Species

KNApSAcK Entry

Organism name Peucedanum ostruthium
Genus Peucedanum
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Peucedanum ostruthium
Linked NCBI taxonomy ID 52477
Linked level species

Family

Family in NCBI taxonomy Apiaceae
ID 4037

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Natural Activity

List (12)

Species Activity
Peucedanum ostruthium (L.) W. D. J. Koch. Antidote, spider
Peucedanum ostruthium (L.) W. D. J. Koch. Antispasmodic
Peucedanum ostruthium (L.) W. D. J. Koch. Aphrodisiac
Peucedanum ostruthium (L.) W. D. J. Koch. Carminative
Peucedanum ostruthium (L.) W. D. J. Koch. Depurative
Peucedanum ostruthium (L.) W. D. J. Koch. Diaphoretic
Peucedanum ostruthium (L.) W. D. J. Koch. Diuretic
Peucedanum ostruthium (L.) W. D. J. Koch. Emmenagogue
Peucedanum ostruthium (L.) W. D. J. Koch. Expectorant
Peucedanum ostruthium (L.) W. D. J. Koch. Sedative
Peucedanum ostruthium (L.) W. D. J. Koch. Stimulant
Peucedanum ostruthium (L.) W. D. J. Koch. Stomachic

Metabolite list (6)

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
C00002488 External link 512 Osthol
/ Osthole
CHEMBL52229
C046627
12 / 6 / 5 7 / 4 No. 466 No. 25
C00035717 External link 512 (+)-Oxypeucedanin
/ Oxypeucedanin hydrate
CHEMBL454060
CHEMBL1438253
13 / 5 / 8 No. 579 No. 25
C00002489 External link 512 Ostruthin
CHEMBL1812645
C008719
No. 1758 No. 25
C00002490 External link 512 Oxypeucedanin
CHEMBL510120
CHEMBL1510267
CHEMBL1609439
C031535
8 / 14 / 11 No. 2896 No. 25
C00013140 External link 512 Alatol
/ Alatol(Euonymus)
No. 4206
C00033066 External link 512 Isooxypeucedanin
No. 4290

Human Protein / Gene in interactions

26 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P56817 Beta-secretase 1 A1A C00002488 C00002490 C00035717 0 / 0
O75496 Geminin Unclassified protein C00002488 C00002490 C00035717 0 / 0
P06746 DNA polymerase beta Enzyme C00002490 C00035717 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002490 C00035717 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002488 C00002490 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002488 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00002488 0 / 0
P02545 Prelamin-A/C Unclassified protein C00002490 11 / 10
P17405 Sphingomyelin phosphodiesterase Enzyme C00035717 2 / 2
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00002488 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002488 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00035717 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00035717 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00002490 3 / 1
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002488 0 / 0
P04062 Glucosylceramidase Enzyme C00002488 6 / 4
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002488 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00035717 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00035717 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00035717 0 / 0
O14980 Exportin-1 Unclassified protein C00002488 0 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002488 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002490 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00035717 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00035717 1 / 4
Q13148 TAR DNA-binding protein 43 Unclassified protein C00035717 1 / 1

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
2180 ACSL1, ACS1, FACL1, FACL2, LACS, LACS1, LACS2 acyl-CoA synthetase long-chain family member 1 (EC:6.2.1.3) C00002488
1374 CPT1A, CPT1, CPT1-L, L-CPT1 carnitine palmitoyltransferase 1A (liver) (EC:2.3.1.21) C00002488
4313 MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) C00002488
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00002488
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002488
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00002488
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002488

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#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
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#168600 Parkinson disease, late-onset; pd P04062
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (24)

KEGG name UniProt
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)
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)
H00036 Osteosarcoma P08684 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
C538231 Adenocarcinoma of lung C00002488
D003920 Diabetes Mellitus C00002488
D006943 Hyperglycemia C00002488
D009361 Neoplasm Invasiveness C00002488