Species

KNApSAcK Entry

Organism name Mentha spicata
Genus Mentha
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Mentha spicata
Linked NCBI taxonomy ID 29719
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 (20)

Species Activity
Mentha spicata L. Allergenic
Mentha spicata L. Analgesic
Mentha spicata L. Antipyretic
Mentha spicata L. Antiseptic
Mentha spicata L. Antispasmodic
Mentha spicata L. Carminative
Mentha spicata L. Decongestant
Mentha spicata L. Deodorant
Mentha spicata L. Dermatitigenic
Mentha spicata L. Diaphoretic
Mentha spicata L. Digestive
Mentha spicata L. Diuretic
Mentha spicata L. Emetic
Mentha spicata L. Expectorant
Mentha spicata L. Insecticide
Mentha spicata L. Neurodepressant
Mentha spicata L. Sedative
Mentha spicata L. Stimulant
Mentha spicata L. Stomachic
Mentha spicata L. Vermifuge

Metabolite list (13)

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
C00003892 External link 512 6-Hydroxyluteolin 7,3'-dimethyl ether
/ 5,6,4'-Trihydroxy-7,3'-dimethoxyflavone
/ 5,6-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one
No. 3 No. 15
C00003927 External link 512 Sideritiflavone
/ 5,3',4'-Trihydroxy-6,7,8-trimethoxyflavone
/ 2-(3,4-Dihydroxyphenyl)-5-hydroxy-6,7,8-trimethoxy-4H-1-benzopyran-4-one
CHEMBL312790
No. 3 No. 15
C00001036 External link 512 Diosmetin
/ 4'-Methylluteolin
/ 5,7,3'-Trihydroxy-4'-methoxyflavone
CHEMBL90568
C039602
11 / 12 / 8 5 / 0 No. 3 No. 15
C00003931 External link 512 Thymonin
/ Majoranin
/ Mucroflavone B
/ 5,6,4'-Trihydroxy-7,8,3'-trimethoxyflavone
/ 5,6-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7,8-dimethoxy-4H-1-benzopyran-4-one
CHEMBL478416
No. 3 No. 15
C00003936 External link 512 Demethylnobiletin
/ 5-Hydroxy-6,7,8,3',4'-pentamethoxyflavone
/ 2-(3,4-Dimethoxyphenyl)-5-hydroxy-6,7,8-trimethoxy-4H-1-benzopyran-4-one
CHEMBL75978
21 / 22 / 16 No. 8 No. 15
C00013339 External link 512 Pebrellin
/ 5,6-Dihydroxy-7,8,3',4'-tetramethoxyflavone
/ 2-(3,4-Dimethoxyphenyl)-5,6-dihydroxy-7,8-dimethoxy-4H-1-benzopyran-4-one
No. 8 No. 15
C00029346 External link 512 (Z)-3-Hexenyl beta-D-glucopyranoside
/ (-)-(Z)-3-Hexenyl-beta-glucopyranoside
/ (Z)-3-Hexen-1-ol-beta-D-glucopyranoside
CHEMBL2152486
C058860
No. 258 No. 73
C00000803 External link 512 (-)-Limonene
CHEMBL15799
CHEMBL449062
7 / 21 / 48 No. 848 No. 35
C00000814 External link 512 (-)-trans-Carveol
CHEMBL1385229
CHEMBL1907992
CHEMBL1908058
6 / 15 / 40 No. 1555 No. 35
C00000807 External link 512 (R)-(-)-Carvone
CHEMBL15676
CHEMBL501949
8 / 9 / 9 No. 1740 No. 35
C00003058 External link 512 (+)-Rotundifolone
No. 5079 No. 35
C00000146 External link 512 (+)-Bottrospicatol
No. 5341
C00010936 External link 512 (-)-cis-Pulegol
/ p-Menth-4(8)-en-3-ol
No. 5592

