Species

KNApSAcK Entry

Organism name Pinus pinaster
Genus Pinus
Family Pinaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pinus pinaster
Linked NCBI taxonomy ID 71647
Linked level species

Family

Family in NCBI taxonomy Pinaceae
ID 3318

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Spermatophyta
ID 58024

Natural Activity

List (37)

Species Activity
Pinus pinaster Aiton Analgesic
Pinus pinaster Aiton Anti-HIV
Pinus pinaster Aiton Antiaggregant
Pinus pinaster Aiton Antiaging
Pinus pinaster Aiton Antiallergic
Pinus pinaster Aiton Antiamyloid
Pinus pinaster Aiton Antianaphylactic
Pinus pinaster Aiton Antianemic
Pinus pinaster Aiton Antiasthmatic
Pinus pinaster Aiton Antiatherogenic
Pinus pinaster Aiton Antibacterial
Pinus pinaster Aiton Anticancer
Pinus pinaster Aiton Antidematotic
Pinus pinaster Aiton Antiedemic
Pinus pinaster Aiton Antiexudative
Pinus pinaster Aiton Antihistaminic
Pinus pinaster Aiton Antiinflammatory
Pinus pinaster Aiton Antioxidant
Pinus pinaster Aiton Antiplaque
Pinus pinaster Aiton Antiradicular
Pinus pinaster Aiton Antiseptic
Pinus pinaster Aiton Antisickling
Pinus pinaster Aiton Antithromboxane
Pinus pinaster Aiton Antiviral
Pinus pinaster Aiton Apoptotic
Pinus pinaster Aiton Cancer Preventive
Pinus pinaster Aiton Capillaritonic
Pinus pinaster Aiton Hemopoietic
Pinus pinaster Aiton Hyaluronidase Inhibitor
Pinus pinaster Aiton Immunomodulator
Pinus pinaster Aiton Lipolytic
Pinus pinaster Aiton Lipoxygenase Inhibitor
Pinus pinaster Aiton NO-Genic
Pinus pinaster Aiton Peroxidase Inhibitor
Pinus pinaster Aiton Retinoprotective
Pinus pinaster Aiton Sunscreen
Pinus pinaster Aiton Xanthine-Oxidase Inhibitor

Metabolite list (3)

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
C00002897 External link 512 Pinosylvin
/ Pinosylvine
/ 3,5-Dihydroxystilbene
CHEMBL101506
CHEMBL2203685
1 / 0 / 1 No. 295 No. 13
C00002898 External link 512 Pinosylvin methyl ether
/ 3-Hydroxy-5-methoxystilbene
CHEMBL186366
18 / 39 / 57 No. 295 No. 13
C00022109 External link 512 Geranyllinalool
No. 706

Human Protein / Gene in interactions

19 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04637 Cellular tumor antigen p53 Transcription Factor C00002898 7 / 37
Q16637 Survival motor neuron protein Unclassified protein C00002898 4 / 1
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002898 0 / 0
P37840 Alpha-synuclein Unclassified protein C00002898 4 / 2
P00352 Retinal dehydrogenase 1 Enzyme C00002898 0 / 0
O75496 Geminin Unclassified protein C00002898 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002898 4 / 2
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002898 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002898 7 / 3
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002898 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002898 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002898 2 / 2
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002898 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00002898 4 / 3
P06239 Tyrosine-protein kinase Lck Src C00002897 0 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002898 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002898 1 / 0
O00255 Menin Unclassified protein C00002898 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002898 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (39)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#127750 Dementia, lewy body; dlb P37840
#119900 Digital clubbing, isolated congenital P15428
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#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
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#211980 Lung cancer P04637
#174800 Mccune-albright syndrome; mas P63092
#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
#166350 Osseous heteroplasia, progressive; poh P63092
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#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
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (58)

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)
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)
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)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
P38398 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
P38398 (related)
H00032 Thyroid cancer P04637 (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)
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)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)
H00455 Spinal muscular atrophy (SMA) Q16637 (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)