(2S,7E,9E)-12-(1,3-benzodioxol-5-yl)dodeca-7,9-dien-2-ol

Details

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Internal ID a11c1647-abcd-444f-b0c9-49337c1c13ab
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (2S,7E,9E)-12-(1,3-benzodioxol-5-yl)dodeca-7,9-dien-2-ol
SMILES (Canonical) CC(CCCCC=CC=CCCC1=CC2=C(C=C1)OCO2)O
SMILES (Isomeric) C[C@@H](CCCC/C=C/C=C/CCC1=CC2=C(C=C1)OCO2)O
InChI InChI=1S/C19H26O3/c1-16(20)10-8-6-4-2-3-5-7-9-11-17-12-13-18-19(14-17)22-15-21-18/h2-3,5,7,12-14,16,20H,4,6,8-11,15H2,1H3/b3-2+,7-5+/t16-/m0/s1
InChI Key SGILAVRZPYCFMT-IONKVUFISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H26O3
Molecular Weight 302.40 g/mol
Exact Mass 302.18819469 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.40
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,7E,9E)-12-(1,3-benzodioxol-5-yl)dodeca-7,9-dien-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.8921 89.21%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6776 67.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9084 90.84%
OATP1B3 inhibitior + 0.9249 92.49%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7602 76.02%
BSEP inhibitior + 0.5828 58.28%
P-glycoprotein inhibitior - 0.4715 47.15%
P-glycoprotein substrate - 0.7632 76.32%
CYP3A4 substrate - 0.5111 51.11%
CYP2C9 substrate - 0.8333 83.33%
CYP2D6 substrate - 0.7115 71.15%
CYP3A4 inhibition - 0.6040 60.40%
CYP2C9 inhibition - 0.7851 78.51%
CYP2C19 inhibition - 0.6322 63.22%
CYP2D6 inhibition - 0.7941 79.41%
CYP1A2 inhibition + 0.5182 51.82%
CYP2C8 inhibition - 0.8799 87.99%
CYP inhibitory promiscuity - 0.6510 65.10%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.4319 43.19%
Eye corrosion - 0.9757 97.57%
Eye irritation - 0.7986 79.86%
Skin irritation - 0.5573 55.73%
Skin corrosion - 0.8567 85.67%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6945 69.45%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.6061 60.61%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8372 83.72%
Acute Oral Toxicity (c) III 0.6836 68.36%
Estrogen receptor binding + 0.8369 83.69%
Androgen receptor binding + 0.8013 80.13%
Thyroid receptor binding + 0.6684 66.84%
Glucocorticoid receptor binding + 0.5662 56.62%
Aromatase binding + 0.6008 60.08%
PPAR gamma + 0.7674 76.74%
Honey bee toxicity - 0.9247 92.47%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9465 94.65%

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
CHEMBL2581 P07339 Cathepsin D 98.11% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 96.93% 92.51%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.80% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.56% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.77% 96.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.76% 94.80%
CHEMBL3401 O75469 Pregnane X receptor 92.29% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.07% 99.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.75% 96.77%
CHEMBL240 Q12809 HERG 88.00% 89.76%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.35% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.82% 96.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.89% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.33% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.15% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.68% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.52% 92.62%

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.
Piper villiramulum

Cross-Links

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PubChem 10086286
LOTUS LTS0260022
wikiData Q105252351