Species

KNApSAcK Entry

Organism name Laurus nobilis L.
Genus Laurus
Family Lauraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Laurus
Linked NCBI taxonomy ID 85222
Linked level genus

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

Natural Activity

List (101)

Species Activity
Laurus nobilis L. Abortifacient
Laurus nobilis L. Allergenic
Laurus nobilis L. Alzheimer's
Laurus nobilis L. Ameorrhea
Laurus nobilis L. Analgesic
Laurus nobilis L. Anorexia
Laurus nobilis L. Antibacterial
Laurus nobilis L. Antipyretic
Laurus nobilis L. Antirheumatic
Laurus nobilis L. Antiseptic
Laurus nobilis L. Arthrosis
Laurus nobilis L. Bacteria
Laurus nobilis L. Bruise
Laurus nobilis L. Bugbite
Laurus nobilis L. Cancer
Laurus nobilis L. Cancer, anus
Laurus nobilis L. Cancer, colon
Laurus nobilis L. Cancer, eye
Laurus nobilis L. Cancer, face
Laurus nobilis L. Cancer, joint
Laurus nobilis L. Cancer, liver
Laurus nobilis L. Cancer, mouth
Laurus nobilis L. Cancer, parotid
Laurus nobilis L. Cancer, spleen
Laurus nobilis L. Cancer, stomach
Laurus nobilis L. Cancer, testicle
Laurus nobilis L. Cancer, uterus
Laurus nobilis L. Candida
Laurus nobilis L. Cheilosis
Laurus nobilis L. Cholagogue
Laurus nobilis L. Colic
Laurus nobilis L. Condyloma
Laurus nobilis L. Cough
Laurus nobilis L. Cramp
Laurus nobilis L. Dandruff
Laurus nobilis L. Deafness
Laurus nobilis L. Debility
Laurus nobilis L. Dermatosis
Laurus nobilis L. Diaphoretic
Laurus nobilis L. Digestive
Laurus nobilis L. Diuretic
Laurus nobilis L. Dyspepsia
Laurus nobilis L. Earache
Laurus nobilis L. Emetic
Laurus nobilis L. Emmenagogue
Laurus nobilis L. Escherichia
Laurus nobilis L. Fibroid
Laurus nobilis L. Fungicide
Laurus nobilis L. Fungus
Laurus nobilis L. Furuncle
Laurus nobilis L. Gas
Laurus nobilis L. Gastrosis
Laurus nobilis L. Gastrotonic
Laurus nobilis L. Hepatosis
Laurus nobilis L. Hepatotonic
Laurus nobilis L. High Blood Pressure
Laurus nobilis L. HIV
Laurus nobilis L. Hypotensive
Laurus nobilis L. Hysteria
Laurus nobilis L. Impostume
Laurus nobilis L. Infection
Laurus nobilis L. Inflammation
Laurus nobilis L. Insectifuge
Laurus nobilis L. Klebsiella
Laurus nobilis L. Leukemia
Laurus nobilis L. Mange
Laurus nobilis L. Melanoma
Laurus nobilis L. Migraine
Laurus nobilis L. Molluscicide
Laurus nobilis L. Mycosis
Laurus nobilis L. Narcotic
Laurus nobilis L. Nervine
Laurus nobilis L. Orchosis
Laurus nobilis L. Pain
Laurus nobilis L. Parasite
Laurus nobilis L. Parasiticide
Laurus nobilis L. Pediculosis
Laurus nobilis L. Polyp
Laurus nobilis L. Proctosis
Laurus nobilis L. Rheumatism
Laurus nobilis L. Rubefacient
Laurus nobilis L. Salmonella
Laurus nobilis L. Scabies
Laurus nobilis L. Sclerosis
Laurus nobilis L. Sedative
Laurus nobilis L. Sore
Laurus nobilis L. Spasm
Laurus nobilis L. Sprain
Laurus nobilis L. Staphylococcus
Laurus nobilis L. Stimulant
Laurus nobilis L. Stomachic
Laurus nobilis L. Stomatosis
Laurus nobilis L. Tonic
Laurus nobilis L. Tumor
Laurus nobilis L. Ulcer
Laurus nobilis L. Uterosis
Laurus nobilis L. Virus
Laurus nobilis L. Water Retention
Laurus nobilis L. Wen
Laurus nobilis L. Wound
Laurus nobilis L. Yeast

Metabolite list (9)

