Species

KNApSAcK Entry

Organism name Sophora alopecuroides
Genus Sophora
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Sophora alopecuroides
Linked NCBI taxonomy ID 200492
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (26)

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
C00008364 External link 512 Norkurarinone
/ Sophoraflavanone G
CHEMBL243148
CHEMBL479477
C064849
3 / 2 / 2 No. 19 No. 14
C00008335 External link 512 Isokurarinone
No. 19 No. 14
C00014193 External link 512 Alopecurone G
/ 7,4'-Dihydroxy-8-lavandulyl-2'-methoxyflavanone
No. 19 No. 14
C00008459 External link 512 Glabrol
CHEMBL462721
7 / 12 / 6 No. 19 No. 14
C00008334 External link 512 Kushenol F
No. 19 No. 14
C00008197 External link 512 Isobavachin
CHEMBL491534
C468753
2 / 0 No. 28 No. 14
C00002227 External link 512 Matrine
/ (+)-Matrine
CHEMBL204860
CHEMBL383443
CHEMBL525227
CHEMBL1396816
CHEMBL1733145
CHEMBL1824581
C034244
5 / 3 / 7 4 / 5 No. 85 No. 3
C00026311 External link 512 14beta-Hydroxymatrine
/ (-)-14beta-Hydroxymatrine
No. 85 No. 3
C00007757 External link 512 Sophoridine
/ (-)-Sophoridine
CHEMBL204860
CHEMBL383443
CHEMBL525227
CHEMBL1396816
CHEMBL1733145
CHEMBL1824581
5 / 3 / 7 No. 85 No. 3
C00007138 External link 512 Ammothamnidin
No. 190 No. 13
C00002212 External link 512 Baptifoline
/ (-)-Baptifoline
C106940
No. 384 No. 3
C00002235 External link 512 Sophoramine
C055681
No. 384 No. 3
C00026319 External link 512 7alpha-Hydroxysophoramine
No. 384 No. 3
C00014268 External link 512 Alopecurone D
No. 669
C00014270 External link 512 Alopecurone F
No. 669
C00014269 External link 512 Alopecurone E
No. 669
C00014265 External link 512 Alopecurone A
/ Alopecurone I
No. 669
C00014267 External link 512 Alopecurone C
/ Alopecurone III
No. 669
C00014266 External link 512 Alopecurone B
/ Alopecurone II
No. 669
C00023309 External link 512 Lemannine
/ Lehmannine
/ (+)-Lehmannine
CHEMBL205311
No. 1721
C00026307 External link 512 12beta-Hydroxysophocarpine
CHEMBL441175
No. 1721
C00007759 External link 512 Sophocarpine
/ (-)-Sophocarpine
CHEMBL377725
CHEMBL380909
C035933
0 / 1 No. 1721
C00001183 External link 512 Fumaric acid
CHEMBL503160
CHEMBL539648
C032005
17 / 14 / 46 0 / 1 No. 3766
C00002205 External link 512 Aloperine
C062701
No. 4113
C00007785 External link 512 11,12-Dehydroaloperine
No. 6990
C00001198 External link 512 Oxalic acid
CHEMBL146755
D019815
2 / 0 / 0 1 / 6 No. 7540

Human Protein / Gene in interactions

32 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00001183 C00008459 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002227 C00007757 1 / 2
O00255 Menin Unclassified protein C00002227 C00007757 2 / 5
O75164 Lysine-specific demethylase 4A Enzyme C00001183 C00008459 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002227 C00007757 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002227 C00007757 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00002227 C00007757 0 / 0
P13866 Sodium/glucose cotransporter 1 Glucose C00008364 1 / 1
P37840 Alpha-synuclein Unclassified protein C00008459 4 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00001183 3 / 2
P00918 Carbonic anhydrase 2 Lyase C00001183 1 / 2
Q9GZT9 Egl nine homolog 1 Enzyme C00001183 1 / 1
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00001183 0 / 0
Q8TDS4 Hydroxycarboxylic acid receptor 2 Hydroxycarboxylic acid receptor C00001183 0 / 0
Q16798 NADP-dependent malic enzyme, mitochondrial Enzyme C00001183 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00008459 2 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00001183 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00001183 0 / 0
P11308 Transcriptional regulator ERG Unclassified protein C00001183 1 / 2
P83916 Chromobox protein homolog 1 Unclassified protein C00001183 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00008459 5 / 3
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00001198 0 / 0
Q99700 Ataxin-2 Unclassified protein C00008459 1 / 1
P56817 Beta-secretase 1 A1A C00008364 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001183 0 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00001198 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001183 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00001183 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00008459 1 / 0
P31639 Sodium/glucose cotransporter 2 Glucose C00008364 1 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00001183 7 / 37
Q9C0B1 Alpha-ketoglutarate-dependent dioxygenase FTO Unclassified protein C00001183 1 / 2

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00002227
4893 NRAS, ALPS4, N-ras, NRAS1, NS6 neuroblastoma RAS viral (v-ras) oncogene homolog C00002227
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00002227
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00002227
5241 PGR, NR3C3, PR progesterone receptor C00008197
7031 TFF1, BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2 trefoil factor 1 C00008197
26762 HAVCR1, HAVCR, HAVCR-1, KIM-1, KIM1, TIM, TIM-1, TIM1, TIMD-1, TIMD1 hepatitis A virus cellular receptor 1 C00001198

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (31)

OMIM preferred title UniProt
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#114500 Colorectal cancer; crc P84022
#127750 Dementia, lewy body; dlb P37840
#609820 Erythrocytosis, familial, 3; ecyt3 Q9GZT9
#133239 Esophageal cancer P04637
#612219 Ewing sarcoma; es P11308
#137800 Glioma susceptibility 1; glm1 O75874
P37231
#606824 Glucose/galactose malabsorption; ggm P13866
#612938 Growth retardation, developmental delay, coarse facies, and early death; gdfd Q9C0B1
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#601665 Obesity P37231
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#260500 Papilloma of choroid plexus; cpp P04637
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#233100 Renal glucosuria; glys1 P31639
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#275355 Squamous cell carcinoma, head and neck; hnscc P04637

KEGG DISEASE (58)

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)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (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)
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)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
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)
H00024 Prostate cancer P11308 (related)
H00035 Ewing's sarcoma P11308 (related)
H01261 Congenital glucose-galactose malabsorption (GGM) P13866 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01126 Familial renal glucosuria (FRG) P31639 (related)
H00409 Type II diabetes mellitus P37231 (related)
Q9C0B1 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (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)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00926 Growth retardation, developmental delay, coarse facies, and early death Q9C0B1 (related)
H00236 Congenital polycythemia Q9GZT9 (related)

Diseases related to CTD interactions

13 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002471 Cell Transformation, Neoplastic C00001183
D002289 Carcinoma, Non-Small-Cell Lung C00002227
D002779 Cholestasis C00002227
D056487 Drug-Induced Liver Injury, Chronic C00002227
D006331 Heart Diseases C00002227
D008113 Liver Neoplasms C00002227
D007249 Inflammation C00007759
D058186 Acute Kidney Injury C00001198
D006959 Hyperoxaluria C00001198
D006960 Hyperoxaluria, Primary C00001198
D009397 Nephrocalcinosis C00001198
D053040 Nephrolithiasis C00001198
D051437 Renal Insufficiency C00001198