Species

KNApSAcK Entry

Organism name Lycium chinense
Genus Lycium
Family Solanaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Lycium chinense
Linked NCBI taxonomy ID 112883
Linked level species

Family

Family in NCBI taxonomy Solanaceae
ID 4070

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Natural Activity

List (17)

Species Activity
Lycium chinense Mill. ACE Inhibitor
Lycium chinense Mill. Analgesic
Lycium chinense Mill. Antiaging
Lycium chinense Mill. Antibacterial
Lycium chinense Mill. Antipyretic
Lycium chinense Mill. Bitter
Lycium chinense Mill. Depurative
Lycium chinense Mill. Hemostat
Lycium chinense Mill. Hepatoprotective
Lycium chinense Mill. Hepatotonic
Lycium chinense Mill. Hypoglycemic
Lycium chinense Mill. Hypotensive
Lycium chinense Mill. Immunosuppressive
Lycium chinense Mill. Mydriatic
Lycium chinense Mill. Nephrotonic
Lycium chinense Mill. Radioprotective
Lycium chinense Mill. Tonic

Metabolite list (17)

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
C00036313 External link 512 (+)-Lyoniresinol 3alpha-O-beta-glucopyranoside
/ (+)-Lyoniresinol 3alpha-O-beta-D-glucopyranoside
CHEMBL464198
CHEMBL1159486
CHEMBL1159487
CHEMBL1813178
CHEMBL1813179
CHEMBL1813180
CHEMBL1813181
CHEMBL2332109
6 / 11 / 5 No. 174 No. 22
C00036866 External link 512 Calystegine B4
CHEMBL526330
CHEMBL513797
CHEMBL1213469
CHEMBL1984376
1 / 6 / 4 No. 643 No. 1
C00036868 External link 512 Calystegine C1
/ (+)-Calystegine C1
CHEMBL1972699
No. 643 No. 1
C00028001 External link 512 Calystegine B1
CHEMBL1965915
C110567
No. 643 No. 1
C00036867 External link 512 Calystegine B5
/ (+)-Calystegine B5
No. 643 No. 1
C00036870 External link 512 Calystegine N1
No. 643 No. 1
C00035552 External link 512 Calystegine B3
/ (+)-Calystegine B3
CHEMBL526330
CHEMBL513797
CHEMBL1213469
CHEMBL1984376
1 / 6 / 4 No. 643 No. 1
C00037556 External link 512 N-Methyl-calystegine B2
CHEMBL447814
No. 643 No. 1
C00036865 External link 512 Calystegine A7
No. 643 No. 1
C00036863 External link 512 Calystegine A5
No. 643 No. 1
C00036864 External link 512 Calystegine A6
No. 643 No. 1
C00036613 External link 512 6-Deoxy-fagomine
/ (-)-6-Deoxy-fagomine
No. 786 No. 1
C00002038 External link 512 Fagomine
CHEMBL303545
CHEMBL108084
CHEMBL456583
CHEMBL505237
CHEMBL1818435
CHEMBL1818436
CHEMBL1818437
CHEMBL1818438
CHEMBL1818439
C105643
5 / 9 / 7 No. 786 No. 1
C00007205 External link 512 (+)-Lyoniresinol
CHEMBL455365
CHEMBL1760594
CHEMBL1761710
No. 4145
C00012761 External link 512 1,2-Dehydro-alpha-cyperone
/ (+)-Eudesma-1,4,11-trien-3-one
/ (4aS-cis)-5,6,7,8-Tetrahydro-1,4a-dimethyl-7-(1-methylethenyl)-2(4aH)-naphthalenone
No. 4452
C00028498 External link 512 Lyciumin A
No. 4771
C00028433 External link 512 Kukoamine A
CHEMBL79129
No. 8476

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P04062 Glucosylceramidase Enzyme C00002038 C00035552 C00036866 6 / 4
P04066 Tissue alpha-L-fucosidase Enzyme C00002038 1 / 2
Q14697 Neutral alpha-glucosidase AB Enzyme C00002038 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002038 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00036313 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00036313 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00036313 7 / 3
Q9P0U3 Sentrin-specific protease 1 Enzyme C00036313 0 / 0
P00734 Prothrombin S1A C00036313 4 / 2
Q9HCG7 Non-lysosomal glucosylceramidase Enzyme C00002038 1 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00036313 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#230000 Fucosidosis P04066
#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
#232300 Glycogen storage disease ii P10253
#174800 Mccune-albright syndrome; mas P63092
#166350 Osseous heteroplasia, progressive; poh P63092
#168600 Parkinson disease, late-onset; pd P04062
#102200 Pituitary adenoma, growth hormone-secreting P63092
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#614409 Spastic paraplegia 46, autosomal recessive; spg46 Q9HCG7
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (12)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (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)
H00141 Fucosidosis P04066 (related)
H00422 Glycoproteinoses P04066 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)