[(1S,2R,5R,6R,9R,10R,13S,15S)-6,10-dimethyl-5-[(1R)-1-[(1R,2R)-2-[(2R)-3-methylbutan-2-yl]cyclopropyl]ethyl]-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-yl] acetate

Details

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Internal ID 27e5420a-d064-4b64-857d-d40c60d3220a
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid esters
IUPAC Name [(1S,2R,5R,6R,9R,10R,13S,15S)-6,10-dimethyl-5-[(1R)-1-[(1R,2R)-2-[(2R)-3-methylbutan-2-yl]cyclopropyl]ethyl]-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H48O4/c1-18(2)19(3)23-16-24(23)20(4)25-8-9-26-28(25,6)12-11-27-29(7)13-10-22(33-21(5)32)17-30(29)14-15-31(26,27)35-34-30/h14-15,18-20,22-27H,8-13,16-17H2,1-7H3/t19-,20-,22+,23-,24-,25-,26-,27-,28-,29-,30-,31+/m1/s1
InChI Key JTWUHDUABHMRCG-UWQKGCGHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C31H48O4
Molecular Weight 484.70 g/mol
Exact Mass 484.35526001 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 7.80
Atomic LogP (AlogP) 7.12
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2R,5R,6R,9R,10R,13S,15S)-6,10-dimethyl-5-[(1R)-1-[(1R,2R)-2-[(2R)-3-methylbutan-2-yl]cyclopropyl]ethyl]-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-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 + 0.9833 98.33%
Caco-2 - 0.6551 65.51%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5703 57.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8467 84.67%
OATP1B3 inhibitior + 0.8806 88.06%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9145 91.45%
P-glycoprotein inhibitior + 0.7153 71.53%
P-glycoprotein substrate - 0.6006 60.06%
CYP3A4 substrate + 0.7317 73.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8513 85.13%
CYP3A4 inhibition - 0.7445 74.45%
CYP2C9 inhibition - 0.8604 86.04%
CYP2C19 inhibition - 0.7834 78.34%
CYP2D6 inhibition - 0.9425 94.25%
CYP1A2 inhibition - 0.6061 60.61%
CYP2C8 inhibition + 0.5482 54.82%
CYP inhibitory promiscuity - 0.9029 90.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6161 61.61%
Eye corrosion - 0.9819 98.19%
Eye irritation - 0.9322 93.22%
Skin irritation - 0.5926 59.26%
Skin corrosion - 0.9106 91.06%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6937 69.37%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5597 55.97%
skin sensitisation - 0.7441 74.41%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7035 70.35%
Acute Oral Toxicity (c) III 0.3880 38.80%
Estrogen receptor binding + 0.7677 76.77%
Androgen receptor binding + 0.7543 75.43%
Thyroid receptor binding + 0.5847 58.47%
Glucocorticoid receptor binding + 0.6895 68.95%
Aromatase binding + 0.6699 66.99%
PPAR gamma + 0.6150 61.50%
Honey bee toxicity - 0.6781 67.81%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9884 98.84%

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 97.86% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.43% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.07% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.47% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.56% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.02% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.85% 82.69%
CHEMBL340 P08684 Cytochrome P450 3A4 87.04% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.29% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.06% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 83.66% 97.79%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.58% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.26% 91.07%
CHEMBL2581 P07339 Cathepsin D 83.13% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.12% 92.62%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.63% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.62% 97.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.59% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.48% 95.56%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.93% 95.71%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.91% 95.89%

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 23252131
LOTUS LTS0219372
wikiData Q105135053