Organism name | Derris robusta |
---|---|
Genus | Derris |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Derris robusta |
---|---|
Linked NCBI taxonomy ID | 1225697 |
Linked level | species |
Family in NCBI taxonomy | Fabaceae |
---|---|
ID | 3803 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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 |
---|---|---|---|---|---|---|---|---|
C00009450
![]() |
5-Hydroxy-7-methoxyisoflavone
|
No. 3 | No. 15 |
![]() |
||||
C00009479
![]() |
Derrugenin
/ 5,4'-Dihydroxy-7,2',5'-trimethoxyisoflavone |
No. 3 | No. 15 |
![]() |
||||
C00009484
![]() |
Robustigenin
/ 5-Hydroxy-7,2',4',5'-tetramethoxyisoflavone |
No. 8 | No. 15 |
![]() |
||||
C00009486
![]() |
Robustigenin methyl ether
/ 5,7,2',4',5'-Pentamethoxyisoflavone |
No. 8 | No. 15 |
![]() |
||||
C00009505
![]() |
Derrubone
/ 5,7-Dihydroxy-3',4'-methylenedioxy-6-prenylisoflavone |
CHEMBL412010
|
11 / 16 / 48 | No. 15 | No. 15 |
![]() |
||
C00009496
![]() |
4'-O-Methylderrone
|
No. 24 | No. 15 |
![]() |
||||
C00009493
![]() |
Derrone
|
CHEMBL393223
|
No. 24 | No. 15 |
![]() |
|||
C00009503
![]() |
Robustone
|
CHEMBL252722
|
3 / 11 / 40 | No. 24 | No. 15 |
![]() |
||
C00009508
![]() |
Robustone methyl ether
|
CHEMBL1403041
|
11 / 31 / 56 | No. 24 | No. 15 |
![]() |
||
C00009504
![]() |
Alpinumisoflavone dimethyl ether
|
No. 24 | No. 15 |
![]() |
||||
C00009466
![]() |
Derrustone
/ 5,7-Dimethoxy-3',4'-methylenedioxyisoflavone |
CHEMBL252721
|
5 / 8 / 5 | No. 27 | No. 15 |
![]() |
||
C00009788
![]() |
Methyl robustate
/ O-Methylrobustic acid / Robustic acid methyl ether |
No. 377 |
![]() |
|||||
C00009787
![]() |
Robustic acid
|
CHEMBL400777
|
C105206
|
11 / 26 / 54 | No. 377 |
![]() |
||
C00009790
![]() |
Robustin methyl ether
|
No. 377 |
![]() |
|||||
C00009789
![]() |
Robustin
|
No. 377 |
![]() |
|||||
C00009786
![]() |
Derrusnin
/ 4,5,7-Trimethoxy-3-(3,4-methylenedioxyphenyl)coumarin |
CHEMBL1526572
|
10 / 32 / 57 | No. 473 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00009466 C00009503 C00009505 C00009508 C00009786 C00009787 | 0 / 1 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00009466 C00009503 C00009505 C00009508 C00009786 C00009787 | 4 / 3 |
P04637 | Cellular tumor antigen p53 | Transcription Factor | C00009503 C00009505 C00009508 C00009786 C00009787 | 7 / 37 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00009466 C00009508 C00009786 C00009787 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00009466 C00009505 C00009508 C00009786 | 0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00009505 C00009508 C00009786 | 2 / 2 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00009466 C00009508 C00009786 | 4 / 1 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00009508 C00009786 C00009787 | 3 / 3 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00009505 C00009508 | 0 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00009505 C00009787 | 1 / 2 |
O00255 | Menin | Unclassified protein | C00009505 C00009787 | 2 / 5 |
P02545 | Prelamin-A/C | Unclassified protein | C00009508 C00009786 | 11 / 10 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00009508 C00009787 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00009505 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00009787 | 6 / 4 |
O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00009787 | 0 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00009787 | 3 / 1 |
P06280 | Alpha-galactosidase A | Enzyme | C00009786 | 1 / 1 |
P07900 | Heat shock protein HSP 90-alpha | Other cytosolic protein | C00009505 | 0 / 0 |
P08238 | Heat shock protein HSP 90-beta | Other cytosolic protein | C00009505 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
#614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 |
P04637
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#133239 | Esophageal cancer |
P04637
|
#301500 | Fabry disease |
P06280
|
#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
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#151623 | Li-fraumeni syndrome 1; lfs1 |
P04637
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#211980 | Lung cancer |
P04637
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#260500 | Papilloma of choroid plexus; cpp |
P04637
|
#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
|
#275355 | Squamous cell carcinoma, head and neck; hnscc |
P04637
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
#274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
#145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
P04637 (related) |
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(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)
|
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)
|
H00004 | Chronic myeloid leukemia (CML) |
P04637
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
P04637
(related)
|
H00006 | Hairy-cell leukemia |
P04637
(related)
|
H00008 | Burkitt lymphoma |
P04637
(related)
|
H00009 | Adult T-cell leukemia |
P04637
(related)
|
H00010 | Multiple myeloma |
P04637
(related)
|
H00013 | Small cell lung cancer |
P04637
(related)
|
H00014 | Non-small cell lung cancer |
P04637
(related)
|
H00015 | Malignant pleural mesothelioma |
P04637
(related)
|
H00016 | Oral cancer |
P04637
(related)
P04637 (marker) |
H00017 | Esophageal cancer |
P04637
(related)
P04637 (marker) |
H00018 | Gastric cancer |
P04637
(related)
|
H00019 | Pancreatic cancer |
P04637
(related)
P04637 (marker) |
H00020 | Colorectal cancer |
P04637
(related)
P04637 (marker) |
H00022 | Bladder cancer |
P04637
(related)
|
H00025 | Penile cancer |
P04637
(related)
P04637 (marker) |
H00026 | Endometrial Cancer |
P04637
(related)
|
H00027 | Ovarian cancer |
P04637
(related)
|
H00028 | Choriocarcinoma |
P04637
(related)
|
H00029 | Vulvar cancer |
P04637
(related)
|
H00031 | Breast cancer |
P04637
(related)
|
H00032 | Thyroid cancer |
P04637
(related)
|
H00036 | Osteosarcoma |
P04637
(related)
P08684 (marker) |
H00038 | Malignant melanoma |
P04637
(related)
|
H00039 | Basal cell carcinoma |
P04637
(related)
|
H00040 | Squamous cell carcinoma |
P04637
(related)
|
H00041 | Kaposi's sarcoma |
P04637
(related)
|
H00042 | Glioma |
P04637
(related)
P04637 (marker) |
H00044 | Cancer of the anal canal |
P04637
(related)
|
H00046 | Cholangiocarcinoma |
P04637
(related)
|
H00047 | Gallbladder cancer |
P04637
(related)
|
H00048 | Hepatocellular carcinoma |
P04637
(related)
|
H00055 | Laryngeal cancer |
P04637
(related)
P04637 (marker) |
H00881 | Li-Fraumeni syndrome |
P04637
(related)
|
H01007 | Choroid plexus papilloma |
P04637
(related)
|
H00021 | Renal cell carcinoma |
P04637
(marker)
|
H00125 | Fabry disease |
P06280
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(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)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(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)
|