3-(3,4,5-Trimethoxyphenyl)prop-2-enyl dec-2-en-4,6-diynoate

Details

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Internal ID fb7b4aa5-9c2a-43da-8623-86595be3b24a
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 3-(3,4,5-trimethoxyphenyl)prop-2-enyl dec-2-en-4,6-diynoate
SMILES (Canonical) CCCC#CC#CC=CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC)OC
SMILES (Isomeric) CCCC#CC#CC=CC(=O)OCC=CC1=CC(=C(C(=C1)OC)OC)OC
InChI InChI=1S/C22H24O5/c1-5-6-7-8-9-10-11-14-21(23)27-15-12-13-18-16-19(24-2)22(26-4)20(17-18)25-3/h11-14,16-17H,5-6,15H2,1-4H3
InChI Key HVLQFFFGJMWZML-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O5
Molecular Weight 368.40 g/mol
Exact Mass 368.16237386 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.63
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(3,4,5-Trimethoxyphenyl)prop-2-enyl dec-2-en-4,6-diynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.5307 53.07%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8461 84.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8785 87.85%
OATP1B3 inhibitior + 0.9686 96.86%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8824 88.24%
P-glycoprotein inhibitior + 0.6665 66.65%
P-glycoprotein substrate - 0.7666 76.66%
CYP3A4 substrate + 0.5687 56.87%
CYP2C9 substrate - 0.6019 60.19%
CYP2D6 substrate - 0.8497 84.97%
CYP3A4 inhibition + 0.5805 58.05%
CYP2C9 inhibition - 0.6910 69.10%
CYP2C19 inhibition - 0.6720 67.20%
CYP2D6 inhibition - 0.9186 91.86%
CYP1A2 inhibition + 0.6734 67.34%
CYP2C8 inhibition + 0.6711 67.11%
CYP inhibitory promiscuity + 0.5595 55.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6743 67.43%
Carcinogenicity (trinary) Non-required 0.5993 59.93%
Eye corrosion - 0.9571 95.71%
Eye irritation - 0.8765 87.65%
Skin irritation - 0.8352 83.52%
Skin corrosion - 0.9750 97.50%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3699 36.99%
Micronuclear - 0.7752 77.52%
Hepatotoxicity - 0.5922 59.22%
skin sensitisation - 0.6420 64.20%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.5170 51.70%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.5924 59.24%
Acute Oral Toxicity (c) III 0.6865 68.65%
Estrogen receptor binding + 0.7903 79.03%
Androgen receptor binding + 0.6127 61.27%
Thyroid receptor binding + 0.7589 75.89%
Glucocorticoid receptor binding + 0.7115 71.15%
Aromatase binding + 0.6984 69.84%
PPAR gamma + 0.6958 69.58%
Honey bee toxicity - 0.8184 81.84%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5745 57.45%
Fish aquatic toxicity + 0.9860 98.60%

Targets

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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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.92% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.32% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.49% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.95% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.70% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.13% 94.45%
CHEMBL2535 P11166 Glucose transporter 82.90% 98.75%

Plants that contains it

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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.
Dimerostemma asperatum
Dimerostemma brasilianum

Cross-Links

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PubChem 86024323
LOTUS LTS0115606
wikiData Q105034335