Metabolite

KNApSAcK Entry

id C00034737
Name Umbelliprenin
CAS RN 23838-17-7
Standard InChI InChI=1S/C24H30O3/c1-18(2)7-5-8-19(3)9-6-10-20(4)15-16-26-22-13-11-21-12-14-24(25)27-23(21)17-22/h7,9,11-15,17H,5-6,8,10,16H2,1-4H3/b19-9+,20-15+
Standard InChI (Main Layer) InChI=1S/C24H30O3/c1-18(2)7-5-8-19(3)9-6-10-20(4)15-16-26-22-13-11-21-12-14-24(25)27-23(21)17-22/h7,9,11-15,17H,5-6,8,10,16H2,1-4H3

Cluster

Phytochemical cluster
KCF-S cluster No. 2038

Link

ChEMBL

By standard InChI CHEMBL156127
By standard InChI Main Layer CHEMBL156127

KEGG

By LinkDB

CTD

By CAS RN

Human Protein / Gene in interaction

8 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P17405 Sphingomyelin phosphodiesterase Enzyme CHEMBL156127 CHEMBL1794495 (1)
2 / 2
P39748 Flap endonuclease 1 Enzyme CHEMBL156127 CHEMBL1794486 (1)
0 / 0
O75496 Geminin Unclassified protein CHEMBL156127 CHEMBL2114780 (1)
0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL156127 CHEMBL1794401 (1)
0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme CHEMBL156127 CHEMBL2091179 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL156127 CHEMBL1794483 (1)
0 / 0
O75164 Lysine-specific demethylase 4A Enzyme CHEMBL156127 CHEMBL1737991 (1)
0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme CHEMBL156127 CHEMBL1614364 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (3)

OMIM preferred title UniProt
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8

KEGG DISEASE (3)

KEGG disease name UniProt
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)