3,10,15-Trimethyl-6-propan-2-yl-14,16-dioxapentacyclo[9.4.1.01,11.03,7.013,15]hexadecane

Details

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Internal ID 877186f4-bc1e-449b-9087-9a5be1c0ab98
Taxonomy Organoheterocyclic compounds > Dioxepanes > 1,4-dioxepanes
IUPAC Name 3,10,15-trimethyl-6-propan-2-yl-14,16-dioxapentacyclo[9.4.1.01,11.03,7.013,15]hexadecane
SMILES (Canonical) CC1CCC2C(CCC2(CC34C1(O3)CC5C4(O5)C)C)C(C)C
SMILES (Isomeric) CC1CCC2C(CCC2(CC34C1(O3)CC5C4(O5)C)C)C(C)C
InChI InChI=1S/C20H32O2/c1-12(2)14-8-9-17(4)11-20-18(5)16(21-18)10-19(20,22-20)13(3)6-7-15(14)17/h12-16H,6-11H2,1-5H3
InChI Key TWQSMTGKQQCPBV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O2
Molecular Weight 304.50 g/mol
Exact Mass 304.240230259 g/mol
Topological Polar Surface Area (TPSA) 25.10 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.56
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,10,15-Trimethyl-6-propan-2-yl-14,16-dioxapentacyclo[9.4.1.01,11.03,7.013,15]hexadecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.7116 71.16%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.3903 39.03%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9305 93.05%
OATP1B3 inhibitior + 0.9713 97.13%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9227 92.27%
P-glycoprotein inhibitior - 0.8386 83.86%
P-glycoprotein substrate - 0.7384 73.84%
CYP3A4 substrate + 0.6306 63.06%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.7103 71.03%
CYP3A4 inhibition - 0.9613 96.13%
CYP2C9 inhibition - 0.7007 70.07%
CYP2C19 inhibition - 0.6288 62.88%
CYP2D6 inhibition - 0.9216 92.16%
CYP1A2 inhibition - 0.5518 55.18%
CYP2C8 inhibition - 0.7128 71.28%
CYP inhibitory promiscuity - 0.9222 92.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6900 69.00%
Eye corrosion - 0.9606 96.06%
Eye irritation - 0.8544 85.44%
Skin irritation - 0.6962 69.62%
Skin corrosion - 0.9366 93.66%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5060 50.60%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.6364 63.64%
skin sensitisation - 0.6048 60.48%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5512 55.12%
Acute Oral Toxicity (c) III 0.6400 64.00%
Estrogen receptor binding + 0.7515 75.15%
Androgen receptor binding + 0.7283 72.83%
Thyroid receptor binding + 0.7153 71.53%
Glucocorticoid receptor binding + 0.5683 56.83%
Aromatase binding + 0.6899 68.99%
PPAR gamma + 0.5978 59.78%
Honey bee toxicity - 0.7248 72.48%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.7113 71.13%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.64% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.20% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.72% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.09% 97.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 89.49% 86.00%
CHEMBL299 P17252 Protein kinase C alpha 89.25% 98.03%
CHEMBL221 P23219 Cyclooxygenase-1 89.22% 90.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.96% 97.14%
CHEMBL259 P32245 Melanocortin receptor 4 86.65% 95.38%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.90% 99.18%
CHEMBL1871 P10275 Androgen Receptor 84.65% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.64% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.36% 100.00%
CHEMBL2094135 Q96BI3 Gamma-secretase 84.13% 98.05%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 83.83% 97.31%
CHEMBL2039 P27338 Monoamine oxidase B 83.22% 92.51%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.53% 93.40%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 82.39% 91.03%
CHEMBL2007625 O75874 Isocitrate dehydrogenase [NADP] cytoplasmic 82.13% 99.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.77% 96.47%
CHEMBL4072 P07858 Cathepsin B 81.38% 93.67%
CHEMBL237 P41145 Kappa opioid receptor 81.22% 98.10%
CHEMBL2996 Q05655 Protein kinase C delta 80.94% 97.79%
CHEMBL3869 P50281 Matrix metalloproteinase 14 80.89% 93.10%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.69% 96.38%
CHEMBL2820 P03951 Coagulation factor XI 80.63% 95.29%

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.
Plicanthus hirtellus

Cross-Links

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PubChem 14707343
LOTUS LTS0126040
wikiData Q105266021