PCIDB

KNApSAcK Metabolite C00037471

Metabolite

KNApSAcK Entry

id C00037471
Name Maltol
CAS RN 118-71-8
Standard InChI InChI=1S/C6H6O3/c1-4-6(8)5(7)2-3-9-4/h2-3,8H,1H3
Standard InChI (Main Layer) InChI=1S/C6H6O3/c1-4-6(8)5(7)2-3-9-4/h2-3,8H,1H3

Cluster

Phytochemical cluster No. 64
KCF-S cluster No. 4868

Link

ChEMBL

By standard InChI CHEMBL31422
By standard InChI Main Layer CHEMBL31422

KEGG

By LinkDB C11918

CTD

By CAS RN C008316

Species

Summary

Plant class

class name count
asterids 1

Family

family name count
Apiaceae 1
Streptomycetaceae 1

List (2)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Prangos tschimganica 52496 Apiaceae asterids Viridiplantae
Streptomyces sp. GW23/1540 1883 Streptomycetaceae Bacteria

Human Protein / Gene in interaction

12 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein CHEMBL31422 CHEMBL1738312 (1)
0 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase CHEMBL31422 CHEMBL1664429 (1)
0 / 0
P22894 Neutrophil collagenase M10A CHEMBL31422 CHEMBL1664434 (1)
0 / 0
P14780 Matrix metalloproteinase-9 M10A CHEMBL31422 CHEMBL1664435 (1)
2 / 2
P02545 Prelamin-A/C Unclassified protein CHEMBL31422 CHEMBL1614544 (1)
11 / 10
P03956 Interstitial collagenase M10A CHEMBL31422 CHEMBL1664431 (1)
0 / 1
P08253 72 kDa type IV collagenase M10A CHEMBL31422 CHEMBL1664432 (1)
1 / 3
O75164 Lysine-specific demethylase 4A Enzyme CHEMBL31422 CHEMBL1737991 (1)
0 / 0
Q04760 Lactoylglutathione lyase Enzyme CHEMBL31422 CHEMBL684310 (1)
0 / 0
P08254 Stromelysin-1 M10A CHEMBL31422 CHEMBL1664433 (1)
1 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL31422 CHEMBL1613914 (2)
0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL31422 CHEMBL1738442 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (15)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603932 Intervertebral disc disease; idd P14780
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (14)

KEGG disease name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00028 Choriocarcinoma P03956 (related)
P08253 (related)
H00025 Penile cancer P08253 (related)
P14780 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00479 Metaphyseal dysplasias P14780 (related)