Species

KNApSAcK Entry

Organism name Annona cherimola
Genus Annona
Family Annonaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Annona cherimola
Linked NCBI taxonomy ID 49314
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 cherimola Mill. Antiprotozoal
Annona cherimola Mill. Antiseptic
Annona cherimola Mill. Cathartic
Annona cherimola Mill. Cytotoxic
Annona cherimola Mill. Emetic
Annona cherimola Mill. Filaricide
Annona cherimola Mill. Insecticide
Annona cherimola Mill. Parasiticide
Annona cherimola Mill. Pediculicide
Annona cherimola Mill. Piscicide
Annona cherimola Mill. Poison
Annona cherimola Mill. Stomachic
Annona cherimola Mill. Uterocontractant

Metabolite list (45)

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
C00001323 External link 512 Squamocin
CHEMBL41177
CHEMBL502366
CHEMBL453405
CHEMBL452936
C059660
No. 6 No. 70
C00038511 External link 512 Aromin A
/ (+)-Aromin A
No. 6 No. 70
C00001872 External link 512 Isocorydine
/ (+)-Isocorydine
/ L-(+)-Isocorydine
/ (S)-(+)-Isocorydine
CHEMBL489525
CHEMBL1376826
14 / 7 / 10 No. 20 No. 4
C00001806 External link 512 Anolobine
/ (-)-Anolobine
CHEMBL257746
No. 20 No. 4
C00027281 External link 512 Anonaine
CHEMBL401798
C098138
1 / 0 / 0 No. 20 No. 4
C00025991 External link 512 O-Nornuciferine
/ (-)-Nornuciferine
/ (-)-N-Methylasimilobine
CHEMBL2316499
No. 20 No. 4
C00001928 External link 512 Xylopine
/ (-)-Xylopine
CHEMBL227689
CHEMBL452201
C062700
No. 20 No. 4
C00025675 External link 512 Lauroscholtzine
/ 2-O-Methylboldine
/ N-Methyllaurotetanine
/ (+)-N-Methyllaurotetanine
CHEMBL464099
1 / 1 / 0 No. 20 No. 4
C00025231 External link 512 Asimilobine
/ (-)-Asimilobine
CHEMBL389271
CHEMBL469423
C054614
1 / 1 / 0 No. 20 No. 4
C00027409 External link 512 Laurotetanin
/ Laurotetanine
/ (+)-Laurotetanine
CHEMBL464098
C008256
No. 20 No. 4
C00027438 External link 512 Sanjoinine Ib
/ Norisocorydine
CHEMBL465212
No. 20 No. 4
C00025241 External link 512 Kikemanin
/ Kikemanine
/ Corydalmine
/ Schefferine
/ (-)-Kikemanine
/ (-)-Corydalmine
CHEMBL448891
CHEMBL1209608
CHEMBL2334894
C058198
5 / 3 / 0 No. 37 No. 4
C00002631 External link 512 (+)-Lirioresinol B
/ (+)-Syringaresinol
CHEMBL361362
CHEMBL402653
C042192
1 / 0 / 0 No. 38 No. 21
C00027457 External link 512 Oxoglaucine
/ O-Methylatheroline
CHEMBL470881
C111587
25 / 27 / 24 No. 74
C00025319 External link 512 Oxoxylopin
/ Oxoxylopine
/ Lanuginosine
CHEMBL389400
1 / 4 / 2 No. 74
C00025935 External link 512 Lysicamine
/ Oxonuciferine
CHEMBL510090
C069090
No. 74
C00027456 External link 512 Oxoanolobine
No. 74
C00001878 External link 512 Liriodenine
/ Oxoushinsunine
/ Spermatheridine
CHEMBL37736
C026980
5 / 3 / 1 No. 74
C00025995 External link 512 Oxonantenine
CHEMBL1270949
No. 74
C00027870 External link 512 Anomoline
No. 253 No. 4
C00029944 External link 512 Cherimolacyclopeptide G
No. 290
C00029941 External link 512 Cherimolacyclopeptide C
/ Cyclo(L-alanyl-L-alanyl-L-tryptophyl-L-isoleucyl-L-prolyl-L-prolylglycyl)
CHEMBL510705
No. 290
C00001910 External link 512 Reticuline
/ (+)-Reticuline
CHEMBL235212
CHEMBL401501
CHEMBL464734
C003298
1 / 0 / 0 No. 345 No. 4
C00026908 External link 512 Cheritamine
No. 442
C00025324 External link 512 N-cis-Feruloyltyramine
/ cis-N-Feruloyltyramine
CHEMBL206555
CHEMBL451720
1 / 4 / 2 No. 499
C00034085 External link 512 N-p-Coumaroyltyramine
CHEMBL64286
No. 499
C00027423 External link 512 N-Formylanonaine
/ (-)-N-Formylanonaine
CHEMBL1170090
1 / 4 / 2 No. 553
C00027444 External link 512 Michelalbine
/ Norushinsunine
CHEMBL464657
CHEMBL1618042
No. 553
C00025258 External link 512 Micheline A
/ (-)-Ushinsunine
CHEMBL221034
CHEMBL1617041
CHEMBL2009013
1 / 0 / 0 No. 553
C00001905 External link 512 Milthanthine
/ Pronuciferine
/ (+)-Pronuciferine
/ N-Methylstepharine
/ N,O-Dimethylcrotonosine
CHEMBL237766
No. 688
C00025272 External link 512 Stepharine
/ (+)-Stepharine
CHEMBL463957
CHEMBL1975436
C009320
No. 688
C00027480 External link 512 Romucosine H
No. 889
C00027477 External link 512 Romucosine
/ (-)-Romucosine
No. 889
C00036730 External link 512 Annocherine B
/ (+)-Annocherine B
No. 1137
C00036729 External link 512 Annocherine A
/ (+)-Annocherine A
No. 1137
C00029939 External link 512 Cherimolacyclopeptide A
No. 1183
C00029940 External link 512 Cherimolacyclopeptide B
No. 1183
C00029943 External link 512 Cherimolacyclopeptide F
No. 1183
C00027167 External link 512 Thalifoline
CHEMBL1813177
No. 2199
C00027321 External link 512 Cherianoine
No. 3076 No. 7
C00036764 External link 512 Artabonatine B
/ (-)-Artabonatine B
CHEMBL458523
1 / 4 / 2 No. 3212
C00027346 External link 512 Doryphornine
No. 3424
C00026406 External link 512 Cherimoline
No. 5258
C00029942 External link 512 Cherimolacyclopeptide D
No. 5577
C00027322 External link 512 Cherinonaine
No. 5792

