| id | C00019561 |
|---|---|
| Name | PPi / Diphosphoric acid / Pyrophosphoric acid |
| CAS RN | 2466-09-3 |
| Standard InChI | InChI=1S/H4O7P2/c1-8(2,3)7-9(4,5)6/h(H2,1,2,3)(H2,4,5,6) |
| Standard InChI (Main Layer) | InChI=1S/H4O7P2/c1-8(2,3)7-9(4,5)6/h(H2,1,2,3)(H2,4,5,6) |
| Phytochemical cluster | |
|---|---|
| KCF-S cluster | No. 8423 |
| By standard InChI | CHEMBL1160571 |
|---|---|
| By standard InChI Main Layer | CHEMBL1160571 |
| By LinkDB | C00013 |
|---|
| By CAS RN | C107241 |
|---|
| class name | count |
|---|
| family name | count |
|---|---|
| Enterobacteriaceae | 1 |
| KNApSAcK organism | *ID | *family | *plant class | *kingdom |
|---|---|---|---|---|
| Escherichia coli | 562 | Enterobacteriaceae | Bacteria |
| accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | CHEMBL1160571 |
CHEMBL1741321
(1)
|
1 / 0 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | CHEMBL1160571 |
CHEMBL1741325
(1)
|
0 / 1 |
| P54132 | Bloom syndrome protein | Enzyme | CHEMBL1160571 |
CHEMBL1614067
(1)
|
1 / 2 |
| P00480 | Ornithine carbamoyltransferase, mitochondrial | Enzyme | CHEMBL1160571 |
CHEMBL753864
(1)
CHEMBL753865
(1)
CHEMBL750183 (1) |
1 / 1 |
| P14324 | Farnesyl pyrophosphate synthase | Transferase | CHEMBL1160571 |
CHEMBL924793
(2)
CHEMBL924794
(2)
|
0 / 0 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | CHEMBL1160571 |
CHEMBL1741322
(1)
|
0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | CHEMBL1160571 |
CHEMBL1741323
(1)
|
1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | CHEMBL1160571 |
CHEMBL1741324
(1)
|
0 / 1 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | CHEMBL1160571 |
CHEMBL1738442
(1)
|
0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | CHEMBL1160571 |
CHEMBL1614364
(1)
|
1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #210900 | Bloom syndrome; blm |
P54132
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #311250 | Ornithine transcarbamylase deficiency, hyperammonemia due to |
P00480
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| KEGG | disease name | UniProt |
|---|---|---|
| H00187 | Ornithine transcarbamylase deficiency |
P00480
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00094 | DNA repair defects |
P54132
(related)
|
| H00296 | Defects in RecQ helicases |
P54132
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|