Haplophyllum perforatum
Species
KNApSAcK Entry
| Organism name | Haplophyllum perforatum |
|---|---|
| Genus | Haplophyllum |
| Family | Rutaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Haplophyllum |
|---|---|
| Linked NCBI taxonomy ID | 266078 |
| Linked level | genus |
Family
| Family in NCBI taxonomy | Rutaceae |
|---|---|
| ID | 23513 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | rosids |
|---|---|
| ID | 71275 |
Metabolite list (17)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00005721
|
Limocitrin 7-neohesperidoside
|
No. 1 | No. 15 |
|
||||
|
C00006037
|
Haploside C
|
No. 1 | No. 15 |
|
||||
|
C00005710
|
Haploside F
|
No. 1 | No. 15 |
|
||||
|
C00006035
|
Haploside D
|
No. 1 | No. 15 |
|
||||
|
C00006036
|
Limocitrin 7-(6''-acetylglucoside)
|
No. 2 | No. 15 |
|
||||
|
C00005708
|
Haploside B
|
No. 2 | No. 15 |
|
||||
|
C00006034
|
Haploside A
|
No. 2 | No. 15 |
|
||||
|
C00004725
|
Haplogenin
|
No. 3 | No. 15 |
|
||||
|
C00000640
|
(+)-Eudesmin
|
CHEMBL519099
CHEMBL512865 CHEMBL523743 CHEMBL464352 CHEMBL1726879 |
C105875
|
2 / 0 / 0 | No. 38 | No. 21 |
|
|
|
C00026404
|
Anhydroevoxine
/ 7-(2,3-Epoxy-3-methylbutyl)oxy-8-methoxy-dictamnine |
No. 600 | No. 7 |
|
||||
|
C00002162
|
Flindersine
|
CHEMBL1507844
|
1 / 3 / 3 | No. 799 | No. 7 |
|
||
|
C00026427
|
Evoxoidine
/ 7-(3-Methylbutan-2-only)oxy-8-methoxydictamnine |
No. 1050 |
|
|||||
|
C00026425
|
Evodine
/ 7-(2-Hydroxy-3-methylbut-3-enyl)oxy-8-methoxydictamnine |
No. 1050 |
|
|||||
|
C00002171
|
Haplophyllidine
|
CHEMBL1864455
|
2 / 0 / 0 | No. 1718 | No. 7 |
|
||
|
C00026419
|
Dihydrohaplamine
|
No. 6495 |
|
|||||
|
C00002166
|
Glycoperine
|
CHEMBL1613094
|
3 / 2 / 2 | No. 6513 | No. 7 |
|
||
|
C00026495
|
Triacetylglycoperine
|
No. 8758 |
|
Human Protein / Gene in interactions
8 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00002166 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00000640 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00002171 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002171 | 0 / 0 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002162 | 3 / 3 |
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002166 | 2 / 2 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00000640 | 0 / 0 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002166 | 0 / 0 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (5)
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #119900 | Digital clubbing, isolated congenital |
P15428
|
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
KEGG DISEASE (5)
| KEGG | name | UniProt |
|---|---|---|
| H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
| H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(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)
|