Metabolite

KNApSAcK Entry

id C00040083
Name Psammaplin F
CAS RN 540466-74-8
Standard InChI InChI=1S/C15H18BrN3O6S2/c16-10-7-9(1-2-12(10)20)8-11(19-25)13(21)17-3-5-26-27-6-4-18-14(22)15(23)24/h1-2,7,20,25H,3-6,8H2,(H,17,21)(H,18,22)(H,23,24)/b19-11-
Standard InChI (Main Layer) InChI=1S/C15H18BrN3O6S2/c16-10-7-9(1-2-12(10)20)8-11(19-25)13(21)17-3-5-26-27-6-4-18-14(22)15(23)24/h1-2,7,20,25H,3-6,8H2,(H,17,21)(H,18,22)(H,23,24)

Cluster

Phytochemical cluster
KCF-S cluster No. 1954

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL150237

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count

Family

family name count
Pseudoceratinidae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Pseudoceratina purpurea 1162763 Pseudoceratinidae Metazoa

Human Protein / Gene in interaction

11 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q9BY41 Histone deacetylase 8 Hydrolase CHEMBL150237 CHEMBL697248 (1)
2 / 0
Q969S8 Histone deacetylase 10 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0
O15379 Histone deacetylase 3 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0
P56524 Histone deacetylase 4 Hydrolase CHEMBL150237 CHEMBL697248 (1)
1 / 1
Q8WUI4 Histone deacetylase 7 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0
Q9UQL6 Histone deacetylase 5 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0
Q9UKV0 Histone deacetylase 9 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0
Q13547 Histone deacetylase 1 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0
Q92769 Histone deacetylase 2 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0
Q9UBN7 Histone deacetylase 6 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0
Q96DB2 Histone deacetylase 11 Hydrolase CHEMBL150237 CHEMBL697248 (1)
0 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (3)

OMIM preferred title UniProt
#600430 Brachydactyly-mental retardation syndrome; bdmr P56524
#300882 Cornelia de lange syndrome 5; cdls5 Q9BY41
#309585 Wilson-turner x-linked mental retardation syndrome; wts Q9BY41

KEGG DISEASE (1)

KEGG disease name UniProt
H00561 Brachydacytly-mental retardation syndrome and Smith-Magenis syndrome P56524 (related)