Metabolite

KNApSAcK Entry

id C00021689
Name Hymenin / Epiparthenin
CAS RN 20555-04-8
Standard InChI InChI=1S/C15H18O4/c1-8-4-5-10-9(2)13(17)19-12(10)14(3)11(16)6-7-15(8,14)18/h6-8,10,12,18H,2,4-5H2,1,3H3/t8-,10-,12+,14-,15+/m0/s1
Standard InChI (Main Layer) InChI=1S/C15H18O4/c1-8-4-5-10-9(2)13(17)19-12(10)14(3)11(16)6-7-15(8,14)18/h6-8,10,12,18H,2,4-5H2,1,3H3

Cluster

Phytochemical cluster No. 38
KCF-S cluster No. 495

Link

ChEMBL

By standard InChI CHEMBL401149
By standard InChI Main Layer CHEMBL312004 CHEMBL401149 CHEMBL1869439

KEGG

By LinkDB C09523

CTD

By CAS RN

Human Protein / Gene in interaction

10 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein CHEMBL1869439 CHEMBL2114784 (1)
1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein CHEMBL1869439 CHEMBL1794584 (1)
2 / 0
O75496 Geminin Unclassified protein CHEMBL1869439 CHEMBL2114843 (1) CHEMBL2114780 (1)
0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor CHEMBL1869439 CHEMBL2114788 (1)
0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL1869439 CHEMBL1794401 (1)
0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme CHEMBL1869439 CHEMBL1963863 (1) CHEMBL2114934 (1)
0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme CHEMBL1869439 CHEMBL2354311 (1)
1 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme CHEMBL1869439 CHEMBL2114859 (1) CHEMBL2114734 (1)
0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein CHEMBL1869439 CHEMBL2114913 (1)
0 / 3
P51531 Probable global transcription activator SNF2L2 Unclassified protein CHEMBL1869439 CHEMBL2354206 (1)
1 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#137800 Glioma susceptibility 1; glm1 O75874
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#601358 Nicolaides-baraitser syndrome; ncbrs P51531
#183090 Spinocerebellar ataxia 2; sca2 Q99700

KEGG DISEASE (4)

KEGG disease name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)