| Organism name | Xylopia parviflora | 
|---|---|
| Genus | Xylopia | 
| Family | Annonaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Xylopia parviflora | 
|---|---|
| Linked NCBI taxonomy ID | 992813 | 
| Linked level | species | 
| Family in NCBI taxonomy | Annonaceae | 
|---|---|
| ID | 22140 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | Magnoliophyta | 
|---|---|
| ID | 3398 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00001806   | Anolobine / (-)-Anolobine | CHEMBL257746 | No. 20 | No. 4 |   | |||
| C00001807   | Anonaine / (-)-Anonaine / (R)-Annonaine | CHEMBL401798 | C098138 | 1 / 0 / 0 | No. 20 | No. 4 |   | |
| C00034986   | (+)-Noroconovine | No. 20 | No. 4 |   | ||||
| C00034984   | (+)-10,11-Dihydroxy-1,2-dimethoxynoraporphine | No. 20 | No. 4 |   | ||||
| C00034982   | (+)-1,2-Dimethoxy-3-hydroxy-9,10-methylenedioxynoraporphine | CHEMBL1618043 | No. 20 | No. 4 |   | |||
| C00027433   | Laurolitsine / (+)-Norboldine / (+)-Laurolitsine | CHEMBL487388 | C109133 | No. 20 | No. 4 |   | ||
| C00027409   | Laurotetanin / Laurotetanine / (+)-Laurotetanine | CHEMBL464098 | C008256 | No. 20 | No. 4 |   | ||
| C00027307   | Calycinine / (-)-Calycinine | CHEMBL226824 | No. 20 | No. 4 |   | |||
| C00025676   | Norglaucin / Norglaucine / (+)-Norglaucine / O,O-Dimethyllaurelliptine | No. 20 | No. 4 |   | ||||
| C00025675   | Lauroscholtzine / 2-O-Methylboldine / N-Methyllaurotetanine / (+)-N-Methyllaurotetanine | CHEMBL464099 | 1 / 1 / 0 | No. 20 | No. 4 |   | ||
| C00025269   | Nornantenine / N-Nornantenine / (+)-Nornantenine | CHEMBL1254951 | 1 / 0 / 0 | No. 20 | No. 4 |   | ||
| C00027304   | Boldine / d-Boldine / (+)-Boldine | CHEMBL388342 CHEMBL1321247 CHEMBL1437753 | C011686 | 34 / 32 / 35 | No. 20 | No. 4 |   | |
| C00025655   | Corytuberine / (+)-Corytuberine | CHEMBL227965 | C013896 | 1 / 0 / 0 | No. 20 | No. 4 |   | |
| C00001928   | Xylopine / (-)-Xylopine | CHEMBL227689 CHEMBL452201 | C062700 | No. 20 | No. 4 |   | ||
| C00025402   | Norargemonine / (-)-Norargemonine / O2-Demetylargemonie / O8-Demethylargemonine | CHEMBL1570385 | 2 / 2 / 0 | No. 37 | No. 4 |   | ||
| C00025397   | Rotundine / (-)-Bisnorargemonine | CHEMBL518908 CHEMBL1494954 | 1 / 0 / 0 | No. 37 | No. 4 |   | ||
| C00025238   | Discretine / (-)-Discretine | CHEMBL513084 | No. 37 | No. 4 |   | |||
| C00025930   | Lindoldhamine / (+)-Lindoldhamine | CHEMBL1375576 | 9 / 8 / 11 | No. 89 | No. 4 |   | ||
| C00027137   | Dehydrocoreximine | No. 155 | No. 4 |   | ||||
| C00001874   | Neprotin / Neprotine / Yatrorizine / Jatrorrhizine | CHEMBL251055 | C055785 | 14 / 27 / 20 | 1 / 0 | No. 155 | No. 4 |   | 
| C00026127   | Dehydrodiscretine / Pseudojatrorrhizine | CHEMBL220527 | No. 155 | No. 4 |   | |||
| C00027159   | Depiline / Palmatine / Berbericinine / O,O-Dimethyldemethyleneberberine | CHEMBL206106 | C005413 | 8 / 13 / 13 | 8 / 0 | No. 155 | No. 4 |   | 
| C00027160   | Phellodendrine | C079418 | No. 234 |   | ||||
| C00034979   | (-)-4'-O-Methylcoclaurine | CHEMBL451723 | No. 253 | No. 4 |   | |||
| C00025652   | d-Coclaurine / Sanjoinine K / (R)-Coclaurine / (+)-Coclaurine / (+)-R-Coclaurine | CHEMBL256448 CHEMBL453291 CHEMBL446211 | 8 / 17 / 10 | No. 253 | No. 4 |   | ||
| C00025619   | (-)-N-Methylcoclaurine / (R)-N-Methylcoclaurine | CHEMBL453292 CHEMBL513109 | No. 253 | No. 4 |   | |||
| C00001885   | Escholin / Escholine / Thalictrin / Thalictrine / Magnoflorine / (+)-Magnoflorine | CHEMBL235428 | C001670 | No. 286 | No. 4 |   | ||
| C00027170   | Xanthoplanine / (+)-Xanthoplanine | CHEMBL1180065 | No. 286 | No. 4 |   | |||
| C00025674   | N-Methylcorydine / (+)-N-Methylcorydine | CHEMBL1617951 | No. 286 | No. 4 |   | |||
| C00027152   | N-Methylphoebine | No. 286 | No. 4 |   | ||||
| C00025654   | Codamine / (+)-Codamine / L-(+)-Codamine / (S)-(+)-Codamine | CHEMBL251624 | No. 345 | No. 4 |   | |||
