Species

KNApSAcK Entry

Organism name Annona reticulata
Genus Annona
Family Annonaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Annona reticulata
Linked NCBI taxonomy ID 301862
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

Natural Activity

List (13)

Species Activity
Annona reticulata L. Anthelmintic
Annona reticulata L. Anticancer
Annona reticulata L. Antiinflammatory
Annona reticulata L. Antineoplastic
Annona reticulata L. Antitumor
Annona reticulata L. Astringent
Annona reticulata L. Cytotoxic
Annona reticulata L. Insecticide
Annona reticulata L. Pediculicide
Annona reticulata L. Poison
Annona reticulata L. Purgative
Annona reticulata L. Tonic
Annona reticulata L. Vermifuge

Metabolite list (25)

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
C00001302 External link 512 Bullatacinone
CHEMBL28898
CHEMBL349802
CHEMBL448053
CHEMBL500765
CHEMBL1967501
CHEMBL1981927
C061021
No. 6 No. 70
C00001323 External link 512 Squamocin
CHEMBL41177
CHEMBL502366
CHEMBL453405
CHEMBL452936
C059660
No. 6 No. 70
C00049020 External link 512 trans-Murisolinone
No. 6 No. 70
C00049019 External link 512 trans-Isomurisolenin
No. 6 No. 70
C00048967 External link 512 cis-Murisolinone
No. 6 No. 70
C00048966 External link 512 cis-Isomurisolenin
No. 6 No. 70
C00048965 External link 512 cis-Bullatacinone
CHEMBL28898
CHEMBL349802
CHEMBL448053
CHEMBL500765
CHEMBL1967501
CHEMBL1981927
No. 6 No. 70
C00048955 External link 512 Annoreticuin-9-one
CHEMBL447923
CHEMBL505178
CHEMBL503350
CHEMBL449247
No. 6 No. 70
C00044198 External link 512 Isoannoreticuin
CHEMBL451459
No. 6 No. 70
C00044048 External link 512 10-Hydroxy-asimicin
/ (+)-10-Hydroxy-asimicin
CHEMBL443639
CHEMBL509800
CHEMBL447889
CHEMBL443955
CHEMBL2007510
No. 6 No. 70
C00038662 External link 512 Bullatacin
/ (+)-Bullatacin
CHEMBL13710
CHEMBL61332
CHEMBL68179
CHEMBL142918
CHEMBL453675
CHEMBL503360
CHEMBL453496
CHEMBL454744
CHEMBL501110
CHEMBL451402
CHEMBL506914
CHEMBL446085
CHEMBL509939
CHEMBL508255
CHEMBL499188
CHEMBL1996175
CHEMBL1999460
CHEMBL2007355
No. 6 No. 70
C00027153 External link 512 Norcorydine
/ (+)-Norcorydine
CHEMBL494053
No. 20 No. 4
C00001861 External link 512 Glaucine
/ S-(+)-Glaucine
/ O,O-Dimethylisoboldine
CHEMBL36536
CHEMBL228082
14 / 8 / 6 No. 20 No. 4
C00025827 External link 512 Corydine
/ Glaucentrin
/ (+)-Corydine
/ Glaucentrine
CHEMBL489524
CHEMBL2002847
C067341
1 / 0 / 0 No. 20 No. 4
C00001928 External link 512 Xylopine
/ (-)-Xylopine
CHEMBL227689
CHEMBL452201
C062700
No. 20 No. 4
C00025231 External link 512 Asimilobine
/ (-)-Asimilobine
CHEMBL389271
CHEMBL469423
C054614
1 / 1 / 0 No. 20 No. 4
C00001807 External link 512 Anonaine
/ (-)-Anonaine
/ (R)-Annonaine
CHEMBL401798
C098138
1 / 0 / 0 No. 20 No. 4
C00025319 External link 512 Oxoxylopin
/ Oxoxylopine
/ Lanuginosine
CHEMBL389400
1 / 4 / 2 No. 74
C00025995 External link 512 Oxonantenine
CHEMBL1270949
No. 74
C00001878 External link 512 Liriodenine
/ Oxoushinsunine
/ Spermatheridine
CHEMBL37736
C026980
5 / 3 / 1 No. 74
C00001910 External link 512 Reticuline
/ (+)-Reticuline
CHEMBL235212
CHEMBL401501
CHEMBL464734
C003298
1 / 0 / 0 No. 345 No. 4
C00044145 External link 512 Dieporeticanin 1
No. 421
C00044146 External link 512 Dieporeticanin 2
No. 421
C00044147 External link 512 Dieporeticenin
No. 421
C00044294 External link 512 Reticulatamone
No. 3105

Human Protein / Gene in interactions

22 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q14761 Protein tyrosine phosphatase receptor type C-associated protein Enzyme C00001807 C00001861 C00001878 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001861 0 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00025827 0 / 0
P30926 Neuronal acetylcholine receptor subunit beta-4 CHRN beta C00001878 0 / 0
P32297 Neuronal acetylcholine receptor subunit alpha-3 CHRN alpha C00001878 1 / 0
P17787 Neuronal acetylcholine receptor subunit beta-2 CHRN beta C00001878 1 / 1
P43681 Neuronal acetylcholine receptor subunit alpha-4 CHRN alpha C00001878 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001861 1 / 0
Q9BQF6 Sentrin-specific protease 7 Enzyme C00001861 0 / 0
Q9GZR1 Sentrin-specific protease 6 Enzyme C00001861 0 / 0
Q96LD8 Sentrin-specific protease 8 Enzyme C00001861 0 / 0
P42574 Caspase-3 C14 C00001861 0 / 0
O75496 Geminin Unclassified protein C00001861 0 / 0
P00734 Prothrombin S1A C00025319 4 / 2
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001861 3 / 3
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001861 0 / 0
P22303 Acetylcholinesterase Hydrolase C00025231 1 / 0
P35372 Mu-type opioid receptor Opioid receptor C00001910 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001861 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001861 4 / 3
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001861 0 / 0
P43351 DNA repair protein RAD52 homolog Unclassified protein C00001861 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (16)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#600513 Epilepsy, nocturnal frontal lobe, 1; enfl1 P43681
#605375 Epilepsy, nocturnal frontal lobe, 3; enfl3 P17787
#600274 Frontotemporal dementia; ftd P10636
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#612052 Smoking as a quantitative trait locus 3; sqtl3 P32297
#601367 Stroke, ischemic P00734
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#112100 Yt blood group antigen P22303

KEGG DISEASE (9)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00807 Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) P17787 (related)
P43681 (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)