Species

KNApSAcK Entry

Organism name Tripterygium wilfordii
Genus Tripterygium
Family Celastraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Tripterygium wilfordii
Linked NCBI taxonomy ID 458696
Linked level species

Family

Family in NCBI taxonomy Celastraceae
ID 4305

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (49)

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
C00000659 External link 512 Medioresinol
/ (+)-Medioresinol
CHEMBL376507
CHEMBL513023
2 / 1 / 1 No. 38 No. 21
C00002631 External link 512 (+)-Lirioresinol B
/ (+)-Syringaresinol
CHEMBL361362
CHEMBL402653
C042192
1 / 0 / 0 No. 38 No. 21
C00046516 External link 512 Wilfornine E
CHEMBL450102
No. 43
C00046977 External link 512 Wilfordinine B
No. 43
C00001987 External link 512 Wilfordin
CHEMBL449308
CHEMBL525628
No. 43
C00046976 External link 512 Wilfordinine A
CHEMBL2335702
No. 43
C00046846 External link 512 Peritassine A
/ (+)-Peritassine A
CHEMBL1951082
No. 43
C00013107 External link 512 Alatusinine
/ (8a)-8-(Acetyloxy)-8-deoxo-26-hydroxyevonimine
CHEMBL508998
CHEMBL501360
No. 43
C00013120 External link 512 Evonine
/ [8R-(8R*,9R*,10R*,11S*,12S*,13R*,14R*,15S*,18S*,19S*,20S*,21S*)]-10,13,14,21-Tetrakis(acetyloxy)-12-[(acetyloxy)methyl]-7,8,9,10,12,13,14,15,18,19-decahydro-20-hydroxy-8,18,19,20-tetramethyl-8,11-epoxy-9,12-ethano-11,15-methano-11H-[1,8]dioxacycloheptadecino[4,3-b]pyridine-5,17,22-trione
CHEMBL449845
CHEMBL1996226
No. 43
C00013126 External link 512 Euonymin
/ Euonymine
CHEMBL346753
CHEMBL503447
No. 43
C00046518 External link 512 Wilfornine G
CHEMBL502166
No. 43
C00046517 External link 512 Wilfornine F
CHEMBL524497
No. 43
C00013158 External link 512 Mayteine
/ [8R-(8R*,9R*,10R*,11S*,12S*,13R*,14R*,15S*,18S*,19S*,20S*,21S*,22R*)]-10,14,21,22-Tetrakis(acetyloxy)-12-[(acetyloxy)methyl]-13-(benzoyloxy)-7,8,9,10,12,13,14,15,18,19-decahydro-20-hydroxy-8,18,19,20-tetramethyl-8,11-epoxy-9,12-ethano-11,15-methano-11H-[1,8]dioxacycloheptadecino[4,3-b]pyridine-5,17-dione
CHEMBL526919
CHEMBL1813072
C096143
No. 43
C00046978 External link 512 Wilfordinine C
No. 43
C00013191 External link 512 Wilforidine
/ (8R,9R,10R,11S,12S,13R,14R,15S,21S,22S,23R)-[partial]-10,13,22,23-Tetrakis(acetyloxy)-12-[(acetyloxy)methyl]-7,8,9,10,12,13,14,15,17,18,19,20-dodecahydro-14,18,21-trihydroxy-8,18,21-trimethyl-8,11-epoxy-9,12-ethano-11,15-methano-5H,11H-[1,9]dioxacyclooctadecino[4,3-b]pyridine-5,17-dione
CHEMBL504312
CHEMBL1950977
No. 43
C00013193 External link 512 Wilforine
/ (8alpha)-8-(Acetyloxy)-O2-benzoyl-O2-deacetyl-8-deoxoevonimine
CHEMBL503312
CHEMBL502742
No. 43
C00013194 External link 512 Wilforzine
/ O6-Deacetylwilforine
/ ((8alpha)-8-(Acetyloxy)-O2-benzoyl-O2,O6-dideacetyl-8-deoxoevonimine
No. 43
C00046515 External link 512 Wilfornine D
No. 43
C00046514 External link 512 Wilfornine C
CHEMBL509162
