Species

KNApSAcK Entry

Organism name Flourensia cernua
Genus Flourensia
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Flourensia
Linked NCBI taxonomy ID 191157
Linked level genus

Family

Family in NCBI taxonomy Asteraceae
ID 4210

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (15)

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
C00006381 External link 512 Isoshaftoside
/ Isoschaftoside
/ Apigenin 6-C-alpha-L-arabinopyranoside-8-C-beta-D-glucopyranoside
No. 1 No. 15
C00006382 External link 512 Neoschaftoside
CHEMBL1537012
7 / 2 / 2 No. 1 No. 15
C00004640 External link 512 Quercetin 3,4'-dimethyl ether
/ 5,7,3'-Trihydroxy-3,4'-dimethoxyflavone
/ 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-methoxy-4H-1-benzopyran-4-one
CHEMBL309263
16 / 8 / 2 No. 3 No. 15
C00004603 External link 512 Penduletin
/ 5,4'-Dihydroxy-3,6,7-trimethoxyflavone
/ 5-Hydroxy-2-(4-hydroxyphenyl)-3,6,7-trimethoxy-4H-1-benzopyran-4-one
CHEMBL165509
3 / 3 / 0 No. 3 No. 15
C00004638 External link 512 Quercetin 3,7-dimethyl ether
/ 5,3',4'-Trihydroxy-3,7-dimethoxyflavone
/ 2-(3,4-Dihydroxyphenyl)-5-hydroxy-3,7-dimethoxy-4H-1-benzopyran-4-one
CHEMBL164861
C065497
2 / 1 / 2 No. 3 No. 15
C00004596 External link 512 6-Methoxykaempferol 3-methyl ether
/ 5,7,4'-Trihydroxy-3,6-dimethoxyflavone
/ 5,7-Dihydroxy-2-(4-hydroxyphenyl)-3,6-dimethoxy-4H-1-benzopyran-4-one
CHEMBL351607
C014868
No. 3 No. 15
C00004646 External link 512 Pachypodol
/ Quercetin 3,3',7-trimethyl ether
/ 5,4'-Dihydroxy-3,7,3'-trimethoxyflavone
/ 5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-1-benzopyran-4-one
CHEMBL165180
C008751
1 / 2 / 0 No. 3 No. 15
C00004571 External link 512 Kaempferol 7,4'-dimethyl ether
/ 3,5-Dihydroxy-7,4'-dimethoxyflavone
/ 3,5-Dihydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
No. 3 No. 15
C00004692 External link 512 Chrysosplenol D
/ Quercetagetin 3,6,7-Trimethyl ether
/ 5,3',4'-Trihydroxy-3,6,7-trimethoxyflavone
/ 2-(3,4-dihydroxyphenyl)-5-hydroxy-3,6,7-trimethoxy-4H-1-benzopyran-4-one
CHEMBL491366
1 / 0 / 0 No. 3 No. 15
C00004693 External link 512 Jaceidin
/ Quercetagetin 3,3',6-trimethyl ether
/ 5,7,4'-Trihydroxy-3,6,3'-trimethoxyflavone
CHEMBL161878
No. 3 No. 15
C00004648 External link 512 Quercetin 3,3',4'-trimethyl ether
/ 5,7-Dihydroxy-3,3',4'-trimethoxyflavone
/ 2-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-3-methoxy-4H-1-benzopyran-4-one
CHEMBL350720
No. 3 No. 15
C00004533 External link 512 Galangin
/ Norizalpinin
/ 3,5,7-Trihydroxyflavone
/ 3,5,7-Trihydroxy-2-phenyl-4H-1-benzopyran-4-one
CHEMBL309490
C037032
35 / 34 / 29 15 / 4 No. 76 No. 15
C00021208 External link 512 Flourensadiol
No. 197 No. 38
C00034475 External link 512 Dehydroflourensic acid
/ (-)-Dehydroflourensic acid
No. 1429
C00017294 External link 512 Flourensic acid
/ 9-Oxo-7xi-eremophil-11(13)-en-12-oic acid
No. 1933

