Metabolite

KNApSAcK Entry

id C00003837
Name Cirsimaritin
CAS RN 6601-62-3
Standard InChI InChI=1S/C17H14O6/c1-21-14-8-13-15(16(20)17(14)22-2)11(19)7-12(23-13)9-3-5-10(18)6-4-9/h3-8,18,20H,1-2H3
Standard InChI (Main Layer) InChI=1S/C17H14O6/c1-21-14-8-13-15(16(20)17(14)22-2)11(19)7-12(23-13)9-3-5-10(18)6-4-9/h3-8,18,20H,1-2H3

Cluster

Phytochemical cluster No. 15
KCF-S cluster No. 3

Link

ChEMBL

By standard InChI CHEMBL348436
By standard InChI Main Layer CHEMBL348436

KEGG

By LinkDB C17785

CTD

By CAS RN C007072

Species

Summary


List (24)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Artemisia vestita 4219 Asteraceae asterids Viridiplantae
Baccharis eleagnoides 41487 Asteraceae asterids Viridiplantae
Brickellia californica 176615 Asteraceae asterids Viridiplantae
Cheilanthes argentea 238825 Pteridaceae Euphyllophyta Viridiplantae
Cirsium brevistylum 196706 Asteraceae asterids Viridiplantae
Digitalis thapsi 285839 Plantaginaceae asterids Viridiplantae
Lippia dulcis TREV. 320344 Verbenaceae asterids Viridiplantae
Ononis vaginalis 798051 Fabaceae rosids Viridiplantae
Plectranthus ecklonii Benth. 41227 Lamiaceae asterids Viridiplantae
Plectranthus fruticosus 306376 Lamiaceae asterids Viridiplantae
Salvia columbariae 95165 Lamiaceae asterids Viridiplantae
Salvia dorrii 207754 Lamiaceae asterids Viridiplantae
Salvia lavandulaefolia 49214 Lamiaceae asterids Viridiplantae
Salvia lavandulifolia 49214 Lamiaceae asterids Viridiplantae
Salvia macrosiphon 21880 Lamiaceae asterids Viridiplantae
Salvia mirzayana 21880 Lamiaceae asterids Viridiplantae
Salvia nicolsoniana 21880 Lamiaceae asterids Viridiplantae
Salvia officinalis 38868 Lamiaceae asterids Viridiplantae
Salvia palaestina 268920 Lamiaceae asterids Viridiplantae
Salvia sapinae 21880 Lamiaceae asterids Viridiplantae
Salvia tomentosa 1132405 Lamiaceae asterids Viridiplantae
Salvia verbenaca 268912 Lamiaceae asterids Viridiplantae
Teucrium polium 1117157 Lamiaceae asterids Viridiplantae
Teucrium ramosissimum 21896 Lamiaceae asterids Viridiplantae

Human Protein / Gene in interaction

13 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein CHEMBL348436 CHEMBL1738312 (1)
0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase CHEMBL348436 CHEMBL1008498 (1)
0 / 3
P33765 Adenosine receptor A3 Adenosine receptor CHEMBL348436 CHEMBL638578 (1) CHEMBL649050 (1)
0 / 0
P06746 DNA polymerase beta Enzyme CHEMBL348436 CHEMBL1614079 (1)
0 / 0
P04062 Glucosylceramidase Enzyme CHEMBL348436 CHEMBL1613818 (1)
6 / 4
P23219 Prostaglandin G/H synthase 1 Oxidoreductase CHEMBL348436 CHEMBL1008497 (1)
0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor CHEMBL348436 CHEMBL2114788 (1)
0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein CHEMBL348436 CHEMBL2114810 (1)
7 / 3
Q9Y253 DNA polymerase eta Enzyme CHEMBL348436 CHEMBL1794569 (1)
1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein CHEMBL348436 CHEMBL1738588 (1) CHEMBL1738317 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL348436 CHEMBL1794483 (1)
0 / 0
P10636 Microtubule-associated protein tau Unclassified protein CHEMBL348436 CHEMBL1614421 (1) CHEMBL1614502 (1)
4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL348436 CHEMBL1613914 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#600274 Frontotemporal dementia; ftd P10636
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#168600 Parkinson disease, late-onset; pd P04062
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (14)

KEGG disease name UniProt
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)