(1S,2R,6R,7R,10R,11R,14S,16S)-7,11-dimethyl-6-[(2R)-6-methylheptan-2-yl]-17,18-dioxapentacyclo[14.2.2.01,10.02,7.011,16]icos-19-en-14-ol

Details

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Internal ID 3c5b2f22-9d75-44b4-b79a-6fb374dba81a
Taxonomy Organoheterocyclic compounds > Dioxanes > 1,2-dioxanes
IUPAC Name (1S,2R,6R,7R,10R,11R,14S,16S)-7,11-dimethyl-6-[(2R)-6-methylheptan-2-yl]-17,18-dioxapentacyclo[14.2.2.01,10.02,7.011,16]icos-19-en-14-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H46O3/c1-19(2)8-6-9-20(3)22-10-7-11-23-25(22,4)14-13-24-26(5)15-12-21(29)18-27(26)16-17-28(23,24)31-30-27/h16-17,19-24,29H,6-15,18H2,1-5H3/t20-,21+,22-,23-,24-,25-,26-,27-,28+/m1/s1
InChI Key VJYHZFNCMYTSNE-WBIZBJRUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H46O3
Molecular Weight 430.70 g/mol
Exact Mass 430.34469533 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 7.80
Atomic LogP (AlogP) 6.84
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2R,6R,7R,10R,11R,14S,16S)-7,11-dimethyl-6-[(2R)-6-methylheptan-2-yl]-17,18-dioxapentacyclo[14.2.2.01,10.02,7.011,16]icos-19-en-14-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.5657 56.57%
Blood Brain Barrier + 0.6316 63.16%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5152 51.52%
OATP2B1 inhibitior - 0.7202 72.02%
OATP1B1 inhibitior + 0.8702 87.02%
OATP1B3 inhibitior + 0.9372 93.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8512 85.12%
P-glycoprotein inhibitior - 0.5259 52.59%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6990 69.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7078 70.78%
CYP3A4 inhibition - 0.7875 78.75%
CYP2C9 inhibition - 0.9046 90.46%
CYP2C19 inhibition - 0.8710 87.10%
CYP2D6 inhibition - 0.9572 95.72%
CYP1A2 inhibition - 0.8198 81.98%
CYP2C8 inhibition - 0.6876 68.76%
CYP inhibitory promiscuity - 0.9510 95.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6628 66.28%
Eye corrosion - 0.9818 98.18%
Eye irritation - 0.9491 94.91%
Skin irritation - 0.6783 67.83%
Skin corrosion - 0.9157 91.57%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7174 71.74%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5897 58.97%
skin sensitisation - 0.6700 67.00%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7674 76.74%
Acute Oral Toxicity (c) III 0.4613 46.13%
Estrogen receptor binding + 0.8218 82.18%
Androgen receptor binding + 0.7498 74.98%
Thyroid receptor binding + 0.6430 64.30%
Glucocorticoid receptor binding + 0.7733 77.33%
Aromatase binding + 0.5833 58.33%
PPAR gamma + 0.5730 57.30%
Honey bee toxicity - 0.8504 85.04%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9198 91.98%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.36% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.12% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.52% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 89.98% 95.93%
CHEMBL2581 P07339 Cathepsin D 89.92% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.64% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.54% 97.09%
CHEMBL237 P41145 Kappa opioid receptor 89.43% 98.10%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.09% 93.56%
CHEMBL2179 P04062 Beta-glucocerebrosidase 89.00% 85.31%
CHEMBL221 P23219 Cyclooxygenase-1 88.45% 90.17%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.38% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.00% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.30% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 86.18% 97.79%
CHEMBL268 P43235 Cathepsin K 85.09% 96.85%
CHEMBL4302 P08183 P-glycoprotein 1 84.98% 92.98%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.67% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.50% 93.04%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.43% 90.71%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.40% 90.08%
CHEMBL2514 O95665 Neurotensin receptor 2 81.20% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.52% 92.62%
CHEMBL4618 P09960 Leukotriene A4 hydrolase 80.25% 97.86%

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.
There are no matching plants.

Cross-Links

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PubChem 162936723
LOTUS LTS0263428
wikiData Q105287596