id | C00006961 |
---|---|
Name | 2',3'-Dihydroxy-4',6'-dimethoxychalcone |
CAS RN | 54299-64-8 |
Standard InChI | InChI=1S/C17H16O5/c1-21-13-10-14(22-2)16(19)17(20)15(13)12(18)9-8-11-6-4-3-5-7-11/h3-10,19-20H,1-2H3/b9-8+ |
Standard InChI (Main Layer) | InChI=1S/C17H16O5/c1-21-13-10-14(22-2)16(19)17(20)15(13)12(18)9-8-11-6-4-3-5-7-11/h3-10,19-20H,1-2H3 |
Phytochemical cluster | |
---|---|
KCF-S cluster | No. 79 |
By standard InChI | CHEMBL1446527 |
---|---|
By standard InChI Main Layer | CHEMBL1446527 |
By LinkDB |
---|
By CAS RN |
---|
class name | count |
---|---|
Magnoliophyta | 1 |
family name | count |
---|---|
Piperaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Piper hispidum | 130401 | Piperaceae | Magnoliophyta | Viridiplantae |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | CHEMBL1446527 |
CHEMBL1738312
(1)
|
0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | CHEMBL1446527 |
CHEMBL2114784
(1)
|
1 / 1 |
P11473 | Vitamin D3 receptor | NR1I1 | CHEMBL1446527 |
CHEMBL1794311
(1)
|
2 / 3 |
O75496 | Geminin | Unclassified protein | CHEMBL1446527 |
CHEMBL2114843
(1)
CHEMBL2114780
(1)
|
0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | CHEMBL1446527 |
CHEMBL2114817
(1)
|
7 / 3 |
Q9Y253 | DNA polymerase eta | Enzyme | CHEMBL1446527 |
CHEMBL1794569
(1)
|
1 / 1 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | CHEMBL1446527 |
CHEMBL1963863
(1)
|
0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | CHEMBL1446527 |
CHEMBL1794483
(1)
|
0 / 0 |
Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | CHEMBL1446527 |
CHEMBL1614052
(1)
|
1 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | CHEMBL1446527 |
CHEMBL1737991
(1)
|
0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL1446527 |
CHEMBL1614421
(1)
|
4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | CHEMBL1446527 |
CHEMBL2114908
(1)
|
0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | CHEMBL1446527 |
CHEMBL2354287
(1)
|
1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#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
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | disease name | UniProt |
---|---|---|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (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)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|