Metabolite

KNApSAcK Entry

id C00032667
Name 6,7,8-Trimethoxy-2H-1-benzopyran-2-one
CAS RN 6035-49-0
Standard InChI InChI=1S/C12H12O5/c1-14-8-6-7-4-5-9(13)17-10(7)12(16-3)11(8)15-2/h4-6H,1-3H3
Standard InChI (Main Layer) InChI=1S/C12H12O5/c1-14-8-6-7-4-5-9(13)17-10(7)12(16-3)11(8)15-2/h4-6H,1-3H3

Cluster

Phytochemical cluster No. 25
KCF-S cluster No. 364

Link

ChEMBL

By standard InChI CHEMBL253551
By standard InChI Main Layer CHEMBL253551

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
asterids 1

Family

family name count
Convolvulaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Cuscuta reflexa 4129 Convolvulaceae asterids Viridiplantae

Human Protein / Gene in interaction

10 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P43166 Carbonic anhydrase 7 Lyase CHEMBL253551 CHEMBL2341285 (1)
0 / 0
Q8N1Q1 Carbonic anhydrase 13 Lyase CHEMBL253551 CHEMBL2341282 (1)
0 / 0
P00918 Carbonic anhydrase 2 Lyase CHEMBL253551 CHEMBL2341286 (1)
1 / 2
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL253551 CHEMBL1614458 (1)
0 / 0
O43570 Carbonic anhydrase 12 Lyase CHEMBL253551 CHEMBL2341283 (1)
1 / 2
P00915 Carbonic anhydrase 1 Lyase CHEMBL253551 CHEMBL2341287 (1)
0 / 0
Q16790 Carbonic anhydrase 9 Lyase CHEMBL253551 CHEMBL2341284 (1)
0 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme CHEMBL253551 CHEMBL1613910 (1)
3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme CHEMBL253551 CHEMBL1614038 (1)
2 / 2
B2RXH2 Lysine-specific demethylase 4E Enzyme CHEMBL253551 CHEMBL1613914 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#119900 Digital clubbing, isolated congenital P15428
#143860 Hyperchlorhidrosis, isolated O43570
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918

KEGG DISEASE (9)

KEGG disease name UniProt
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)