Metabolite

KNApSAcK Entry

id C00010196
Name Serratin / 5,7-Dihydroxy-4-phenylcoumarin
CAS RN 7758-73-8
Standard InChI InChI=1S/C15H10O4/c16-10-6-12(17)15-11(9-4-2-1-3-5-9)8-14(18)19-13(15)7-10/h1-8,16-17H
Standard InChI (Main Layer) InChI=1S/C15H10O4/c16-10-6-12(17)15-11(9-4-2-1-3-5-9)8-14(18)19-13(15)7-10/h1-8,16-17H

Cluster

Phytochemical cluster No. 17
KCF-S cluster No. 54

Link

ChEMBL

By standard InChI CHEMBL600635
By standard InChI Main Layer CHEMBL600635

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
rosids 1

Family

family name count
Passifloraceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Passiflora serratodigitata 231192 Passifloraceae rosids Viridiplantae

Human Protein / Gene in interaction

8 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein CHEMBL600635 CHEMBL2114784 (1)
1 / 1
P37840 Alpha-synuclein Unclassified protein CHEMBL600635 CHEMBL2354282 (1)
4 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein CHEMBL600635 CHEMBL1614166 (1)
1 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme CHEMBL600635 CHEMBL1738606 (1)
0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor CHEMBL600635 CHEMBL1072092 (1)
0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein CHEMBL600635 CHEMBL1738588 (1)
0 / 0
Q9GZV3 High affinity choline transporter 1 Choline Na-symporter CHEMBL600635 CHEMBL1794362 (1)
1 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein CHEMBL600635 CHEMBL2114913 (1)
0 / 3

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#127750 Dementia, lewy body; dlb P37840
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#158580 Neuronopathy, distal hereditary motor, type viia; hmn7a Q9GZV3
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (6)

KEGG disease name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)