3,7-Dimethyl-9-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)nona-1,6-dien-3-ol

Details

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Internal ID 0636d661-583e-4779-9338-164bf657d5ee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 3,7-dimethyl-9-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)nona-1,6-dien-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H32O3/c1-8-18(7,19)13-9-10-14(2)11-12-15-16(3,4)21-17(5,6)20-15/h8,10,15,19H,1,9,11-13H2,2-7H3
InChI Key PMQKDUOLNIZGFG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H32O3
Molecular Weight 296.40 g/mol
Exact Mass 296.23514488 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.36
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7-Dimethyl-9-(2,2,5,5-tetramethyl-1,3-dioxolan-4-yl)nona-1,6-dien-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9804 98.04%
Caco-2 + 0.7690 76.90%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5741 57.41%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.8942 89.42%
OATP1B3 inhibitior + 0.8862 88.62%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.5952 59.52%
P-glycoprotein inhibitior - 0.8487 84.87%
P-glycoprotein substrate - 0.8305 83.05%
CYP3A4 substrate + 0.5851 58.51%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.8010 80.10%
CYP3A4 inhibition - 0.6646 66.46%
CYP2C9 inhibition - 0.7714 77.14%
CYP2C19 inhibition - 0.7864 78.64%
CYP2D6 inhibition - 0.9314 93.14%
CYP1A2 inhibition - 0.7282 72.82%
CYP2C8 inhibition - 0.5907 59.07%
CYP inhibitory promiscuity - 0.8595 85.95%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8028 80.28%
Carcinogenicity (trinary) Non-required 0.6193 61.93%
Eye corrosion - 0.9700 97.00%
Eye irritation - 0.6304 63.04%
Skin irritation - 0.5513 55.13%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis - 0.5754 57.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3926 39.26%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.6799 67.99%
skin sensitisation + 0.4776 47.76%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5772 57.72%
Acute Oral Toxicity (c) III 0.6496 64.96%
Estrogen receptor binding + 0.6553 65.53%
Androgen receptor binding - 0.5617 56.17%
Thyroid receptor binding + 0.6184 61.84%
Glucocorticoid receptor binding + 0.5694 56.94%
Aromatase binding + 0.5690 56.90%
PPAR gamma + 0.6271 62.71%
Honey bee toxicity - 0.7435 74.35%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9675 96.75%

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 92.93% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 91.07% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.34% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.79% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.84% 97.25%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.60% 90.93%
CHEMBL2039 P27338 Monoamine oxidase B 81.37% 92.51%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.87% 96.47%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.11% 96.90%
CHEMBL1951 P21397 Monoamine oxidase A 80.09% 91.49%

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 162787734
LOTUS LTS0136897
wikiData Q104195049