Species

KNApSAcK Entry

Organism name Menispermum dauricum
Genus Menispermum
Family Menispermaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Menispermum dauricum
Linked NCBI taxonomy ID 49683
Linked level species

Family

Family in NCBI taxonomy Menispermaceae
ID 3455

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (13)

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
C00001817 External link 512 Berbamine
/ d-Berbamine
/ (+)-Berbamine
CHEMBL504323
CHEMBL507540
CHEMBL1198334
C027870
4 / 3 / 4 9 / 1 No. 10 No. 4
C00027338 External link 512 Daurioxoisoporphine C
CHEMBL1651051
No. 74
C00027337 External link 512 Daurioxoisoporphine B
CHEMBL446816
No. 74
C00027339 External link 512 Daurioxoisoporphine D
No. 74
C00028131 External link 512 Dauricine
CHEMBL442717
CHEMBL1721004
CHEMBL1995008
C035934
2 / 2 / 2 1 / 2 No. 89 No. 4
C00001845 External link 512 Dauricine
CHEMBL442717
CHEMBL1721004
CHEMBL1995008
C035934
2 / 2 / 2 1 / 2 No. 89 No. 4
C00002310 External link 512 Acutumidine
CHEMBL237548
CHEMBL237765
No. 915
C00027340 External link 512 Dechloroacutumine
CHEMBL237764
No. 915
C00027334 External link 512 Dauricumidine
CHEMBL237548
CHEMBL237765
No. 915
C00027335 External link 512 Dauricumine
CHEMBL391628
CHEMBL391835
CHEMBL1716763
1 / 0 / 0 No. 915
C00035573 External link 512 Dechlorodauricumine
/ (+)-Dechlorodauricumine
CHEMBL237764
No. 915
C00003486 External link 512 Strigol
/ (+)-Strigol
No. 1816 No. 38
C00027336 External link 512 Daurioxoisoporphine A
CHEMBL523250
No. 8327

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001845 C00027335 C00028131 0 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00001845 C00028131 2 / 2
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001817 3 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00001817 0 / 0
P54750 Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A PDE_1A C00001817 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001817 0 / 1

10 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00001845 C00028131
1147 CHUK, IKBKA, IKK-alpha, IKK1, IKKA, NFKBIKA, TCF16 conserved helix-loop-helix ubiquitous kinase (EC:2.7.11.10) C00001817
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00001817
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00001817
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00001817
637 BID, FP497 BH3 interacting domain death agonist C00001817
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00001817
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00001817
7128 TNFAIP3, A20, OTUD7C, TNFA1P2 tumor necrosis factor, alpha-induced protein 3 (EC:3.4.19.12) C00001817
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00001817

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#613688 Long qt syndrome 2; lqt2 Q12809
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#609620 Short qt syndrome 1; sqt1 Q12809

KEGG DISEASE (6)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
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)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00001845
C00028131
D001145 Arrhythmias, Cardiac C00001845
C00028131
D015473 Leukemia, Promyelocytic, Acute C00001817