Species

KNApSAcK Entry

Organism name Magnolia denudata
Genus Magnolia
Family Magnoliaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Magnolia denudata
Linked NCBI taxonomy ID 85856
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

Metabolite list (33)

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
C00031449 External link 512 (-)-Methylpiperitol
CHEMBL462822
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
C00000642 External link 512 (+)-Yangambin
CHEMBL510536
CHEMBL454592
CHEMBL1412125
4 / 2 / 0 No. 38 No. 21
C00000643 External link 512 Kobusin
/ (+)-Kobusin
/ (+)-Spinescin
/ Methylpiperitol
CHEMBL462822
No. 38 No. 21
C00030244 External link 512 Fargesin
CHEMBL462822
No. 38 No. 21
C00007190 External link 512 (+)-Pinoresinol
CHEMBL267963
CHEMBL487611
CHEMBL460862
C103298
7 / 5 / 6 No. 38 No. 21
C00007212 External link 512 Galgravin
CHEMBL56800
CHEMBL57542
CHEMBL418309
CHEMBL291515
CHEMBL56856
CHEMBL56917
CHEMBL112481
CHEMBL469500
C084077
1 / 0 / 0 No. 38 No. 21
C00002607 External link 512 Grandisin
/ (-)-Grandisin
CHEMBL459404
CHEMBL459405
CHEMBL1377609
CHEMBL2204392
C074346
4 / 3 / 7 No. 38 No. 21
C00002633 External link 512 (+)-Veraguensin
CHEMBL56800
CHEMBL57542
CHEMBL418309
CHEMBL291515
CHEMBL56856
CHEMBL56917
CHEMBL112481
CHEMBL469500
1 / 0 / 0 No. 38 No. 21
C00032698 External link 512 Acuminatin
/ (+)-Acuminatin
CHEMBL571195
C077860
No. 215 No. 23
C00000696 External link 512 Licarin B
CHEMBL259386
CHEMBL578403
C119225
No. 215 No. 23
C00000601 External link 512 (+)-Sesamin
CHEMBL43469
CHEMBL252915
CHEMBL1572261
CHEMBL1591714
CHEMBL1708854
CHEMBL1904496
CHEMBL1968861
C054125
20 / 24 / 15 0 / 5 No. 621 No. 21
C00007213 External link 512 (-)-Galbacin
CHEMBL1980140
CHEMBL2151191
2 / 0 / 0 No. 621 No. 21
C00000602 External link 512 (+)-Lariciresinol
CHEMBL518421
2 / 1 / 1 No. 700 No. 21
C00032901 External link 512 Denudatin A
CHEMBL606463
No. 1419 No. 23
C00000671 External link 512 (+)-Denudatin B
CHEMBL30122
CHEMBL296958
CHEMBL571196
CHEMBL2114380
No. 1419 No. 23
C00031846 External link 512 Hancinone
CHEMBL606463
No. 1419 No. 23
C00033250 External link 512 Nirandin A
CHEMBL30352
CHEMBL570291
No. 1419 No. 23
C00032896 External link 512 Denudadione C
No. 1497
C00032894 External link 512 Denudadione A
No. 1497
C00032895 External link 512 Denudadione B
No. 1497
C00031994 External link 512 Magnolone
/ (-)-Magnolone
No. 1587
C00033060 External link 512 Isodihydrofutoquinol B
/ (+)-Isodihydrofutoquinol B
CHEMBL290066
No. 2047 No. 23
C00033059 External link 512 Isodihydrofutoquinol A
CHEMBL290066
No. 2047 No. 23
C00002610 External link 512 Kadsurin A
/ (+)-Kadsurin A
CHEMBL37432
No. 2788 No. 23
C00032897 External link 512 Denudanolide A
No. 2876
C00032898 External link 512 Denudanolide B
No. 2876
C00032900 External link 512 Denudanolide D
No. 2876
C00032899 External link 512 Denudanolide C
No. 2876
C00031784 External link 512 Fargesone B
No. 3583 No. 23
C00001259 External link 512 Naphthalene
CHEMBL16293
C031721
6 / 5 / 4 43 / 18 No. 5021
C00031639 External link 512 Burcellin
No. 6551

Human Protein / Gene in interactions

39 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00000601 C00000642 C00001259 C00002607 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000601 C00000642 C00007190 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00002633 C00007212 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000601 C00000602 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00000601 C00002607 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000601 C00000602 1 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00000640 C00000642 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000601 C00000642 2 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000601 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00002631 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000601 2 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00000601 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00001259 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00000640 0 / 0
P42574 Caspase-3 C14 C00001259 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00007190 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000601 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000601 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00000601 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000601 0 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00007190 5 / 3
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00001259 2 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000601 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001259 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000601 2 / 2
P45984 Mitogen-activated protein kinase 9 Jnk C00007213 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00007213 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000601 1 / 1
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00007190 0 / 3
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00007190 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000601 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000601 0 / 0
P10275 Androgen receptor NR3C4 C00001259 3 / 4
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00007190 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00000601 4 / 1
O00255 Menin Unclassified protein C00002607 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002607 1 / 2
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00007190 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000601 1 / 1

