Species

KNApSAcK Entry

Organism name Daphniphyllum oldhami
Genus Daphniphyllum
Family Daphniphyllaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Daphniphyllum oldhamii
Linked NCBI taxonomy ID 1008903
Linked level species

Family

Family in NCBI taxonomy Daphniphyllaceae
ID 4386

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (37)

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
C00002227 External link 512 Matrine
/ (+)-Matrine
CHEMBL204860
CHEMBL383443
CHEMBL525227
CHEMBL1396816
CHEMBL1733145
CHEMBL1824581
C034244
5 / 3 / 7 4 / 5 No. 85 No. 3
C00002207 External link 512 Anagyrine
/ (-)-Anagyrine
CHEMBL203399
CHEMBL509692
CHEMBL1324708
CHEMBL1454284
C012736
7 / 8 / 11 No. 384 No. 3
C00002215 External link 512 Camoensine
No. 384 No. 3
C00040720 External link 512 Yuzurimine B
No. 584
C00040721 External link 512 Yuzurimine E
/ (-)-Yuzurimine E
No. 584
C00039690 External link 512 Macrodaphniphyllidine
No. 584
C00038684 External link 512 Calyciphylline B
No. 1167
C00038943 External link 512 Daphnioldhanin J
/ (-)-Daphnioldhanin J
CHEMBL465875
No. 1167
C00038986 External link 512 Deoxycalyciphylline B
/ (-)-Deoxycalyciphylline B
No. 1167
C00038932 External link 512 Daphnilactone B
/ (-)-Daphnilactone B
No. 1167
C00039435 External link 512 Isodaphnilactone B
No. 1167
C00038989 External link 512 Deoxyisocalyciphylline B
/ (-)-Deoxyisocalyciphylline B
No. 1167
C00007758 External link 512 Oxymatrine
/ Ammothamnine
/ Matrine N-oxide
/ (+)-Matrine N-oxide
/ Matrine 1beta-oxide
CHEMBL458337
CHEMBL1358502
C037573
3 / 11 / 6 0 / 4 No. 1211 No. 3
C00038942 External link 512 Daphnioldhanin I
No. 1333
C00038926 External link 512 Daphmacrine
No. 1333
C00038927 External link 512 Daphmacropodine
No. 1333
C00038941 External link 512 Daphnioldhanin G
/ (-)-Daphnioldhanin G
CHEMBL1078304
No. 1333
C00038938 External link 512 Daphnioldhanin D
No. 1333
C00038940 External link 512 Daphnioldhanin F
/ (-)-Daphnioldhanin F
No. 1333
C00038939 External link 512 Daphnioldhanin E
/ (-)-Daphnioldhanin E
No. 1333
C00040267 External link 512 Secodaphniphylline
No. 1457
C00038818 External link 512 Codaphniphylline
/ (+)-Codaphniphylline
No. 1457
C00038934 External link 512 Daphnimacropine
No. 1457
C00038933 External link 512 Daphnilongeranin D
No. 1457
C00038957 External link 512 Dehydrodaphnigraciline
CHEMBL465534
No. 1714
C00040722 External link 512 Yuzurine
No. 1714
C00038931 External link 512 Daphnigraciline
No. 1714
C00007759 External link 512 Sophocarpine
/ (-)-Sophocarpine
CHEMBL377725
CHEMBL380909
C035933
0 / 1 No. 1721
C00039756 External link 512 Methyl homosecodaphniphyllate
No. 2618
C00038928 External link 512 Daphmanidin A
/ (-)-Daphmanidin A
CHEMBL519114
No. 2948
C00038937 External link 512 Daphnioldhanin C
No. 3743
C00038935 External link 512 Daphnioldhanin A
/ (-)-Daphnioldhanin A
No. 3743
C00038936 External link 512 Daphnioldhanin B
/ (-)-Daphnioldhanin B
No. 3743
C00047838 External link 512 Dapholdhamine A
CHEMBL563837
No. 4190
C00047839 External link 512 Dapholdhamine B
/ (-)-Dapholdhamine B
CHEMBL561787
No. 4190
C00047840 External link 512 Dapholdhamine C
/ (-)-Dapholdhamine C
CHEMBL552401
No. 5234
C00047841 External link 512 Dapholdhamine D
/ (-)-Dapholdhamine D
CHEMBL563419
No. 5234

Human Protein / Gene in interactions

13 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002207 C00002227 1 / 2
O00255 Menin Unclassified protein C00002207 C00002227 2 / 5
P28482 Mitogen-activated protein kinase 1 Erk C00002227 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002227 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00007758 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00007758 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002207 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002207 3 / 3
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002207 1 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00007758 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002207 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00002227 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002207 1 / 0

4 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00002227
4893 NRAS, ALPS4, N-ras, NRAS1, NS6 neuroblastoma RAS viral (v-ras) oncogene homolog C00002227
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00002227
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00002227

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
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#166350 Osseous heteroplasia, progressive; poh P63092
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (17)

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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (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)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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

9 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D007249 Inflammation C00007759
C00007758
D008113 Liver Neoplasms C00002227
D056487 Drug-Induced Liver Injury, Chronic C00002227
D006331 Heart Diseases C00002227
D002779 Cholestasis C00002227
D002289 Carcinoma, Non-Small-Cell Lung C00002227
D003092 Colitis C00007758
D019694 Hepatitis B, Chronic C00007758
D008106 Liver Cirrhosis, Experimental C00007758