Metabolite

KNApSAcK Entry

id C00011304
Name Ditryptophenaline
CAS RN 64947-43-9
Standard InChI InChI=1S/C42H40N6O4/c1-45-31(21-25-13-5-3-6-14-25)37(51)47-33(35(45)49)23-41(27-17-9-11-19-29(27)43-39(41)47)42-24-34-36(50)46(2)32(22-26-15-7-4-8-16-26)38(52)48(34)40(42)44-30-20-12-10-18-28(30)42/h3-20,31-34,39-40,43-44H,21-24H2,1-2H3/t31-,32+,33-,34+,39-,40+,41?,42?
Standard InChI (Main Layer) InChI=1S/C42H40N6O4/c1-45-31(21-25-13-5-3-6-14-25)37(51)47-33(35(45)49)23-41(27-17-9-11-19-29(27)43-39(41)47)42-24-34-36(50)46(2)32(22-26-15-7-4-8-16-26)38(52)48(34)40(42)44-30-20-12-10-18-28(30)42/h3-20,31-34,39-40,43-44H,21-24H2,1-2H3

Cluster

Phytochemical cluster
KCF-S cluster No. 2371

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL501675 CHEMBL1457214

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count

Family

family name count
Aspergillaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Aspergillus flavus 5059 Aspergillaceae Fungi

Human Protein / Gene in interaction

6 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein CHEMBL1457214 CHEMBL1794584 (1)
2 / 0
O75496 Geminin Unclassified protein CHEMBL1457214 CHEMBL2114780 (1)
0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein CHEMBL1457214 CHEMBL1738588 (1)
0 / 0
P25103 Substance-P receptor Neurokinin receptor CHEMBL501675 CHEMBL1013871 (1)
0 / 0
O75164 Lysine-specific demethylase 4A Enzyme CHEMBL1457214 CHEMBL1737991 (1)
0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein CHEMBL1457214 CHEMBL2114913 (1)
0 / 3

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (2)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc P84022
#613795 Loeys-dietz syndrome, type 3; lds3 P84022

KEGG DISEASE (3)

KEGG disease name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)