No. 43
C00046513 External link 512 Wilfornine B
CHEMBL525210
No. 43
C00039395 External link 512 Hyponine D
CHEMBL504037
No. 43
C00041008 External link 512 Hypoglaunine C
/ (+)-Hypoglaunine C
CHEMBL501891
No. 43
C00041944 External link 512 Tripfordine A
CHEMBL504312
CHEMBL1950977
No. 43
C00041945 External link 512 Tripfordine B
CHEMBL453463
No. 43
C00046511 External link 512 Wilfordinine J
CHEMBL511075
No. 43
C00046512 External link 512 Wilfornine A
CHEMBL502989
No. 43
C00046510 External link 512 Wilfordinine I
CHEMBL508482
No. 43
C00041946 External link 512 Tripfordine C
CHEMBL505030
No. 43
C00013156 External link 512 Triptofordin D 1
/ [3R-(3alpha,5alpha,5aalpha,6alpha,9beta,9aalpha,10R*)]-10-(Acetyloxy)-5a-[(acetyloxy)methyl]-5-(benzoyloxy)octahydro-9-hydroxy-2,2,9-trimethyl-4-oxo-2H-3,9a-methano-1-benzoxepin-6-yl ester 3-phenyl-2-propenoic acid
No. 168
C00013148 External link 512 Triptofordin D 2
/ [3R-(3alpha,4alpha,5alpha,5aalpha,6alpha,9beta,9aalpha,10R*)]-4,10-bis(Acetyloxy)-5a-[(acetyloxy)methyl]-5-(benzoyloxy)octahydro-9-hydroxy-2,2,9-trimethyl-2H-3,9a-methano-1-benzoxepin-6-yl ester 3-phenyl-2-propenoic acid
No. 168
C00049687 External link 512 (-)-17-Hydroxy-16alpha-kauran-19-oic acid
CHEMBL511892
CHEMBL481645
CHEMBL448617
CHEMBL456957
No. 203 No. 41
C00049686 External link 512 (-)-16alpha-Hydroxykauran-19-oic acid
CHEMBL207260
CHEMBL480070
CHEMBL604095
CHEMBL1760135
C060419
1 / 0 / 0 No. 203 No. 41
C00049689 External link 512 16alpha,19-Dihydroxy-ent-kaurane
CHEMBL1760128
No. 203 No. 41
C00049759 External link 512 Triptobenzene N
/ (-)-Triptobenzene N
CHEMBL444235
No. 355
C00049757 External link 512 Triptobenzene L
/ (+)-Triptobenzene L
No. 359 No. 40
C00049755 External link 512 Triptobenzene A
No. 760
C00049758 External link 512 Triptobenzene M
/ (+)-Triptobenzene M
No. 760
C00002609 External link 512 Hinokiol
/ (+)-Hinokiol
CHEMBL16901
26 / 24 / 20 No. 761 No. 23
C00041947 External link 512 Tripterifordin
CHEMBL484043
C074970
No. 925
C00049760 External link 512 Triptoquinone C
No. 1436
C00035883 External link 512 Triptoquinone B
No. 1436
C00013189 External link 512 Triptofordin A
/ (+)-Triptofordin A
/ [3R-(3alpha,5beta,5aalpha,6alpha,9beta,9aalpha)]-6-(Benzoyloxy)octahydro-9-hydroxy-2,2,5a,9-tetramethyl-2H-3,9a-methano-1-benzoxepin-5-yl ester 3-phenyl-2-propenoic acid
No. 1678
C00002322 External link 512 Celabenzine
No. 2404
C00049756 External link 512 Triptobenzene H
No. 2898
C00035770 External link 512 Triptinin B
/ (+)-Triptinin B
No. 2898
C00003494 External link 512 Triptolide
CHEMBL463763
CHEMBL444360
C001899
6 / 13 / 18 20 / 15 No. 3698 No. 41
C00003493 External link 512 Tripdiolide
CHEMBL486403
C001898
No. 3698 No. 41
C00035774 External link 512 Triptoquinone A
C100591
No. 4560
C00049761 External link 512 Triptotin B
/ (+)-Triptotin B
No. 7621