| C00025666   | (S)-Laudanine / (+)-Laudanidine / L-(+)-Laudanidine | CHEMBL251625 CHEMBL1425007 | 2 / 0 / 0 | No. 345 | No. 4 |   | ||
| C00034987   | (+)-Parvinine | CHEMBL452500 | No. 345 | No. 4 |   | |||
| C00001910   | Reticuline / (+)-Reticuline | CHEMBL235212 CHEMBL401501 CHEMBL464734 | C003298 | 1 / 0 / 0 | No. 345 | No. 4 |   | |
| C00026017   | Protosinomenine / (S)-Protosinomenine | No. 345 | No. 4 |   | ||||
| C00001862   | Glaziovine / L-Glaziovine / N-Methylcrotsparine / L-(-)-N-Methylcrotsparine | CHEMBL1980854 | C007847 | No. 688 |   | |||
| C00025272   | Stepharine / (+)-Stepharine | CHEMBL463957 CHEMBL1975436 | C009320 | No. 688 |   | |||
| C00025934   | Lotusine / (-)-Lotusine / D-(-)-Lotusine | No. 896 |   | |||||
| C00025982   | Oblongine / (+)-Oblongine | CHEMBL457373 | C081049 | No. 896 |   | |||
| C00025347   | Tembetarine / (+)-Tembetarine | C003383 | No. 896 |   | ||||
| C00035166   | Yuzirine | C417577 | No. 1137 |   | ||||
| C00027167   | Thalifoline | CHEMBL1813177 | No. 2199 |   | ||||
| C00027111   | 1,2-Dehydroreticuline | No. 2440 |   | |||||
| C00001879   | Longifolonine | No. 3542 |   | |||||
| C00001815   | Backebergine | No. 4224 |   | |||||
| C00026021   | Pycnarrhine / Dehydrocorypalline | CHEMBL1618006 | No. 4925 |   | ||||
| C00027140   | Dihydrobackebergine / 3,4-Dihydrobackebergine / 3,4-Dihydro-6,7-dimethoxyisoquinoline / 6,7-Dimethoxy-3,4-dihydroisoquinoline | CHEMBL1998359 | No. 4925 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| O75496 | Geminin | Unclassified protein | C00025402 C00025652 C00025666 C00027304 | 0 / 0 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001874 C00025397 C00025652 C00025666 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001874 C00025652 C00025930 C00027304 | 0 / 0 | 
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00001874 C00025652 C00025930 C00027304 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00001874 C00025652 C00025930 C00027304 | 4 / 3 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00001874 C00027159 C00027304 | 11 / 10 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001874 C00027159 C00027304 | 0 / 1 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00027159 C00027304 | 0 / 1 | 
| P04062 | Glucosylceramidase | Enzyme | C00001874 C00025652 | 6 / 4 | 
| P14618 | Pyruvate kinase PKM | Enzyme | C00025652 C00025930 | 0 / 0 | 
| O00255 | Menin | Unclassified protein | C00025930 C00027304 | 2 / 5 | 
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00001874 C00027304 | 1 / 1 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00025930 C00027304 | 0 / 0 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00001874 C00027304 | 0 / 0 | 
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00001874 C00027304 | 1 / 0 | 
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00025930 C00027304 | 0 / 0 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00027159 C00027304 | 1 / 1 | 
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00027159 C00027304 | 0 / 0 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00001874 C00027304 | 0 / 0 | 
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00027159 C00027304 | 0 / 0 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00025930 C00027304 | 1 / 2 | 
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00027159 C00027304 | 1 / 0 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00027304 | 1 / 1 | 
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00025652 | 7 / 3 | 
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00027304 | 0 / 0 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00025402 | 2 / 0 | 
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00027159 | 0 / 0 | 
| P36544 | Neuronal acetylcholine receptor subunit alpha-7 | CHRN alpha | C00027304 | 0 / 0 | 
