id | C00030423 |
---|---|
Name | Gossypetin |
CAS RN | 489-35-0 |
Standard InChI | InChI=1S/C15H10O8/c16-6-2-1-5(3-7(6)17)14-13(22)12(21)10-8(18)4-9(19)11(20)15(10)23-14/h1-4,16-20,22H |
Standard InChI (Main Layer) | InChI=1S/C15H10O8/c16-6-2-1-5(3-7(6)17)14-13(22)12(21)10-8(18)4-9(19)11(20)15(10)23-14/h1-4,16-20,22H |
Phytochemical cluster | No. 15 |
---|---|
KCF-S cluster | No. 3 |
By standard InChI | CHEMBL253570 |
---|---|
By standard InChI Main Layer | CHEMBL253570 |
By LinkDB | C04109 |
---|
By CAS RN | C059922 |
---|
class name | count |
---|---|
asterids | 1 |
eudicotyledons | 1 |
family name | count |
---|---|
Rubiaceae | 1 |
Crassulaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Adina cordifolia Roxb. | 170034 | Rubiaceae | asterids | Viridiplantae |
Sinocrassula indica | 91157 | Crassulaceae | eudicotyledons | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P11309 | Serine/threonine-protein kinase pim-1 | Pim | CHEMBL253570 |
CHEMBL926333
(1)
|
0 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | CHEMBL253570 |
CHEMBL1794311
(1)
|
2 / 3 |
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL253570 |
CHEMBL1614458
(1)
|
0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | CHEMBL253570 |
CHEMBL1794467
(1)
|
0 / 0 |
P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | CHEMBL253570 |
CHEMBL987970
(1)
|
2 / 2 |
P06280 | Alpha-galactosidase A | Enzyme | CHEMBL253570 |
CHEMBL1614217
(1)
|
1 / 1 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | CHEMBL253570 |
CHEMBL1614038
(1)
|
2 / 2 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | CHEMBL253570 |
CHEMBL1614240
(1)
|
0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | CHEMBL253570 |
CHEMBL1614466
(1)
CHEMBL1614211
(1)
|
0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL253570 |
CHEMBL1614250
(1)
CHEMBL1614421
(1)
CHEMBL1614502 (1) |
4 / 3 |
Q9UBT6 | DNA polymerase kappa | Enzyme | CHEMBL253570 |
CHEMBL1794536
(1)
|
0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL253570 |
CHEMBL1613914
(1)
|
0 / 0 |
O00255 | Menin | Unclassified protein | CHEMBL253570 |
CHEMBL1614257
(1)
|
2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | CHEMBL253570 |
CHEMBL1614257
(1)
|
1 / 3 |
compound | gene | gene name | gene description | interaction | interaction type | form |
reference
pmid |
---|---|---|---|---|---|---|---|
C059922 | 142 |
PARP1
ADPRT ADPRT_1 ADPRT1 ARTD1 PARP PARP-1 PPOL pADPRT-1 |
poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) | gossypetin results in decreased activity of PARP1 protein |
decreases activity
|
protein |
17884996
|
OMIM | preferred title | UniProt |
---|---|---|
#613546 | Aromatase deficiency |
P11511
|
#139300 | Aromatase excess syndrome; aexs |
P11511
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#301500 | Fabry disease |
P06280
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
KEGG | disease 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)
|
H00125 | Fabry disease |
P06280
(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)
|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P11511
(related)
|
H00794 | Aromatase excess syndrome |
P11511
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(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)
|