Human Protein / Gene in interactions

36 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000659 1 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00049686 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002609 1 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002609 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00003494 0 / 3
P06746 DNA polymerase beta Enzyme C00002609 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002609 1 / 1
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002609 0 / 0
P02545 Prelamin-A/C Unclassified protein C00003494 11 / 10
P37840 Alpha-synuclein Unclassified protein C00002609 4 / 2
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00002609 0 / 0
P47870 Gamma-aminobutyric acid receptor subunit beta-2 GABA-A beta C00002609 0 / 0
P14867 Gamma-aminobutyric acid receptor subunit alpha-1 GABA-A alpha C00002609 1 / 1
P11387 DNA topoisomerase 1 Isomerase C00002631 0 / 0
P34972 Cannabinoid receptor 2 Cannabinoid receptor C00002609 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002609 2 / 2
P39748 Flap endonuclease 1 Enzyme C00002609 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002609 2 / 0
O75496 Geminin Unclassified protein C00002609 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00003494 0 / 0
Q9Y2T6 G-protein coupled receptor 55 Lysophosphatidylinositol receptor C00002609 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002609 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00002609 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00002609 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002609 5 / 3
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00002609 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00003494 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000659 0 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00002609 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002609 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002609 4 / 3
Q9GZV3 High affinity choline transporter 1 Choline Na-symporter C00002609 1 / 0
O00255 Menin Unclassified protein C00002609 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002609 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00003494 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00003494 1 / 4

20 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
330 BIRC3, AIP1, API2, CIAP2, HAIP1, HIAP1, MALT2, MIHC, RNF49, c-IAP2 baculoviral IAP repeat containing 3 C00003494
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00003494
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00003494
941 CD80, B7, B7-1, B7.1, BB1, CD28LG, CD28LG1, LAB7 CD80 molecule C00003494
942 CD86, B7-2, B7.2, B70, CD28LG2, LAB72 CD86 molecule C00003494
1082 CGB, CGB3, CGB5, CGB7, CGB8, hCGB chorionic gonadotropin, beta polypeptide C00003494
1843 DUSP1, CL100, HVH1, MKP-1, MKP1, PTPN10 dual specificity phosphatase 1 (EC:3.1.3.16 3.1.3.48) C00003494
2146 EZH2, ENX-1, ENX1, EZH1, EZH2b, KMT6, KMT6A, WVS, WVS2 enhancer of zeste homolog 2 (Drosophila) (EC:2.1.1.43) C00003494
3303 HSPA1A, HSP70-1, HSP70-1A, HSP70I, HSP72, HSPA1 heat shock 70kDa protein 1A C00003494
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00003494
3592 IL12A, CLMF, IL-12A, NFSK, NKSF1, P35 interleukin 12A (natural killer cell stimulatory factor 1, cytotoxic lymphocyte maturation factor 1, p35) C00003494
3593 IL12B, CLMF, CLMF2, IL-12B, NKSF, NKSF2 interleukin 12B (natural killer cell stimulatory factor 2, cytotoxic lymphocyte maturation factor 2, p40) C00003494
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00003494
1432 MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA mitogen-activated protein kinase 14 (EC:2.7.11.24) C00003494
2908 NR3C1, GCCR, GCR, GR, GRL nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) C00003494
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00003494
6839 SUV39H1, H3-K9-HMTase_1, KMT1A, MG44, SUV39H suppressor of variegation 3-9 homolog 1 (Drosophila) (EC:2.1.1.43) C00003494
6863 TAC1, Hs.2563, NK2, NKNA, NPK, TAC2 tachykinin, precursor 1 C00003494
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00003494
331 XIAP, API3, BIRC4, IAP-3, ILP1, MIHA, XLP2, hIAP-3, hIAP3 X-linked inhibitor of apoptosis C00003494

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (38)

OMIM preferred title UniProt
%606641 Body mass index; bmi P37231
#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
#127750 Dementia, lewy body; dlb P37840
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#611136 Epilepsy, juvenile myoclonic, susceptibility to, 5; ejm5 P14867
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 P37231
#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
#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
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#158580 Neuronopathy, distal hereditary motor, type viia; hmn7a Q9GZV3
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (37)

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)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
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)
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)
H00808 Idiopathic generalized epilepsies (IGEs) P14867 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (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)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (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)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)

Diseases related to CTD interactions

15 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D058186 Acute Kidney Injury C00003494
D000855 Anorexia C00003494
D003967 Diarrhea C00003494
D056486 Drug-Induced Liver Injury C00003494
D005234 Fatty Liver C00003494
D007249 Inflammation C00003494
D007674 Kidney Diseases C00003494
D015470 Leukemia, Myeloid, Acute C00003494
D009101 Multiple Myeloma C00003494
D009102 Multiple Organ Failure C00003494
D009369 Neoplasms C00003494
D010049 Ovarian Diseases C00003494
D011014 Pneumonia C00003494
D011507 Proteinuria C00003494
D013163 Splenomegaly C00003494