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00027304 | 0 / 0 | 
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00027304 | 3 / 3 | 
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00027304 | 2 / 2 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00027304 | 0 / 0 | 
| P28223 | 5-hydroxytryptamine receptor 2A | Serotonin receptor | C00025269 | 0 / 0 | 
| P35372 | Mu-type opioid receptor | Opioid receptor | C00001910 | 0 / 0 | 
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00027304 | 0 / 0 | 
| Q14761 | Protein tyrosine phosphatase receptor type C-associated protein | Enzyme | C00001807 | 0 / 0 | 
| P43681 | Neuronal acetylcholine receptor subunit alpha-4 | CHRN alpha | C00027304 | 1 / 1 | 
| P17787 | Neuronal acetylcholine receptor subunit beta-2 | CHRN beta | C00027304 | 1 / 1 | 
| P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00025655 | 0 / 0 | 
| P08908 | 5-hydroxytryptamine receptor 1A | Serotonin receptor | C00025675 | 1 / 0 | 
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00027304 | 0 / 0 | 
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00027304 | 0 / 0 | 
| P06746 | DNA polymerase beta | Enzyme | C00001874 | 0 / 0 | 
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00025930 | 1 / 1 | 
| Q99700 | Ataxin-2 | Unclassified protein | C00027304 | 1 / 1 | 
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00027304 | 0 / 1 | 
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00027304 | 1 / 4 | 
| Q16637 | Survival motor neuron protein | Unclassified protein | C00001874 | 4 / 1 | 
| P43351 | DNA repair protein RAD52 homolog | Unclassified protein | C00001874 | 0 / 0 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 332 | BIRC5, API4, EPR-1 | baculoviral IAP repeat containing 5 | C00001874
                          C00027159 | 
| 6352 | CCL5, D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228, eoCP | chemokine (C-C motif) ligand 5 | C00027159 | 
| 6348 | CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 | chemokine (C-C motif) ligand 3 | C00027159 | 
| 6351 | CCL4, ACT2, AT744.1, G-26, HC21, LAG-1, LAG1, MIP-1-beta, MIP1B, MIP1B1, SCYA2, SCYA4 | chemokine (C-C motif) ligand 4 | C00027159 | 
| 6347 | CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF | chemokine (C-C motif) ligand 2 | C00027159 | 
| 3570 | IL6R, CD126, IL-6R-1, IL-6RA, IL6Q, IL6RA, IL6RQ, gp80 | interleukin 6 receptor | C00027159 | 
| 3576 | IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 | interleukin 8 | C00027159 | 
| 7422 | VEGFA, MVCD1, VEGF, VPF | vascular endothelial growth factor A | C00027159 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency | Q99714 | 
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah | P63092 | 
| #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 | P84022 | 
| #119900 | Digital clubbing, isolated congenital | P15428 | 
| #609535 | Drug metabolism, poor, cyp2c19-related | P33261 | 
| #608902 | Drug metabolism, poor, cyp2d6-related | P10635 | 
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 | P02545 | 
| #600513 | Epilepsy, nocturnal frontal lobe, 1; enfl1 | P43681 | 
| #605375 | Epilepsy, nocturnal frontal lobe, 3; enfl3 | P17787 | 
| #600274 | Frontotemporal dementia; ftd | P10636 | 
| #608013 | Gaucher disease, perinatal lethal | P04062 | 
| #230800 | Gaucher disease, type i | P04062 | 
| #230900 | Gaucher disease, type ii | P04062 | 
| #231000 | Gaucher disease, type iii | P04062 | 
| #231005 | Gaucher disease, type iiic | P04062 | 
| #232300 | Glycogen storage disease ii | P10253 | 
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | Q03164 | 
| #610140 | Heart-hand syndrome, slovenian type | P02545 | 
| #176670 | Hutchinson-gilford progeria syndrome; hgps | P02545 | 
| #145000 | Hyperparathyroidism 1; hrpt1 | O00255 | 
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 | P15428 | 
