Metabolite

KNApSAcK Entry

id C00026716
Name Tuberostemonine H / (+)-Tuberostemonine H / (9alpha)-Neotuberostemonine
CAS RN 670254-76-9
Standard InChI InChI=1S/C22H33NO4/c1-4-13-14-7-5-6-8-23-16(17-9-11(2)21(24)26-17)10-15(19(14)23)18-12(3)22(25)27-20(13)18/h11-20H,4-10H2,1-3H3/t11-,12-,13+,14-,15-,16-,17-,18-,19-,20+/m0/s1
Standard InChI (Main Layer) InChI=1S/C22H33NO4/c1-4-13-14-7-5-6-8-23-16(17-9-11(2)21(24)26-17)10-15(19(14)23)18-12(3)22(25)27-20(13)18/h11-20H,4-10H2,1-3H3

Cluster

Phytochemical cluster
KCF-S cluster No. 733

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL517375 CHEMBL479493 CHEMBL1317235

KEGG

By LinkDB

CTD

By CAS RN

Species

Summary

Plant class

class name count
Liliopsida 1

Family

family name count
Stemonaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Stemona tuberosa 167572 Stemonaceae Liliopsida Viridiplantae

Human Protein / Gene in interaction

2 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 CHEMBL1317235 CHEMBL1614110 (1)
1 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme CHEMBL1317235 CHEMBL1614227 (1)
3 / 3

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (4)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#608902 Drug metabolism, poor, cyp2d6-related P10635
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714

KEGG DISEASE (3)

KEGG disease name UniProt
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)