Species

KNApSAcK Entry

Organism name Frullania tamarisci
Genus Frullania
Family Jubulaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Frullania tamarisci
Linked NCBI taxonomy ID 95764
Linked level species

Family

Family in NCBI taxonomy Frullaniaceae
ID 400721

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Embryophyta
ID 3193

Metabolite list (25)

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
C00014074 External link 512 6-C-Rhamnopyranosylrhamnetin 3-O-glucopyranoside
No. 1 No. 15
C00004266 External link 512 Cinaroside
/ Luteolin 7-glucoside
/ Luteolin-7-O-glucoside
/ Luteolin 7-O-beta-D-glucopyranoside
CHEMBL233929
CHEMBL574683
CHEMBL1159535
CHEMBL1317166
C066408
26 / 31 / 53 No. 2 No. 15
C00003242 External link 512 (+)-beta-Cyclocostunolide
/ beta-Cyclocostunolide[3aS-(3aalpha,5abeta,9aalpha,9bbeta)]-Decahydro-5a-methyl-3,9-bis(methylene)-naphtho[1,2-b]furan-2(3H)-one
No. 69 No. 38
C00003241 External link 512 alpha-Cyclocostunolide
CHEMBL218788
C002603
No. 69 No. 38
C00015321 External link 512 3,4'-Dimethoxybibenzyl
/ Lunularine dimethyl ether
CHEMBL477915
No. 96 No. 26
C00016975 External link 512 Eremophilene
No. 151 No. 38
C00013031 External link 512 (+)-Frullanolide
/ [3aR-(3aalpha,5abeta,9balpha)]-3a,4,5,5a,6,7,8,9b-Octahydro-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2(3H)-one
No. 178 No. 38
C00003287 External link 512 (-)-Frullanolide
/ Tournefortiolide
/ [3aS-(3aalpha,5abeta,9balpha)]-3a,4,5,5a,6,7,8,9b-Octahydro-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2(3H)-one
C007787
No. 178 No. 38
C00003161 External link 512 Ledol
/ (+)-Ledol
CHEMBL2171207
1 / 2 / 3 No. 197 No. 38
C00021213 External link 512 Globulol
/ (-)-Globulol
CHEMBL2171207
1 / 2 / 3 No. 197 No. 38
C00020066 External link 512 T-Cadinol
/ epi-alpha-Cadinol
CHEMBL486795
C072576
No. 205 No. 38
C00002889 External link 512 Lunularin
/ 3,4'-Dihydroxybibenzyl
CHEMBL445252
C121619
No. 242 No. 26
C00003118 External link 512 Copaene
/ alpha-Copaene
/ (-)-alpha-Copaene
No. 333 No. 38
C00021886 External link 512 beta-Pompene
/ Gymnomitrene
/ beta-Barbatene
/ beta-Gymnomitrene
No. 365 No. 38
C00012810 External link 512 Rosifoliol
/ (+)-Rosifoliol
/ [2R-(2alpha,4abeta,8beta)]-2,3,4,4a,5,6,7,8-octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol
No. 613 No. 38
C00036399 External link 512 11-Bourbonene
No. 640
C00036290 External link 512 (-)-Tamariscene
No. 640
C00036308 External link 512 (+)-Germacrene A
No. 701 No. 38
C00037126 External link 512 Eudesma-4,11-diene
/ (+)-Selina-4,11-diene
No. 748
C00036286 External link 512 (-)-Pacifigorgia-1(9),10-diene
No. 1391
C00036271 External link 512 (-)-beta-Elemene
CHEMBL448502
CHEMBL479707
No. 1400
C00036291 External link 512 (-)-Tamariscol
No. 2857
C00021436 External link 512 Tamariscol
No. 2857
C00020383 External link 512 gamma-Gurjunene
/ (+)-gamma-Gurjunene
CHEMBL455046
No. 3712 No. 38
C00036285 External link 512 (-)-Pacifigorgia-1(6),10-diene
No. 8531

Human Protein / Gene in interactions

27 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00003161 C00021213 2 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00004266 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00004266 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00004266 0 / 0
P39748 Flap endonuclease 1 Enzyme C00004266 0 / 0
O75496 Geminin Unclassified protein C00004266 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00004266 4 / 2
Q9Y253 DNA polymerase eta Enzyme C00004266 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00004266 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00004266 0 / 0
P14679 Tyrosinase Oxidoreductase C00004266 4 / 2
P04637 Cellular tumor antigen p53 Transcription Factor C00004266 7 / 37
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00004266 3 / 3
Q99700 Ataxin-2 Unclassified protein C00004266 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00004266 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00004266 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00004266 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00004266 4 / 3
Q9UBT6 DNA polymerase kappa Enzyme C00004266 0 / 0
P24298 Alanine aminotransferase 1 Enzyme C00004266 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004266 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00004266 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00004266 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00004266 1 / 0
O00255 Menin Unclassified protein C00004266 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00004266 1 / 2
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00004266 2 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (33)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#114500 Colorectal cancer; crc Q14191
#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
#114550 Hepatocellular carcinoma P08581
#145000 Hyperparathyroidism 1; hrpt1 O00255
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#211980 Lung cancer P04637
#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
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (53)

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)
P08581 (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)
H00038 Malignant melanoma P04637 (related)
P14679 (marker)
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)
P08581 (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)
P08581 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (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)
H00296 Defects in RecQ helicases Q14191 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)