PCIDB

KNApSAcK Metabolite C00030987

Metabolite

KNApSAcK Entry

id C00030987
Name Phellopterin
CAS RN 2543-94-4
Standard InChI InChI=1S/C17H16O5/c1-10(2)6-8-21-17-15-12(7-9-20-15)14(19-3)11-4-5-13(18)22-16(11)17/h4-7,9H,8H2,1-3H3
Standard InChI (Main Layer) InChI=1S/C17H16O5/c1-10(2)6-8-21-17-15-12(7-9-20-15)14(19-3)11-4-5-13(18)22-16(11)17/h4-7,9H,8H2,1-3H3

Cluster

Phytochemical cluster No. 25
KCF-S cluster No. 606

Link

ChEMBL

By standard InChI CHEMBL452751
By standard InChI Main Layer CHEMBL452751

KEGG

By LinkDB C17047

CTD

By CAS RN C104601

Human Protein / Gene in interaction

7 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P37840 Alpha-synuclein Unclassified protein CHEMBL452751 CHEMBL2354282 (1)
4 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein CHEMBL452751 CHEMBL1614166 (1)
1 / 0
P11413 Glucose-6-phosphate 1-dehydrogenase Enzyme CHEMBL452751 CHEMBL1737961 (1)
1 / 2
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein CHEMBL452751 CHEMBL2114810 (1)
7 / 3
P56817 Beta-secretase 1 A1A CHEMBL452751 CHEMBL1936881 (1)
0 / 0
P10636 Microtubule-associated protein tau Unclassified protein CHEMBL452751 CHEMBL1614421 (1)
4 / 3
Q13148 TAR DNA-binding protein 43 Unclassified protein CHEMBL452751 CHEMBL2354287 (1)
1 / 1

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300908 Anemia, nonspherocytic hemolytic, due to g6pd deficiency P11413
#127750 Dementia, lewy body; dlb P37840
#600274 Frontotemporal dementia; ftd P10636
#174800 Mccune-albright syndrome; mas P63092
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#166350 Osseous heteroplasia, progressive; poh P63092
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (10)

KEGG disease name UniProt
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00101 Other phagocyte defects P11413 (related)
H00668 Anemia due to disorders of glutathione metabolism P11413 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)