Metabolite

KNApSAcK Entry

id C00016655
Name Radicinin / Stemphylone
CAS RN 10088-95-6
Standard InChI InChI=1S/C12H12O5/c1-3-4-7-5-8-9(12(15)17-7)11(14)10(13)6(2)16-8/h3-6,10,13H,1-2H3/b4-3+/t6-,10-/m0/s1
Standard InChI (Main Layer) InChI=1S/C12H12O5/c1-3-4-7-5-8-9(12(15)17-7)11(14)10(13)6(2)16-8/h3-6,10,13H,1-2H3

Cluster

Phytochemical cluster
KCF-S cluster No. 2439

Link

ChEMBL

By standard InChI CHEMBL1994984
By standard InChI Main Layer CHEMBL1894884 CHEMBL1994984

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count

Family

family name count
Pleosporaceae 2

List (2)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Alternaria chrysanthemi 5598 Pleosporaceae Fungi
Curvularia sp. AB 2090A-11 (NRRL 22559) 5502 Pleosporaceae Fungi

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 CHEMBL1894884 CHEMBL2114784 (1)
1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme CHEMBL1894884 CHEMBL1794585 (1)
0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme CHEMBL1894884 CHEMBL1794495 (1)
2 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein CHEMBL1894884 CHEMBL1794584 (1)
2 / 0
O75496 Geminin Unclassified protein CHEMBL1894884 CHEMBL2114843 (1) CHEMBL2114780 (1)
0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor CHEMBL1894884 CHEMBL2114788 (1)
0 / 0
Q9Y253 DNA polymerase eta Enzyme CHEMBL1894884 CHEMBL1794569 (1)
1 / 1
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme CHEMBL1894884 CHEMBL1963863 (1)
0 / 0
Q9UNA4 DNA polymerase iota Enzyme CHEMBL1894884 CHEMBL1794483 (1)
0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein CHEMBL1894884 CHEMBL2114913 (1)
0 / 3

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (7)

KEGG disease name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)