Species

KNApSAcK Entry

Organism name Delphinium stapeliosum
Genus Delphinium
Family Ranunculaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Delphinium
Linked NCBI taxonomy ID 46246
Linked level genus

Family

Family in NCBI taxonomy Ranunculaceae
ID 3440

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (18)

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
C00031727 External link 512 Delbonine
No. 31 No. 10
C00001632 External link 512 Delcosine
CHEMBL2141282
2 / 7 / 3 No. 31 No. 10
C00028671 External link 512 Neoline
CHEMBL1242346
No. 31 No. 10
C00046562 External link 512 14-Demethyltuguaconitine
/ (+)-14-Demethyltuguaconitine
No. 31 No. 10
C00028038 External link 512 Chasmanine
No. 31 No. 10
C00031729 External link 512 Deltatsine
No. 31 No. 10
C00046560 External link 512 14-Acetylchasmanine
No. 31 No. 10
C00001633 External link 512 Delphinine
CHEMBL1995442
No. 138 No. 10
C00001629 External link 512 14-Deacetylnudicauline
CHEMBL443248
C086739
No. 166 No. 10
C00028578 External link 512 Methyllycaconitine
CHEMBL223494
CHEMBL387362
CHEMBL510275
CHEMBL1412391
CHEMBL1592980
CHEMBL1620703
CHEMBL1869403
CHEMBL2094019
C054634
21 / 12 / 8 15 / 7 No. 166 No. 10
C00046606 External link 512 Ajadine
CHEMBL1240988
No. 166 No. 10
C00035462 External link 512 14-Deacetyl-14-isobutyrylnudicauline
No. 166 No. 10
C00043157 External link 512 14-Deacetyl-14-isobutyrylajadine
/ (+)-14-Deacetyl-14-isobutyrylajadine
No. 166 No. 10
C00046561 External link 512 14-Deacetylajadine
CHEMBL1240987
No. 166 No. 10
C00001658 External link 512 Nudicauline
CHEMBL2112854
No. 166 No. 10
C00043256 External link 512 Ajacine
CHEMBL1240989
No. 166 No. 10
C00024882 External link 512 Dihydroatisine
/ F-Dihydroatisine
No. 274 No. 10
C00027913 External link 512 Azitine
No. 619 No. 10

Human Protein / Gene in interactions

23 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00028578 1 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00028578 2 / 0
P23415 Glycine receptor subunit alpha-1 GLR alpha C00028578 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00028578 0 / 1
P30926 Neuronal acetylcholine receptor subunit beta-4 CHRN beta C00028578 0 / 0
P32297 Neuronal acetylcholine receptor subunit alpha-3 CHRN alpha C00028578 1 / 0
P43681 Neuronal acetylcholine receptor subunit alpha-4 CHRN alpha C00028578 1 / 1
P17787 Neuronal acetylcholine receptor subunit beta-2 CHRN beta C00028578 1 / 1
O75496 Geminin Unclassified protein C00001632 0 / 0
P46098 5-hydroxytryptamine receptor 3A NS C00028578 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00001632 7 / 3
P36544 Neuronal acetylcholine receptor subunit alpha-7 CHRN alpha C00028578 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00028578 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00028578 3 / 3
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00028578 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00028578 0 / 1
Q15822 Neuronal acetylcholine receptor subunit alpha-2 CHRN alpha C00028578 1 / 1
Q8WXA8 5-hydroxytryptamine receptor 3C NS C00028578 0 / 0
Q70Z44 5-hydroxytryptamine receptor 3D NS C00028578 0 / 0
O95264 5-hydroxytryptamine receptor 3B NS C00028578 0 / 0
A5X5Y0 5-hydroxytryptamine receptor 3E NS C00028578 0 / 0
Q9UGM1 Neuronal acetylcholine receptor subunit alpha-9 CHRN alpha C00028578 0 / 0
Q9GZZ6 Neuronal acetylcholine receptor subunit alpha-10 CHRN alpha C00028578 0 / 0

15 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00028578
627 BDNF, ANON2, BULN2 brain-derived neurotrophic factor C00028578
1137 CHRNA4, BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 cholinergic receptor, nicotinic, alpha 4 (neuronal) C00028578
1139 CHRNA7, CHRNA7-2, NACHRA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) C00028578
1141 CHRNB2, EFNL3, nAChRB2 cholinergic receptor, nicotinic, beta 2 (neuronal) C00028578
1621 DBH, DBM dopamine beta-hydroxylase (dopamine beta-monooxygenase) (EC:1.14.17.1) C00028578
3674 ITGA2B, BDPLT16, BDPLT2, CD41, CD41B, GP2B, GPIIb, GT, GTA, HPA3 integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) C00028578
3690 ITGB3, BDPLT16, BDPLT2, CD61, GP3A, GPIIIa, GT integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) C00028578
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00028578
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00028578
4915 NTRK2, GP145-TrkB, TRKB, trk-B neurotrophic tyrosine kinase, receptor, type 2 (EC:2.7.10.1) C00028578
6774 STAT3, APRF, HIES signal transducer and activator of transcription 3 (acute-phase response factor) C00028578
7054 TH, DYT14, DYT5b, TYH tyrosine hydroxylase (EC:1.14.16.2) C00028578
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00028578
7538 ZFP36, G0S24, GOS24, NUP475, RNF162A, TIS11, TTP, zfp-36 ZFP36 ring finger protein C00028578

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (19)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#600513 Epilepsy, nocturnal frontal lobe, 1; enfl1 P43681
#605375 Epilepsy, nocturnal frontal lobe, 3; enfl3 P17787
#610353 Epilepsy, nocturnal frontal lobe, 4; enfl4 Q15822
#149400 Hyperekplexia, hereditary 1; hkpx1 P23415
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#612052 Smoking as a quantitative trait locus 3; sqtl3 P32297

KEGG DISEASE (11)

KEGG name UniProt
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00807 Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) P17787 (related)
P43681 (related)
Q15822 (related)
H00769 Hyperekplexia P23415 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)

Diseases related to CTD interactions

7 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D001259 Ataxia C00028578
D001919 Bradycardia C00028578
D006973 Hypertension C00028578
D018908 Muscle Weakness C00028578
D012640 Seizures C00028578
D013610 Tachycardia C00028578
D014202 Tremor C00028578