Metabolite

KNApSAcK Entry

id C00044826
Name Isovanillin
CAS RN 621-59-0
Standard InChI InChI=1S/C8H8O3/c1-11-8-3-2-6(5-9)4-7(8)10/h2-5,10H,1H3
Standard InChI (Main Layer) InChI=1S/C8H8O3/c1-11-8-3-2-6(5-9)4-7(8)10/h2-5,10H,1H3

Cluster

Phytochemical cluster
KCF-S cluster No. 1003

Link

ChEMBL

By standard InChI CHEMBL275563
By standard InChI Main Layer CHEMBL275563

KEGG

By LinkDB

CTD

By CAS RN C093382

Species

Summary

Plant class

class name count
Magnoliophyta 1

Family

family name count
Lauraceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Neolitsea acuminatissima 128654 Lauraceae Magnoliophyta Viridiplantae

Human Protein / Gene in interaction

7 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase CHEMBL275563 CHEMBL1014040 (1)
1 / 1
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL275563 CHEMBL1614458 (1)
0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein CHEMBL275563 CHEMBL2114810 (1)
7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL275563 CHEMBL1794401 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL275563 CHEMBL1794483 (1)
0 / 0
Q06278 Aldehyde oxidase Enzyme CHEMBL275563 CHEMBL1640077 (1)
0 / 1
O94925 Glutaminase kidney isoform, mitochondrial Enzyme CHEMBL275563 CHEMBL2114738 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#174800 Mccune-albright syndrome; mas P63092
#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
#278300 Xanthinuria, type i P47989

KEGG DISEASE (4)

KEGG disease name UniProt
H00192 Xanthinuria P47989 (related)
Q06278 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)