PCIDB

KNApSAcK Metabolite C00034054

Metabolite

KNApSAcK Entry

id C00034054
Name Methyl benzoate
CAS RN 93-58-3
Standard InChI InChI=1S/C8H8O2/c1-10-8(9)7-5-3-2-4-6-7/h2-6H,1H3
Standard InChI (Main Layer) InChI=1S/C8H8O2/c1-10-8(9)7-5-3-2-4-6-7/h2-6H,1H3

Cluster

Phytochemical cluster
KCF-S cluster No. 4170

Link

ChEMBL

By standard InChI CHEMBL16435
By standard InChI Main Layer CHEMBL16435

KEGG

By LinkDB

CTD

By CAS RN C044605

Human Protein / Gene in interaction

4 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL16435 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
P10145 Interleukin-8 Secreted protein CHEMBL16435 CHEMBL2114835 (1)
0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL16435 CHEMBL2114890 (1)
0 / 0
P10275 Androgen receptor NR3C4 CHEMBL16435 CHEMBL1794321 (1) 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)