Human Protein / Gene in interactions

47 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04637 Cellular tumor antigen p53 Transcription Factor C00000803 C00000814 7 / 37
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000803 C00000807 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000807 C00003936 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00000803 C00000807 3 / 1
P02545 Prelamin-A/C Unclassified protein C00000803 C00003936 11 / 10
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00000803 C00001036 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003936 0 / 1
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000803 0 / 3
P16473 Thyrotropin receptor Glycohormone receptor C00000814 3 / 2
P49798 Regulator of G-protein signaling 4 Unclassified protein C00000807 2 / 0
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00000803 0 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00001036 0 / 0
P33527 Multidrug resistance-associated protein 1 drugs C00001036 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00000814 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00000814 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00001036 5 / 3
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00001036 4 / 4
P04745 Alpha-amylase 1 Enzyme C00001036 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00003936 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001036 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00001036 2 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00001036 1 / 1
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00000807 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003936 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001036 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00000814 5 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00003936 4 / 3
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00000814 3 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00001036 0 / 0
O00255 Menin Unclassified protein C00000807 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000807 1 / 2
Q13748 Tubulin alpha-3C/D chain Structural C00003936 0 / 0
P68366 Tubulin alpha-4A chain Structural C00003936 0 / 0
Q9H4B7 Tubulin beta-1 chain Structural C00003936 1 / 0
P04350 Tubulin beta-4A chain Structural C00003936 2 / 0
Q3ZCM7 Tubulin beta-8 chain Structural C00003936 0 / 0
P07437 Tubulin beta chain Structural C00003936 0 / 0
Q71U36 Tubulin alpha-1A chain Structural C00003936 1 / 1
P68371 Tubulin beta-4B chain Structural C00003936 0 / 0
Q13509 Tubulin beta-3 chain Structural C00003936 2 / 1
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000807 1 / 1
P68363 Tubulin alpha-1B chain Unclassified protein C00003936 0 / 0
Q13885 Tubulin beta-2A chain Structural C00003936 0 / 0
Q6PEY2 Tubulin alpha-3E chain Unclassified protein C00003936 0 / 0
Q9BQE3 Tubulin alpha-1C chain Unclassified protein C00003936 0 / 0
Q9BUF5 Tubulin beta-6 chain Structural C00003936 0 / 0
Q9BVA1 Tubulin beta-2B chain Structural C00003936 1 / 0

5 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00001036
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00001036
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00001036
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00001036
1577 CYP3A5, CP35, CYPIIIA5, P450PCN3, PCN3 cytochrome P450, family 3, subfamily A, polypeptide 5 (EC:1.14.14.1) C00001036

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (58)

OMIM preferred title UniProt
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#614490 Blood group, junior system; jr Q9UNQ0
%606641 Body mass index; bmi P37231
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#614039 Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 Q13509
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#237500 Dubin-johnson syndrome; djs Q92887
#128101 Dystonia 4, torsion, autosomal dominant; dyt4 P04350
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#600638 Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a Q13509
#600274 Frontotemporal dementia; ftd P10636
#143500 Gilbert syndrome P22309
P22310
#137750 Glaucoma 1, open angle, a; glc1a Q16678
#231300 Glaucoma 3, primary congenital, a; glc3a Q16678
#137760 Glaucoma, primary open angle; poag Q16678
#137800 Glioma susceptibility 1; glm1 P37231
#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
#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
#612438 Leukodystrophy, hypomyelinating, 6; hld6 P04350
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#611603 Lissencephaly 3; lis3 Q71U36
#211980 Lung cancer P04637
#613112 Macrothrombocytopenia, autosomal dominant, tubb1-related Q9H4B7
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#601665 Obesity P37231
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#604229 Peters anomaly Q16678
#172700 Pick disease of brain P10636
#610031 Polymicrogyria, symmetric or asymmetric; pmgysa Q9BVA1
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0

KEGG DISEASE (67)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (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)
P37231 (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)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
P35354 (related)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P35354 (related)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
P35354 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00208 Hyperbilirubinemia P22309 (related)
Q92887 (related)
H00409 Type II diabetes mellitus P37231 (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)
H00838 Congenital fibrosis of the extraocular muscles (CFEOM) Q13509 (related)
H00612 Primary open angle glaucoma Q16678 (related)
H01075 Peters anomaly Q16678 (related)
H01159 Anterior segment dysgenesis (ASD) Q16678 (related)
H01203 Primary congenital glaucoma (PCG) Q16678 (related)
H00268 Lissencephaly (LIS) Q71U36 (related)