Organism name | Citrullus colocynthis (L.) |
---|---|
Genus | Citrullus |
Family | Cucurbitaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Citrullus |
---|---|
Linked NCBI taxonomy ID | 3653 |
Linked level | genus |
Family in NCBI taxonomy | Cucurbitaceae |
---|---|
ID | 3650 |
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 |
---|---|---|---|---|---|---|---|---|
C00001059
![]() |
Isovitexin
/ Saponaretin / Homovitexin / 6-C-beta-D-Glucopyranosylapigenin / 6-beta-D-Glucopyranosyl-4',5,7-trihydroxyflavone / 6-beta-D-Glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one |
CHEMBL465360
CHEMBL1601394 |
C049772
|
28 / 20 / 19 | No. 22 | No. 15 |
![]() |
|
C00030466
![]() |
Helicid
/ 4-(beta-D-glucopyranosyloxy) benzaldehyde |
CHEMBL201358
CHEMBL461515 |
C055677
|
2 / 2 / 2 | No. 45 | No. 72 |
![]() |
|
C00029534
![]() |
4-Hydroxybenzyl beta-D-glucopyranoside
|
No. 45 | No. 72 |
![]() |
||||
C00029516
![]() |
Gastrodin
/ (-)-Gastrodin / 4-(beta-D-Glucopyranosyloxy) benzyl alcohol |
CHEMBL274739
|
C045345
|
2 / 2 / 2 | 0 / 2 | No. 45 | No. 72 |
![]() |
C00029812
![]() |
Benzyl beta-D-glucopyranoside
/ (-)-Benzyl-O-beta-D-glucopyranoside |
CHEMBL1170453
CHEMBL2336738 |
C410942
|
No. 45 | No. 72 |
![]() |
||
C00030034
![]() |
Cucurbitacin l 2-O-beta-D-glucopyranoside
|
CHEMBL449483
|
1 / 4 / 2 | No. 315 |
![]() |
|||
C00030001
![]() |
Colocynthoside A
/ (-)-Colocynthoside A |
No. 315 |
![]() |
|||||
C00030032
![]() |
Cucurbitacin K 2-O-beta-glucopyranoside
/ Cucurbitacin K 2-O-beta-D-glucopyranoside |
CHEMBL1923785
CHEMBL1923786 |
No. 315 |
![]() |
||||
C00030029
![]() |
Elaterinide
/ Gratiotoxin / Cucurbitacin E-2-O-glucoside / alpha-Elaterin 2-D-glucopyranoside / Cucurbitacin E 2-O-beta-D-glucopyranoside |
CHEMBL1455367
CHEMBL1765381 |
8 / 5 / 3 | No. 315 |
![]() |
|||
C00030031
![]() |
Cucurbitacin I 2-O-beta-D-glucopyranoside
|
CHEMBL1723294
CHEMBL1765380 |
2 / 0 / 0 | No. 315 |
![]() |
|||
C00030608
![]() |
Khekadaengoside E
/ (-)-Khekadaengoside E |
No. 315 |
![]() |
|||||
C00030002
![]() |
Colocynthoside B
/ (-)-Colocynthoside B |
No. 675 | No. 51 |
![]() |
||||
C00029478
![]() |
3,4'-Dihydroxypropiophenone
/ 4-Hydroxy-(3-hydroxypropionyl)benzene |
CHEMBL1417159
|
25 / 10 / 7 | No. 2849 |
![]() |
|||
C00029477
![]() |
beta-Hydroxypropiovanillone
/ omega-Hydroxypropioguaiacone / 3,4'-Dihydroxy-3'-methoxypropiophenone / 3-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)-1-propanone |
CHEMBL485875
|
No. 2959 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00001059 C00030029 C00030031 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00001059 C00029478 C00030029 | 0 / 0 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00001059 C00029478 C00030029 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00001059 C00029478 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00001059 C00029478 | 1 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00001059 C00029478 | 0 / 0 |
P51649 | Succinate-semialdehyde dehydrogenase, mitochondrial | Oxidoreductase | C00029516 C00030466 | 1 / 1 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001059 C00029478 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00001059 C00029478 | 1 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00001059 C00029478 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00001059 C00030029 | 1 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00001059 C00029478 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00001059 C00029478 | 1 / 1 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00001059 C00029478 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001059 C00029478 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00001059 C00029478 | 1 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00001059 C00029478 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001059 C00029478 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00001059 C00029478 | 2 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00029478 C00030031 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00001059 C00029478 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00001059 C00029478 | 0 / 0 |
P80404 | 4-aminobutyrate aminotransferase, mitochondrial | Transferase | C00029516 C00030466 | 1 / 1 |
Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00029478 | 0 / 0 |
P30989 | Neurotensin receptor type 1 | Neurotensin receptor | C00001059 | 0 / 0 |
P10696 | Alkaline phosphatase, placental-like | Enzyme | C00029478 | 0 / 1 |
P14679 | Tyrosinase | Oxidoreductase | C00030034 | 4 / 2 |
P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00029478 | 3 / 1 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00001059 | 0 / 0 |
P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00029478 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00001059 | 7 / 3 |
O75496 | Geminin | Unclassified protein | C00030029 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00029478 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00030029 | 2 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00001059 | 2 / 2 |
O00255 | Menin | Unclassified protein | C00001059 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00001059 | 1 / 2 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00001059 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00001059 | 1 / 4 |
P54132 | Bloom syndrome protein | Enzyme | C00029478 | 1 / 2 |
Q99700 | Ataxin-2 | Unclassified protein | C00030029 | 1 / 1 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00030029 | 1 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
#203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
#606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
#210900 | Bloom syndrome; blm |
P54132
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#613163 | Gaba-transaminase deficiency |
P80404
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#146300 | Hypophosphatasia, adult |
P05186
|
#241510 | Hypophosphatasia, childhood |
P05186
|
#241500 | Hypophosphatasia, infantile |
P05186
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#271980 | Succinic semialdehyde dehydrogenase deficiency; ssadhd |
P51649
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
H00213 | Hypophosphatasia |
P05186
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00023 | Testicular cancer |
P10696
(marker)
|
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00038 | Malignant melanoma |
P14679
(marker)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00835 | Succinic semialdehyde dehydrogenase (SSADH) deficiency |
P51649
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
Q14191 (related) |
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H01257 | GABA-transaminase deficiency |
P80404
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) Q03164 (related) Q03164 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00032 | Thyroid cancer |
Q06710
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
Q06710
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|