Species

KNApSAcK Entry

Organism name Peucedanum praeruptorum
Genus Peucedanum
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Peucedanum praeruptorum
Linked NCBI taxonomy ID 312531
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

Metabolite list (8)

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
C00019997 External link 512 Peucedanocoumarin I
CHEMBL2104448
No. 224 No. 25
C00019998 External link 512 Peucedanocoumarin II
CHEMBL71876
CHEMBL1376728
CHEMBL1494966
CHEMBL1884860
16 / 18 / 45 No. 224 No. 25
C00019999 External link 512 Peucedanocoumarin III
CHEMBL71876
CHEMBL1376728
CHEMBL1494966
CHEMBL1884860
16 / 18 / 45 No. 224 No. 25
C00020008 External link 512 Praeroside II
/ (-)-Praeroside II
No. 399 No. 25
C00020036 External link 512 Praeroside V
No. 399 No. 25
C00020009 External link 512 Praeroside III
No. 399 No. 25
C00020010 External link 512 Praeroside IV
CHEMBL1159445
2 / 0 / 0 No. 399 No. 25
C00020007 External link 512 Praeroside I
No. 2585

Human Protein / Gene in interactions

17 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00019998 C00019999 C00020010 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00019998 C00019999 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00019998 C00019999 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00019998 C00019999 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00019998 C00019999 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00019998 C00019999 2 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00019998 C00019999 7 / 37
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00019998 C00019999 0 / 0
Q99700 Ataxin-2 Unclassified protein C00019998 C00019999 1 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00019998 C00019999 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00019998 C00019999 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00019998 C00019999 2 / 2
B2RXH2 Lysine-specific demethylase 4E Enzyme C00019998 C00019999 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00019998 C00019999 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00019998 C00019999 0 / 0
P06280 Alpha-galactosidase A Enzyme C00019998 C00019999 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00020010 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114500 Colorectal cancer; crc P84022
#119900 Digital clubbing, isolated congenital P15428
#133239 Esophageal cancer P04637
#301500 Fabry disease P06280
#232300 Glycogen storage disease ii P10253
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#260500 Papilloma of choroid plexus; cpp P04637
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#275355 Squamous cell carcinoma, head and neck; hnscc P04637

KEGG DISEASE (45)

KEGG name UniProt
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)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00033 Adrenal carcinoma 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)
H00125 Fabry disease P06280 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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)