Species

KNApSAcK Entry

Organism name Xylopia parviflora
Genus Xylopia
Family Annonaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Xylopia parviflora
Linked NCBI taxonomy ID 992813
Linked level species

Family

Family in NCBI taxonomy Annonaceae
ID 22140

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

Metabolite list (47)

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 External link 512 Anolobine
/ (-)-Anolobine
CHEMBL257746
No. 20 No. 4
C00001807 External link 512 Anonaine
/ (-)-Anonaine
/ (R)-Annonaine
CHEMBL401798
C098138
1 / 0 / 0 No. 20 No. 4
C00034986 External link 512 (+)-Noroconovine
No. 20 No. 4
C00034984 External link 512 (+)-10,11-Dihydroxy-1,2-dimethoxynoraporphine
No. 20 No. 4
C00034982 External link 512 (+)-1,2-Dimethoxy-3-hydroxy-9,10-methylenedioxynoraporphine
CHEMBL1618043
No. 20 No. 4
C00027433 External link 512 Laurolitsine
/ (+)-Norboldine
/ (+)-Laurolitsine
CHEMBL487388
C109133
No. 20 No. 4
C00027409 External link 512 Laurotetanin
/ Laurotetanine
/ (+)-Laurotetanine
CHEMBL464098
C008256
No. 20 No. 4
C00027307 External link 512 Calycinine
/ (-)-Calycinine
CHEMBL226824
No. 20 No. 4
C00025676 External link 512 Norglaucin
/ Norglaucine
/ (+)-Norglaucine
/ O,O-Dimethyllaurelliptine
No. 20 No. 4
C00025675 External link 512 Lauroscholtzine
/ 2-O-Methylboldine
/ N-Methyllaurotetanine
/ (+)-N-Methyllaurotetanine
CHEMBL464099
1 / 1 / 0 No. 20 No. 4
C00025269 External link 512 Nornantenine
/ N-Nornantenine
/ (+)-Nornantenine
CHEMBL1254951
1 / 0 / 0 No. 20 No. 4
C00027304 External link 512 Boldine
/ d-Boldine
/ (+)-Boldine
CHEMBL388342
CHEMBL1321247
CHEMBL1437753
C011686
34 / 32 / 35 No. 20 No. 4
C00025655 External link 512 Corytuberine
/ (+)-Corytuberine
CHEMBL227965
C013896
1 / 0 / 0 No. 20 No. 4
C00001928 External link 512 Xylopine
/ (-)-Xylopine
CHEMBL227689
CHEMBL452201
C062700
No. 20 No. 4
C00025402 External link 512 Norargemonine
/ (-)-Norargemonine
/ O2-Demetylargemonie
/ O8-Demethylargemonine
CHEMBL1570385
2 / 2 / 0 No. 37 No. 4
C00025397 External link 512 Rotundine
/ (-)-Bisnorargemonine
CHEMBL518908
CHEMBL1494954
1 / 0 / 0 No. 37 No. 4
C00025238 External link 512 Discretine
/ (-)-Discretine
CHEMBL513084
No. 37 No. 4
C00025930 External link 512 Lindoldhamine
/ (+)-Lindoldhamine
CHEMBL1375576
9 / 8 / 11 No. 89 No. 4
C00027137 External link 512 Dehydrocoreximine
No. 155 No. 4
C00001874 External link 512 Neprotin
/ Neprotine
/ Yatrorizine
/ Jatrorrhizine
CHEMBL251055
C055785
14 / 27 / 20 1 / 0 No. 155 No. 4
C00026127 External link 512 Dehydrodiscretine
/ Pseudojatrorrhizine
CHEMBL220527
No. 155 No. 4
C00027159 External link 512 Depiline
/ Palmatine
/ Berbericinine
/ O,O-Dimethyldemethyleneberberine
CHEMBL206106
C005413
8 / 13 / 13 8 / 0 No. 155 No. 4
C00027160 External link 512 Phellodendrine
C079418
No. 234
C00034979 External link 512 (-)-4'-O-Methylcoclaurine
CHEMBL451723
No. 253 No. 4
C00025652 External link 512 d-Coclaurine
/ Sanjoinine K
/ (R)-Coclaurine
/ (+)-Coclaurine
/ (+)-R-Coclaurine
CHEMBL256448
CHEMBL453291
CHEMBL446211
8 / 17 / 10 No. 253 No. 4
C00025619 External link 512 (-)-N-Methylcoclaurine
/ (R)-N-Methylcoclaurine
CHEMBL453292
CHEMBL513109
No. 253 No. 4
C00001885 External link 512 Escholin
/ Escholine
/ Thalictrin
/ Thalictrine
/ Magnoflorine
/ (+)-Magnoflorine
CHEMBL235428
C001670
No. 286 No. 4
C00027170 External link 512 Xanthoplanine
/ (+)-Xanthoplanine
CHEMBL1180065
No. 286 No. 4
C00025674 External link 512 N-Methylcorydine
/ (+)-N-Methylcorydine
CHEMBL1617951
No. 286 No. 4
C00027152 External link 512 N-Methylphoebine
No. 286 No. 4
C00025654 External link 512 Codamine
/ (+)-Codamine
/ L-(+)-Codamine
/ (S)-(+)-Codamine
CHEMBL251624
No. 345 No. 4
C00025666 External link 512 (S)-Laudanine
/ (+)-Laudanidine
/ L-(+)-Laudanidine
CHEMBL251625
CHEMBL1425007
2 / 0 / 0 No. 345 No. 4
C00034987 External link 512 (+)-Parvinine
CHEMBL452500
No. 345 No. 4
C00001910 External link 512 Reticuline
/ (+)-Reticuline
CHEMBL235212
CHEMBL401501
CHEMBL464734
C003298
1 / 0 / 0 No. 345 No. 4
C00026017 External link 512 Protosinomenine
/ (S)-Protosinomenine
No. 345 No. 4
C00001862 External link 512 Glaziovine
/ L-Glaziovine
/ N-Methylcrotsparine
/ L-(-)-N-Methylcrotsparine
CHEMBL1980854
C007847
No. 688
C00025272 External link 512 Stepharine
/ (+)-Stepharine
CHEMBL463957
CHEMBL1975436
C009320
No. 688
C00025934 External link 512 Lotusine
/ (-)-Lotusine
/ D-(-)-Lotusine
No. 896
C00025982 External link 512 Oblongine
/ (+)-Oblongine
CHEMBL457373
C081049
No. 896
C00025347 External link 512 Tembetarine
/ (+)-Tembetarine
C003383
No. 896
C00035166 External link 512 Yuzirine
C417577
No. 1137
C00027167 External link 512 Thalifoline
CHEMBL1813177
No. 2199
C00027111 External link 512 1,2-Dehydroreticuline
No. 2440
C00001879 External link 512 Longifolonine
No. 3542
C00001815 External link 512 Backebergine
No. 4224
C00026021 External link 512 Pycnarrhine
/ Dehydrocorypalline
CHEMBL1618006
No. 4925
C00027140 External link 512 Dihydrobackebergine
/ 3,4-Dihydrobackebergine
/ 3,4-Dihydro-6,7-dimethoxyisoquinoline
/ 6,7-Dimethoxy-3,4-dihydroisoquinoline
CHEMBL1998359
No. 4925

Human Protein / Gene in interactions

49 ChEMBL Protein in interactions

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

8 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (53)

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 DISEASE (43)

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)