Metabolite

KNApSAcK Entry

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)

Cluster

Phytochemical cluster
KCF-S cluster No. 8423

Link

ChEMBL

By standard InChI CHEMBL1160571
By standard InChI Main Layer CHEMBL1160571

KEGG

By LinkDB C00013

CTD

By CAS RN C107241

Species

Summary

Plant class

class name count

Family

family name count
Enterobacteriaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Escherichia coli 562 Enterobacteriaceae Bacteria

Human Protein / Gene in interaction

10 ChEMBL Protein in interactions

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

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (5)

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 (7)

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)