Gymnoconjugatin B

Details

Top
Internal ID a85dffcf-0c9a-4c5d-8f96-d4a8c45a341c
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 6-[(1E,3E,5E,7E)-8-(furan-2-yl)octa-1,3,5,7-tetraenyl]-4-methoxy-3-methylpyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O4/c1-15-18(21-2)14-17(23-19(15)20)11-8-6-4-3-5-7-10-16-12-9-13-22-16/h3-14H,1-2H3/b5-3+,6-4+,10-7+,11-8+
InChI Key FKOMBLMMNSQCAJ-FPTHMUSISA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H18O4
Molecular Weight 310.30 g/mol
Exact Mass 310.12050905 g/mol
Topological Polar Surface Area (TPSA) 48.70 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.39
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

Top
Gymnoconjugatin B
6-[(1E,3E,5E,7E)-8-(furan-2-yl)octa-1,3,5,7-tetraenyl]-4-methoxy-3-methylpyran-2-one

2D Structure

Top
2D Structure of Gymnoconjugatin B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.6523 65.23%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7993 79.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9195 91.95%
OATP1B3 inhibitior + 0.9744 97.44%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8510 85.10%
P-glycoprotein inhibitior + 0.7394 73.94%
P-glycoprotein substrate - 0.9161 91.61%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6203 62.03%
CYP2D6 substrate - 0.8701 87.01%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.7735 77.35%
CYP2C19 inhibition + 0.8808 88.08%
CYP2D6 inhibition - 0.7950 79.50%
CYP1A2 inhibition + 0.8062 80.62%
CYP2C8 inhibition - 0.6537 65.37%
CYP inhibitory promiscuity + 0.8452 84.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8868 88.68%
Carcinogenicity (trinary) Danger 0.4624 46.24%
Eye corrosion - 0.9198 91.98%
Eye irritation - 0.6332 63.32%
Skin irritation - 0.7027 70.27%
Skin corrosion - 0.9735 97.35%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8376 83.76%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8034 80.34%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6045 60.45%
Acute Oral Toxicity (c) II 0.4481 44.81%
Estrogen receptor binding + 0.9309 93.09%
Androgen receptor binding + 0.5273 52.73%
Thyroid receptor binding + 0.6412 64.12%
Glucocorticoid receptor binding + 0.5973 59.73%
Aromatase binding + 0.8776 87.76%
PPAR gamma + 0.6776 67.76%
Honey bee toxicity - 0.8882 88.82%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9600 96.00%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.41% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.02% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.16% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.48% 94.00%
CHEMBL2039 P27338 Monoamine oxidase B 89.19% 92.51%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.90% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 86.49% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.38% 89.00%
CHEMBL2581 P07339 Cathepsin D 84.98% 98.95%

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.
There are no matching plants.

Cross-Links

Top
PubChem 12161900
LOTUS LTS0019695
wikiData Q77520655