PCIDB

KNApSAcK Metabolite C00042277

Metabolite

KNApSAcK Entry

id C00042277
Name Benzamide
CAS RN 55-21-0
Standard InChI InChI=1S/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)
Standard InChI (Main Layer) InChI=1S/C7H7NO/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)

Cluster

Phytochemical cluster No. 9
KCF-S cluster No. 2578

Link

ChEMBL

By standard InChI CHEMBL267373
By standard InChI Main Layer CHEMBL267373

KEGG

By LinkDB C09815

CTD

By CAS RN

Species

Summary

Plant class

class name count
rosids 1

Family

family name count
Rutaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Boronella koniambiensis 1226048 Rutaceae rosids Viridiplantae

Human Protein / Gene in interaction

19 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein CHEMBL267373 CHEMBL2114784 (1)
1 / 1
P06746 DNA polymerase beta Enzyme CHEMBL267373 CHEMBL1614079 (1)
0 / 0
Q86W56 Poly(ADP-ribose) glycohydrolase Enzyme CHEMBL267373 CHEMBL1814966 (1) CHEMBL1814972 (1)
0 / 0
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL267373 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
P54132 Bloom syndrome protein Enzyme CHEMBL267373 CHEMBL1614522 (1) CHEMBL1614067 (1)
1 / 2
O75496 Geminin Unclassified protein CHEMBL267373 CHEMBL2114843 (1) CHEMBL2114780 (1)
0 / 0
P09874 Poly [ADP-ribose] polymerase 1 Enzyme CHEMBL267373 CHEMBL763795 (1) CHEMBL761610 (1)
CHEMBL1814965 (1)
0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein CHEMBL267373 CHEMBL1614280 (1)
0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL267373 CHEMBL1794401 (1)
0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme CHEMBL267373 CHEMBL1614227 (1)
3 / 3
Q01453 Peripheral myelin protein 22 Unclassified protein CHEMBL267373 CHEMBL1614171 (1)
5 / 2
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 CHEMBL267373 CHEMBL1613777 (1)
1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 CHEMBL267373 CHEMBL1614108 (1) CHEMBL1613886 (1)
0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme CHEMBL267373 CHEMBL1614211 (1)
0 / 0
P10636 Microtubule-associated protein tau Unclassified protein CHEMBL267373 CHEMBL1614250 (1)
4 / 3
Q99549 M-phase phosphoprotein 8 Unclassified protein CHEMBL267373 CHEMBL1738402 (1)
0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL267373 CHEMBL1737980 (1)
0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme CHEMBL267373 CHEMBL1614330 (1)
0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme CHEMBL267373 CHEMBL1614364 (2)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (19)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#210900 Bloom syndrome; blm P54132
#118300 Charcot-marie-tooth disease and deafness Q01453
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#609535 Drug metabolism, poor, cyp2c19-related P33261
#600274 Frontotemporal dementia; ftd P10636
#139393 Guillain-barre syndrome, familial; gbs Q01453
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (15)

KEGG disease name UniProt
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00264 Charcot-Marie-Tooth disease (CMT) Q01453 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)