PCIDB

KNApSAcK Metabolite C00032013

Metabolite

KNApSAcK Entry

id C00032013
Name Methyl p-formylbenzoate
CAS RN 1571-08-0
Standard InChI InChI=1S/C9H8O3/c1-12-9(11)8-4-2-7(6-10)3-5-8/h2-6H,1H3
Standard InChI (Main Layer) InChI=1S/C9H8O3/c1-12-9(11)8-4-2-7(6-10)3-5-8/h2-6H,1H3

Cluster

Phytochemical cluster
KCF-S cluster No. 2169

Link

ChEMBL

By standard InChI CHEMBL1607943
By standard InChI Main Layer CHEMBL1607943

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
rosids 1

Family

family name count
Malvaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Hibiscus taiwanensis 47605 Malvaceae rosids Viridiplantae

Human Protein / Gene in interaction

7 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 CHEMBL1607943 CHEMBL1794552 (1)
0 / 0
P10828 Thyroid hormone receptor beta NR1A2 CHEMBL1607943 CHEMBL1794399 (1)
3 / 1
P11473 Vitamin D3 receptor NR1I1 CHEMBL1607943 CHEMBL1794339 (1)
2 / 3
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL1607943 CHEMBL1614458 (1)
0 / 0
P04150 Glucocorticoid receptor NR3C1 CHEMBL1607943 CHEMBL1794382 (1)
0 / 1
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor CHEMBL1607943 CHEMBL2114853 (1)
0 / 0
P10275 Androgen receptor NR3C4 CHEMBL1607943 CHEMBL1794321 (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
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (9)

KEGG disease name UniProt
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
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)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)