Species

KNApSAcK Entry

Organism name Ferula szowitsiana
Genus Ferula
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Ferula szowitsiana
Linked NCBI taxonomy ID 555415
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 (12)

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
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00003674 External link 512 Stigmasterol
/ beta-Stigmasterol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00034703 External link 512 Szowitsiacoumarin A
/ (+)-Szowitsiacoumarin A
No. 209
C00034704 External link 512 Szowitsiacoumarin B
/ (+)-Szowitsiacoumarin B
CHEMBL270298
No. 209
C00029763 External link 512 Auraptene
CHEMBL307341
C105832
28 / 25 / 26 3 / 0 No. 335
C00034380 External link 512 2-Epihelmanticine
No. 1913
C00034507 External link 512 Farnesiferol B
CHEMBL272886
CHEMBL1082630
CHEMBL1083019
No. 1958
C00034508 External link 512 Farnesiferol C
CHEMBL177697
CHEMBL270486
No. 2027
C00034520 External link 512 Galbanic acid
CHEMBL1078509
C048972
No. 2027
C00034737 External link 512 Umbelliprenin
CHEMBL156127
8 / 3 / 3 No. 2038
C00034601 External link 512 Methyl galbanate
No. 2552
C00034625 External link 512 Persicasulfide A
/ (-)-Persicasulfide A
No. 8909

Human Protein / Gene in interactions

49 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003672 C00029763 C00034737 1 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme C00029763 C00034737 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00029763 C00034737 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003672 C00029763 0 / 1
P06746 DNA polymerase beta Enzyme C00003672 C00003674 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00029763 C00034737 0 / 0
O75496 Geminin Unclassified protein C00029763 C00034737 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00029763 C00034737 2 / 2
P14679 Tyrosinase Oxidoreductase C00003672 4 / 2
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00003674 0 / 0
P08183 Multidrug resistance protein 1 drug C00003672 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003672 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00029763 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003672 0 / 0
P39748 Flap endonuclease 1 Enzyme C00034737 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00029763 2 / 0
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00029763 1 / 4
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00029763 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00029763 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00029763 0 / 0
P04062 Glucosylceramidase Enzyme C00029763 6 / 4
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00029763 0 / 0
P00734 Prothrombin S1A C00003672 4 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00003672 3 / 2
P06280 Alpha-galactosidase A Enzyme C00029763 1 / 1
Q96RI1 Bile acid receptor NR1H4 C00029763 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00029763 0 / 0
P56817 Beta-secretase 1 A1A C00029763 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003672 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00029763 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00029763 2 / 2
P03372 Estrogen receptor NR3A1 C00003672 1 / 1
P09884 DNA polymerase alpha catalytic subunit Transferase C00003674 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003672 1 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003672 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
Q9UNA4 DNA polymerase iota Enzyme C00034737 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00029763 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00029763 4 / 3
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00029763 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00029763 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00029763 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00029763 1 / 4
P11388 DNA topoisomerase 2-alpha Isomerase C00003674 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00003674 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00029763 1 / 1

4 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00029763
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00029763
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00029763
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00003674

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (43)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#218030 Apparent mineralocorticoid excess; ame P80365
#208900 Ataxia-telangiectasia; at Q13315
#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
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#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
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (36)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00026 Endometrial Cancer P03372 (marker)
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)
H00125 Fabry disease P06280 (related)
H00036 Osteosarcoma P08684 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (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)
H00259 Apparent mineralocorticoid excess syndrome P80365 (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)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)