Species

KNApSAcK Entry

Organism name Origanum vulgare
Genus Origanum
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Origanum vulgare
Linked NCBI taxonomy ID 39352
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 (32)

Species Activity
Origanum vulgare L. Analgesic
Origanum vulgare L. Antialzheimeran
Origanum vulgare L. Antiarthritic
Origanum vulgare L. Antibacterial
Origanum vulgare L. Anticancer
Origanum vulgare L. Antiinflammatory
Origanum vulgare L. Antimutagenic
Origanum vulgare L. Antioxidant
Origanum vulgare L. Antipyretic
Origanum vulgare L. Antiseptic
Origanum vulgare L. Antispasmodic
Origanum vulgare L. Carminative
Origanum vulgare L. Choleretic
Origanum vulgare L. COX-2 Inhibitor
Origanum vulgare L. Decongestant
Origanum vulgare L. Diaphoretic
Origanum vulgare L. Digestive
Origanum vulgare L. Diuretic
Origanum vulgare L. Emmenagogue
Origanum vulgare L. Expectorant
Origanum vulgare L. Fungicide
Origanum vulgare L. Laxative
Origanum vulgare L. Narcotic
Origanum vulgare L. Nervine
Origanum vulgare L. Orexigenic
Origanum vulgare L. Pectoral
Origanum vulgare L. Propecic
Origanum vulgare L. Sedative
Origanum vulgare L. Stimulant
Origanum vulgare L. Stomachic
Origanum vulgare L. Tonic
Origanum vulgare L. Vermicide

Metabolite list (5)

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
C00000983 External link 512 Naringin
CHEMBL451532
CHEMBL451512
CHEMBL1742953
CHEMBL1970019
C005274
18 / 12 / 6 12 / 4 No. 48 No. 14
C00000156 External link 512 Carvacrol
CHEMBL281202
C073316
10 / 6 / 1 4 / 2 No. 969 No. 35
C00010934 External link 512 p-Menth-3-en-1-ol
No. 2215
C00036174 External link 512 Nepetoidin A
No. 2442
C00036175 External link 512 Nepetoidin B
CHEMBL2335274
No. 2442

Human Protein / Gene in interactions

25 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00000156 C00000983 3 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00000156 C00000983 5 / 1
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00000156 C00000983 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000983 0 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00000156 0 / 0
P08183 Multidrug resistance protein 1 drug C00000983 1 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000156 0 / 0
O75496 Geminin Unclassified protein C00000983 0 / 0
P46721 Solute carrier organic anion transporter family member 1A2 Unclassified protein C00000983 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00000156 0 / 0
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter C00000983 1 / 0
P11308 Transcriptional regulator ERG Unclassified protein C00000983 1 / 2
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00000983 0 / 0
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter C00000983 1 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00000983 2 / 2
O75762 Transient receptor potential cation channel subfamily A member 1 Unclassified protein C00000156 1 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00000156 0 / 0
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00000156 0 / 0
P61088 Ubiquitin-conjugating enzyme E2 N Enzyme C00000983 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000983 0 / 0
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00000156 0 / 0
Q9Y251 Heparanase Enzyme C00000983 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000983 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00000983 1 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000983 1 / 1

15 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00000156 C00000983
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) C00000983
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00000983
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00000983
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00000983
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00000983
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00000983
581 BAX, BCL2L4 BCL2-associated X protein C00000983
8772 FADD, MORT1 Fas (TNFRSF6)-associated via death domain C00000983
355 FAS, ALPS1A, APO-1, APT1, CD95, FAS1, FASTM, TNFRSF6 Fas cell surface death receptor C00000983
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00000983
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00000983
8989 TRPA1, ANKTM1, FEPS transient receptor potential cation channel, subfamily A, member 1 C00000156
162514 TRPV3, OLMS, VRL3 transient receptor potential cation channel, subfamily V, member 3 C00000156
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00000156

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (13)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#615040 Episodic pain syndrome, familial, 1; feps1 O75762
#612219 Ewing sarcoma; es P11308
#143500 Gilbert syndrome P22309
P22310
#137800 Glioma susceptibility 1; glm1 O75874
#237450 Hyperbilirubinemia, rotor type; hblrr Q9NPD5
Q9Y6L6
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#612244 Inflammatory bowel disease 13; ibd13 P08183

KEGG DISEASE (6)

KEGG name UniProt
H00024 Prostate cancer P11308 (related)
H00035 Ewing's sarcoma P11308 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H00208 Hyperbilirubinemia P22309 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)

Diseases related to CTD interactions

6 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D058186 Acute Kidney Injury C00000983
D056486 Drug-Induced Liver Injury C00000983
D009203 Myocardial Infarction C00000983
D002583 Uterine Cervical Neoplasms C00000983
D003866 Depressive Disorder C00000156
D010146 Pain C00000156