Human Protein / Gene in interactions

49 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001872 C00027457 1 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001872 C00027457 0 / 0
P08908 5-hydroxytryptamine receptor 1A Serotonin receptor C00025241 C00025675 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001872 C00027457 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001872 C00027457 1 / 1
P14679 Tyrosinase Oxidoreductase C00025324 C00027423 4 / 2
P00734 Prothrombin S1A C00025319 C00036764 4 / 2
O75496 Geminin Unclassified protein C00001872 C00027457 0 / 0
Q14761 Protein tyrosine phosphatase receptor type C-associated protein Enzyme C00001878 C00027281 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001872 C00027457 0 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00027457 1 / 2
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 C00027457 1 / 0
P11387 DNA topoisomerase 1 Isomerase C00002631 0 / 0
P14416 D(2) dopamine receptor Dopamine receptor C00025241 2 / 0
P24941 Cyclin-dependent kinase 2 Cdc2 C00001872 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001872 0 / 0
P39748 Flap endonuclease 1 Enzyme C00027457 0 / 0
P42858 Huntingtin Unclassified protein C00027457 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00027457 2 / 0
P02545 Prelamin-A/C Unclassified protein C00027457 11 / 10
Q9Y253 DNA polymerase eta Enzyme C00027457 1 / 1
P30926 Neuronal acetylcholine receptor subunit beta-4 CHRN beta C00001878 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00027457 0 / 0
Q92793 CREB-binding protein Enzyme C00027457 1 / 1
O14757 Serine/threonine-protein kinase Chk1 Chk1 C00025258 0 / 0
P13726 Tissue factor Membrane receptor C00025241 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00027457 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001872 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001872 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00027457 2 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00027457 0 / 0
P22303 Acetylcholinesterase Hydrolase C00025231 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00025241 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00001910 0 / 0
P29466 Caspase-1 C14 C00027457 0 / 0
P06746 DNA polymerase beta Enzyme C00027457 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00027457 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00027457 4 / 3
P21728 D(1A) dopamine receptor Dopamine receptor C00025241 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00027457 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00027457 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00027457 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00001872 1 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00001872 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001872 1 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001872 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (47)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#103780 Alcohol dependence P14416
#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
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#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
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#159900 Myoclonic dystonia P14416
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260540 Parkinson-dementia syndrome P10636
#614674 Periodic fever, menstrual cycle-dependent P08908
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#275210 Restrictive dermopathy, lethal P02545
#180849 Rubinstein-taybi syndrome 1; rsts1 Q92793
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#612052 Smoking as a quantitative trait locus 3; sqtl3 P32297
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (35)

KEGG name UniProt
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)
H00036 Osteosarcoma P08684 (marker)
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)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
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)
H00059 Huntington's disease (HD) P42858 (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)
H00504 Rubinstein-Taybi syndrome Q92793 (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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)