Species

KNApSAcK Entry

Organism name Schinopsis lorentzii
Genus Schinopsis
Family Anacardiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Schinopsis lorentzii
Linked NCBI taxonomy ID 289763
Linked level species

Family

Family in NCBI taxonomy Anacardiaceae
ID 4011

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

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
C00004582 External link 512 Fisetin 4'-methyl ether
CHEMBL2017117
No. 3 No. 15
C00009141 External link 512 ent-Fisetinidol-(4alpha->8)-catechin
No. 16 No. 19
C00009136 External link 512 ent-Fisetinidol-(4alpha->6)-catechin
No. 16 No. 19
C00009152 External link 512 ent-Fisetinidol-(4alpha->8)-catechin-(6->4alpha)-ent-fisetinidol
No. 29 No. 19
C00002921 External link 512 ent-Fisetinidol-(4beta->8)-catechin-(6->4beta)-ent-fisetinidol
No. 29 No. 19
C00009153 External link 512 ent-Fisetinidol-(4beta->8)-catechin-(6->4alpha)-ent-fisetinidol
No. 29 No. 19
C00000963 External link 512 (2R,3R)-fustin
CHEMBL470267
CHEMBL508731
2 / 3 / 5 No. 42 No. 14
C00008999 External link 512 ent-Epifisetinidol-4beta-ol
No. 52 No. 14
C00008998 External link 512 ent-Fisetinidol-4beta-ol
No. 52 No. 14
C00004540 External link 512 Resokaempferol
CHEMBL242383
19 / 22 / 55 No. 76 No. 15
C00008069 External link 512 2,6,3'-Trihydroxy-4'-methoxy-2-benzylcoumaranone
No. 1085

Human Protein / Gene in interactions

21 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00004540 1 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00004540 7 / 37
P29466 Caspase-1 C14 C00004540 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00004540 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00004540 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00004540 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00000963 0 / 1
P28482 Mitogen-activated protein kinase 1 Erk C00004540 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00004540 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00004540 2 / 2
P55210 Caspase-7 C14 C00004540 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00004540 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00004540 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00004540 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00004540 4 / 3
P10275 Androgen receptor NR3C4 C00000963 3 / 4
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004540 0 / 0
O00255 Menin Unclassified protein C00004540 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00004540 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00004540 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00004540 1 / 4

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#211980 Lung cancer P04637
#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
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (60)

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)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (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)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
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 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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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)