PCIDB

KNApSAcK Metabolite C00002752

Metabolite

KNApSAcK Entry

id C00002752
Name Isoferulic acid
CAS RN 537-73-5
Standard InChI InChI=1S/C10H10O4/c1-14-9-4-2-7(6-8(9)11)3-5-10(12)13/h2-6,11H,1H3,(H,12,13)/b5-3+
Standard InChI (Main Layer) InChI=1S/C10H10O4/c1-14-9-4-2-7(6-8(9)11)3-5-10(12)13/h2-6,11H,1H3,(H,12,13)

Cluster

Phytochemical cluster No. 6
KCF-S cluster No. 1366

Link

ChEMBL

By standard InChI CHEMBL233295
By standard InChI Main Layer CHEMBL233295

KEGG

By LinkDB C10470

CTD

By CAS RN C008180

Human Protein / Gene in interaction

5 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein CHEMBL233295 CHEMBL2114810 (1)
7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL233295 CHEMBL1794401 (1)
0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein CHEMBL233295 CHEMBL1738588 (1)
0 / 0
P03372 Estrogen receptor NR3A1 CHEMBL233295 CHEMBL1941568 (1) CHEMBL1941569 (1)
1 / 1
Q12794 Hyaluronidase-1 Enzyme CHEMBL233295 CHEMBL1111859 (1)
1 / 2

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#615363 Estrogen resistance; estrr P03372
#174800 Mccune-albright syndrome; mas P63092
#601492 Mucopolysaccharidosis, type ix; mps9 Q12794
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092

KEGG DISEASE (6)

KEGG disease name UniProt
H00026 Endometrial Cancer P03372 (marker)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00133 Mucopolysaccharidosis type IX (MPS9) Q12794 (related)
H00421 Mucopolysaccharidosis (MPS) Q12794 (related)

Diseases related to CTD interactions

1 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D000647 C008180 Amnesia therapeutic
12880915