Species

KNApSAcK Entry

Organism name Mentha pulegium L.
Genus Mentha
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Mentha pulegium
Linked NCBI taxonomy ID 294739
Linked level species

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Natural Activity

List (25)

Species Activity
Mentha pulegium L. Abortifacient
Mentha pulegium L. Antipyretic
Mentha pulegium L. Antiseptic
Mentha pulegium L. Antispasmodic
Mentha pulegium L. Carminative
Mentha pulegium L. Cholagogue
Mentha pulegium L. Decongestant
Mentha pulegium L. Depurative
Mentha pulegium L. Diaphoretic
Mentha pulegium L. Digestive
Mentha pulegium L. Diuretic
Mentha pulegium L. Ecbolic
Mentha pulegium L. Emmenagogue
Mentha pulegium L. Expectorant
Mentha pulegium L. Hepatotoxic
Mentha pulegium L. Insecticide
Mentha pulegium L. Insectifuge
Mentha pulegium L. Nervine
Mentha pulegium L. Pectoral
Mentha pulegium L. Poison
Mentha pulegium L. Purgative
Mentha pulegium L. Refrigerant
Mentha pulegium L. Stimulant
Mentha pulegium L. Sudorific
Mentha pulegium L. Uterotonic

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
C00003110 External link 512 Caryophyllene
/ (E)-Caryophyllene
/ beta-Caryophyllene
/ (-)-(E)-Caryophyllene
/ (E)-beta-Caryophyllene
CHEMBL445740
CHEMBL448700
2 / 3 / 7 No. 478 No. 38
C00029674 External link 512 alpha-Terpineol
CHEMBL447597
CHEMBL449810
C016775
3 / 16 / 11 No. 983 No. 35
C00035341 External link 512 Menthone
CHEMBL276311
CHEMBL1719455
C019466
1 / 0 / 0 3 / 0 No. 1288 No. 35
C00029544 External link 512 4-Terpineol
/ Terpin-4-ol
/ Terpineol-4
/ Terpinen-4-ol
CHEMBL507795
C034019
1 / 3 / 0 No. 2215
C00029844 External link 512 Bornyl acetate
CHEMBL1439452
C071528
4 / 1 / 4 No. 4140 No. 35
C00035369 External link 512 Piperitenone oxide
No. 5079 No. 35
C00000136 External link 512 1,8-Cineole
CHEMBL485259
CHEMBL1397305
99 / 57 / 50 No. 5413 No. 35
C00035329 External link 512 Isophorene
No. 8911

Human Protein / Gene in interactions

107 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00029544 C00029674 3 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00029844 C00035341 0 / 0
P02545 Prelamin-A/C Unclassified protein C00000136 C00029674 11 / 10
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00000136 1 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000136 0 / 3
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00000136 2 / 2
P08246 Neutrophil elastase S1A C00000136 2 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00000136 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00000136 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00000136 0 / 0
P29466 Caspase-1 C14 C00000136 0 / 0
P17252 Protein kinase C alpha type Alpha C00000136 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00000136 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00000136 2 / 2
Q7Z2W7 Transient receptor potential cation channel subfamily M member 8 Unclassified protein C00000136 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00000136 3 / 2
P00918 Carbonic anhydrase 2 Lyase C00000136 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00000136 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00000136 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00000136 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00000136 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00000136 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00000136 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00000136 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00000136 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00000136 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00000136 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00000136 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000136 0 / 1
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000136 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00000136 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000136 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00000136 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00000136 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00000136 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00000136 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00000136 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00000136 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00000136 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00000136 1 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000136 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000136 1 / 0
O75496 Geminin Unclassified protein C00000136 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00000136 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00000136 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00000136 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00000136 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00000136 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00000136 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00000136 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00000136 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00000136 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00000136 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00000136 1 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00000136 0 / 0
P08311 Cathepsin G S1A C00000136 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00000136 1 / 0
P03956 Interstitial collagenase M10A C00000136 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00000136 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000136 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00000136 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00000136 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00000136 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00000136 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00000136 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00000136 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00000136 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00000136 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00000136 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00000136 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00000136 0 / 0
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00000136 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00000136 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000136 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00000136 2 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000136 0 / 0
P55055 Oxysterols receptor LXR-beta NR1H3 C00000136 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00000136 0 / 0
P03372 Estrogen receptor NR3A1 C00000136 1 / 1
P21728 D(1A) dopamine receptor Dopamine receptor C00000136 0 / 0
P22303 Acetylcholinesterase Hydrolase C00000136 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00000136 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00000136 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00000136 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00000136 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00000136 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00000136 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00000136 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000136 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000136 0 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00000136 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00029674 5 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00000136 4 / 3
P10275 Androgen receptor NR3C4 C00000136 3 / 4
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00000136 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00000136 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00000136 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00000136 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00000136 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00000136 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00000136 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00029844 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000136 0 / 0
O00255 Menin Unclassified protein C00003110 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003110 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00029844 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00029844 1 / 4

3 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
2554 GABRA1, ECA4, EJM, EJM5 gamma-aminobutyric acid (GABA) A receptor, alpha 1 C00035341
2561 GABRB2 gamma-aminobutyric acid (GABA) A receptor, beta 2 C00035341
2566 GABRG2, CAE2, ECA2, GEFSP3 gamma-aminobutyric acid (GABA) A receptor, gamma 2 C00035341

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (66)

OMIM preferred title UniProt
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#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
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#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
#600274 Frontotemporal dementia; ftd P10636
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#143500 Gilbert syndrome P22309
P22310
#137800 Glioma susceptibility 1; glm1 P04626
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#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
%300852 Mental retardation, x-linked 88; mrx88 P50052
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#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
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#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
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (61)

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)
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)
H00031 Breast cancer P04626 (related)
P04626 (marker)
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)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (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)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00548 Brunner syndrome P21397 (related)
H00208 Hyperbilirubinemia P22309 (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)
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)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)