| Organism name | Stephania epigaea H.S.Lo |
|---|---|
| Genus | Stephania |
| Family | Menispermaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Stephania |
|---|---|
| Linked NCBI taxonomy ID | 147243 |
| Linked level | genus |
| Family in NCBI taxonomy | Menispermaceae |
|---|---|
| ID | 3455 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | eudicotyledons |
|---|---|
| ID | 71240 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00001870
|
Isobebeerin
/ Isobebeerine / Isochondodendrine |
CHEMBL509310
CHEMBL1169628 |
No. 10 | No. 4 |
|
|||
|
C00025602
|
l-Curine
/ (-)-Curine / l-Bebeerine / Aristolochine / (-)-Bebeerine / Aristolochine(C36 alkaloid) |
CHEMBL1169627
|
13 / 6 / 5 | No. 10 | No. 4 |
|
||
|
C00025604
|
Cycleanine
/ (-)-Cycleanine |
CHEMBL1711244
CHEMBL1983719 |
C037098
|
7 / 1 / 1 | No. 10 | No. 4 |
|
|
|
C00025607
|
NSC 251699
/ L-Dicentrine / (-)-Dicentrine / (R)-(-)-Dicentrine |
CHEMBL464748
CHEMBL478754 |
15 / 20 / 16 | No. 20 | No. 4 |
|
||
|
C00025630
|
Stephanine
/ l-Stephanine / (-)-Stephanine / (R)-(-)-Stephanine |
CHEMBL601020
|
C054160
|
1 / 0 / 0 | No. 20 | No. 4 |
|
|
|
C00026150
|
Tetrahydropalmatine
/ dl-Tetrahydropalmatine / (+/-)-Tetrahydropalmatine |
CHEMBL187892
CHEMBL487182 CHEMBL2334889 |
8 / 5 / 2 | No. 37 | No. 4 |
|
||
|
C00025913
|
Isostephodeline
/ (+)-Isostephodeline / (+)-14-Epierromangine |
No. 346 | No. 4 |
|
||||
|
C00025846
|
Dehydrostephanine
/ 1,2-Methylenedioxy-8-methoxydehydroaporphine |
C030171
|
No. 416 |
|
||||
|
C00025842
|
Dehydrodicentrine
|
CHEMBL456942
|
No. 416 |
|
||||
|
C00025629
|
Sinoacutine
/ (-)-Sinoacutine / (-)-Salutaridine |
CHEMBL402782
CHEMBL404097 |
3 / 4 / 2 | No. 426 | No. 4 |
|
||
|
C00026072
|
Ushinsunine
/ Micheline A / (-)-Ushinsunine |
CHEMBL221034
CHEMBL1617041 CHEMBL2009013 |
1 / 0 / 0 | No. 553 |
|
|||
|
C00025984
|
Oliveroline
/ (-)-Oliveroline |
CHEMBL221034
CHEMBL1617041 CHEMBL2009013 |
1 / 0 / 0 | No. 553 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00025607 C00025629 C00025630 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00025602 C00025604 C00025607 | 0 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00025602 C00025604 C00025607 | 0 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00025604 C00025607 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00025602 C00025607 | 4 / 3 |
| O14757 | Serine/threonine-protein kinase Chk1 | Chk1 | C00025984 C00026072 | 0 / 0 |
| P35372 | Mu-type opioid receptor | Opioid receptor | C00025602 C00025629 | 0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00025602 C00025604 | 1 / 1 |
| P43351 | DNA repair protein RAD52 homolog | Unclassified protein | C00025602 C00025607 | 0 / 0 |
| P00734 | Prothrombin | S1A | C00025629 | 4 / 2 |
| P14416 | D(2) dopamine receptor | Dopamine receptor | C00026150 | 2 / 0 |
| P39748 | Flap endonuclease 1 | Enzyme | C00025607 | 0 / 0 |
| P42858 | Huntingtin | Unclassified protein | C00025602 | 1 / 1 |
| P47898 | 5-hydroxytryptamine receptor 5A | Serotonin receptor | C00025602 | 0 / 0 |
| P41143 | Delta-type opioid receptor | Opioid receptor | C00025602 | 0 / 0 |
| Q99720 | Sigma non-opioid intracellular receptor 1 | Membrane receptor | C00026150 | 1 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00025604 | 0 / 0 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00025607 | 1 / 2 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00025607 | 1 / 0 |
| P13726 | Tissue factor | Membrane receptor | C00026150 | 0 / 0 |
| P03372 | Estrogen receptor | NR3A1 | C00026150 | 1 / 1 |
| P28223 | 5-hydroxytryptamine receptor 2A | Serotonin receptor | C00026150 | 0 / 0 |
| P02545 | Prelamin-A/C | Unclassified protein | C00025607 | 11 / 10 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00026150 | 0 / 1 |
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00025604 | 0 / 0 |
| P06746 | DNA polymerase beta | Enzyme | C00025607 | 0 / 0 |
| P21728 | D(1A) dopamine receptor | Dopamine receptor | C00026150 | 0 / 0 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00025607 | 0 / 0 |
| P08908 | 5-hydroxytryptamine receptor 1A | Serotonin receptor | C00026150 | 1 / 0 |
| O43603 | Galanin receptor type 2 | Galanin receptor | C00025602 | 0 / 0 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00025602 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00025607 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00025602 | 0 / 0 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00025607 | 1 / 0 |
| Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00025604 | 0 / 0 |
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00025607 | 2 / 1 |
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00025602 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #103780 | Alcohol dependence |
P14416
|
| #614373 | Amyotrophic lateral sclerosis 16, juvenile; als16 |
Q99720
|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #114500 | Colorectal cancer; crc |
Q14191
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #615363 | Estrogen resistance; estrr |
P03372
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #143100 | Huntington disease; hd |
P42858
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #159900 | Myoclonic dystonia |
P14416
|
| #160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #614674 | Periodic fever, menstrual cycle-dependent |
P08908
|
| #172700 | Pick disease of brain |
P10636
|
| #614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
| #613679 | Prothrombin deficiency, congenital |
P00734
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #601367 | Stroke, ischemic |
P00734
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|
| #277700 | Werner syndrome; wrn |
Q14191
|
| KEGG | name | UniProt |
|---|---|---|
| H00223 | Inherited thrombophilia |
P00734
(related)
|
| H01254 | Congenital prothrombin deficiency |
P00734
(related)
|
| H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
| H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
| H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
| H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
| H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
| H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
| H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
| H00663 | Restrictive dermopathy |
P02545
(related)
|
| H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
| H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
| H00026 | Endometrial Cancer |
P03372
(marker)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H00059 | Huntington's disease (HD) |
P42858
(related)
|
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
| H00296 | Defects in RecQ helicases |
Q14191
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|