Species

KNApSAcK Entry

Organism name Sophora subprostrata
Genus Sophora
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Sophora
Linked NCBI taxonomy ID 3896
Linked level genus

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 (14)

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
C00006199 External link 512 Sophoraflavone A
No. 1 No. 15
C00004117 External link 512 Sophoraflavone B
No. 2 No. 15
C00008196 External link 512 7,4'-Dihydroxy-6,8-di-C-prenylflavanone
CHEMBL560504
No. 19 No. 14
C00006083 External link 512 Bayin
/ 8-beta-D-Glucopyranosyl-4',7-dihydroxyflavone
No. 22 No. 15
C00003749 External link 512 Lupeol
/ Lupenol
/ (+)-Lupenol
CHEMBL289191
CHEMBL459702
C010480
3 / 0 / 0 2 / 6 No. 23 No. 51
C00008251 External link 512 Sophoranochromene
No. 39
C00002227 External link 512 Matrine
/ (+)-Matrine
CHEMBL204860
CHEMBL383443
CHEMBL525227
CHEMBL1396816
CHEMBL1733145
CHEMBL1824581
C034244
5 / 3 / 7 4 / 5 No. 85 No. 3
C00001005 External link 512 Sophoranone
/ (-)-Sophoranone
No. 170 No. 14
C00007092 External link 512 2,4,2'-Trihydroxy-6'',6''-dimethyl-3'-prenylpyrano[2'',3'':4',5']chalcone
No. 186
C00007075 External link 512 Sophoradochromene
No. 186
C00010188 External link 512 6'-O-Acetyltrifolirhizin
/ Trifolirhizin 6'-monoacetate
No. 557 No. 15
C00010186 External link 512 Trifolirhizin
/ Sophojaponicin B1
/ (-)-Maackiain 3-O-glucoside
CHEMBL454878
No. 557 No. 15
C00007758 External link 512 Oxymatrine
/ Ammothamnine
/ Matrine N-oxide
/ (+)-Matrine N-oxide
/ Matrine 1beta-oxide
CHEMBL458337
CHEMBL1358502
C037573
3 / 11 / 6 0 / 4 No. 1211 No. 3
C00007074 External link 512 Sophoradin
No. 1780

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P11387 DNA topoisomerase 1 Isomerase C00002227 C00003749 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00007758 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00003749 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002227 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00007758 7 / 3
P08047 Transcription factor Sp1 Unclassified protein C00003749 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002227 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00007758 4 / 3
O00255 Menin Unclassified protein C00002227 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002227 1 / 2

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1499 CTNNB1, CTNNB, MRD19, armadillo catenin (cadherin-associated protein), beta 1, 88kDa C00003749
5728 PTEN, 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, TEP1 phosphatase and tensin homolog (EC:3.1.3.67 3.1.3.16 3.1.3.48) C00003749
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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (14)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#174800 Mccune-albright syndrome; mas P63092
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#166350 Osseous heteroplasia, progressive; poh P63092
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (13)

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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (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)

Diseases related to CTD interactions

15 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006528 Carcinoma, Hepatocellular C00003749
D009202 Cardiomyopathies C00003749
D006937 Hypercholesterolemia C00003749
D009374 Neoplasms, Experimental C00003749
D012878 Skin Neoplasms C00003749
D014947 Wounds and Injuries C00003749
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
D003092 Colitis C00007758
D019694 Hepatitis B, Chronic C00007758
D007249 Inflammation C00007758
D008106 Liver Cirrhosis, Experimental C00007758