Species

KNApSAcK Entry

Organism name Ficus beecheyana
Genus Ficus
Family Moraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Moraceae
Linked NCBI taxonomy ID 3487
Linked level family

Family

Family in NCBI taxonomy Moraceae
ID 3487

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (7)

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
C00001105 External link 512 Tangeretin
/ 4',5,6,7,8-Pentamethoxyflavone
CHEMBL73930
C059006
12 / 11 / 11 2 / 0 No. 8 No. 15
C00000970 External link 512 Hesperidin
CHEMBL265606
CHEMBL449317
CHEMBL1314714
CHEMBL1328143
CHEMBL1535112
CHEMBL1574000
CHEMBL2140112
D006569
24 / 9 / 14 10 / 5 No. 48 No. 14
C00035212 External link 512 2,3-Dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone
No. 1180
C00035306 External link 512 erythro-2,3-Bis(4-hydroxy-3-methoxyphenyl)-3-ethoxypropan-1-ol
No. 2211
C00035413 External link 512 threo-2,3-Bis(4-hydroxy-3-methoxyphenyl)-3-ethoxypropan-1-ol
/ (+)-threo-2,3-Bis(4-hydroxy-3-methoxyphenyl)-3-ethoxypropan-1-ol
No. 2211
C00035419 External link 512 trans-4,5-Bis(4-hydroxy-3-methoxyphenyl)-1,3-dioxacyclohexane
No. 2211
C00035414 External link 512 threo-3-(4-Hydroxy-3,5-dimethoxyphenyl)-3-ethoxypropane-1,2-diol
No. 5619

Human Protein / Gene in interactions

32 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P83916 Chromobox protein homolog 1 Unclassified protein C00000970 C00001105 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000970 C00001105 1 / 2
O00255 Menin Unclassified protein C00000970 C00001105 2 / 5
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000970 C00001105 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000970 0 / 0
P62158 Calmodulin Unclassified protein C00000970 1 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00001105 1 / 1
P10828 Thyroid hormone receptor beta NR1A2 C00001105 3 / 1
P08183 Multidrug resistance protein 1 drug C00001105 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000970 0 / 1
Q9GZU7 Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 Enzyme C00000970 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001105 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00000970 1 / 1
P11308 Transcriptional regulator ERG Unclassified protein C00000970 1 / 2
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000970 1 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00001105 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000970 0 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00001105 2 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000970 1 / 1
P06746 DNA polymerase beta Enzyme C00000970 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000970 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00000970 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000970 0 / 0
Q9Y251 Heparanase Enzyme C00000970 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00000970 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000970 1 / 1
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00001105 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00000970 0 / 0
Q02410 Amyloid beta A4 precursor protein-binding family A member 1 Unclassified protein C00000970 0 / 0
Q00975 Voltage-dependent N-type calcium channel subunit alpha-1B N-TYPE C00000970 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00000970 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00001105 1 / 1

12 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00001105
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00001105
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00000970
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00000970
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00000970
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00000970
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00000970
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00000970
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00000970
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00000970
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00000970
7412 VCAM1, CD106, INCAM-100 vascular cell adhesion molecule 1 C00000970

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614490 Blood group, junior system; jr Q9UNQ0
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#612219 Ewing sarcoma; es P11308
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#612244 Inflammatory bowel disease 13; ibd13 P08183
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#614916 Ventricular tachycardia, catecholaminergic polymorphic, 4; cpvt4 P62158
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (17)

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)
H00036 Osteosarcoma P08684 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00024 Prostate cancer P11308 (related)
H00035 Ewing's sarcoma P11308 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00192 Xanthinuria P47989 (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)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

5 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D058186 Acute Kidney Injury C00000970
D055371 Acute Lung Injury C00000970
D056486 Drug-Induced Liver Injury C00000970
D008171 Lung Diseases C00000970
D012128 Respiratory Distress Syndrome, Adult C00000970