Aureol Acetate

Details

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Internal ID 2053818d-d1f6-4049-84e0-e853b44e01f4
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthenes
IUPAC Name [(1S,10R,11S,14S)-10,11,15,15-tetramethyl-2-oxatetracyclo[8.8.0.01,14.03,8]octadeca-3(8),4,6-trien-6-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H32O3/c1-15-7-10-20-21(3,4)11-6-12-23(20)22(15,5)14-17-13-18(25-16(2)24)8-9-19(17)26-23/h8-9,13,15,20H,6-7,10-12,14H2,1-5H3/t15-,20-,22+,23-/m0/s1
InChI Key MQRRSNNZKRHXGT-QMEZDXFZSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C23H32O3
Molecular Weight 356.50 g/mol
Exact Mass 356.23514488 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.55
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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aureol acetate
CHEMBL457078

2D Structure

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2D Structure of Aureol Acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.7825 78.25%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8078 80.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8678 86.78%
OATP1B3 inhibitior + 0.9778 97.78%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8744 87.44%
P-glycoprotein inhibitior - 0.5208 52.08%
P-glycoprotein substrate - 0.8541 85.41%
CYP3A4 substrate + 0.6571 65.71%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.7626 76.26%
CYP3A4 inhibition - 0.8392 83.92%
CYP2C9 inhibition - 0.6901 69.01%
CYP2C19 inhibition + 0.5325 53.25%
CYP2D6 inhibition - 0.9151 91.51%
CYP1A2 inhibition - 0.5713 57.13%
CYP2C8 inhibition + 0.5737 57.37%
CYP inhibitory promiscuity - 0.8961 89.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6790 67.90%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.9434 94.34%
Skin irritation - 0.6911 69.11%
Skin corrosion - 0.9583 95.83%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8852 88.52%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.6709 67.09%
skin sensitisation - 0.8162 81.62%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4862 48.62%
Acute Oral Toxicity (c) IV 0.6059 60.59%
Estrogen receptor binding + 0.9157 91.57%
Androgen receptor binding + 0.6741 67.41%
Thyroid receptor binding + 0.7818 78.18%
Glucocorticoid receptor binding + 0.7714 77.14%
Aromatase binding + 0.8297 82.97%
PPAR gamma + 0.6743 67.43%
Honey bee toxicity - 0.7727 77.27%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9939 99.39%

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 99.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.94% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.88% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.23% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.12% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.93% 97.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.58% 94.80%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.05% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.88% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.72% 97.25%
CHEMBL2243 O00519 Anandamide amidohydrolase 88.37% 97.53%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.58% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.06% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.81% 89.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.09% 95.71%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 82.99% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.80% 92.62%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.72% 99.18%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.35% 94.00%
CHEMBL4208 P20618 Proteasome component C5 80.86% 90.00%

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 44566991
LOTUS LTS0125856
wikiData Q104402177