Species

KNApSAcK Entry

Organism name Fibraurea chloroleuca Miers
Genus Fibraurea
Family Menispermaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Fibraurea chloroleuca
Linked NCBI taxonomy ID 527504
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 (8)

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
C00026149 External link 512 Corypalmine
/ Tetrahydrojatrorrhizine
CHEMBL2334885
CHEMBL2334886
4 / 3 / 0 No. 37 No. 4
C00026150 External link 512 Tetrahydropalmatine
/ dl-Tetrahydropalmatine
/ (+/-)-Tetrahydropalmatine
CHEMBL187892
CHEMBL487182
CHEMBL2334889
8 / 5 / 2 No. 37 No. 4
C00026143 External link 512 Govanine
/ Pseudocolumbamine
CHEMBL1197451
No. 155 No. 4
C00026142 External link 512 Palmatrubine
/ Palmaturbine
No. 155 No. 4
C00026124 External link 512 Dehydrocorydalmine
CHEMBL1618061
No. 155 No. 4
C00024667 External link 512 Columbamine
/ Dehydroisocorypalmine
CHEMBL400345
C055786
1 / 0 / 1 8 / 1 No. 155 No. 4
C00026111 External link 512 Berberrubine
/ 9-Berberoline
CHEMBL203135
CHEMBL2160119
5 / 10 / 6 No. 155 No. 4
C00026154 External link 512 Thalifendine
CHEMBL1187148
C477156
No. 155 No. 4

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P21728 D(1A) dopamine receptor Dopamine receptor C00026149 C00026150 0 / 0
P08908 5-hydroxytryptamine receptor 1A Serotonin receptor C00026149 C00026150 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00024667 C00026150 0 / 1
P14416 D(2) dopamine receptor Dopamine receptor C00026149 C00026150 2 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00026149 C00026150 0 / 0
P03372 Estrogen receptor NR3A1 C00026150 1 / 1
P13726 Tissue factor Membrane receptor C00026150 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00026150 1 / 0
Q09428 ATP-binding cassette sub-family C member 8 K C00026111 5 / 3
Q99700 Ataxin-2 Unclassified protein C00026111 1 / 1
Q14654 ATP-sensitive inward rectifier potassium channel 11 K C00026111 3 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00026111 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00026111 2 / 1

8 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1003 CDH5, 7B4, CD144 cadherin 5, type 2 (vascular endothelium) C00024667
1021 CDK6, PLSTIRE cyclin-dependent kinase 6 (EC:2.7.11.22) C00024667
1437 CSF2, GMCSF colony stimulating factor 2 (granulocyte-macrophage) C00024667
2048 EPHB2, CAPB, DRT, EK5, EPHT3, ERK, Hek5, PCBC, Tyro5 EPH receptor B2 (EC:2.7.10.1) C00024667
9500 MAGED1, DLXIN-1, NRAGE melanoma antigen family D, 1 C00024667
4313 MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) C00024667
64321 SOX17, VUR3 SRY (sex determining region Y)-box 17 C00024667
6774 STAT3, APRF, HIES signal transducer and activator of transcription 3 (acute-phase response factor) C00024667

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (15)

OMIM preferred title UniProt
#103780 Alcohol dependence P14416
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#114500 Colorectal cancer; crc Q14191
#606176 Diabetes mellitus, permanent neonatal; pndm Q09428
Q14654
#610374 Diabetes mellitus, transient neonatal, 2 Q09428
#610582 Diabetes mellitus, transient neonatal, 3 Q14654
#615363 Estrogen resistance; estrr P03372
#256450 Hyperinsulinemic hypoglycemia, familial, 1; hhf1 Q09428
#601820 Hyperinsulinemic hypoglycemia, familial, 2; hhf2 Q14654
#602485 Hyperinsulinemic hypoglycemia, familial, 3; hhf3 Q09428
#240800 Hypoglycemia, leucine-induced; lih Q09428
#159900 Myoclonic dystonia P14416
#614674 Periodic fever, menstrual cycle-dependent P08908
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#277700 Werner syndrome; wrn Q14191

KEGG DISEASE (8)

KEGG name UniProt
H00026 Endometrial Cancer P03372 (marker)
H00036 Osteosarcoma P08684 (marker)
H00512 Permanent neonatal diabetes mellitus (PNDM) Q09428 (related)
Q14654 (related)
H00513 Transient neonatal diabetes mellitus (TNDM) Q09428 (related)
Q14654 (related)
H01267 Familial hyperinsulinemic hypoglycemia (HHF) Q09428 (related)
Q14654 (related)
H00296 Defects in RecQ helicases Q14191 (related)
H00409 Type II diabetes mellitus Q14654 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D009361 Neoplasm Invasiveness C00024667