Methyl 2-hexa-2,4-diynyl-6-methoxybenzoate

Details

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Internal ID 095163ad-76fe-4a2a-8acc-3dbaa6507f9a
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > O-methoxybenzoic acids and derivatives
IUPAC Name methyl 2-hexa-2,4-diynyl-6-methoxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H14O3/c1-4-5-6-7-9-12-10-8-11-13(17-2)14(12)15(16)18-3/h8,10-11H,9H2,1-3H3
InChI Key IAKJWTWZFAUOIR-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O3
Molecular Weight 242.27 g/mol
Exact Mass 242.094294304 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 2-hexa-2,4-diynyl-6-methoxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.7362 73.62%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.9142 91.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9445 94.45%
OATP1B3 inhibitior + 0.9744 97.44%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8811 88.11%
P-glycoprotein inhibitior - 0.9151 91.51%
P-glycoprotein substrate - 0.7039 70.39%
CYP3A4 substrate + 0.5152 51.52%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.8299 82.99%
CYP3A4 inhibition - 0.8573 85.73%
CYP2C9 inhibition - 0.9656 96.56%
CYP2C19 inhibition - 0.7990 79.90%
CYP2D6 inhibition - 0.9593 95.93%
CYP1A2 inhibition + 0.5256 52.56%
CYP2C8 inhibition + 0.4819 48.19%
CYP inhibitory promiscuity - 0.5119 51.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6004 60.04%
Carcinogenicity (trinary) Non-required 0.6448 64.48%
Eye corrosion + 0.6215 62.15%
Eye irritation - 0.6851 68.51%
Skin irritation - 0.5796 57.96%
Skin corrosion - 0.9593 95.93%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5095 50.95%
Micronuclear - 0.6193 61.93%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8871 88.71%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6503 65.03%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6719 67.19%
Acute Oral Toxicity (c) III 0.7707 77.07%
Estrogen receptor binding - 0.5464 54.64%
Androgen receptor binding + 0.5223 52.23%
Thyroid receptor binding + 0.5181 51.81%
Glucocorticoid receptor binding - 0.6010 60.10%
Aromatase binding + 0.5784 57.84%
PPAR gamma - 0.6605 66.05%
Honey bee toxicity - 0.9034 90.34%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9542 95.42%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.22% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 92.26% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.75% 96.00%
CHEMBL2535 P11166 Glucose transporter 91.40% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.27% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.17% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.14% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.50% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.38% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.47% 95.56%

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.
Argyranthemum adauctum
Argyranthemum frutescens
Datura innoxia
Duboisia leichhardtii
Glebionis segetum

Cross-Links

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PubChem 15559375
LOTUS LTS0036245
wikiData Q104991849