Metabolite

KNApSAcK Entry

id C00002673
Name Sesamol
CAS RN 533-31-3
Standard InChI InChI=1S/C7H6O3/c8-5-1-2-6-7(3-5)10-4-9-6/h1-3,8H,4H2
Standard InChI (Main Layer) InChI=1S/C7H6O3/c8-5-1-2-6-7(3-5)10-4-9-6/h1-3,8H,4H2

Cluster

Phytochemical cluster
KCF-S cluster No. 4093

Link

ChEMBL

By standard InChI CHEMBL1517998
By standard InChI Main Layer CHEMBL1517998

KEGG

By LinkDB C10832

CTD

By CAS RN C025583

Species

Summary

Plant class

class name count
asterids 1

Family

family name count
Pedaliaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Sesamum indicum 4182 Pedaliaceae asterids Viridiplantae

Human Protein / Gene in interaction

3 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 CHEMBL1517998 CHEMBL1794510 (1)
5 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 CHEMBL1517998 CHEMBL1614108 (1) CHEMBL1613886 (1)
0 / 1
P10275 Androgen receptor NR3C4 CHEMBL1517998 CHEMBL1794321 (1) CHEMBL1794560 (1)
3 / 4

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#137800 Glioma susceptibility 1; glm1 P37231
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#601665 Obesity P37231
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275

KEGG DISEASE (8)

KEGG disease name UniProt
H00036 Osteosarcoma P08684 (marker)
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)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)

Diseases related to CTD interactions

1 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D009203 C025583 Myocardial Infarction therapeutic
20196927