adrenergic receptor Adrenergic receptor C00027150 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00027150 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00027150 0 / 0
P46098 5-hydroxytryptamine receptor 3A NS C00027150 0 / 0
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00027150 0 / 0
Q9H3N8 Histamine H4 receptor Histamine receptor C00027150 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00027304 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00027304 1 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00027150 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00027150 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00027150 2 / 0
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00027150 1 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00027150 0 / 0
P36544 Neuronal acetylcholine receptor subunit alpha-7 CHRN alpha C00027304 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00027304 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00027304 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00027304 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00027304 0 / 0
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00027150 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00027150 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00027150 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00027150 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00027150 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00027304 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00027304 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00027304 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00027304 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00027304 4 / 3
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00027150 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00027150 0 / 0
P28221 5-hydroxytryptamine receptor 1D Serotonin receptor C00027150 0 / 0
P35368 Alpha-1B adrenergic receptor Adrenergic receptor C00027150 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00027150 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00027304 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00027304 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00027304 0 / 0
O00255 Menin Unclassified protein C00027304 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00027304 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00027304 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00027304 1 / 4

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (42)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103780 Alcohol dependence P08172
P14416
P31645
#606798 Blepharospasm, benign essential P21918
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#600513 Epilepsy, nocturnal frontal lobe, 1; enfl1 P43681
#605375 Epilepsy, nocturnal frontal lobe, 3; enfl3 P17787
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#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
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#608516 Major depressive disorder; mdd P08172
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#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
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#159900 Myoclonic dystonia P14416
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#190300 Tremor, hereditary essential, 1; etm1 P35462
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (37)

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)
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)
H00079 Asthma P07550 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00807 Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) P17787 (related)
P43681 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)