Gnetumelin A

Details

Top
Internal ID 52a5015d-77d8-42c3-8c14-c11da392add0
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-benzyl-5-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol
SMILES (Canonical) C1=CC=C(C=C1)CC2=C(C=C(C=C2O)O)C=CC3=CC(=C(C=C3)O)O
SMILES (Isomeric) C1=CC=C(C=C1)CC2=C(C=C(C=C2O)O)/C=C/C3=CC(=C(C=C3)O)O
InChI InChI=1S/C21H18O4/c22-17-12-16(8-6-15-7-9-19(23)21(25)11-15)18(20(24)13-17)10-14-4-2-1-3-5-14/h1-9,11-13,22-25H,10H2/b8-6+
InChI Key UGUXUAIOUHJDFR-SOFGYWHQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C21H18O4
Molecular Weight 334.40 g/mol
Exact Mass 334.12050905 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

Top
1004321-83-8
GnetumelinA

2D Structure

Top
2D Structure of Gnetumelin A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9180 91.80%
Caco-2 - 0.7437 74.37%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.5279 52.79%
OATP2B1 inhibitior - 0.5604 56.04%
OATP1B1 inhibitior + 0.8609 86.09%
OATP1B3 inhibitior + 0.9616 96.16%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior + 0.7864 78.64%
P-glycoprotein inhibitior - 0.8418 84.18%
P-glycoprotein substrate - 0.9404 94.04%
CYP3A4 substrate - 0.5784 57.84%
CYP2C9 substrate + 0.5764 57.64%
CYP2D6 substrate - 0.6648 66.48%
CYP3A4 inhibition - 0.5615 56.15%
CYP2C9 inhibition - 0.5673 56.73%
CYP2C19 inhibition - 0.8719 87.19%
CYP2D6 inhibition - 0.9185 91.85%
CYP1A2 inhibition + 0.7616 76.16%
CYP2C8 inhibition + 0.8159 81.59%
CYP inhibitory promiscuity + 0.6961 69.61%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8123 81.23%
Carcinogenicity (trinary) Non-required 0.6110 61.10%
Eye corrosion - 0.9722 97.22%
Eye irritation + 0.9345 93.45%
Skin irritation + 0.4899 48.99%
Skin corrosion - 0.7286 72.86%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6778 67.78%
Micronuclear + 0.6959 69.59%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation + 0.9056 90.56%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7241 72.41%
Acute Oral Toxicity (c) III 0.7928 79.28%
Estrogen receptor binding + 0.9394 93.94%
Androgen receptor binding + 0.9345 93.45%
Thyroid receptor binding + 0.7564 75.64%
Glucocorticoid receptor binding + 0.8269 82.69%
Aromatase binding + 0.8873 88.73%
PPAR gamma + 0.9487 94.87%
Honey bee toxicity - 0.8045 80.45%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9859 98.59%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.65% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.11% 91.49%
CHEMBL3194 P02766 Transthyretin 93.66% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.69% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.13% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.83% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.33% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.95% 94.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.74% 99.15%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 89.62% 91.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.02% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.70% 99.17%
CHEMBL1929 P47989 Xanthine dehydrogenase 84.97% 96.12%
CHEMBL240 Q12809 HERG 84.60% 89.76%
CHEMBL3401 O75469 Pregnane X receptor 83.25% 94.73%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.64% 95.17%
CHEMBL221 P23219 Cyclooxygenase-1 82.06% 90.17%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.56% 96.25%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Gnetum montanum

Cross-Links

Top
PubChem 101839191
LOTUS LTS0247920
wikiData Q105272578