Organism name | Dracaena cochinchinensis |
---|---|
Genus | Dracaena |
Family | Dracaenaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Dracaena cochinchinensis |
---|---|
Linked NCBI taxonomy ID | 593754 |
Linked level | species |
Family in NCBI taxonomy | Asparagaceae |
---|---|
ID | 40552 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Liliopsida |
---|---|
ID | 4447 |
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 |
---|---|---|---|---|---|---|---|---|
C00014604
![]() |
4,4'-Dihydroxy-2,6-dimethoxydihydrochalcone
|
CHEMBL400283
|
No. 90 | No. 13 |
![]() |
|||
C00014597
![]() |
4'-Hydroxy-2,6-dimethoxydihydrochalcone
|
No. 90 | No. 13 |
![]() |
||||
C00006927
![]() |
Isoliquiritigenin 2'-methy ether
/ 4,4'-Dihydroxy-2'-methoxychalcone |
CHEMBL253777
|
7 / 20 / 19 | No. 92 | No. 13 |
![]() |
||
C00038096
![]() |
(2S)-4',5-Dihydroxy-7-methoxy-8-methylflavan
|
CHEMBL253562
|
No. 179 | No. 15 |
![]() |
|||
C00040540
![]() |
trans-3,5-Dihydroxy-4'-methoxystilbene
|
CHEMBL291501
CHEMBL313687 |
6 / 13 / 13 | No. 295 | No. 13 |
![]() |
||
C00038095
![]() |
(2R)-8-Methylsocotrin-4'-ol
|
CHEMBL254647
|
2 / 4 / 3 | No. 435 |
![]() |
|||
C00014639
![]() |
Cochinchinenin
/ 3-[2,4-Dihydroxy-5-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]phenyl]-1-(4-hydroxyphenyl)-1-propanone |
No. 435 |
![]() |
|||||
C00038812
![]() |
Cochinchinenene A
/ (+)-Cochinchinenene A |
CHEMBL254229
|
2 / 4 / 3 | No. 435 |
![]() |
|||
C00038813
![]() |
Cochinchinenene B
/ (+)-Cochinchinenene B |
CHEMBL399481
|
2 / 4 / 3 | No. 435 |
![]() |
|||
C00038817
![]() |
Cochinchinenin C
/ (+)-Cochinchinenin C |
CHEMBL254649
|
2 / 4 / 3 | No. 435 |
![]() |
|||
C00038815
![]() |
Cochinchinenene D
/ (+)-Cochinchinenene D |
CHEMBL254440
|
2 / 4 / 3 | No. 435 |
![]() |
|||
C00038816
![]() |
Cochinchinenin B
/ (+)-Cochinchinenin B |
CHEMBL254648
|
2 / 4 / 3 | No. 435 |
![]() |
|||
C00038814
![]() |
Cochinchinenene C
/ (+)-Cochinchinenene C |
CHEMBL254439
|
2 / 4 / 3 | No. 435 |
![]() |
|||
C00014596
![]() |
2,4,4'-Trihydroxydihydrochalcone
|
CHEMBL253564
|
No. 548 | No. 13 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P27487 | Dipeptidyl peptidase 4 | S9B | C00038095 C00038812 C00038813 C00038814 C00038815 C00038816 C00038817 | 0 / 1 |
P00734 | Prothrombin | S1A | C00038095 C00038812 C00038813 C00038814 C00038815 C00038816 C00038817 | 4 / 2 |
P12931 | Proto-oncogene tyrosine-protein kinase Src | Src | C00006927 | 0 / 0 |
P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00006927 | 1 / 8 |
P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00040540 | 0 / 0 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00040540 | 0 / 3 |
P21802 | Fibroblast growth factor receptor 2 | TK tyrosine-protein kinase TLK subfamily | C00006927 | 9 / 3 |
P02545 | Prelamin-A/C | Unclassified protein | C00040540 | 11 / 10 |
P35968 | Vascular endothelial growth factor receptor 2 | Vegfr | C00006927 | 1 / 0 |
P18054 | Arachidonate 12-lipoxygenase, 12S-type | Enzyme | C00040540 | 2 / 0 |
P08581 | Hepatocyte growth factor receptor | TK tyrosine-protein kinase MET subfamily | C00006927 | 2 / 3 |
P11362 | Fibroblast growth factor receptor 1 | Fgfr | C00006927 | 4 / 5 |
O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00040540 | 0 / 0 |
P10721 | Mast/stem cell growth factor receptor Kit | Pdgfr | C00006927 | 4 / 3 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00040540 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#207410 | Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 |
P21802
|
#101200 | Apert syndrome |
P21802
|
#123790 | Beare-stevenson cutis gyrata syndrome; bstvs |
P21802
|
#614592 | Bent bone dysplasia syndrome; bbds |
P21802
|
#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 |
P18054
|
#123500 | Crouzon syndrome |
P21802
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#133239 | Esophageal cancer |
P18054
|
#606764 | Gastrointestinal stromal tumor; gist |
P10721
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#602089 | Hemangioma, capillary infantile |
P35968
|
#114550 | Hepatocellular carcinoma |
P08581
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#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
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#211980 | Lung cancer |
P00533
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#166250 | Osteoglophonic dysplasia; ogd |
P11362
|
#101600 | Pfeiffer syndrome |
P11362
P21802 |
#172800 | Piebald trait; pbt |
P10721
|
#614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
#613679 | Prothrombin deficiency, congenital |
P00734
|
#605074 | Renal cell carcinoma, papillary, 1; rccp1 |
P08581
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#609579 | Scaphocephaly, maxillary retrusion, and mental retardation |
P21802
|
#601367 | Stroke, ischemic |
P00734
|
#273300 | Testicular germ cell tumor; tgct |
P10721
|
#188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|
#190440 | Trigonocephaly 1; trigno1 |
P11362
|
KEGG | name | UniProt |
---|---|---|
H00016 | Oral cancer |
P00533
(related)
P00533 (marker) |
H00017 | Esophageal cancer |
P00533
(related)
P35354 (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) |
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)
|
H00021 | Renal cell carcinoma |
P08581
(related)
|
H00046 | Cholangiocarcinoma |
P08581
(related)
P35354 (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)
|
H00642 | Lacrimo-auriculo-dento-digital syndrome (LADD) |
P21802
(related)
|
H00032 | Thyroid cancer |
P27487
(marker)
|
H00025 | Penile cancer |
P35354
(related)
|