Species

KNApSAcK Entry

Organism name Inula royleana
Genus Inula
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Inula
Linked NCBI taxonomy ID 41589
Linked level genus

Family

Family in NCBI taxonomy Asteraceae
ID 4210

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (17)

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
C00001653 External link 512 Lycoctonine
/ (+)-Lycoctonine
CHEMBL517003
CHEMBL1242718
CHEMBL1303310
CHEMBL1975737
CHEMBL2356607
C093992
3 / 10 / 7 No. 31 No. 10
C00003306 External link 512 Isohelenin
/ Isoalantolactone
/ Isoallantolactone
CHEMBL273254
CHEMBL137803
CHEMBL1410671
CHEMBL1451900
CHEMBL2000732
C032787
6 / 4 / 5 No. 69 No. 38
C00029526 External link 512 4-epi-Isoinuviscolide
No. 69 No. 38
C00021698 External link 512 8-epi-Isovangustin
No. 69 No. 38
C00021699 External link 512 9beta-Hydroxy costunolide
No. 107 No. 38
C00020347 External link 512 Carabrol
/ 4-Dihydrocarabrone
No. 144 No. 38
C00021695 External link 512 Acetylivalin
No. 157 No. 38
C00001615 External link 512 Anthranoyllycoctonine
CHEMBL359227
CHEMBL451362
CHEMBL1499239
CHEMBL1968141
11 / 33 / 28 No. 166 No. 10
C00021697 External link 512 8-epi-Ivangustin
No. 178 No. 38
C00021704 External link 512 4beta,5alpha-Epoxy-4,5-cis-inunolide
No. 227 No. 38
C00021701 External link 512 9beta-(2-Methyl butyryloxy)-costunolide
No. 249 No. 38
C00021700 External link 512 9beta-Propionyloxy costunolide
No. 249 No. 38
C00012896 External link 512 2-Oxoalantolactone
/ [3aR-(3aalpha,5beta,8abeta,9aalpha)]-3,3a,5,6,8,8a,9,9a-Octahydro-5,8a-dimethyl-3-methylenenaphtho[2,3-b]furan-2,7-dione
No. 358 No. 38
C00012893 External link 512 Eupatal
/ Alant camphor
/ Inula camphor
/ (+)-Alantolactone
/ Elecampane camphor
CHEMBL8831
CHEMBL136356
CHEMBL1592975
C004363
5 / 21 / 50 10 / 0 No. 358 No. 38
C00012895 External link 512 2alpha-Hydroxy alantolactone
CHEMBL486020
C044996
No. 358 No. 38
C00003480 External link 512 Royleanone
CHEMBL1813341
No. 792 No. 40
C00021709 External link 512 4-Dihydrotomentosin
CHEMBL1912041
CHEMBL1912056
No. 857 No. 38

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00001615 C00001653 7 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003306 C00012893 0 / 1
P03372 Estrogen receptor NR3A1 C00003306 C00012893 1 / 1
P02545 Prelamin-A/C Unclassified protein C00001615 C00012893 11 / 10
P11473 Vitamin D3 receptor NR1I1 C00001653 C00012893 2 / 3
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003306 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003306 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00001615 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00001615 2 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00001615 2 / 0
P07237 Protein disulfide-isomerase Enzyme C00001615 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001615 1 / 2
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00001615 2 / 2
P04062 Glucosylceramidase Enzyme C00001615 6 / 4
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003306 1 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00012893 7 / 37
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001615 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003306 1 / 1
O00255 Menin Unclassified protein C00001615 2 / 5
Q13148 TAR DNA-binding protein 43 Unclassified protein C00001653 1 / 1

10 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
578 BAK1, BAK, BAK-LIKE, BCL2L7, CDN1 BCL2-antagonist/killer 1 C00012893
581 BAX, BCL2L4 BCL2-associated X protein C00012893
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00012893
637 BID, FP497 BH3 interacting domain death agonist C00012893
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00012893
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00012893
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00012893
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00012893
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00012893
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00012893

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (47)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#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
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#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
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#166350 Osseous heteroplasia, progressive; poh P63092
#260500 Papilloma of choroid plexus; cpp P04637
#168600 Parkinson disease, late-onset; pd P04062
#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
#275210 Restrictive dermopathy, lethal P02545
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (71)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (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)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
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)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H01171 Poor drug metabolism (PM) P33261 (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)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)