PCIDB

KNApSAcK Metabolite C00029680

Metabolite

KNApSAcK Entry

id C00029680
Name Ammajin / Marmesinin / (-)-Marmesinin
CAS RN 495-30-7
Standard InChI InChI=1S/C20H24O9/c1-20(2,29-19-18(25)17(24)16(23)13(8-21)28-19)14-6-10-5-9-3-4-15(22)27-11(9)7-12(10)26-14/h3-5,7,13-14,16-19,21,23-25H,6,8H2,1-2H3/t13-,14?,16-,17+,18-,19+/m1/s1
Standard InChI (Main Layer) InChI=1S/C20H24O9/c1-20(2,29-19-18(25)17(24)16(23)13(8-21)28-19)14-6-10-5-9-3-4-15(22)27-11(9)7-12(10)26-14/h3-5,7,13-14,16-19,21,23-25H,6,8H2,1-2H3

Cluster

Phytochemical cluster No. 25
KCF-S cluster No. 399

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL459825

KEGG

By LinkDB

CTD

By CAS RN

Human Protein / Gene in interaction

11 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P10253 Lysosomal alpha-glucosidase Hydrolase CHEMBL459825 CHEMBL1614103 (1) CHEMBL1614031 (1)
1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein CHEMBL459825 CHEMBL1614166 (1)
1 / 0
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL459825 CHEMBL1614458 (1)
0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme CHEMBL459825 CHEMBL1794495 (1)
2 / 2
O75496 Geminin Unclassified protein CHEMBL459825 CHEMBL2114780 (1)
0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein CHEMBL459825 CHEMBL1614280 (1)
0 / 0
P06280 Alpha-galactosidase A Enzyme CHEMBL459825 CHEMBL1614369 (1)
1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme CHEMBL459825 CHEMBL1614038 (1)
2 / 2
P22303 Acetylcholinesterase Hydrolase CHEMBL459825 CHEMBL1003053 (1)
1 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL459825 CHEMBL1794483 (1)
0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL459825 CHEMBL1738442 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#119900 Digital clubbing, isolated congenital P15428
#301500 Fabry disease P06280
#232300 Glycogen storage disease ii P10253
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#112100 Yt blood group antigen P22303

KEGG DISEASE (6)

KEGG disease name UniProt
H00125 Fabry disease P06280 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)