id | C00001874 |
---|---|
Name | Neprotin / Neprotine / Yatrorizine / Jatrorrhizine |
CAS RN | 3621-38-3 |
Standard InChI | InChI=1S/C20H19NO4/c1-23-18-5-4-12-8-16-14-10-19(24-2)17(22)9-13(14)6-7-21(16)11-15(12)20(18)25-3/h4-5,8-11H,6-7H2,1-3H3/p+1 |
Standard InChI (Main Layer) | InChI=1S/C20H19NO4/c1-23-18-5-4-12-8-16-14-10-19(24-2)17(22)9-13(14)6-7-21(16)11-15(12)20(18)25-3/h4-5,8-11H,6-7H2,1-3H3 |
Phytochemical cluster | No. 4 |
---|---|
KCF-S cluster | No. 155 |
By standard InChI | CHEMBL251055 |
---|---|
By standard InChI Main Layer | CHEMBL251055 |
By LinkDB | C09553 |
---|
By CAS RN | C055785 |
---|
class name | count |
---|---|
eudicotyledons | 23 |
Magnoliophyta | 2 |
rosids | 1 |
family name | count |
---|---|
Berberidaceae | 14 |
Menispermaceae | 4 |
Ranunculaceae | 4 |
Pieridae | 1 |
Magnoliaceae | 1 |
Papaveraceae | 1 |
Annonaceae | 1 |
Rutaceae | 1 |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | CHEMBL251055 |
CHEMBL1613842
(1)
|
4 / 2 |
P06746 | DNA polymerase beta | Enzyme | CHEMBL251055 |
CHEMBL1614079
(1)
|
0 / 0 |
P04062 | Glucosylceramidase | Enzyme | CHEMBL251055 |
CHEMBL1613818
(1)
|
6 / 4 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | CHEMBL251055 |
CHEMBL1614175
(1)
|
1 / 1 |
P02545 | Prelamin-A/C | Unclassified protein | CHEMBL251055 |
CHEMBL1614544
(1)
|
11 / 10 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | CHEMBL251055 |
CHEMBL1614166
(1)
|
1 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | CHEMBL251055 |
CHEMBL1794486
(1)
|
0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | CHEMBL251055 |
CHEMBL942995
(1)
|
0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | CHEMBL251055 |
CHEMBL1794483
(1)
|
0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL251055 |
CHEMBL1614421
(1)
|
4 / 3 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL251055 |
CHEMBL1613914
(1)
|
0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | CHEMBL251055 |
CHEMBL1738442
(1)
|
0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | CHEMBL251055 |
CHEMBL2114738
(1)
|
0 / 0 |
P43351 | DNA repair protein RAD52 homolog | Unclassified protein | CHEMBL251055 |
CHEMBL2354285
(1)
|
0 / 0 |
compound | gene | gene name | gene description | interaction | interaction type | form |
reference
pmid |
---|---|---|---|---|---|---|---|
C055785 | 332 |
BIRC5
API4 EPR-1 |
baculoviral IAP repeat containing 5 | jatrorrhizine binds to BIRC5 promoter |
affects binding
|
promoter |
17968851
|
OMIM | preferred title | UniProt |
---|---|---|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#608013 | Gaucher disease, perinatal lethal |
P04062
|
#230800 | Gaucher disease, type i |
P04062
|
#230900 | Gaucher disease, type ii |
P04062
|
#231000 | Gaucher disease, type iii |
P04062
|
#231005 | Gaucher disease, type iiic |
P04062
|
#232300 | Glycogen storage disease ii |
P10253
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#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
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | disease name | UniProt |
---|---|---|
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)
|
H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
Q16637 (related) |