(4S)-4-[(E)-1-(1,3-benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one

Details

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Internal ID 02fb695b-7ade-4bb0-8f0c-2893dcb82194
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (4S)-4-[(E)-1-(1,3-benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one
SMILES (Canonical) CC(=CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC
SMILES (Isomeric) C/C(=C\C1=CC2=C(C=C1)OCO2)/[C@]3(C=C(C(=O)C=C3OC)CC=C)OC
InChI InChI=1S/C21H22O5/c1-5-6-16-12-21(24-4,20(23-3)11-17(16)22)14(2)9-15-7-8-18-19(10-15)26-13-25-18/h5,7-12H,1,6,13H2,2-4H3/b14-9+/t21-/m0/s1
InChI Key AOZTYYBGNNXAOI-PBAKHKOTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O5
Molecular Weight 354.40 g/mol
Exact Mass 354.14672380 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.82
H-Bond Acceptor 5
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-[(E)-1-(1,3-benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-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 + 0.9930 99.30%
Caco-2 + 0.7688 76.88%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6973 69.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8939 89.39%
OATP1B3 inhibitior + 0.9278 92.78%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8940 89.40%
P-glycoprotein inhibitior + 0.7730 77.30%
P-glycoprotein substrate - 0.8060 80.60%
CYP3A4 substrate + 0.5879 58.79%
CYP2C9 substrate - 0.8041 80.41%
CYP2D6 substrate - 0.8420 84.20%
CYP3A4 inhibition + 0.9617 96.17%
CYP2C9 inhibition + 0.6648 66.48%
CYP2C19 inhibition + 0.9184 91.84%
CYP2D6 inhibition - 0.6660 66.60%
CYP1A2 inhibition + 0.5449 54.49%
CYP2C8 inhibition - 0.6130 61.30%
CYP inhibitory promiscuity + 0.9465 94.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4904 49.04%
Eye corrosion - 0.9804 98.04%
Eye irritation - 0.8569 85.69%
Skin irritation - 0.7487 74.87%
Skin corrosion - 0.9500 95.00%
Ames mutagenesis - 0.5670 56.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8161 81.61%
Micronuclear + 0.6033 60.33%
Hepatotoxicity + 0.7053 70.53%
skin sensitisation + 0.4934 49.34%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6293 62.93%
Acute Oral Toxicity (c) III 0.4732 47.32%
Estrogen receptor binding + 0.9020 90.20%
Androgen receptor binding + 0.8122 81.22%
Thyroid receptor binding + 0.6591 65.91%
Glucocorticoid receptor binding + 0.8226 82.26%
Aromatase binding + 0.7873 78.73%
PPAR gamma + 0.5400 54.00%
Honey bee toxicity - 0.7597 75.97%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9904 99.04%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.22% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.35% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.35% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 97.02% 94.80%
CHEMBL1951 P21397 Monoamine oxidase A 96.34% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.13% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.95% 86.33%
CHEMBL2039 P27338 Monoamine oxidase B 95.40% 92.51%
CHEMBL240 Q12809 HERG 93.30% 89.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.27% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.86% 98.95%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 91.58% 85.30%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.12% 96.09%
CHEMBL4208 P20618 Proteasome component C5 87.33% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.27% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 83.22% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.14% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.53% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.16% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.97% 95.89%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 80.67% 80.96%

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.
Castilleja sulphurea
Dioscorea villosa
Forsythia japonica
Gymnosporia pyria
Huperzia miyoshiana
Lindera aggregata
Piper kadsura
Piper schmidtii
Pseudobrickellia brasiliensis
Rhododendron latoucheae

Cross-Links

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PubChem 101833872
NPASS NPC253714
LOTUS LTS0258386
wikiData Q104916107