| 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) |