(-)-(2R,3R,4aR)-altenuene-3-acetoxy ester

Details

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Internal ID 104f8fdc-b712-4905-99bc-1a26f4523db6
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name [(2R,3R,4aR)-2,7-dihydroxy-9-methoxy-4a-methyl-6-oxo-3,4-dihydro-2H-benzo[c]chromen-3-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H18O7/c1-8(18)23-14-7-17(2)11(6-12(14)19)10-4-9(22-3)5-13(20)15(10)16(21)24-17/h4-6,12,14,19-20H,7H2,1-3H3/t12-,14-,17-/m1/s1
InChI Key NRCQFDXVYVENDF-SUYBPPKGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O7
Molecular Weight 334.30 g/mol
Exact Mass 334.10525291 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (-)-(2R,3R,4aR)-altenuene-3-acetoxy ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9808 98.08%
Caco-2 + 0.5194 51.94%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6259 62.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8577 85.77%
OATP1B3 inhibitior + 0.8706 87.06%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4790 47.90%
P-glycoprotein inhibitior - 0.7987 79.87%
P-glycoprotein substrate - 0.7617 76.17%
CYP3A4 substrate + 0.6686 66.86%
CYP2C9 substrate + 0.5924 59.24%
CYP2D6 substrate - 0.8461 84.61%
CYP3A4 inhibition - 0.8233 82.33%
CYP2C9 inhibition - 0.7361 73.61%
CYP2C19 inhibition - 0.7249 72.49%
CYP2D6 inhibition - 0.8991 89.91%
CYP1A2 inhibition - 0.5579 55.79%
CYP2C8 inhibition + 0.4596 45.96%
CYP inhibitory promiscuity - 0.7728 77.28%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9818 98.18%
Carcinogenicity (trinary) Non-required 0.4674 46.74%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.7154 71.54%
Skin irritation - 0.7038 70.38%
Skin corrosion - 0.9403 94.03%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6185 61.85%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.5170 51.70%
skin sensitisation - 0.7703 77.03%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.7768 77.68%
Acute Oral Toxicity (c) I 0.3910 39.10%
Estrogen receptor binding + 0.7770 77.70%
Androgen receptor binding + 0.6924 69.24%
Thyroid receptor binding - 0.4944 49.44%
Glucocorticoid receptor binding + 0.8217 82.17%
Aromatase binding - 0.4949 49.49%
PPAR gamma + 0.5494 54.94%
Honey bee toxicity - 0.7910 79.10%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9732 97.32%

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 99.50% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.85% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.04% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.55% 98.95%
CHEMBL4208 P20618 Proteasome component C5 94.16% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.50% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.29% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.37% 99.15%
CHEMBL340 P08684 Cytochrome P450 3A4 88.71% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.27% 97.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.03% 91.07%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.38% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.05% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.60% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.40% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.71% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.60% 95.89%
CHEMBL2535 P11166 Glucose transporter 82.36% 98.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.27% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.97% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.65% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.01% 95.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.82% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139588595
LOTUS LTS0263029
wikiData Q105184406