Organism name | Bryonia dioica |
---|---|
Genus | Bryonia |
Family | Cucurbitaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Bryonia dioica |
---|---|
Linked NCBI taxonomy ID | 3652 |
Linked level | species |
Family in NCBI taxonomy | Cucurbitaceae |
---|---|
ID | 3650 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
Species | Activity |
---|---|
Bryonia dioica Jacq. | Antitumor |
Bryonia dioica Jacq. | Cytotoxic |
Bryonia dioica Jacq. | Diuretic |
Bryonia dioica Jacq. | Emetic |
Bryonia dioica Jacq. | Laxative |
Bryonia dioica Jacq. | toxic |
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 |
---|---|---|---|---|---|---|---|---|
C00006224
![]() |
Saponarin
|
C457771
|
No. 1 | No. 15 |
![]() |
|||
C00014076
![]() |
Isovitexin 7-O-(6'''-caffeoyl)-beta-D-glucopyranoside
|
No. 7 | No. 15 |
![]() |
||||
C00029859
![]() |
Bryonolic acid
|
CHEMBL482596
CHEMBL1982562 |
C074984
|
No. 13 | No. 51 |
![]() |
||
C00038091
![]() |
(24R)-24-Hydroxy-24-vinyllathosterol
|
No. 111 | No. 11 |
![]() |
||||
C00038092
![]() |
(24S)-24-Hydroxy-24-vinyllathosterol
|
No. 111 | No. 11 |
![]() |
||||
C00003678
![]() |
Bryodulcosigenin
|
CHEMBL465204
|
No. 119 | No. 51 |
![]() |
|||
C00045246
![]() |
Bryonioside E
/ (+)-Bryonioside E |
CHEMBL503377
|
No. 202 |
![]() |
||||
C00045245
![]() |
Bryonioside D
/ (+)-Bryonioside D |
CHEMBL507538
|
No. 202 |
![]() |
||||
C00045247
![]() |
Bryonioside F
/ (+)-Bryonioside F |
CHEMBL451089
|
No. 202 |
![]() |
||||
C00045242
![]() |
Bryonioside A
/ (+)-Bryonioside A |
CHEMBL450045
|
No. 202 |
![]() |
||||
C00045249
![]() |
Cabenoside D
|
CHEMBL510167
CHEMBL1996311 |
No. 202 |
![]() |
||||
C00031748
![]() |
Dihydrocucurbitacin B
|
CHEMBL553851
|
1 / 1 / 2 | No. 220 | No. 11 |
![]() |
||
C00003683
![]() |
Cucurbitacin B
|
CHEMBL367917
CHEMBL508185 CHEMBL507237 CHEMBL1708265 CHEMBL1728549 |
C041246
|
22 / 30 / 28 | No. 220 | No. 11 |
![]() |
|
C00003690
![]() |
Cucurbitacin J
|
CHEMBL1923789
CHEMBL1923790 CHEMBL1984707 |
No. 220 | No. 11 |
![]() |
|||
C00003689
![]() |
Cucurbitacin I
|
CHEMBL387737
CHEMBL1317135 CHEMBL1717364 |
C038106
|
20 / 15 / 15 | 2 / 0 | No. 220 | No. 11 |
![]() |
C00003685
![]() |
Cucurbitacin D
|
CHEMBL493646
CHEMBL492404 |
C038105
|
1 / 0 / 0 | No. 220 | No. 11 |
![]() |
|
C00003686
![]() |
Cucurbitacin E
|
CHEMBL455056
|
C102326
|
3 / 1 / 2 | No. 220 | No. 11 |
![]() |
|
C00032785
![]() |
Bryoamaride
/ Cucurbitacin l 2-O-beta-D-glucopyranoside |
CHEMBL449483
|
1 / 4 / 2 | No. 315 |
![]() |
|||
C00045243
![]() |
Bryonioside B
/ (+)-Bryonioside B |
CHEMBL464459
CHEMBL1991496 |
No. 675 | No. 51 |
![]() |
|||
C00045244
![]() |
Bryonioside C
/ (+)-Bryonioside C |
CHEMBL454236
|
No. 675 | No. 51 |
![]() |
|||
C00045248
![]() |
Bryonioside G
/ (+)-Bryonioside G |
CHEMBL472126
|
No. 675 | No. 51 |
![]() |
|||
C00003694
![]() |
Cucurbitacin S
|
D054728
|
No. 7002 | No. 11 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P20701 | Integrin alpha-L | Membrane receptor | C00003683 C00003685 C00003686 C00003689 | 0 / 0 |
P40763 | Signal transducer and activator of transcription 3 | Transcription Factor | C00003683 C00003686 C00031748 | 1 / 2 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003683 C00003689 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00003683 C00003689 | 1 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003683 C00003689 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00003683 C00003689 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003683 C00003689 | 2 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00003683 C00003689 | 2 / 3 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00003683 C00003689 | 4 / 1 |
P23528 | Cofilin-1 | Unclassified protein | C00003686 C00003689 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00003683 C00003689 | 0 / 0 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00003683 C00003689 | 1 / 2 |
P42858 | Huntingtin | Unclassified protein | C00003683 | 1 / 1 |
P39748 | Flap endonuclease 1 | Enzyme | C00003683 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00003683 | 0 / 0 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00003689 | 0 / 0 |
P11387 | DNA topoisomerase 1 | Isomerase | C00003683 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00003689 | 0 / 1 |
P11308 | Transcriptional regulator ERG | Unclassified protein | C00003689 | 1 / 2 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00003683 | 0 / 0 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00003683 | 0 / 0 |
P14679 | Tyrosinase | Oxidoreductase | C00032785 | 4 / 2 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00003689 | 0 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00003683 | 1 / 1 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003683 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00003689 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00003689 | 0 / 1 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00003683 | 4 / 3 |
P02545 | Prelamin-A/C | Unclassified protein | C00003683 | 11 / 10 |
P31939 | Bifunctional purine biosynthesis protein PURH | Enzyme | C00003689 | 1 / 1 |
Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00003683 | 1 / 4 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00003689 | 0 / 3 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003689 | 1 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
3717 | JAK2, JTK10, THCYT3 | Janus kinase 2 (EC:2.7.10.2) |
C00003689
|
6774 | STAT3, APRF, HIES | signal transducer and activator of transcription 3 (acute-phase response factor) |
C00003689
|
OMIM | preferred title | UniProt |
---|---|---|
#608688 | Aicar transformylase/imp cyclohydrolase deficiency |
P31939
|
#103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
#203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
#606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
#208900 | Ataxia-telangiectasia; at |
Q13315
|
#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 |
P84022
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#612219 | Ewing sarcoma; es |
P11308
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#143100 | Huntington disease; hd |
P42858
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#147060 | Hyper-ige recurrent infection syndrome, autosomal dominant |
P40763
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#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
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#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
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
Q06710 (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)
|
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)
|
H00024 | Prostate cancer |
P11308
(related)
|
H00035 | Ewing's sarcoma |
P11308
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00038 | Malignant melanoma |
P14679
(marker)
|
H00966 | AICA-ribosiduria |
P31939
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00016 | Oral cancer |
P40763
(related)
|
H00107 | Other well-defined immunodeficiency syndromes |
P40763
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00032 | Thyroid cancer |
Q06710
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
H00094 | DNA repair defects |
Q13315
(related)
|
H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|