Organism name | Croton hemiargyreus |
---|---|
Genus | Croton |
Family | Euphorbiaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Croton hemiargyreus |
---|---|
Linked NCBI taxonomy ID | 765397 |
Linked level | species |
Family in NCBI taxonomy | Euphorbiaceae |
---|---|
ID | 3977 |
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 |
---|---|---|---|---|---|---|---|---|
C00001861
![]() |
Glaucine
/ S-(+)-Glaucine / O,O-Dimethylisoboldine |
CHEMBL36536
CHEMBL228082 |
14 / 8 / 6 | No. 20 | No. 4 |
![]() |
||
C00001872
![]() |
Isocorydine
/ (+)-Isocorydine / L-(+)-Isocorydine / (S)-(+)-Isocorydine |
CHEMBL489525
CHEMBL1376826 |
14 / 7 / 10 | No. 20 | No. 4 |
![]() |
||
C00025827
![]() |
Corydine
/ Glaucentrin / (+)-Corydine / Glaucentrine |
CHEMBL489524
CHEMBL2002847 |
C067341
|
1 / 0 / 0 | No. 20 | No. 4 |
![]() |
|
C00027153
![]() |
Norcorydine
/ (+)-Norcorydine |
CHEMBL494053
|
No. 20 | No. 4 |
![]() |
|||
C00027374
![]() |
Hemiargyrine
|
No. 37 | No. 4 |
![]() |
||||
C00001929
![]() |
Xylopinine
/ O-Methylgovanine / S-(-)-Xylopinine / O,O-Dimethylgovadine |
CHEMBL465824
CHEMBL2357282 |
C008672
|
1 / 0 / 0 | No. 37 | No. 4 |
![]() |
|
C00026150
![]() |
Tetrahydropalmatine
/ dl-Tetrahydropalmatine / (+/-)-Tetrahydropalmatine |
CHEMBL187892
CHEMBL487182 CHEMBL2334889 |
8 / 5 / 2 | No. 37 | No. 4 |
![]() |
||
C00027457
![]() |
Oxoglaucine
/ O-Methylatheroline |
CHEMBL470881
|
C111587
|
25 / 27 / 24 | No. 74 |
![]() |
||
C00001916
![]() |
Salutaridine
/ (+)-Salutaridine |
CHEMBL402782
CHEMBL404097 |
C009270
|
3 / 4 / 2 | No. 426 | No. 4 |
![]() |
|
C00027443
![]() |
Norsalutaridine
|
No. 426 | No. 4 |
![]() |
||||
C00027154
![]() |
Norlaudanosine
/ Tetrahydropapaverine / S-(-)-N-Norlaudanosine |
CHEMBL160919
|
No. 4059 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001861 C00001872 C00027457 | 0 / 0 |
P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00001872 C00001916 C00025827 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00001861 C00001872 C00027457 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001872 C00026150 C00027457 | 0 / 1 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00001861 C00001872 | 3 / 3 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00001861 C00027457 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001872 C00027457 | 1 / 1 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00001861 C00001872 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00001861 C00027457 | 4 / 3 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001872 C00027457 | 1 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001872 C00027457 | 0 / 1 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00001861 C00027457 | 1 / 0 |
P43351 | DNA repair protein RAD52 homolog | Unclassified protein | C00001861 C00001929 | 0 / 0 |
Q9GZR1 | Sentrin-specific protease 6 | Enzyme | C00001861 | 0 / 0 |
P14416 | D(2) dopamine receptor | Dopamine receptor | C00026150 | 2 / 0 |
Q14761 | Protein tyrosine phosphatase receptor type C-associated protein | Enzyme | C00001861 | 0 / 0 |
Q9BQF6 | Sentrin-specific protease 7 | Enzyme | C00001861 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00027457 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00027457 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00027457 | 2 / 0 |
P42574 | Caspase-3 | C14 | C00001861 | 0 / 0 |
Q99720 | Sigma non-opioid intracellular receptor 1 | Membrane receptor | C00026150 | 1 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00027457 | 1 / 1 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00027457 | 1 / 2 |
Q96LD8 | Sentrin-specific protease 8 | Enzyme | C00001861 | 0 / 0 |
P00734 | Prothrombin | S1A | C00001916 | 4 / 2 |
P13726 | Tissue factor | Membrane receptor | C00026150 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00027457 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001872 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00027457 | 11 / 10 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00027457 | 2 / 2 |
Q92793 | CREB-binding protein | Enzyme | C00027457 | 1 / 1 |
P03372 | Estrogen receptor | NR3A1 | C00026150 | 1 / 1 |
P28223 | 5-hydroxytryptamine receptor 2A | Serotonin receptor | C00026150 | 0 / 0 |
P35372 | Mu-type opioid receptor | Opioid receptor | C00001916 | 0 / 0 |
P29466 | Caspase-1 | C14 | C00027457 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00027457 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00001861 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00027457 | 0 / 0 |
P21728 | D(1A) dopamine receptor | Dopamine receptor | C00026150 | 0 / 0 |
P08908 | 5-hydroxytryptamine receptor 1A | Serotonin receptor | C00026150 | 1 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00027457 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00027457 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00027457 | 1 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00001872 | 1 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00001872 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00001872 | 1 / 4 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001872 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00027457 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#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 |
P84022
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#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
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#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
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#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
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
#613679 | Prothrombin deficiency, congenital |
P00734
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#180849 | Rubinstein-taybi syndrome 1; rsts1 |
Q92793
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601367 | Stroke, ischemic |
P00734
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
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)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(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)
|
H00504 | Rubinstein-Taybi syndrome |
Q92793
(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)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|