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
C00001076 External link 512 Nobiletin
/ 3',4',5,6,7,8-Hexamethoxyflavone
CHEMBL76447
C008661
22 / 23 / 20 5 / 2 No. 8 No. 15
C00001105 External link 512 Tangeretin
/ 4',5,6,7,8-Pentamethoxyflavone
CHEMBL73930
C059006
12 / 11 / 11 2 / 0 No. 8 No. 15
C00004804 External link 512 3,3',4',5,6,7,8-Heptamethoxyflavone
/ 3,5,6,7,8,3',4'-Heptamethoxyflavone
/ 2-(3,4-Dimethoxyphenyl)-3,5,6,7,8-pentamethoxy-4H-1-benzopyran-4-one
CHEMBL77993
C059294
17 / 10 / 2 No. 8 No. 15
C00013040 External link 512 Reynosin
/ Reinosin
/ (+)-Reynosin
CHEMBL272178
C016715
No. 69 No. 38
C00032545 External link 512 Zaluzanin D
CHEMBL371402
3 / 0 / 0 No. 206 No. 38
C00003245 External link 512 Dehydrocostus lactone
CHEMBL88985
CHEMBL487201
CHEMBL1939730
C083030
1 / 1 / 1 No. 306 No. 38
C00003256 External link 512 Eremanthine
/ (-)-Eremanthin
CHEMBL451364
C002601
0 / 2 No. 306 No. 38
C00003397 External link 512 Zaluzanin C
CHEMBL461700
CHEMBL462318
CHEMBL1988754
C009697
No. 306 No. 38
C00032567 External link 512 (1R,4S)-1-Hydroperoxy-p-menth-2-en-8-ol acetate
No. 6817

Human Protein / Gene in interactions

44 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00001076 C00001105 C00004804 2 / 0
P08183 Multidrug resistance protein 1 drug C00001076 C00001105 C00004804 1 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00001076 C00001105 1 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001076 C00001105 1 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00001076 C00001105 1 / 1
O00255 Menin Unclassified protein C00001076 C00001105 2 / 5
P00352 Retinal dehydrogenase 1 Enzyme C00001076 C00001105 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001076 C00001105 0 / 1
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00001076 C00001105 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001076 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00032545 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00001105 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00001105 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00001076 5 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00001076 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001076 3 / 3
O75496 Geminin Unclassified protein C00001076 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00001076 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001076 0 / 0
P03372 Estrogen receptor NR3A1 C00003245 1 / 1
Q92830 Histone acetyltransferase KAT2A Enzyme C00001076 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001076 4 / 3
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00001076 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001076 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001076 1 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00001105 3 / 1
Q00653 Nuclear factor NF-kappa-B p100 subunit Transcription Factor C00032545 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00032545 0 / 0
Q13748 Tubulin alpha-3C/D chain Structural C00004804 0 / 0
P68366 Tubulin alpha-4A chain Structural C00004804 0 / 0
Q9H4B7 Tubulin beta-1 chain Structural C00004804 1 / 0
P04350 Tubulin beta-4A chain Structural C00004804 2 / 0
Q3ZCM7 Tubulin beta-8 chain Structural C00004804 0 / 0
P07437 Tubulin beta chain Structural C00004804 0 / 0
Q71U36 Tubulin alpha-1A chain Structural C00004804 1 / 1
P68371 Tubulin beta-4B chain Structural C00004804 0 / 0
Q13509 Tubulin beta-3 chain Structural C00004804 2 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00001076 0 / 0
P68363 Tubulin alpha-1B chain Unclassified protein C00004804 0 / 0
Q13885 Tubulin beta-2A chain Structural C00004804 0 / 0
Q6PEY2 Tubulin alpha-3E chain Unclassified protein C00004804 0 / 0
Q9BQE3 Tubulin alpha-1C chain Unclassified protein C00004804 0 / 0
Q9BUF5 Tubulin beta-6 chain Structural C00004804 0 / 0
Q9BVA1 Tubulin beta-2B chain Structural C00004804 1 / 0

5 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00001076 C00001105
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00001076 C00001105
972 CD74, DHLAG, HLADG, II, Ia-GAMMA CD74 molecule, major histocompatibility complex, class II invariant chain C00001076
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00001076
4316 MMP7, MMP-7, MPSL1, PUMP-1 matrix metallopeptidase 7 (matrilysin, uterine) (EC:3.4.24.23) C00001076

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (34)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614490 Blood group, junior system; jr Q9UNQ0
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#614039 Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 Q13509
#119900 Digital clubbing, isolated congenital P15428
#128101 Dystonia 4, torsion, autosomal dominant; dyt4 P04350
#615363 Estrogen resistance; estrr P03372
#600638 Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a Q13509
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#612244 Inflammatory bowel disease 13; ibd13 P08183
#612438 Leukodystrophy, hypomyelinating, 6; hld6 P04350
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#611603 Lissencephaly 3; lis3 Q71U36
#613112 Macrothrombocytopenia, autosomal dominant, tubb1-related Q9H4B7
#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
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#601665 Obesity P37231
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#610031 Polymicrogyria, symmetric or asymmetric; pmgysa Q9BVA1
#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
#278300 Xanthinuria, type i P47989

KEGG DISEASE (24)

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)
H00026 Endometrial Cancer P03372 (marker)
H00036 Osteosarcoma P08684 (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)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00192 Xanthinuria P47989 (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)
H00268 Lissencephaly (LIS) Q71U36 (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)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003921 Diabetes Mellitus, Experimental C00003256
D050171 Dyslipidemias C00003256
D003110 Colonic Neoplasms C00001076
D011230 Precancerous Conditions C00001076