Human Protein / Gene in interactions

61 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08183 Multidrug resistance protein 1 drug C00004533 C00004603 1 / 0
Q9UNA4 DNA polymerase iota Enzyme C00004533 C00006382 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00004603 C00004646 2 / 0
P15121 Aldose reductase Enzyme C00004603 C00004692 0 / 0
Q13748 Tubulin alpha-3C/D chain Structural C00004640 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00004533 0 / 0
P06746 DNA polymerase beta Enzyme C00006382 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00006382 1 / 1
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00004533 1 / 1
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00004533 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00004533 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00004533 0 / 1
P11388 DNA topoisomerase 2-alpha Isomerase C00004533 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00004533 0 / 0
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00004533 1 / 1
P39748 Flap endonuclease 1 Enzyme C00006382 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00004533 2 / 0
O75496 Geminin Unclassified protein C00004533 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00004533 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00004533 4 / 2
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00004533 0 / 0
Q9NPH5 NADPH oxidase 4 Enzyme C00004638 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00006382 1 / 1
P04150 Glucocorticoid receptor NR3C1 C00004533 0 / 1
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00004533 2 / 2
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00004533 4 / 4
P06276 Cholinesterase Hydrolase C00004533 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00004533 0 / 0
O75795 UDP-glucuronosyltransferase 2B17 Enzyme C00004533 1 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00004533 0 / 0
O14763 Tumor necrosis factor receptor superfamily member 10B Unclassified protein C00004640 1 / 0
P22303 Acetylcholinesterase Hydrolase C00004533 1 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00004533 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00004533 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00004533 0 / 1
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00004533 3 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00006382 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00004533 5 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00004533 4 / 3
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00004533 0 / 0
P10275 Androgen receptor NR3C4 C00004533 3 / 4
P06239 Tyrosine-protein kinase Lck Src C00004533 0 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00006382 0 / 0
O00255 Menin Unclassified protein C00004533 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00004533 1 / 2
P00747 Plasminogen S1A C00004638 1 / 2
P68366 Tubulin alpha-4A chain Structural C00004640 0 / 0
Q9H4B7 Tubulin beta-1 chain Structural C00004640 1 / 0
P04350 Tubulin beta-4A chain Structural C00004640 2 / 0
Q3ZCM7 Tubulin beta-8 chain Structural C00004640 0 / 0
P07437 Tubulin beta chain Structural C00004640 0 / 0
Q71U36 Tubulin alpha-1A chain Structural C00004640 1 / 1
P68371 Tubulin beta-4B chain Structural C00004640 0 / 0
Q13509 Tubulin beta-3 chain Structural C00004640 2 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00004533 0 / 0
P68363 Tubulin alpha-1B chain Unclassified protein C00004640 0 / 0
Q13885 Tubulin beta-2A chain Structural C00004640 0 / 0
Q6PEY2 Tubulin alpha-3E chain Unclassified protein C00004640 0 / 0
Q9BQE3 Tubulin alpha-1C chain Unclassified protein C00004640 0 / 0
Q9BUF5 Tubulin beta-6 chain Structural C00004640 0 / 0
Q9BVA1 Tubulin beta-2B chain Structural C00004640 1 / 0

15 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4363 ABCC1, ABC29, ABCC, GS-X, MRP, MRP1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1 C00004533
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00004533
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00004533
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00004533
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) C00004533
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) C00004533
2034 EPAS1, ECYT4, HIF2A, HLF, MOP2, PASD2, bHLHe73 endothelial PAS domain protein 1 C00004533
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00004533
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00004533
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00004533
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00004533
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00004533
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00004533
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00004533
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00004533

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (47)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#614490 Blood group, junior system; jr Q9UNQ0
#612560 Bone mineral density quantitative trait locus 12; bmnd12 O75795
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#114500 Colorectal cancer; crc P84022
#614039 Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 Q13509
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#128101 Dystonia 4, torsion, autosomal dominant; dyt4 P04350
#600638 Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a Q13509
#600274 Frontotemporal dementia; ftd P10636
#143500 Gilbert syndrome P22309
P22310
#137750 Glaucoma 1, open angle, a; glc1a Q16678
#231300 Glaucoma 3, primary congenital, a; glc3a Q16678
#137760 Glaucoma, primary open angle; poag Q16678
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#145000 Hyperparathyroidism 1; hrpt1 O00255
#612244 Inflammatory bowel disease 13; ibd13 P08183
#601626 Leukemia, acute myeloid; aml P36888
#612438 Leukodystrophy, hypomyelinating, 6; hld6 P04350
#611603 Lissencephaly 3; lis3 Q71U36
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#613112 Macrothrombocytopenia, autosomal dominant, tubb1-related Q9H4B7
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260540 Parkinson-dementia syndrome P10636
#604229 Peters anomaly Q16678
#172700 Pick disease of brain P10636
#217090 Plasminogen deficiency, type i P00747
#610031 Polymicrogyria, symmetric or asymmetric; pmgysa Q9BVA1
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#275355 Squamous cell carcinoma, head and neck; hnscc O14763
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (35)

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)
H00223 Inherited thrombophilia P00747 (related)
H01206 Plasminogen deficiency P00747 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00208 Hyperbilirubinemia P22309 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00003 Acute myeloid leukemia (AML) P36888 (related)
H00027 Ovarian cancer P38398 (related)
H00031 Breast cancer P38398 (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)
H00612 Primary open angle glaucoma Q16678 (related)
H01075 Peters anomaly Q16678 (related)
H01159 Anterior segment dysgenesis (ASD) Q16678 (related)
H01203 Primary congenital glaucoma (PCG) Q16678 (related)
H00268 Lissencephaly (LIS) Q71U36 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006943 Hyperglycemia C00004533
D006946 Hyperinsulinism C00004533
D015228 Hypertriglyceridemia C00004533
D007333 Insulin Resistance C00004533