Metabolite

KNApSAcK Entry

id C00036456
Name 2,4,5-Trimethoxybenzaldehyde / 3,4,6-Trimethoxybenzaldehyde
CAS RN 4460-86-0
Standard InChI InChI=1S/C10H12O4/c1-12-8-5-10(14-3)9(13-2)4-7(8)6-11/h4-6H,1-3H3
Standard InChI (Main Layer) InChI=1S/C10H12O4/c1-12-8-5-10(14-3)9(13-2)4-7(8)6-11/h4-6H,1-3H3

Cluster

Phytochemical cluster
KCF-S cluster No. 856

Link

ChEMBL

By standard InChI CHEMBL1164301
By standard InChI Main Layer CHEMBL1164301

KEGG

By LinkDB

CTD

By CAS RN C034031

Species

Summary

Plant class

class name count
Liliopsida 1

Family

family name count
Zingiberaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Alpinia flabellata Ridley 4642 Zingiberaceae Liliopsida Viridiplantae

Human Protein / Gene in interaction

9 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 CHEMBL1164301 CHEMBL1794524 (1)
0 / 0
P16473 Thyrotropin receptor Glycohormone receptor CHEMBL1164301 CHEMBL1614281 (1) CHEMBL1614361 (1)
3 / 2
P10828 Thyroid hormone receptor beta NR1A2 CHEMBL1164301 CHEMBL1794399 (1)
3 / 1
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL1164301 CHEMBL1614458 (1)
0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein CHEMBL1164301 CHEMBL2114810 (1)
7 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein CHEMBL1164301 CHEMBL1738588 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL1164301 CHEMBL1794483 (1)
0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL1164301 CHEMBL1613914 (1)
0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme CHEMBL1164301 CHEMBL1614364 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (14)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#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
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#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

KEGG DISEASE (7)

KEGG disease name UniProt
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)