Metabolite

KNApSAcK Entry

id C00000706
Name Phyllanthin
CAS RN 10351-88-9
Standard InChI InChI=1S/C24H34O6/c1-25-15-19(11-17-7-9-21(27-3)23(13-17)29-5)20(16-26-2)12-18-8-10-22(28-4)24(14-18)30-6/h7-10,13-14,19-20H,11-12,15-16H2,1-6H3/t19-,20-/m0/s1
Standard InChI (Main Layer) InChI=1S/C24H34O6/c1-25-15-19(11-17-7-9-21(27-3)23(13-17)29-5)20(16-26-2)12-18-8-10-22(28-4)24(14-18)30-6/h7-10,13-14,19-20H,11-12,15-16H2,1-6H3

Cluster

Phytochemical cluster No. 21
KCF-S cluster No. 1232

Link

ChEMBL

By standard InChI CHEMBL453568
By standard InChI Main Layer CHEMBL453568 CHEMBL1253999

KEGG

By LinkDB C10746

CTD

By CAS RN

Human Protein / Gene in interaction

3 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P24530 Endothelin B receptor Endothelin receptor CHEMBL453568 CHEMBL937908 (1)
4 / 4
P25101 Endothelin-1 receptor Endothelin receptor CHEMBL453568 CHEMBL937907 (1)
0 / 0
O14746 Telomerase reverse transcriptase Enzyme CHEMBL453568 CHEMBL1251398 (1)
5 / 5

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#600501 Abcd syndrome; abcds P24530
#609135 Aplastic anemia O14746
#613989 Dyskeratosis congenita, autosomal dominant, 2; dkca2 O14746
#142623 Hirschsprung disease, susceptibility to, 1; hscr1 P24530
#600155 Hirschsprung disease, susceptibility to, 2; hscr2 P24530
#615134 Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 O14746
#614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 O14746
#178500 Pulmonary fibrosis, idiopathic; ipf O14746
#277580 Waardenburg syndrome, type 4a; ws4a P24530

KEGG DISEASE (9)

KEGG disease name UniProt
H00764 Cri du chat syndrome O14746 (related)
H01132 Aplastic anemia (AA) O14746 (related)
H01299 Idiopathic pulmonary fibrosis O14746 (related)
H00022 Bladder cancer O14746 (marker)
H00024 Prostate cancer O14746 (marker)
H00054 Nasopharyngeal cancer P24530 (related)
H00759 Waardenburg syndrome (WS) P24530 (related)
H00823 ABCD syndrome P24530 (related)
H00910 Hirschsprung disease (HD) P24530 (related)