Species

KNApSAcK Entry

Organism name Liriodendron tulipifera
Genus Liriodendron
Family Magnoliaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Liriodendron tulipifera
Linked NCBI taxonomy ID 3415
Linked level species

Family

Family in NCBI taxonomy Magnoliaceae
ID 3401

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

Natural Activity

List (18)

Species Activity
Liriodendron tulipifera L. Analgesic
Liriodendron tulipifera L. Antibacterial
Liriodendron tulipifera L. Antiinflammatory
Liriodendron tulipifera L. Antipyretic
Liriodendron tulipifera L. Antiseptic
Liriodendron tulipifera L. Aphrodisiac
Liriodendron tulipifera L. Bitter
Liriodendron tulipifera L. Candidicide
Liriodendron tulipifera L. Cardiotonic
Liriodendron tulipifera L. Depurative
Liriodendron tulipifera L. Diaphoretic
Liriodendron tulipifera L. Digitalic
Liriodendron tulipifera L. Diuretic
Liriodendron tulipifera L. Fungicide
Liriodendron tulipifera L. Positive Inotropic
Liriodendron tulipifera L. Stimulant
Liriodendron tulipifera L. Tonic
Liriodendron tulipifera L. Vermifuge

Metabolite list (24)

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
C00028475 External link 512 Lirioferine
No. 20 No. 4
C00025675 External link 512 Lauroscholtzine
/ 2-O-Methylboldine
/ N-Methyllaurotetanine
/ (+)-N-Methyllaurotetanine
CHEMBL464099
1 / 1 / 0 No. 20 No. 4
C00001861 External link 512 Glaucine
/ S-(+)-Glaucine
/ O,O-Dimethylisoboldine
CHEMBL36536
CHEMBL228082
14 / 8 / 6 No. 20 No. 4
C00025931 External link 512 Liriotulipiferine
CHEMBL1996399
No. 20 No. 4
C00001825 External link 512 Caaverine
/ (-)-Caaverine
No. 20 No. 4
C00000659 External link 512 Medioresinol
/ (+)-Medioresinol
CHEMBL376507
CHEMBL513023
2 / 1 / 1 No. 38 No. 21
C00000642 External link 512 (+)-Yangambin
CHEMBL510536
CHEMBL454592
CHEMBL1412125
4 / 2 / 0 No. 38 No. 21
C00007190 External link 512 (+)-Pinoresinol
CHEMBL267963
CHEMBL487611
CHEMBL460862
C103298
7 / 5 / 6 No. 38 No. 21
C00002631 External link 512 (+)-Lirioresinol B
/ (+)-Syringaresinol
CHEMBL361362
CHEMBL402653
C042192
1 / 0 / 0 No. 38 No. 21
C00000640 External link 512 (+)-Eudesmin
CHEMBL519099
CHEMBL512865
CHEMBL523743
CHEMBL464352
CHEMBL1726879
C105875
2 / 0 / 0 No. 38 No. 21
C00001878 External link 512 Liriodenine
/ Oxoushinsunine
/ Spermatheridine
CHEMBL37736
C026980
5 / 3 / 1 No. 74
C00012975 External link 512 alpha-Liriodenolide
/ [3aR-(3aalpha,4beta,5abeta,6beta,9aalpha,9bbeta)]-4-(acetyloxy)-3a,4,5,5a,6,7,9a,9b-octahydro-6-hydroxy-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2(3H)-one
No. 157 No. 38
C00012978 External link 512 gamma-Liriodenolide
/ [3aR-(3aalpha,4beta,5abeta,6beta,9bbeta)]-4-(acetyloxy)-3a,4,5,5a,6,7,8,9b-Octahydro-6-hydroxy-5a,9-dimethyl-3-methylenenaphtho[1,2-b]furan-2(3H)-one
No. 157 No. 38
C00012982 External link 512 beta-Liriodenolide
/ [3aR-(3aalpha,4beta,5abeta,6beta,9aalpha,9bbeta)]-4-(Acetyloxy)decahydro-6-hydroxy-5a-methyl-3,9-bis(methylene)-naphtho[1,2-b]furan-2(3H)-one
No. 157 No. 38
C00020472 External link 512 Michefuscalide
/ beta-Cyclolipiferolide
C059287
No. 157 No. 38
C00003378 External link 512 Tulipinolide
CHEMBL520114
No. 249 No. 38
C00012329 External link 512 Tulirinol
No. 249 No. 38
C00003379 External link 512 epi-Tulipinolide
CHEMBL520114
No. 249 No. 38
C00001164 External link 512 Myoinositol
/ myo-Inositol
CHEMBL278373
CHEMBL468154
CHEMBL1222251
CHEMBL1231671
CHEMBL1950780
8 / 17 / 18 No. 795
C00003347 External link 512 1-Peroxyferolide
CHEMBL518136
No. 843 No. 38
C00003319 External link 512 Lipiferolide
No. 843 No. 38
C00002498 External link 512 Scoparone
/ 6,7-Dimethoxycoumarin
/ Aesculetin dimethyl ether
CHEMBL325864
C018145
4 / 2 / 2 6 / 0 No. 864 No. 25
C00003380 External link 512 epi-Tulipinolide diepoxide
No. 1056 No. 38
C00012037 External link 512 Elemanolide
/ Epitulipdienolide
No. 1132

