(4S)-4,5-dimethoxy-4-(3-methylbut-2-enyl)-2-prop-2-enylcyclohexa-2,5-dien-1-one

Details

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Internal ID 1111a15e-5d50-48ae-8903-129d6221169d
Taxonomy Organic acids and derivatives > Vinylogous esters
IUPAC Name (4S)-4,5-dimethoxy-4-(3-methylbut-2-enyl)-2-prop-2-enylcyclohexa-2,5-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H22O3/c1-6-7-13-11-16(19-5,9-8-12(2)3)15(18-4)10-14(13)17/h6,8,10-11H,1,7,9H2,2-5H3/t16-/m0/s1
InChI Key CPXLLBFWGUPGGS-INIZCTEOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H22O3
Molecular Weight 262.34 g/mol
Exact Mass 262.15689456 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S)-4,5-dimethoxy-4-(3-methylbut-2-enyl)-2-prop-2-enylcyclohexa-2,5-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8520 85.20%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8154 81.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8922 89.22%
OATP1B3 inhibitior + 0.9135 91.35%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6269 62.69%
P-glycoprotein inhibitior - 0.9266 92.66%
P-glycoprotein substrate - 0.8663 86.63%
CYP3A4 substrate + 0.5414 54.14%
CYP2C9 substrate - 0.7861 78.61%
CYP2D6 substrate - 0.8428 84.28%
CYP3A4 inhibition - 0.8480 84.80%
CYP2C9 inhibition - 0.8830 88.30%
CYP2C19 inhibition - 0.5863 58.63%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.8312 83.12%
CYP2C8 inhibition - 0.8772 87.72%
CYP inhibitory promiscuity - 0.7996 79.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7214 72.14%
Carcinogenicity (trinary) Non-required 0.5715 57.15%
Eye corrosion - 0.9399 93.99%
Eye irritation + 0.6199 61.99%
Skin irritation - 0.6145 61.45%
Skin corrosion - 0.9826 98.26%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4284 42.84%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6870 68.70%
skin sensitisation + 0.6885 68.85%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.7886 78.86%
Acute Oral Toxicity (c) III 0.6797 67.97%
Estrogen receptor binding + 0.6845 68.45%
Androgen receptor binding - 0.5276 52.76%
Thyroid receptor binding - 0.5230 52.30%
Glucocorticoid receptor binding - 0.6359 63.59%
Aromatase binding + 0.6484 64.84%
PPAR gamma - 0.5494 54.94%
Honey bee toxicity - 0.7032 70.32%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9509 95.09%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.66% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.37% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.53% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.95% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.40% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.26% 95.56%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.57% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 83.88% 94.73%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.32% 85.30%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 44463981
LOTUS LTS0044058
wikiData Q104967829