Metabolite

KNApSAcK Entry

id C00044987
Name p-(Acetylamino)benzoic acid
CAS RN 556-08-1
Standard InChI InChI=1S/C9H9NO3/c1-6(11)10-8-4-2-7(3-5-8)9(12)13/h2-5H,1H3,(H,10,11)(H,12,13)
Standard InChI (Main Layer) InChI=1S/C9H9NO3/c1-6(11)10-8-4-2-7(3-5-8)9(12)13/h2-5H,1H3,(H,10,11)(H,12,13)

Cluster

Phytochemical cluster
KCF-S cluster No. 8182

Link

ChEMBL

By standard InChI CHEMBL112687
By standard InChI Main Layer CHEMBL112687

KEGG

By LinkDB

CTD

By CAS RN C023730

Species

Summary

Plant class

class name count

Family

family name count
Streptomycetaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Streptomyces venezuelae 54571 Streptomycetaceae Bacteria

Human Protein / Gene in interaction

6 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL112687 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
Q9UQ49 Sialidase-3 Enzyme CHEMBL112687 CHEMBL751097 (2)
0 / 0
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL112687 CHEMBL1614458 (1)
0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL112687 CHEMBL1794401 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL112687 CHEMBL1794483 (1)
0 / 0
P10275 Androgen receptor NR3C4 CHEMBL112687 CHEMBL1794560 (1)
3 / 4

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275

KEGG DISEASE (6)

KEGG disease name UniProt
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)