[(1R,5R,6R,7S,9S,11R,13R)-11-(furan-3-yl)-7-hydroxy-9,13-dimethyl-4-oxospiro[10,14-dioxatetracyclo[9.2.1.01,6.09,13]tetradecane-5,2'-oxirane]-6-yl]methyl acetate

Details

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Internal ID 1493b6ac-be24-444d-a761-69f989fb8e9e
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name [(1R,5R,6R,7S,9S,11R,13R)-11-(furan-3-yl)-7-hydroxy-9,13-dimethyl-4-oxospiro[10,14-dioxatetracyclo[9.2.1.01,6.09,13]tetradecane-5,2'-oxirane]-6-yl]methyl acetate
SMILES (Canonical) CC(=O)OCC12C(CC3(C4(C1(CCC(=O)C25CO5)OC(C4)(O3)C6=COC=C6)C)C)O
SMILES (Isomeric) CC(=O)OC[C@@]12[C@H](C[C@]3([C@@]4([C@@]1(CCC(=O)[C@]25CO5)O[C@@](C4)(O3)C6=COC=C6)C)C)O
InChI InChI=1S/C22H26O8/c1-13(23)27-11-19-16(25)8-18(3)17(2)10-21(29-18,14-5-7-26-9-14)30-22(17,19)6-4-15(24)20(19)12-28-20/h5,7,9,16,25H,4,6,8,10-12H2,1-3H3/t16-,17+,18-,19-,20+,21+,22+/m0/s1
InChI Key YJFASSMQGOHSIM-OVMODOJMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O8
Molecular Weight 418.40 g/mol
Exact Mass 418.16276778 g/mol
Topological Polar Surface Area (TPSA) 108.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 8
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 [(1R,5R,6R,7S,9S,11R,13R)-11-(furan-3-yl)-7-hydroxy-9,13-dimethyl-4-oxospiro[10,14-dioxatetracyclo[9.2.1.01,6.09,13]tetradecane-5,2'-oxirane]-6-yl]methyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9516 95.16%
Caco-2 - 0.5236 52.36%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8286 82.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8093 80.93%
OATP1B3 inhibitior + 0.8008 80.08%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7537 75.37%
BSEP inhibitior + 0.6253 62.53%
P-glycoprotein inhibitior - 0.4860 48.60%
P-glycoprotein substrate - 0.6091 60.91%
CYP3A4 substrate + 0.6723 67.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8384 83.84%
CYP3A4 inhibition + 0.5656 56.56%
CYP2C9 inhibition - 0.7258 72.58%
CYP2C19 inhibition - 0.7542 75.42%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.8985 89.85%
CYP2C8 inhibition + 0.5219 52.19%
CYP inhibitory promiscuity - 0.9205 92.05%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5706 57.06%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9304 93.04%
Skin irritation - 0.7003 70.03%
Skin corrosion - 0.9412 94.12%
Ames mutagenesis - 0.6424 64.24%
Human Ether-a-go-go-Related Gene inhibition + 0.6776 67.76%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.6100 61.00%
skin sensitisation - 0.9222 92.22%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6163 61.63%
Acute Oral Toxicity (c) I 0.6730 67.30%
Estrogen receptor binding + 0.8442 84.42%
Androgen receptor binding + 0.7598 75.98%
Thyroid receptor binding + 0.6070 60.70%
Glucocorticoid receptor binding + 0.7588 75.88%
Aromatase binding + 0.8342 83.42%
PPAR gamma + 0.6070 60.70%
Honey bee toxicity - 0.7415 74.15%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9753 97.53%

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 97.74% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.16% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.68% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.03% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.64% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.50% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.46% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.19% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.16% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.65% 89.00%
CHEMBL3524 P56524 Histone deacetylase 4 85.89% 92.97%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.60% 97.25%
CHEMBL1951 P21397 Monoamine oxidase A 83.11% 91.49%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.99% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.80% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.77% 90.17%
CHEMBL340 P08684 Cytochrome P450 3A4 81.16% 91.19%
CHEMBL1937 Q92769 Histone deacetylase 2 80.87% 94.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.44% 95.71%
CHEMBL5028 O14672 ADAM10 80.33% 97.50%

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.
Teucrium orientale

Cross-Links

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PubChem 162890338
LOTUS LTS0014790
wikiData Q105349216