Species

KNApSAcK Entry

Organism name Sinodielsia yunnanensis
Genus Sinodielsia
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Meeboldia yunnanensis
Linked NCBI taxonomy ID 496675
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 (11)

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
C00002499 External link 512 Scopoletin
CHEMBL71851
D012603
48 / 37 / 34 9 / 0 No. 864 No. 25
C00001283 External link 512 Falcarindiol
CHEMBL69018
CHEMBL1094112
C034379
3 / 0 / 0 No. 940 No. 69
C00032154 External link 512 Sinodielide E
/ (+)-Sinodielide E
No. 1016
C00032153 External link 512 Sinodielide D
/ (-)-Sinodielide D
No. 1016
C00032155 External link 512 Sinodielide F
/ (-)-Sinodielide F
No. 1016
C00032150 External link 512 Sinodielide A
No. 1140
C00000575 External link 512 Bergaptan
CHEMBL24171
C022909
22 / 22 / 17 0 / 3 No. 1282 No. 25
C00032156 External link 512 Sinodielide G
/ (+)-Sinodielide G
No. 1990
C00032157 External link 512 Sinodielide H
/ (-)-Sinodielide H
No. 1990
C00032151 External link 512 Sinodielide B
/ (-)-Sinodielide B
No. 2161
C00032152 External link 512 Sinodielide C
/ (-)-Sinodielide C
No. 2161

Human Protein / Gene in interactions

65 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000575 C00002499 1 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000575 C00002499 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000575 C00002499 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000575 C00002499 1 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000575 C00002499 3 / 3
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000575 C00002499 7 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00000575 C00002499 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000575 C00002499 0 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002499 2 / 2
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002499 0 / 3
P22001 Potassium voltage-gated channel subfamily A member 3 KCNA, Kv1.x (Shaker) C00000575 0 / 0
P04062 Glucosylceramidase Enzyme C00002499 6 / 4
P10253 Lysosomal alpha-glucosidase Hydrolase C00002499 1 / 1
P43166 Carbonic anhydrase 7 Lyase C00002499 0 / 0
P29466 Caspase-1 C14 C00002499 0 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00002499 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002499 0 / 0
Q8N1Q1 Carbonic anhydrase 13 Lyase C00002499 0 / 0
P20813 Cytochrome P450 2B6 Cytochrome P450 2B6 C00000575 1 / 0
P17658 Potassium voltage-gated channel subfamily A member 6 K C00000575 0 / 0
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme C00002499 1 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00000575 3 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00002499 1 / 1
P00918 Carbonic anhydrase 2 Lyase C00002499 1 / 2
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00001283 0 / 0
P08183 Multidrug resistance protein 1 drug C00000575 1 / 0
Q99700 Ataxin-2 Unclassified protein C00002499 1 / 1
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00001283 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00001283 0 / 0
P16389 Potassium voltage-gated channel subfamily A member 2 KCNA, Kv1.x (Shaker) C00000575 0 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00002499 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00002499 1 / 2
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000575 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00002499 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002499 0 / 0
O75496 Geminin Unclassified protein C00002499 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00002499 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00002499 0 / 0
P15121 Aldose reductase Enzyme C00002499 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00002499 0 / 0
P48547 Potassium voltage-gated channel subfamily C member 1 K C00000575 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00002499 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000575 0 / 0
P06280 Alpha-galactosidase A Enzyme C00002499 1 / 1
P56817 Beta-secretase 1 A1A C00000575 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002499 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00002499 0 / 1
O75795 UDP-glucuronosyltransferase 2B17 Enzyme C00002499 1 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002499 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00002499 0 / 0
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00002499 0 / 0
P22303 Acetylcholinesterase Hydrolase C00002499 1 / 0
Q00796 Sorbitol dehydrogenase Enzyme C00002499 0 / 0
P55210 Caspase-7 C14 C00002499 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00002499 0 / 0
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00002499 3 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00002499 5 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000575 0 / 0
P10275 Androgen receptor NR3C4 C00000575 3 / 4
P22460 Potassium voltage-gated channel subfamily A member 5 KCNA, Kv1.x (Shaker) C00000575 1 / 1
Q09470 Potassium voltage-gated channel subfamily A member 1 KCNA, Kv1.x (Shaker) C00000575 1 / 1
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002499 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002499 0 / 0
O00255 Menin Unclassified protein C00002499 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002499 1 / 2

9 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00002499
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002499
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002499
54578 UGT1A6, GNT1, HLUGP, HLUGP1, UDPGT, UDPGT_1-6, UGT1, UGT1A6S, UGT1F UDP glucuronosyltransferase 1 family, polypeptide A6 (EC:2.4.1.17) C00002499
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002499
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00002499
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00002499
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00002499
7508 XPC, RAD4, XP3, XPCC xeroderma pigmentosum, complementation group C C00002499

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (47)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#612240 Atrial fibrillation, familial, 7; atfb7 P22460
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#612560 Bone mineral density quantitative trait locus 12; bmnd12 O75795
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#614546 Efavirenz, poor metabolism of P20813
#160120 Episodic ataxia, type 1; ea1 Q09470
#301500 Fabry disease P06280
#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
#143500 Gilbert syndrome P22309
P22310
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#145000 Hyperparathyroidism 1; hrpt1 O00255
#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
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#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
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#278300 Xanthinuria, type i P47989
#112100 Yt blood group antigen P22303

KEGG DISEASE (42)

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)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (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)
H00125 Fabry disease P06280 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H01205 Coumarin resistance P11712 (related)
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)
H00208 Hyperbilirubinemia P22309 (related)
H00731 Atrial fibrillation P22460 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00192 Xanthinuria P47989 (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)
H00749 Episodic ataxias Q09470 (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)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006505 Hepatitis C00000575
D010787 Photosensitivity Disorders C00000575
D011565 Psoriasis C00000575