43 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00001259
196 AHR, bHLHe76 aryl hydrocarbon receptor C00001259
429 ASCL1, ASH1, HASH1, MASH1, bHLHa46 achaete-scute family bHLH transcription factor 1 C00001259
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00001259
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00001259
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00001259
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00001259
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00001259
1557 CYP2C19, CPCJ, CYP2C, P450C2C, P450IIC19 cytochrome P450, family 2, subfamily C, polypeptide 19 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00001259
1558 CYP2C8, CPC8, CYPIIC8, MP-12/MP-20 cytochrome P450, family 2, subfamily C, polypeptide 8 (EC:1.14.14.1) C00001259
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00001259
1565 CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) C00001259
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00001259
13107 C00001259
29785 CYP2S1 cytochrome P450, family 2, subfamily S, polypeptide 1 (EC:1.14.14.1) C00001259
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00001259
1577 CYP3A5, CP35, CYPIIIA5, P450PCN3, PCN3 cytochrome P450, family 3, subfamily A, polypeptide 5 (EC:1.14.14.1) C00001259
2052 EPHX1, EPHX, EPOX, HYL1, MEH epoxide hydrolase 1, microsomal (xenobiotic) (EC:3.3.2.9) C00001259
2053 EPHX2, CEH, SEH epoxide hydrolase 2, cytoplasmic (EC:3.3.2.10 3.1.3.76) C00001259
2252 FGF7, HBGF-7, KGF fibroblast growth factor 7 C00001259
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00001259
2521 FUS, ALS6, ETM4, FUS1, HNRNPP2, POMP75, TLS fused in sarcoma C00001259
2642 GCGR, GGR glucagon receptor C00001259
2944 GSTM1, GST1, GSTM1-1, GSTM1a-1a, GSTM1b-1b, GTH4, GTM1, H-B, MU, MU-1 glutathione S-transferase mu 1 (EC:2.5.1.18) C00001259
8870 IER3, DIF-2, DIF2, GLY96, IEX-1, IEX-1L, IEX1, PRG1 immediate early response 3 C00001259
3565 IL4, BCGF-1, BCGF1, BSF-1, BSF1, IL-4 interleukin 4 C00001259
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001259
3725 JUN, AP-1, AP1, c-Jun jun proto-oncogene C00001259
3956 LGALS1, GAL1, GBP lectin, galactoside-binding, soluble, 1 C00001259
4157 MC1R, CMM5, MSH-R, SHEP2 melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) C00001259
4159 MC3R, BMIQ9, MC3, MC3-R, OB20, OQTL melanocortin 3 receptor C00001259
4160 MC4R melanocortin 4 receptor C00001259
4161 MC5R, MC2 melanocortin 5 receptor C00001259
10403 NDC80, HEC, HEC1, HsHec1, KNTC2, TID3, hsNDC80 NDC80 kinetochore complex component C00001259
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00001259
5053 PAH, PH, PKU, PKU1 phenylalanine hydroxylase (EC:1.14.16.1) C00001259
5894 RAF1, CRAF, NS5, Raf-1, c-Raf v-raf-1 murine leukemia viral oncogene homolog 1 (EC:2.7.11.1) C00001259
389 RHOC, ARH9, ARHC, H9, RHOH9 ras homolog family member C C00001259
7356 SCGB1A1, CC10, CC16, CCPBP, CCSP, UGB, UP-1, UP1 secretoglobin, family 1A, member 1 (uteroglobin) C00001259
6855 SYP, MRXSYP synaptophysin C00001259
6932 TCF7, TCF-1 transcription factor 7 (T-cell specific, HMG-box) C00001259
7076 TIMP1, CLGI, EPA, EPO, HCI, TIMP TIMP metallopeptidase inhibitor 1 C00001259
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00001259

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (36)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#114500 Colorectal cancer; crc P18054
P84022
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#133239 Esophageal cancer P18054
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (32)

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)
H00036 Osteosarcoma P08684 (marker)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (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)
H00420 Familial partial lipodystrophy (FPL) P37231 (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) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)

Diseases related to CTD interactions

23 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000014 Abnormalities, Drug-Induced C00001259
D058186 Acute Kidney Injury C00001259
D055371 Acute Lung Injury C00001259
D000743 Anemia, Hemolytic C00001259
D002386 Cataract C00001259
D006456 Hemoglobinuria C00001259
D006529 Hepatomegaly C00001259
D006959 Hyperoxaluria C00001259
D006965 Hyperplasia C00001259
D008114 Liver Neoplasms, Experimental C00001259
D055370 Lung Injury C00001259
D008175 Lung Neoplasms C00001259
D048629 Micronuclei, Chromosome-Defective C00001259
D009336 Necrosis C00001259
D009362 Neoplasm Metastasis C00001259
D011041 Poisoning C00001259
D014133 Tracheal Diseases C00001259
D015431 Weight Loss C00001259
D001930 Brain Injuries C00000601
D002375 Catalepsy C00000601
D018476 Hypokinesia C00000601
D020244 Infarction, Middle Cerebral Artery C00000601
D020734 Parkinsonian Disorders C00000601