Species

KNApSAcK Entry

Organism name Croton hemiargyreus
Genus Croton
Family Euphorbiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Croton hemiargyreus
Linked NCBI taxonomy ID 765397
Linked level species

Family

Family in NCBI taxonomy Euphorbiaceae
ID 3977

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (11)

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 External link 512 Glaucine
/ S-(+)-Glaucine
/ O,O-Dimethylisoboldine
CHEMBL36536
CHEMBL228082
14 / 8 / 6 No. 20 No. 4
C00001872 External link 512 Isocorydine
/ (+)-Isocorydine
/ L-(+)-Isocorydine
/ (S)-(+)-Isocorydine
CHEMBL489525
CHEMBL1376826
14 / 7 / 10 No. 20 No. 4
C00025827 External link 512 Corydine
/ Glaucentrin
/ (+)-Corydine
/ Glaucentrine
CHEMBL489524
CHEMBL2002847
C067341
1 / 0 / 0 No. 20 No. 4
C00027153 External link 512 Norcorydine
/ (+)-Norcorydine
CHEMBL494053
No. 20 No. 4
C00027374 External link 512 Hemiargyrine
No. 37 No. 4
C00001929 External link 512 Xylopinine
/ O-Methylgovanine
/ S-(-)-Xylopinine
/ O,O-Dimethylgovadine
CHEMBL465824
CHEMBL2357282
C008672
1 / 0 / 0 No. 37 No. 4
C00026150 External link 512 Tetrahydropalmatine
/ dl-Tetrahydropalmatine
/ (+/-)-Tetrahydropalmatine
CHEMBL187892
CHEMBL487182
CHEMBL2334889
8 / 5 / 2 No. 37 No. 4
C00027457 External link 512 Oxoglaucine
/ O-Methylatheroline
CHEMBL470881
C111587
25 / 27 / 24 No. 74
C00001916 External link 512 Salutaridine
/ (+)-Salutaridine
CHEMBL402782
CHEMBL404097
C009270
3 / 4 / 2 No. 426 No. 4
C00027443 External link 512 Norsalutaridine
No. 426 No. 4
C00027154 External link 512 Norlaudanosine
/ Tetrahydropapaverine
/ S-(-)-N-Norlaudanosine
CHEMBL160919
No. 4059

Human Protein / Gene in interactions

49 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (41)

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 DISEASE (33)

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)