Species

KNApSAcK Entry

Organism name Haplophyllum tuberculatum (Forssk.) Al Juss.
Genus Haplophyllum
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Haplophyllum
Linked NCBI taxonomy ID 266078
Linked level genus

Family

Family in NCBI taxonomy Rutaceae
ID 23513

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (11)

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
C00002159 External link 512 gamma-Fagarine
/ 4,8-Dimethoxyfuro[2,3-b]quinoline
CHEMBL252925
C049193
8 / 14 / 7 No. 368 No. 7
C00037236 External link 512 Haplotubine
No. 600 No. 7
C00002162 External link 512 Flindersine
CHEMBL1507844
1 / 3 / 3 No. 799 No. 7
C00036304 External link 512 (+)-Dihydroperfamine
No. 1718 No. 7
C00037536 External link 512 N-(2-Phenylethyl)benzamide
No. 2550
C00018703 External link 512 Tuberin
/ Tuberine
CHEMBL1967986
No. 2748 No. 6
C00037965 External link 512 Tubacetine
CHEMBL477734
CHEMBL1991947
No. 5525
C00037966 External link 512 Tubasenecine
CHEMBL476701
CHEMBL2005221
No. 5525
C00030143 External link 512 Diphyllin
CHEMBL1752
CHEMBL1488819
D004400
93 / 51 / 42 0 / 1 No. 7304
C00036842 External link 512 Buchapine
CHEMBL511557
No. 8095
C00037237 External link 512 Haplotubinone
No. 8803

Human Protein / Gene in interactions

102 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00030143 1 / 0
Q16637 Survival motor neuron protein Unclassified protein C00030143 4 / 1
P21728 D(1A) dopamine receptor Dopamine receptor C00030143 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00030143 0 / 3
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00030143 2 / 2
P08246 Neutrophil elastase S1A C00030143 2 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00030143 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00030143 0 / 0
P06746 DNA polymerase beta Enzyme C00030143 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00030143 0 / 0
P29466 Caspase-1 C14 C00030143 0 / 0
P17252 Protein kinase C alpha type Alpha C00030143 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00030143 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00030143 2 / 2
P02545 Prelamin-A/C Unclassified protein C00030143 11 / 10
P00918 Carbonic anhydrase 2 Lyase C00030143 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00030143 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00030143 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00030143 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00030143 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00030143 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00030143 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00030143 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00030143 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00030143 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00030143 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00030143 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00030143 0 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002159 1 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00030143 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00030143 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00030143 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00030143 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00030143 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00030143 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00030143 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00030143 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00030143 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00030143 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00030143 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002159 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00030143 0 / 0
O75496 Geminin Unclassified protein C00030143 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002159 4 / 2
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00030143 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00030143 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00030143 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00030143 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00030143 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00030143 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00030143 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00030143 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00030143 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00030143 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00030143 1 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00030143 0 / 0
P08311 Cathepsin G S1A C00030143 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00030143 1 / 0
P03956 Interstitial collagenase M10A C00030143 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00030143 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002159 7 / 3
P04150 Glucocorticoid receptor NR3C1 C00030143 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00030143 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00030143 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00030143 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00030143 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00030143 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00030143 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00030143 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00030143 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00030143 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00030143 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00030143 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00030143 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00030143 2 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00030143 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002162 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002159 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002159 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00030143 0 / 0
P03372 Estrogen receptor NR3A1 C00030143 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00030143 1 / 0
P22303 Acetylcholinesterase Hydrolase C00030143 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00030143 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00030143 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00030143 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00030143 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00030143 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00030143 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00030143 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00030143 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00030143 0 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00030143 0 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00030143 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00030143 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00030143 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00030143 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00030143 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00030143 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00030143 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002159 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002159 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (67)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#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
#615363 Estrogen resistance; estrr P03372
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#137800 Glioma susceptibility 1; glm1 P04626
#610140 Heart-hand syndrome, slovenian type P02545
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#603932 Intervertebral disc disease; idd P14780
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
#608516 Major depressive disorder; mdd P08172
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
%300852 Mental retardation, x-linked 88; mrx88 P50052
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#126200 Multiple sclerosis, susceptibility to; ms P08575
#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
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#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
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#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
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (49)

KEGG name UniProt
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (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)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00019 Pancreatic cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
P38398 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
P38398 (related)
H00046 Cholangiocarcinoma P04626 (related)
P35354 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00548 Brunner syndrome P21397 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006973 Hypertension C00030143