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 |
Phytochemical cluster | No. 15 |
---|---|
KCF-S cluster | No. 3 |
By standard InChI | CHEMBL348436 |
---|---|
By standard InChI Main Layer | CHEMBL348436 |
By LinkDB | C17785 |
---|
By CAS RN | C007072 |
---|
class name | count |
---|---|
asterids | 22 |
Euphyllophyta | 1 |
rosids | 1 |
family name | count |
---|---|
Lamiaceae | 16 |
Asteraceae | 4 |
Pteridaceae | 1 |
Verbenaceae | 1 |
Plantaginaceae | 1 |
Fabaceae | 1 |
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 |
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 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)
|