11beta-Acetoxyselin-4alpha-ol

Details

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Internal ID 27bbd346-0cd3-4076-8c32-caa3bd0689b8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 2-[(2R,4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]propan-2-yl acetate
SMILES (Canonical) CC(=O)OC(C)(C)C1CCC2(CCCC(C2C1)(C)O)C
SMILES (Isomeric) CC(=O)OC(C)(C)[C@@H]1CC[C@]2(CCC[C@@]([C@@H]2C1)(C)O)C
InChI InChI=1S/C17H30O3/c1-12(18)20-15(2,3)13-7-10-16(4)8-6-9-17(5,19)14(16)11-13/h13-14,19H,6-11H2,1-5H3/t13-,14-,16-,17-/m1/s1
InChI Key YJUFRKRDRWIRBO-MUIFIZLQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H30O3
Molecular Weight 282.40 g/mol
Exact Mass 282.21949481 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.69
H-Bond Acceptor 3
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 11beta-Acetoxyselin-4alpha-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.6565 65.65%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8430 84.30%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.9335 93.35%
OATP1B3 inhibitior + 0.9716 97.16%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.5697 56.97%
P-glycoprotein inhibitior - 0.8073 80.73%
P-glycoprotein substrate - 0.8876 88.76%
CYP3A4 substrate + 0.6455 64.55%
CYP2C9 substrate - 0.6408 64.08%
CYP2D6 substrate - 0.8633 86.33%
CYP3A4 inhibition - 0.9073 90.73%
CYP2C9 inhibition - 0.5771 57.71%
CYP2C19 inhibition - 0.7809 78.09%
CYP2D6 inhibition - 0.9699 96.99%
CYP1A2 inhibition - 0.8537 85.37%
CYP2C8 inhibition - 0.6828 68.28%
CYP inhibitory promiscuity - 0.9786 97.86%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6324 63.24%
Eye corrosion - 0.9775 97.75%
Eye irritation - 0.6459 64.59%
Skin irritation + 0.5207 52.07%
Skin corrosion - 0.9464 94.64%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5770 57.70%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6352 63.52%
skin sensitisation + 0.4917 49.17%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6342 63.42%
Acute Oral Toxicity (c) III 0.8207 82.07%
Estrogen receptor binding + 0.6490 64.90%
Androgen receptor binding - 0.6885 68.85%
Thyroid receptor binding + 0.5518 55.18%
Glucocorticoid receptor binding + 0.5529 55.29%
Aromatase binding + 0.5391 53.91%
PPAR gamma - 0.6977 69.77%
Honey bee toxicity - 0.7641 76.41%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9741 97.41%

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 98.56% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 93.32% 97.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.82% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.23% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.25% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.96% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 87.88% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.36% 82.69%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 85.83% 98.99%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.35% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.96% 99.23%
CHEMBL2581 P07339 Cathepsin D 84.94% 98.95%
CHEMBL284 P27487 Dipeptidyl peptidase IV 84.83% 95.69%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 84.61% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.45% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 83.76% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.77% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.47% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.85% 100.00%

Cross-Links

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PubChem 10660570
NPASS NPC265125
LOTUS LTS0009641
wikiData Q105349481