Human Protein / Gene in interactions

41 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00000642 C00001164 C00001861 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000642 C00001861 C00007190 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001164 C00001861 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00000640 C00000642 0 / 0
Q14761 Protein tyrosine phosphatase receptor type C-associated protein Enzyme C00001861 C00001878 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00000640 0 / 0
Q96LD8 Sentrin-specific protease 8 Enzyme C00001861 0 / 0
P42574 Caspase-3 C14 C00001861 0 / 0
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00002498 1 / 1
P16278 Beta-galactosidase Enzyme C00001164 4 / 6
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
P11387 DNA topoisomerase 1 Isomerase C00002631 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000659 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001861 0 / 0
P02545 Prelamin-A/C Unclassified protein C00001164 11 / 10
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000642 2 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00007190 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00007190 5 / 3
P06280 Alpha-galactosidase A Enzyme C00001164 1 / 1
P56817 Beta-secretase 1 A1A C00002498 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001861 3 / 3
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00007190 0 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000659 0 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00007190 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001861 4 / 3
O43451 Maltase-glucoamylase, intestinal Hydrolase C00001164 0 / 0
P08908 5-hydroxytryptamine receptor 1A Serotonin receptor C00025675 1 / 0
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00007190 0 / 0
P10323 Acrosin S1A C00001164 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001861 0 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00002498 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002498 1 / 1
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00007190 0 / 0
P43351 DNA repair protein RAD52 homolog Unclassified protein C00001861 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00001164 1 / 1

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00002498
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00002498
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00002498
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002498
5966 REL, C-Rel v-rel avian reticuloendotheliosis viral oncogene homolog C00002498
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002498

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (39)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#610251 Alcohol sensitivity, acute P05091
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
%606641 Body mass index; bmi P37231
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#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
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#230500 Gm1-gangliosidosis, type i P16278
#230600 Gm1-gangliosidosis, type ii P16278
#230650 Gm1-gangliosidosis, type iii P16278
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#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
#253010 Mucopolysaccharidosis type ivb P16278
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#601665 Obesity P37231
#260540 Parkinson-dementia syndrome P10636
#614674 Periodic fever, menstrual cycle-dependent P08908
#172700 Pick disease of brain P10636
#275210 Restrictive dermopathy, lethal P02545
#612052 Smoking as a quantitative trait locus 3; sqtl3 P32297
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (32)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (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)
H01071 Acute alcohol sensitivity P05091 (related)
H00125 Fabry disease P06280 (related)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00123 Mucopolysaccharidosis type IV (MPS4) P16278 (related)
H00276 Galactosialidosis P16278 (related)
H00281 GM1 gangliosidosis P16278 (related)
H00421 Mucopolysaccharidosis (MPS) P16278 (related)
H00422 Glycoproteinoses P16278 (related)
H00426 Defects in the degradation of ganglioside P16278 (related)
H00807 Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) P17787 (related)
P43681 (related)
H00548 Brunner syndrome P21397 (related)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (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)