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 | P02545 | 
| #613795 | Loeys-dietz syndrome, type 3; lds3 | P84022 | 
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada | P02545 | 
| #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 | 
| #613205 | Muscular dystrophy, congenital, lmna-related | P02545 | 
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b | P02545 | 
| #160900 | Myotonic dystrophy 1; dm1 | Q9NR56 | 
| #166350 | Osseous heteroplasia, progressive; poh | P63092 | 
| #168600 | Parkinson disease, late-onset; pd | P04062 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #614674 | Periodic fever, menstrual cycle-dependent | P08908 | 
| #172700 | Pick disease of brain | P10636 | 
| #102200 | Pituitary adenoma, growth hormone-secreting | P63092 | 
| #601399 | Platelet disorder, familial, with associated myeloid malignancy | Q01196 | 
| #103580 | Pseudohypoparathyroidism, type ia; php1a | P63092 | 
| #603233 | Pseudohypoparathyroidism, type ib; php1b | P63092 | 
| #612462 | Pseudohypoparathyroidism, type ic; php1c | P63092 | 
| #275210 | Restrictive dermopathy, lethal | P02545 | 
| #253300 | Spinal muscular atrophy, type i; sma1 | Q16637 | 
| #253550 | Spinal muscular atrophy, type ii; sma2 | Q16637 | 
| #253400 | Spinal muscular atrophy, type iii; sma3 | Q16637 | 
| #271150 | Spinal muscular atrophy, type iv; sma4 | Q16637 | 
| #183090 | Spinocerebellar ataxia 2; sca2 | Q99700 | 
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 | Q9NUW8 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #278750 | Xeroderma pigmentosum, variant type; xpv | Q9Y253 | 
| 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) | 
| 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) | 
| H00066 | Lewy body dementia (LBD) | P04062
                            (related) | 
| H00126 | Gaucher disease | P04062
                            (related) | 
| H00426 | Defects in the degradation of ganglioside | P04062
                            (related) | 
| H00810 | Progressive myoclonic epilepsy (PME) | P04062
                            (related) | 
| H00036 | Osteosarcoma | P08684
                            (marker) | 
| H00069 | Glycogen storage diseases (GSD) | P10253
                            (related) | 
| H00058 | Amyotrophic lateral sclerosis (ALS) | P10636
                            (related) | 
| H00077 | Progressive supranuclear palsy (PSP) | P10636
                            (related) | 
| H00078 | Frontotemporal lobar degeneration (FTLD) | P10636
                            (related) | 
| H01205 | Coumarin resistance | P11712
                            (related) | 
| H00457 | Primary hypertrophic osteoarthropathy (PHO) | P15428
                            (related) | 
| H01246 | Isolated congenital nail clubbing (ICNC) | P15428
                            (related) | 
| H00807 | Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) | P17787
                            (related) P43681 (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) | Q01196
                            (related) Q01196 (marker) Q03164 (related) Q03164 (marker) | 
| H00003 | Acute myeloid leukemia (AML) | Q01196
                            (related) Q01196 (marker) Q13951 (marker) | 
| H00004 | Chronic myeloid leukemia (CML) | Q01196
                            (related) | 
| H00978 | Thrombocytopenia (THC) | Q01196
                            (related) | 
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) | Q03164
                            (related) | 
| H00455 | Spinal muscular atrophy (SMA) | Q16637
                            (related) | 
| H00063 | Spinocerebellar ataxia (SCA) | Q99700
                            (related) Q9NUW8 (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) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |