Species

KNApSAcK Entry

Organism name Dorstenia poinsettifolia
Genus Dorstenia
Family Moraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Dorstenia
Linked NCBI taxonomy ID 106722
Linked level genus

Family

Family in NCBI taxonomy Moraceae
ID 3487

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (10)

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
C00004090 External link 512 Licoflavone C
/ 8-Prenylapigenin
/ 5,7,4'-Trihydroxy-8-prenylflavone
/ 5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one
CHEMBL371562
1 / 0 / 0 No. 15 No. 15
C00003776 External link 512 Lutein
/ (all-E)-Lutein
/ all-trans-(+)-Xanthophyll
/ (3R,3'R,6'R)-beta,epsilon-Carotene-3,3'-diol
CHEMBL173929
CHEMBL172477
CHEMBL1559643
CHEMBL1979448
D014975
4 / 2 / 3 7 / 2 No. 26 No. 59
C00011161 External link 512 Poinsettifolin A
/ 2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-8-methyl-6-(3-methyl-2-butenyl)-8-(4-methyl-3-pentenyl)-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one
No. 44
C00011163 External link 512 Butyrospermol
/ (-)-Butyrospermol
CHEMBL1835433
No. 119 No. 51
C00008399 External link 512 4'-Hydroxyisolonchocarpin
No. 127 No. 14
C00014224 External link 512 Dorspoinsettifolin
/ 4'-Methoxy-6'',6''-dimethyldihydropyrano[2'',3'':7,8]flavanone
No. 127 No. 14
C00007061 External link 512 Isobavachromene
/ 4-Hydroxylonchocarpin
CHEMBL362378
1 / 0 / 0 No. 130
C00036580 External link 512 4-Hydroxylonchocarpin
CHEMBL362378
1 / 0 / 0 No. 130
C00002381 External link 512 Corylifolinin
/ Isobavachalcone
/ 2',4,4'-Trihydroxy-3'-(3-methyl-2-butenyl)chalcone
CHEMBL253467
C468754
8 / 22 / 21 No. 133 No. 13
C00011162 External link 512 Poinsettifolin B
No. 186

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P11926 Ornithine decarboxylase Lyase C00007061 C00036580 0 / 0
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00002381 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00003776 2 / 3
P21802 Fibroblast growth factor receptor 2 TK tyrosine-protein kinase TLK subfamily C00002381 9 / 3
O75496 Geminin Unclassified protein C00003776 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00003776 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00002381 2 / 2
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002381 1 / 8
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00002381 1 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00002381 2 / 3
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00004090 0 / 0
P11362 Fibroblast growth factor receptor 1 Fgfr C00002381 4 / 5
P10721 Mast/stem cell growth factor receptor Kit Pdgfr C00002381 4 / 3
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00003776 0 / 0

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
581 BAX, BCL2L4 BCL2-associated X protein C00003776
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00003776
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00003776
847 CAT catalase (EC:1.11.1.6) C00003776
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00003776
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00003776
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00003776

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (24)

OMIM preferred title UniProt
#207410 Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 P21802
#101200 Apert syndrome P21802
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#123790 Beare-stevenson cutis gyrata syndrome; bstvs P21802
#614592 Bent bone dysplasia syndrome; bbds P21802
#123500 Crouzon syndrome P21802
#606764 Gastrointestinal stromal tumor; gist P10721
#602089 Hemangioma, capillary infantile P35968
#114550 Hepatocellular carcinoma P08581
#147950 Hypogonadotropic hypogonadism 2 with or without anosmia; hh2 P11362
#123150 Jackson-weiss syndrome; jws P21802
#149730 Lacrimoauriculodentodigital syndrome; ladd P21802
#601626 Leukemia, acute myeloid; aml P10721
#211980 Lung cancer P00533
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166250 Osteoglophonic dysplasia; ogd P11362
#101600 Pfeiffer syndrome P11362
P21802
#172800 Piebald trait; pbt P10721
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#609579 Scaphocephaly, maxillary retrusion, and mental retardation P21802
#273300 Testicular germ cell tumor; tgct P10721
#190440 Trigonocephaly 1; trigno1 P11362
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (24)

KEGG name UniProt
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
H00018 Gastric cancer P00533 (related)
P08581 (related)
P21802 (related)
H00022 Bladder cancer P00533 (related)
H00028 Choriocarcinoma P00533 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00021 Renal cell carcinoma P08581 (related)
H00046 Cholangiocarcinoma P08581 (related)
H00003 Acute myeloid leukemia (AML) P10721 (related)
P10721 (marker)
H00170 Piebaldism P10721 (related)
H00023 Testicular cancer P10721 (marker)
H00255 Hypogonadotropic hypogonadism P11362 (related)
H00443 Osteoglophonic dysplasia (OD) P11362 (related)
H00458 Craniosynostosis P11362 (related)
P21802 (related)
H00516 Isolated orofacial clefts P11362 (related)
H01207 Trigonocephaly P11362 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H00642 Lacrimo-auriculo-dento-digital syndrome (LADD) P21802 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D007939 Leukemia L1210 C00003776
D014605 Uveitis C00003776