(5,9,13-Trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-5-yl)methanol

Details

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Internal ID d6dd4c60-72fb-423c-9d0c-54c67a312f6c
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name (5,9,13-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-5-yl)methanol
SMILES (Canonical) CC12CCC3C4(CCCC(C4CCC3(C1)C5C2O5)(C)CO)C
SMILES (Isomeric) CC12CCC3C4(CCCC(C4CCC3(C1)C5C2O5)(C)CO)C
InChI InChI=1S/C20H32O2/c1-17-9-5-14-19(3)8-4-7-18(2,12-21)13(19)6-10-20(14,11-17)16-15(17)22-16/h13-16,21H,4-12H2,1-3H3
InChI Key WWQSLMHDPLEJSY-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) 32.80 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.16
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5,9,13-Trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-5-yl)methanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9820 98.20%
Caco-2 + 0.7704 77.04%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.5440 54.40%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8845 88.45%
OATP1B3 inhibitior + 0.8915 89.15%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5939 59.39%
P-glycoprotein inhibitior - 0.8209 82.09%
P-glycoprotein substrate - 0.8802 88.02%
CYP3A4 substrate + 0.5847 58.47%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.7346 73.46%
CYP3A4 inhibition - 0.7975 79.75%
CYP2C9 inhibition + 0.6217 62.17%
CYP2C19 inhibition - 0.5128 51.28%
CYP2D6 inhibition - 0.8907 89.07%
CYP1A2 inhibition - 0.6043 60.43%
CYP2C8 inhibition - 0.7801 78.01%
CYP inhibitory promiscuity - 0.8062 80.62%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.7083 70.83%
Eye corrosion - 0.9583 95.83%
Eye irritation - 0.8015 80.15%
Skin irritation - 0.8062 80.62%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis - 0.6670 66.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5390 53.90%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6956 69.56%
skin sensitisation - 0.6689 66.89%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6019 60.19%
Acute Oral Toxicity (c) III 0.6029 60.29%
Estrogen receptor binding + 0.7766 77.66%
Androgen receptor binding + 0.5999 59.99%
Thyroid receptor binding + 0.6591 65.91%
Glucocorticoid receptor binding + 0.7379 73.79%
Aromatase binding + 0.6844 68.44%
PPAR gamma - 0.6479 64.79%
Honey bee toxicity - 0.8746 87.46%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.7807 78.07%

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 96.81% 97.25%
CHEMBL237 P41145 Kappa opioid receptor 95.56% 98.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.84% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.11% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.45% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.34% 97.09%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 88.16% 95.50%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 86.10% 96.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.63% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.60% 93.04%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.35% 96.77%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.00% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.13% 92.62%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.81% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.51% 100.00%

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.
Baccharis tola
Helichrysum tenax

Cross-Links

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PubChem 74034169
LOTUS LTS0193284
wikiData Q105314224