[(1S,2R,4R,5S,8R,9S,13R,14S,17S,18S,20S)-9-(hydroxymethyl)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.01,20.04,17.05,14.08,13]tetracosan-2-yl] acetate

Details

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Internal ID 80bd4a9d-d9e7-491e-bc4f-38cde67eb3eb
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name [(1S,2R,4R,5S,8R,9S,13R,14S,17S,18S,20S)-9-(hydroxymethyl)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.01,20.04,17.05,14.08,13]tetracosan-2-yl] acetate
SMILES (Canonical) CC(=O)OC1CC2C(CCC3C2(CCC4C3(CCCC4(C)CO)C)C)C5OC6C1(O5)CC(=O)O6
SMILES (Isomeric) CC(=O)O[C@@H]1C[C@@H]2[C@H](CC[C@H]3[C@]2(CC[C@@H]4[C@@]3(CCC[C@]4(C)CO)C)C)[C@@H]5O[C@@H]6[C@]1(O5)CC(=O)O6
InChI InChI=1S/C27H40O7/c1-15(29)31-20-12-17-16(22-33-23-27(20,34-22)13-21(30)32-23)6-7-19-25(17,3)11-8-18-24(2,14-28)9-5-10-26(18,19)4/h16-20,22-23,28H,5-14H2,1-4H3/t16-,17+,18-,19-,20+,22+,23+,24+,25-,26-,27-/m0/s1
InChI Key XLOSRKDRMWLLGT-BBTNSOHDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H40O7
Molecular Weight 476.60 g/mol
Exact Mass 476.27740361 g/mol
Topological Polar Surface Area (TPSA) 91.30 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.95
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2R,4R,5S,8R,9S,13R,14S,17S,18S,20S)-9-(hydroxymethyl)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.01,20.04,17.05,14.08,13]tetracosan-2-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9564 95.64%
Caco-2 - 0.6500 65.00%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7769 77.69%
OATP2B1 inhibitior - 0.7151 71.51%
OATP1B1 inhibitior + 0.8038 80.38%
OATP1B3 inhibitior + 0.8785 87.85%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5614 56.14%
BSEP inhibitior + 0.9467 94.67%
P-glycoprotein inhibitior + 0.5862 58.62%
P-glycoprotein substrate - 0.7502 75.02%
CYP3A4 substrate + 0.7226 72.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8670 86.70%
CYP3A4 inhibition - 0.8248 82.48%
CYP2C9 inhibition - 0.7023 70.23%
CYP2C19 inhibition - 0.7844 78.44%
CYP2D6 inhibition - 0.9636 96.36%
CYP1A2 inhibition - 0.8594 85.94%
CYP2C8 inhibition + 0.5992 59.92%
CYP inhibitory promiscuity - 0.9265 92.65%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6023 60.23%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.9090 90.90%
Skin irritation - 0.6958 69.58%
Skin corrosion - 0.9433 94.33%
Ames mutagenesis - 0.6278 62.78%
Human Ether-a-go-go-Related Gene inhibition - 0.4854 48.54%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.6657 66.57%
skin sensitisation - 0.9386 93.86%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.8446 84.46%
Acute Oral Toxicity (c) III 0.4467 44.67%
Estrogen receptor binding + 0.8337 83.37%
Androgen receptor binding + 0.7122 71.22%
Thyroid receptor binding + 0.5270 52.70%
Glucocorticoid receptor binding + 0.7667 76.67%
Aromatase binding + 0.7750 77.50%
PPAR gamma + 0.6740 67.40%
Honey bee toxicity - 0.7527 75.27%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9398 93.98%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.52% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.28% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.54% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.13% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 88.44% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.13% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.05% 89.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.93% 93.04%
CHEMBL2996 Q05655 Protein kinase C delta 87.79% 97.79%
CHEMBL2581 P07339 Cathepsin D 86.34% 98.95%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.81% 93.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.39% 96.77%
CHEMBL237 P41145 Kappa opioid receptor 83.61% 98.10%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.24% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.23% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.68% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.66% 97.25%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.49% 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.
There are no matching plants.

Cross-Links

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PubChem 162934414
LOTUS LTS0147655
wikiData Q105330106