Species

KNApSAcK Entry

Organism name Stemona sessilifolia
Genus Stemona
Family Stemonaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Stemona sessilifolia
Linked NCBI taxonomy ID 339784
Linked level species

Family

Family in NCBI taxonomy Stemonaceae
ID 49662

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Liliopsida
ID 4447

Metabolite list (4)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00029153 External link 512 Tuberostemonine A
CHEMBL517375
CHEMBL479493
CHEMBL1317235
2 / 4 / 3 No. 733
C00029049 External link 512 Stemoninine
/ (-)-Stemoninine
CHEMBL482474
No. 1884
C00028860 External link 512 Protostemonine
No. 1884
C00028861 External link 512 Maistemonine
/ Protostemotinine
CHEMBL1394235
3 / 2 / 0 No. 2562

Human Protein / Gene in interactions

5 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00029153 1 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00028861 2 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00028861 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00029153 3 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00028861 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#114500 Colorectal cancer; crc P84022
#608902 Drug metabolism, poor, cyp2d6-related P10635
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714

KEGG DISEASE (3)

KEGG 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)