KNApSAcK Entry

Organism name Fucus vesiculosus
Genus Fucus
Family Fucaceae
Kingdom Plantae

NCBI taxonomy


Linked NCBI taxonomy name Fucus vesiculosus
Linked NCBI taxonomy ID 49266
Linked level species


Family in NCBI taxonomy Fucaceae
ID 3010

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Eukaryota
ID 2759

Plant class

Plant class

Natural Activity

List (15)

Species Activity
Fucus vesiculosus L. Alterative
Fucus vesiculosus L. Antiaggregant
Fucus vesiculosus L. Antihypothyroid
Fucus vesiculosus L. Antiobesity
Fucus vesiculosus L. Antirheumatic
Fucus vesiculosus L. Antiseptic
Fucus vesiculosus L. Demulcent
Fucus vesiculosus L. Depurative
Fucus vesiculosus L. Emollient
Fucus vesiculosus L. Hemagglutinant
Fucus vesiculosus L. Hypoglycemic
Fucus vesiculosus L. Immunomodulator
Fucus vesiculosus L. Laxative
Fucus vesiculosus L. Metal-Chelator
Fucus vesiculosus L. Tonic

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
C00000931 External link 512 Zeaxanthin
/ all-trans-Zeaxanthin
4 / 2 / 3 1 / 0 No. 26 No. 59
C00003653 External link 512 Fucosterol
/ (24R)24-Ethylcholesta-5,24(28)-dien-3beta-ol
No. 53 No. 11
C00003773 External link 512 Fucoxanthin
12 / 17 / 46 6 / 3 No. 114 No. 59
C00040472 External link 512 Tetrafucol A
No. 270
C00040473 External link 512 Tetrafucol B
No. 270

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000931 C00003773 0 / 0
O75496 Geminin Unclassified protein C00000931 C00003773 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000931 C00003773 2 / 3
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000931 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00003773 2 / 0
Q99700 Ataxin-2 Unclassified protein C00003773 1 / 1
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00003773 0 / 1
P06280 Alpha-galactosidase A Enzyme C00003773 1 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00003773 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00003773 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00003773 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00003773 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00003773 7 / 37

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC: C00000931
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00003773
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC: C00003773
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC: C00003773
2697 GJA1, AVSD3, CMDR, CX43, DFNB38, GJAL, HLHS1, HSS, ODDD gap junction protein, alpha 1, 43kDa C00003773
2705 GJB1, CMTX, CMTX1, CX32 gap junction protein, beta 1, 32kDa C00003773
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC: C00003773

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

OMIM preferred title UniProt
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114500 Colorectal cancer; crc P84022
#133239 Esophageal cancer P04637
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473


KEGG name UniProt
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)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
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)
H00125 Fabry disease P06280 (related)
H00079 Asthma P07550 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)

Diseases related to CTD interactions

3 disease in interactions with metabolites

D056486 Drug-Induced Liver Injury C00003773
D006949 Hyperlipidemias C00003773
D015430 Weight Gain C00003773