Metabolite

KNApSAcK Entry

id C00011332
Name Paspalin-P / Cytochalasin H / Kodocytochalasin 1
CAS RN 53760-19-3
Standard InChI InChI=1S/C30H39NO5/c1-18-10-9-13-23-27(33)20(3)19(2)26-24(16-22-11-7-6-8-12-22)31-28(34)30(23,26)25(36-21(4)32)14-15-29(5,35)17-18/h6-9,11-15,18-19,23-27,33,35H,3,10,16-17H2,1-2,4-5H3,(H,31,34)/b13-9+,15-14+/t18-,19+,23-,24-,25+,26-,27+,29-,30+/m0/s1
Standard InChI (Main Layer) InChI=1S/C30H39NO5/c1-18-10-9-13-23-27(33)20(3)19(2)26-24(16-22-11-7-6-8-12-22)31-28(34)30(23,26)25(36-21(4)32)14-15-29(5,35)17-18/h6-9,11-15,18-19,23-27,33,35H,3,10,16-17H2,1-2,4-5H3,(H,31,34)

Cluster

Phytochemical cluster
KCF-S cluster No. 245

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL75141 CHEMBL1702179 CHEMBL2003636

KEGG

By LinkDB

CTD

By CAS RN C034891

Species

Summary

Plant class

class name count

Family

family name count
Valsaceae 2

List (3)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Geniculosporium sp.
Phomopsis paspalli 34399 Valsaceae Fungi
Phomopsis spp. 34399 Valsaceae Fungi

Human Protein / Gene in interaction

6 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein CHEMBL1702179 CHEMBL2114784 (1)
1 / 1
P33765 Adenosine receptor A3 Adenosine receptor CHEMBL75141 CHEMBL641515 (1)
0 / 0
O75496 Geminin Unclassified protein CHEMBL1702179 CHEMBL2114843 (1) CHEMBL2114780 (1)
0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor CHEMBL1702179 CHEMBL2114788 (1)
0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL1702179 CHEMBL1738184 (1)
0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein CHEMBL1702179 CHEMBL2114913 (1)
0 / 3

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (1)

OMIM preferred title UniProt
#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)