24-O-Acetylacerionol

Details

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Internal ID 41af4894-9b75-4e98-8d08-770d8e105474
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [2-hydroxy-2-methyl-1-[(1S,6R,7R,8R,12R,14R,18S,20S)-6,8,14,19,19-pentamethyl-13-oxo-11,23-dioxahexacyclo[18.2.1.01,18.03,15.06,14.07,12]tricos-3(15)-en-10-yl]propyl] acetate
SMILES (Canonical) CC1CC(OC2C1C3(CCC4=C(C3(C2=O)C)CCC5C(C6CCC5(C4)O6)(C)C)C)C(C(C)(C)O)OC(=O)C
SMILES (Isomeric) C[C@@H]1CC(O[C@@H]2[C@H]1[C@]3(CCC4=C([C@@]3(C2=O)C)CC[C@@H]5[C@@]6(C4)CC[C@@H](C5(C)C)O6)C)C(C(C)(C)O)OC(=O)C
InChI InChI=1S/C32H48O6/c1-17-15-21(27(29(5,6)35)36-18(2)33)37-25-24(17)30(7)13-11-19-16-32-14-12-23(38-32)28(3,4)22(32)10-9-20(19)31(30,8)26(25)34/h17,21-25,27,35H,9-16H2,1-8H3/t17-,21?,22+,23+,24+,25-,27?,30-,31-,32+/m1/s1
InChI Key OIEMVDHLEKUVRF-OBBIKUBESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H48O6
Molecular Weight 528.70 g/mol
Exact Mass 528.34508925 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 4.50
Atomic LogP (AlogP) 5.54
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 24-O-Acetylacerionol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9733 97.33%
Caco-2 - 0.7088 70.88%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.8398 83.98%
OATP2B1 inhibitior - 0.7190 71.90%
OATP1B1 inhibitior + 0.7975 79.75%
OATP1B3 inhibitior - 0.2644 26.44%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.5839 58.39%
P-glycoprotein inhibitior + 0.7388 73.88%
P-glycoprotein substrate - 0.5371 53.71%
CYP3A4 substrate + 0.7361 73.61%
CYP2C9 substrate - 0.8114 81.14%
CYP2D6 substrate - 0.8623 86.23%
CYP3A4 inhibition - 0.7899 78.99%
CYP2C9 inhibition - 0.8301 83.01%
CYP2C19 inhibition - 0.8861 88.61%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.5811 58.11%
CYP2C8 inhibition + 0.6741 67.41%
CYP inhibitory promiscuity - 0.9198 91.98%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4691 46.91%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9152 91.52%
Skin irritation + 0.5353 53.53%
Skin corrosion - 0.8948 89.48%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4928 49.28%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.6246 62.46%
skin sensitisation - 0.8242 82.42%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5850 58.50%
Acute Oral Toxicity (c) III 0.3872 38.72%
Estrogen receptor binding + 0.7270 72.70%
Androgen receptor binding + 0.7300 73.00%
Thyroid receptor binding + 0.5752 57.52%
Glucocorticoid receptor binding + 0.7604 76.04%
Aromatase binding + 0.7665 76.65%
PPAR gamma + 0.6532 65.32%
Honey bee toxicity - 0.6668 66.68%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9916 99.16%

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 99.35% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.12% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.43% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 93.47% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.41% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.59% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.87% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.95% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.97% 97.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.81% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.72% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.45% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 89.34% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.08% 97.09%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 88.63% 90.93%
CHEMBL1951 P21397 Monoamine oxidase A 86.95% 91.49%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.74% 91.07%
CHEMBL5028 O14672 ADAM10 85.14% 97.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.10% 93.04%
CHEMBL226 P30542 Adenosine A1 receptor 83.95% 95.93%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.22% 95.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.75% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.29% 93.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.14% 96.77%
CHEMBL3401 O75469 Pregnane X receptor 82.11% 94.73%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.56% 97.28%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.51% 95.89%
CHEMBL1902 P62942 FK506-binding protein 1A 81.32% 97.05%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.12% 92.62%

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.
Actaea cimicifuga
Actaea dahurica
Actaea simplex

Cross-Links

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PubChem 101596791
NPASS NPC239147