KNApSAcK Metabolite C00029478
Metabolite
KNApSAcK Entry
| id | C00029478 |
|---|---|
| Name | 3,4'-Dihydroxypropiophenone / 4-Hydroxy-(3-hydroxypropionyl)benzene |
| CAS RN | 53170-93-7 |
| Standard InChI | InChI=1S/C9H10O3/c10-6-5-9(12)7-1-3-8(11)4-2-7/h1-4,10-11H,5-6H2 |
| Standard InChI (Main Layer) | InChI=1S/C9H10O3/c10-6-5-9(12)7-1-3-8(11)4-2-7/h1-4,10-11H,5-6H2 |
Cluster
| Phytochemical cluster | |
|---|---|
| KCF-S cluster | No. 2849 |
Link
ChEMBL
| By standard InChI | CHEMBL1417159 |
|---|---|
| By standard InChI Main Layer | CHEMBL1417159 |
KEGG
| By LinkDB |
|---|
CTD
| By CAS RN |
|---|
Species
Summary
Plant class
| class name | count |
|---|---|
| rosids | 1 |
Family
| family name | count |
|---|---|
| Cucurbitaceae | 1 |
List (1)
* NCBI
| KNApSAcK organism | *ID | *family | *plant class | *kingdom |
|---|---|---|---|---|
| Citrullus colocynthis (L.) | 3653 | Cucurbitaceae | rosids | Viridiplantae |
Human Protein / Gene in interaction
25 ChEMBL Protein in interactions
| accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|---|
| Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | CHEMBL1417159 |
CHEMBL1614529
(1)
|
0 / 0 |
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | CHEMBL1417159 |
CHEMBL1738312
(1)
|
0 / 0 |
| P06746 | DNA polymerase beta | Enzyme | CHEMBL1417159 |
CHEMBL1614079
(1)
|
0 / 0 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | CHEMBL1417159 |
CHEMBL1614076
(1)
|
1 / 1 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | CHEMBL1417159 |
CHEMBL1794585
(1)
|
0 / 0 |
| P54132 | Bloom syndrome protein | Enzyme | CHEMBL1417159 |
CHEMBL1614067
(1)
|
1 / 2 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | CHEMBL1417159 |
CHEMBL1614166
(1)
CHEMBL1738096
(1)
CHEMBL1738622 (1) |
1 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL1417159 |
CHEMBL1614458
(1)
|
0 / 0 |
| P39748 | Flap endonuclease 1 | Enzyme | CHEMBL1417159 |
CHEMBL1794486
(1)
|
0 / 0 |
| Q9Y253 | DNA polymerase eta | Enzyme | CHEMBL1417159 |
CHEMBL1794569
(1)
|
1 / 1 |
| P09923 | Intestinal-type alkaline phosphatase | Enzyme | CHEMBL1417159 |
CHEMBL1738315
(1)
|
0 / 0 |
| P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | CHEMBL1417159 |
CHEMBL1738602
(1)
|
3 / 1 |
| Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | CHEMBL1417159 |
CHEMBL1614280
(1)
|
0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | CHEMBL1417159 |
CHEMBL1794401
(1)
|
0 / 0 |
| P10696 | Alkaline phosphatase, placental-like | Enzyme | CHEMBL1417159 |
CHEMBL1738514
(1)
|
0 / 1 |
| Q9UNA4 | DNA polymerase iota | Enzyme | CHEMBL1417159 |
CHEMBL1794483
(1)
|
0 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | CHEMBL1417159 |
CHEMBL1737991
(1)
|
0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | CHEMBL1417159 |
CHEMBL1614466
(1)
CHEMBL1614211
(1)
|
0 / 0 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | CHEMBL1417159 |
CHEMBL1794536
(1)
|
0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL1417159 |
CHEMBL1613914
(1)
|
0 / 0 |
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | CHEMBL1417159 |
CHEMBL1613829
(1)
|
0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | CHEMBL1417159 |
CHEMBL1738442
(1)
|
0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | CHEMBL1417159 |
CHEMBL1614364
(1)
|
1 / 1 |
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | CHEMBL1417159 |
CHEMBL2114738
(1)
|
0 / 0 |
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | CHEMBL1417159 |
CHEMBL2114796
(1)
|
2 / 1 |
Related Disease
Diseases related to proteins in ChEMBL interactions
OMIM (10)
| OMIM | preferred title | UniProt |
|---|---|---|
| #210900 | Bloom syndrome; blm |
P54132
|
| #114500 | Colorectal cancer; crc |
Q14191
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #146300 | Hypophosphatasia, adult |
P05186
|
| #241510 | Hypophosphatasia, childhood |
P05186
|
| #241500 | Hypophosphatasia, infantile |
P05186
|
| #160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #277700 | Werner syndrome; wrn |
Q14191
|
| #278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG DISEASE (7)
| KEGG | disease name | UniProt |
|---|---|---|
| H00213 | Hypophosphatasia |
P05186
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00023 | Testicular cancer |
P10696
(marker)
|
| H00094 | DNA repair defects |
P54132
(related)
|
| H00296 | Defects in RecQ helicases |
P54132
(related)
Q14191 (related) |
| H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|